Randi Jenssen Hagerman

Title(s)Professor, MED: Pediatrics
SchoolSchool of Medicine
AddressMIND Bldg/UCDMC
CA 95817
Phone916-703-0247
ORCID ORCID Icon0000-0001-5029-8448 Additional info
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    Stanford Medical School, Stanford CalifMD1975Medicine

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Parkinson's Disease Polygenic Risk Score and Neurological Involvement in Carriers of the FMR1 Premutation Allele: A Case for Genetic Modifier. Mol Genet Genomic Med. 2024 Nov; 12(11):e70043. Loesch DZ, Chafota F, Bui MQ, Storey E, Atkinson A, Martin NG, Gordon SD, Rentería ME, Hagerman RJ, Tassone F. PMID: 39588919; PMCID: PMC11590032.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Negative effect of treatment with mGluR5 negative allosteric modulator AFQ056 on blood biomarkers in young individuals with Fragile X syndrome. SAGE Open Med. 2024; 12:20503121241282401. Protic D, Breeze E, Mendoza G, Zafarullah M, Abbeduto L, Hagerman R, Coffey C, Cudkowicz M, Durbin-Johnson B, Ashwood P, Berry-Kravis E, Erickson CA, Filipink R, Gropman A, Lehwald L, Maxwell-Horn A, Morris S, Bennett AP, Prock L, Talboy A, Tartaglia N, Veenstra-VanderWeele J, Tassone F. PMID: 39483619; PMCID: PMC11526204.
      View in: PubMed   Mentions:
    3. Knowledge and perceptions about fragile X syndrome and fragile X-premutation-associated conditions among medical doctors in Nigeria. Clin Genet. 2025 Jan; 107(1):56-66. Mbachu CNP, Hagerman R, Eseigbe E, Odita A, Mbachu I, Ilikanu S, Akowundu K, Ndukwu C, Echezona M, Okereke O, Echendu S, Udigwe I. PMID: 39295073; PMCID: PMC11608841.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. Specific EEG resting state biomarkers in FXS and ASD. J Neurodev Disord. 2024 Sep 09; 16(1):53. Proteau-Lemieux M, Knoth IS, Davoudi S, Martin CO, Bélanger AM, Fontaine V, Côté V, Agbogba K, Vachon K, Whitlock K, Biag HMB, Thurman AJ, Rosenfelt C, Tassone F, Frei J, Capano L, Abbeduto L, Jacquemont S, Hessl D, Hagerman RJ, Schneider A, Bolduc F, Anagnostou E, Lippe S. PMID: 39251926; PMCID: PMC11382468.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. Language use predicts symptoms of fragile X-associated tremor/ataxia syndrome in men and women with the FMR1 premutation. Sci Rep. 2024 09 05; 14(1):20707. Maltman N, Sterling A, Santos E, Hagerman R. PMID: 39237554; PMCID: PMC11377817.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Psychiatric Manifestations in Early to Middle Stages of Fragile X-Associated Tremor-Ataxia Syndrome (FXTAS). J Neuropsychiatry Clin Neurosci. 2024 Aug 08; appineuropsych20230215. Chi MH, Bourgeois JA, Santos E, Kim K, Ponzini MD, Mendoza G, Schneider A, Hessl D, Tassone F, Hagerman RJ. PMID: 39113493.
      View in: PubMed   Mentions:    Fields:    
    7. Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome. Int J Mol Sci. 2024 Jul 25; 25(15). Winarni TI, Hwang YH, Rivera SM, Hessl D, Durbin-Johnson BP, Utari A, Hagerman R, Tassone F. PMID: 39125677; PMCID: PMC11312271.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. Longitudinal follow-up of metformin treatment in Fragile X Syndrome. Front Psychol. 2024; 15:1305597. Seng P, Montanaro FAM, Biag HMB, Salcedo-Arellano MJ, Kim K, Ponzini MD, Tassone F, Schneider A, Abbeduto L, Thurman AJ, Hessl D, Bolduc FV, Jacquemont S, Lippé S, Hagerman RJ. PMID: 38939222; PMCID: PMC11210589.
      View in: PubMed   Mentions:
    9. A Comprehensive Review of Fragile X Syndrome and Fragile X Premutation Associated Conditions in Africa. Genes (Basel). 2024 May 25; 15(6). Mbachu CNP, Mbachu II, Hagerman R. PMID: 38927619; PMCID: PMC11203117.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    10. Enlarged perivascular spaces and their association with motor, cognition, MRI markers and cerebrovascular risk factors in male fragile X premutation carriers. J Neurol Sci. 2024 Jun 15; 461:123056. Elias-Mas A, Wang JY, Rodríguez-Revenga L, Kim K, Tassone F, Hessl D, Rivera SM, Hagerman R. PMID: 38772058.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. Mitochondrial dysfunction in brain tissues and Extracellular Vesicles Fragile X-associated tremor/ataxia syndrome. Ann Clin Transl Neurol. 2024 Jun; 11(6):1420-1429. Yao PJ, Manolopoulos A, Eren E, Rivera SM, Hessl DR, Hagerman R, Martinez-Cerdeno V, Tassone F, Kapogiannis D. PMID: 38717724; PMCID: PMC11187838.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    12. Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health. J Autism Dev Disord. 2024 Apr 23. Minhas A, Whitlock K, Rosenfelt C, Shatto J, Finlay B, Zwicker J, Lippe S, Jacquemont S, Hagerman R, Murias K, Bolduc FV. PMID: 38653851.
      View in: PubMed   Mentions: 1     Fields:    
    13. An Update on Psychopharmacological Treatment of Autism Spectrum Disorder. Focus (Am Psychiatr Publ). 2024 Apr; 22(2):198-211. Aishworiya R, Valica T, Hagerman R, Restrepo B. PMID: 38680976; PMCID: PMC11046717.
      View in: PubMed   Mentions:
    14. FMR1 Protein Expression Correlates with Intelligence Quotient in Both Peripheral Blood Mononuclear Cells and Fibroblasts from Individuals with an FMR1 Mutation. J Mol Diagn. 2024 Jun; 26(6):498-509. Jiraanont P, Zafarullah M, Sulaiman N, Espinal GM, Randol JL, Durbin-Johnson B, Schneider A, Hagerman RJ, Hagerman PJ, Tassone F. PMID: 38522837.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    15. Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome. Genes (Basel). 2024 03 13; 15(3). Randol JL, Kim K, Ponzini MD, Tassone F, Falcon AK, Hagerman RJ, Hagerman PJ. PMID: 38540415; PMCID: PMC10969917.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    16. Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome. Genes (Basel). 2024 03 03; 15(3). Tak Y, Schneider A, Santos E, Randol JL, Tassone F, Hagerman P, Hagerman RJ. PMID: 38540390; PMCID: PMC10970065.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    17. State-of-the-art therapies for fragile X syndrome. Dev Med Child Neurol. 2024 Jul; 66(7):863-871. Protic D, Hagerman R. PMID: 38385885; PMCID: PMC11144093.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Case Series: Vestibular Migraines in Fragile X Premutation Carriers. J Clin Med. 2024 Jan 16; 13(2). Tak Y, Tassone F, Hagerman RJ. PMID: 38256638; PMCID: PMC10816080.
      View in: PubMed   Mentions:
    19. FXTAS Neuropathology Includes Widespread Reactive Astrogliosis and White Matter Specific Astrocyte Degeneration. Ann Neurol. 2024 Mar; 95(3):558-575. Dufour BD, Bartley T, McBride E, Allen E, McLennan YA, Hagerman RJ, Martínez-Cerdeño V. PMID: 38069470; PMCID: PMC10922917.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    20. FMR1 Carriers Report Executive Function Changes Prior to Fragile X-Associated Tremor/Ataxia Syndrome: A Longitudinal Study. Mov Disord. 2024 Mar; 39(3):519-525. Hessl D, Mandujano Rojas K, Ferrer E, Espinal G, Famula J, Schneider A, Hagerman R, Tassone F, Rivera SM. PMID: 38124331; PMCID: PMC11268876.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    21. Neurodegeneration of White and Gray Matter in the Hippocampus with FXTAS. Int J Mol Sci. 2023 Dec 08; 24(24). Kargar M, Hagerman RJ, Martínez-Cerdeño V. PMID: 38139097; PMCID: PMC10743470.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    22. Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells. 2023 12 05; 12(24). Santos E, Clark C, Biag HMB, Tang SJ, Kim K, Ponzini MD, Schneider A, Giulivi C, Montanaro FAM, Gipe JT, Dayton J, Randol JL, Yao PJ, Manolopoulos A, Kapogiannis D, Hwang YH, Hagerman P, Hagerman R, Tassone F. PMID: 38132093; PMCID: PMC10741398.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    23. Fragile X syndrome in Democratic Republic of Congo: dysmorphic, cognitive and behavioral findings in 14 subjects from three families. Clin Dysmorphol. 2024 Jan 01; 33(1):9-15. Kasole Lubala T, Kayembe-Kitenge T, Lubala N, Kanteng G, Luboya O, Hagerman R, Lukusa-Tshilobo P, Lumaka A. PMID: 38038060.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    24. Corrigendum: The incidence and clinical characteristics of fragile X syndrome in China. Front Pediatr. 2023; 11:1296110. Mei L, Hu C, Li D, Wang Y, Li H, Zhang K, Zhou B, Zhu R, Hagerman RJ, Xu X, Xu Q. PMID: 37920795; PMCID: PMC10619711.
      View in: PubMed   Mentions:
    25. Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation. Cells. 2023 09 21; 12(18). Tassone F, Protic D, Allen EG, Archibald AD, Baud A, Brown TW, Budimirovic DB, Cohen J, Dufour B, Eiges R, Elvassore N, Gabis LV, Grudzien SJ, Hall DA, Hessl D, Hogan A, Hunter JE, Jin P, Jiraanont P, Klusek J, Kooy RF, Kraan CM, Laterza C, Lee A, Lipworth K, Losh M, Loesch D, Lozano R, Mailick MR, Manolopoulos A, Martinez-Cerdeno V, McLennan Y, Miller RM, Montanaro FAM, Mosconi MW, Potter SN, Raspa M, Rivera SM, Shelly K, Todd PK, Tutak K, Wang JY, Wheeler A, Winarni TI, Zafarullah M, Hagerman RJ. PMID: 37759552; PMCID: PMC10529056.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    26. Adaptive, behavioral, and cognitive outcomes in individuals with fragile X syndrome with varying autism severity. Int J Dev Neurosci. 2023 Dec; 83(8):715-727. Aishworiya R, Tak YE, Ponzini MD, Biag HMB, Salcedo-Arellano MJ, Kim K, Tassone F, Schneider A, Thurman AJ, Abbeduto L, Hessl D, Randol JL, Bolduc FV, Lippe S, Hagerman P, Hagerman R. PMID: 37724826; PMCID: PMC10868665.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    27. A Longitudinal Study of Executive Function in Daily Life in Male Fragile X Premutation Carriers and Association with FXTAS Conversion. medRxiv. 2023 Sep 02. Hessl D, Rojas KM, Ferrer E, Espinal G, Famula J, Schneider A, Elagerman R, Tassone F, Rivera SM. PMID: 37693384; PMCID: PMC10491369.
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    28. Effects of AFQ056 on language learning in fragile X syndrome. J Clin Invest. 2023 Aug 31; 134(5). Berry-Kravis E, Abbeduto L, Hagerman R, Coffey CS, Cudkowicz M, Erickson CA, McDuffie A, Hessl D, Ethridge L, Tassone F, Kaufmann WE, Friedmann K, Bullard L, Hoffmann A, Veenstra-VanderWeele J, Staley K, Klements D, Moshinsky M, Harkey B, Long J, Fedler J, Klingner E, Ecklund D, Costigan M, Huff T, Pearson B, NeuroNEXT FXLEARN Investigators. PMID: 37651202; PMCID: PMC10904045.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimals
    29. Blood Proteome Profiling Reveals Biomarkers and Pathway Alterations in Fragile X PM at Risk for Developing FXTAS. Int J Mol Sci. 2023 Aug 30; 24(17). Zafarullah M, Li J, Salemi MR, Phinney BS, Durbin-Johnson BP, Hagerman R, Hessl D, Rivera SM, Tassone F. PMID: 37686279; PMCID: PMC10488017.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    30. Brain Metabolomics in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS). Cells. 2023 08 23; 12(17). Salcedo-Arellano MJ, Johnson MD, McLennan YA, Hwang YH, Juarez P, McBride EL, Pantoja AP, Durbin-Johnson B, Tassone F, Hagerman RJ, Martínez-Cerdeño V. PMID: 37681866; PMCID: PMC10487256.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    31. Fragile X Syndrome and Fetal Alcohol Syndrome: Occurrence of Dual Diagnosis in a Set of Triplets. J Dev Behav Pediatr. 2023 09 01; 44(7):e470-e475. Aishworiya R, Biag HMB, Salcedo-Arellano MJ, Musa Z, Schneider A, Clark C, Santos E, Tassone F, Hagerman R. PMID: 37556593; PMCID: PMC10527597.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. Usefulness of automated image analysis for recognition of the fragile X syndrome gestalt in Congolese subjects. Eur J Med Genet. 2023 Sep; 66(9):104819. Lubala TK, Kayembe-Kitenge T, Mubungu G, Lumaka A, Kanteng G, Savage S, Luboya O, Hagerman R, Devriendt K, Lukusa-Tshilobo P. PMID: 37532084.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    33. Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome. Cells. 2023 07 24; 12(14). Aishworiya R, Chi MH, Zafarullah M, Mendoza G, Ponzini MD, Kim K, Biag HMB, Thurman AJ, Abbeduto L, Hessl D, Randol JL, Bolduc FV, Jacquemont S, Lippé S, Hagerman P, Hagerman R, Schneider A, Tassone F. PMID: 37508583; PMCID: PMC10377864.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    34. A Postmortem MRI Study of Cerebrovascular Disease and Iron Content at End-Stage of Fragile X-Associated Tremor/Ataxia Syndrome. Cells. 2023 07 20; 12(14). Wang JY, Sonico GJ, Salcedo-Arellano MJ, Hagerman RJ, Martinez-Cerdeno V. PMID: 37508562; PMCID: PMC10377990.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    35. Excitatory neuron-specific suppression of the integrated stress response contributes to autism-related phenotypes in fragile X syndrome. Neuron. 2023 10 04; 111(19):3028-3040.e6. Hooshmandi M, Sharma V, Thörn Perez C, Sood R, Krimbacher K, Wong C, Lister KC, Ureña Guzmán A, Bartley TD, Rocha C, Maussion G, Nadler E, Roque PM, Gantois I, Popic J, Lévesque M, Kaufman RJ, Avoli M, Sanz E, Nader K, Hagerman RJ, Durcan TM, Costa-Mattioli M, Prager-Khoutorsky M, Lacaille JC, Martinez-Cerdeno V, Gibson JR, Huber KM, Sonenberg N, Gkogkas CG, Khoutorsky A. PMID: 37473758; PMCID: PMC10592416.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    36. Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation. Cells. 2023 06 24; 12(13). Protic D, Polli R, Hwang YH, Mendoza G, Hagerman R, Durbin-Johnson B, Hayward BE, Usdin K, Murgia A, Tassone F. PMID: 37443745; PMCID: PMC10341054.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
    37. Meta-analysis of the Modified Checklist for Autism in Toddlers, Revised/Follow-up for Screening. Pediatrics. 2023 06 01; 151(6). Aishworiya R, Ma VK, Stewart S, Hagerman R, Feldman HM. PMID: 37203373; PMCID: PMC10233738.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansPHPublic Health
    38. Fragile X Syndrome in children. Colomb Med (Cali). 2023 Apr-Jun; 54(2):e4005089. Acero-Garcés DO, Saldarriaga W, Cabal-Herrera AM, Rojas CA, Hagerman RJ. PMID: 37664646; PMCID: PMC10469670.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    39. Clinical implications of somatic allele expansion in female FMR1 premutation carriers. Sci Rep. 2023 04 29; 13(1):7050. Aishworiya R, Hwang YH, Santos E, Hayward B, Usdin K, Durbin-Johnson B, Hagerman R, Tassone F. PMID: 37120588; PMCID: PMC10148869.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    40. The incidence and clinical characteristics of fragile X syndrome in China. Front Pediatr. 2023; 11:1064104. Mei L, Hu C, Li D, Wang Y, Li H, Zhang K, Zhou B, Zhu R, Hagerman RJ, Xu X, Xu Q. PMID: 36861076; PMCID: PMC9969088.
      View in: PubMed   Mentions:
    41. A postmortem MRI study of cerebrovascular disease and iron content at end-stage of fragile X-associated tremor/ataxia syndrome. Res Sq. 2023 Jan 11. Wang JY, Sonico GJ, Salcedo-Arellano MJ, Hagerman RJ, Martínez-Cerdeño V. PMID: 36711694; PMCID: PMC9882645.
      View in: PubMed   Mentions:
    42. Role of the endocannabinoid system in fragile X syndrome: potential mechanisms for benefit from cannabidiol treatment. J Neurodev Disord. 2023 01 09; 15(1):1. Palumbo JM, Thomas BF, Budimirovic D, Siegel S, Tassone F, Hagerman R, Faulk C, O'Quinn S, Sebree T. PMID: 36624400; PMCID: PMC9830713.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    43. Targeted Treatments for Fragile X Syndrome. Adv Neurobiol. 2023; 30:225-253. Johnson D, Clark C, Hagerman R. PMID: 36928853.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    44. Drosophila melanogaster as a Model to Study Fragile X-Associated Disorders. Genes (Basel). 2022 12 28; 14(1). Trajkovic J, Makevic V, Pesic M, Pavkovic-Lucic S, Milojevic S, Cvjetkovic S, Hagerman R, Budimirovic DB, Protic D. PMID: 36672829; PMCID: PMC9859539.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
    45. Fragile X-Associated Neuropsychiatric Disorders (FXAND) in Young Fragile X Premutation Carriers. Genes (Basel). 2022 12 17; 13(12). Aishworiya R, Protic D, Tang SJ, Schneider A, Tassone F, Hagerman R. PMID: 36553666; PMCID: PMC9778214.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    46. Family and Caregiver Characteristics Contribute to Caregiver Change in Use of Strategies and Growth in Child Spoken Language in a Parent-Implemented Language Intervention in Fragile X Syndrome. Perspect ASHA Spec Interest Groups. 2022 Dec; 7(6):1630-1644. Potter SN, Bullard L, Banasik A, Feigles RT, Nguyen V, McDuffie A, Thurman AJ, Hagerman R, Abbeduto L. PMID: 36778100; PMCID: PMC9910303.
      View in: PubMed   Mentions: 2  
    47. Artificial neural network applied to fragile X-associated tremor/ataxia syndrome stage diagnosis based on peripheral mitochondrial bioenergetics and brain imaging outcomes. Sci Rep. 2022 Dec 10; 12(1):21382. Giulivi C, Wang JY, Hagerman RJ. PMID: 36496525; PMCID: PMC9741636.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    48. Tophaceous gout of the nose in a male FMR1 premutation carrier. Clin Case Rep. 2022 Nov; 10(11):e6586. Tang SJ, Giri S, Pahlavan N, Han SH, Santos ER, Espinal G, Aishworiya R, Schneider A, Hessl D, Rivera SM, Hagerman RJ. PMID: 36447664; PMCID: PMC9701845.
      View in: PubMed   Mentions: 1  
    49. A randomized, controlled trial of ZYN002 cannabidiol transdermal gel in children and adolescents with fragile X syndrome (CONNECT-FX). J Neurodev Disord. 2022 11 25; 14(1):56. Berry-Kravis E, Hagerman R, Budimirovic D, Erickson C, Heussler H, Tartaglia N, Cohen J, Tassone F, Dobbins T, Merikle E, Sebree T, Tich N, Palumbo JM, O'Quinn S. PMID: 36434514; PMCID: PMC9700889.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCellsCTClinical Trials
    50. The aberrant behavior profile in Indonesian individuals with fragile X syndrome with limited genetic services. Intractable Rare Dis Res. 2022 Nov; 11(4):215-218. Winarni TI, Sumekar TA, Sarjana W, Hardian H, Hagerman RJ, Faradz SM. PMID: 36457587; PMCID: PMC9709619.
      View in: PubMed   Mentions:
    51. Fragile X-associated tremor ataxia syndrome rating scale: Revision and content validity using a mixed method approach. Front Neurol. 2022; 13:977380. Tosin MHS, Stebbins GT, Goetz CG, Hagerman RJ, Hessl D, Zolecki MA, Todd PK, Leehey MA, Hall DA. PMID: 36188408; PMCID: PMC9515309.
      View in: PubMed   Mentions:
    52. Case Reports of Aortic Aneurism in Fragile X Syndrome. Genes (Basel). 2022 08 30; 13(9). Lewis S, DePass A, Hagerman RJ, Lozano R. PMID: 36140728; PMCID: PMC9498845.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    53. Screening for Fragile X Syndrome Among Filipino Children with Autism Spectrum Disorder. J Autism Dev Disord. 2023 Nov; 53(11):4465-4473. Dy ABC, Tanchanco LBS, Sy JCY, Levantino MD, Hagerman RJ. PMID: 35972625.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    54. Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosome. BMJ Case Rep. 2022 Jul 26; 15(7). Tassanakijpanich N, Wright R, Tassone F, Shankar SP, Hagerman R. PMID: 35882436; PMCID: PMC9330300.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    55. Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Mol Genet Genomic Med. 2022 08; 10(8):e2001. Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, Jin P, Allen EG. PMID: 35852003; PMCID: PMC9356544.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    56. Maturation Delay of Human GABAergic Neurogenesis in Fragile X Syndrome Pluripotent Stem Cells. Stem Cells Transl Med. 2022 06 22; 11(6):613-629. Zhang A, Sokolova I, Domissy A, Davis J, Rao L, Hana Utami K, Wang Y, Hagerman RJ, Pouladi MA, Sanna P, Boland MJ, Loring JF. PMID: 35556144; PMCID: PMC9216490.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    57. Autism spectrum disorder in the fragile X premutation state: possible mechanisms and implications. J Neurol. 2022 Sep; 269(9):4676-4683. Aishworiya R, Protic D, Hagerman R. PMID: 35723724.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    58. Prosaccade and Antisaccade Behavior in Fragile X-Associated Tremor/Ataxia Syndrome Progression. Mov Disord Clin Pract. 2022 May; 9(4):473-478. McLennan YA, Mosconi MW, McKenzie FJ, Famula J, Krawchuk B, Kim K, Clark CJ, Hessl D, Rivera SM, Simon TJ, Tassone F, Hagerman RJ. PMID: 35586536; PMCID: PMC9092736.
      View in: PubMed   Mentions: 1     Fields:    
    59. Neuropsychological changes in FMR1 premutation carriers and onset of fragile X-associated tremor/ataxia syndrome. J Neurodev Disord. 2022 03 23; 14(1):23. Famula J, Ferrer E, Hagerman RJ, Tassone F, Schneider A, Rivera SM, Hessl D. PMID: 35321639; PMCID: PMC8942145.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    60. Corrigendum: EEG Signal Complexity Is Reduced During Resting-State in Fragile X Syndrome. Front Psychiatry. 2022; 13:867000. Proteau-Lemieux M, Knoth IS, Agbogba K, Côté V, Barlahan Biag HM, Thurman AJ, Martin CO, Bélanger AM, Rosenfelt C, Tassone F, Abbeduto LJ, Jacquemont S, Hagerman R, Bolduc F, Hessl D, Schneider A, Lippé S. PMID: 35280176; PMCID: PMC8908967.
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    62. Clinical and Molecular Correlates of Abnormal Changes in the Cerebellum and Globus Pallidus in Fragile X Premutation. Front Neurol. 2022; 13:797649. Wang JY, Grigsby J, Placido D, Wei H, Tassone F, Kim K, Hessl D, Rivera SM, Hagerman RJ. PMID: 35211082; PMCID: PMC8863211.
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    63. Increased Pain Symptomatology Among Females vs. Males With Fragile X-Associated Tremor/Ataxia Syndrome. Front Psychiatry. 2021; 12:762915. Johnson D, Santos E, Kim K, Ponzini MD, McLennan YA, Schneider A, Tassone F, Hagerman RJ. PMID: 35126193; PMCID: PMC8811376.
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    64. An Update on Psychopharmacological Treatment of Autism Spectrum Disorder. Neurotherapeutics. 2022 01; 19(1):248-262. Aishworiya R, Valica T, Hagerman R, Restrepo B. PMID: 35029811; PMCID: PMC9130393.
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    65. Raising Knowledge and Awareness of Fragile X Syndrome in Serbia, Georgia, and Colombia: A Model for Other Developing Countries? Yale J Biol Med. 2021 12; 94(4):559-571. Protic D, Salcedo-Arellano MJ, Stojkovic M, Saldarriaga W, Ávila Vidal LA, Miller RM, Tabatadze N, Peric M, Hagerman R, Budimirovic DB. PMID: 34970093; PMCID: PMC8686783.
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    66. Fragile X Premutation: Medications, Therapy and Lifestyle Advice. Pharmgenomics Pers Med. 2021; 14:1689-1699. Sodhi DK, Hagerman R. PMID: 35002287; PMCID: PMC8721286.
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    67. Recent research in fragile X-associated tremor/ataxia syndrome. Curr Opin Neurobiol. 2022 02; 72:155-159. Salcedo-Arellano MJ, Hagerman RJ. PMID: 34890957.
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    68. Eye Movements in Fragile X-Associated Tremor/Ataxia Syndrome. J Neuroophthalmol. 2021 12 01; 41(4):e661-e664. Hall DA, Leehey MA, Hagerman RJ, Pelak VS. PMID: 33110011.
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    69. EEG Signal Complexity Is Reduced During Resting-State in Fragile X Syndrome. Front Psychiatry. 2021; 12:716707. Proteau-Lemieux M, Knoth IS, Agbogba K, Côté V, Barlahan Biag HM, Thurman AJ, Martin CO, Bélanger AM, Rosenfelt C, Tassone F, Abbeduto LJ, Jacquemont S, Hagerman R, Bolduc F, Hessl D, Schneider A, Lippé S. PMID: 34858220; PMCID: PMC8632368.
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    70. FMRP Levels in Human Peripheral Blood Leukocytes Correlates with Intellectual Disability. Diagnostics (Basel). 2021 Sep 28; 11(10). Roth M, Ronco L, Cadavid D, Durbin-Johnson B, Hagerman RJ, Tassone F. PMID: 34679478; PMCID: PMC8534530.
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    71. Case Report: Coexistence of Alzheimer-Type Neuropathology in Fragile X-Associated Tremor Ataxia Syndrome. Front Neurosci. 2021; 15:720253. Salcedo-Arellano MJ, Sanchez D, Wang JY, McLennan YA, Clark CJ, Juarez P, Schneider A, Tassone F, Hagerman RJ, Martínez-Cerdeño V. PMID: 34602969; PMCID: PMC8485779.
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    72. Hispano-American Brain Bank on Neurodevelopmental Disorders: An initiative to promote brain banking, research, education, and outreach in the field of neurodevelopmental disorders. Brain Pathol. 2022 03; 32(2):e13019. Dufour BD, Albores-Gallo L, Luna-Muñoz J, Hagerman R, Miquelajauregui A, Buriticá E, Saldarriaga W, Pacheco-Herrero M, Yris Silvestre-Sosa A, Mazefsky C, Gastgeb H, Kofler J, Casanova M, Hof PR, London E, Hagerman P, Martínez-Cerdeño V. PMID: 34515386; PMCID: PMC8877728.
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    73. Fragile X Syndrome: Lessons Learned and What New Treatment Avenues Are on the Horizon. Annu Rev Pharmacol Toxicol. 2022 01 06; 62:365-381. Hagerman RJ, Hagerman PJ. PMID: 34499526.
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    74. Brain Atrophy and White Matter Damage Linked to Peripheral Bioenergetic Deficits in the Neurodegenerative Disease FXTAS. Int J Mol Sci. 2021 Aug 25; 22(17). Wang J, Napoli E, Kim K, McLennan YA, Hagerman RJ, Giulivi C. PMID: 34502080; PMCID: PMC8431233.
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    75. Fragile X-associated tremor/ataxia syndrome: pathophysiology and management. Curr Opin Neurol. 2021 08 01; 34(4):541-546. Hagerman R, Hagerman P. PMID: 33990099; PMCID: PMC8412174.
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    76. Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series. J Med Genet. 2022 07; 59(7):687-690. Tassanakijpanich N, McKenzie FJ, McLennan YA, Makhoul E, Tassone F, Jasoliya MJ, Romney C, Petrasic IC, Napalinga K, Buchanan CB, Hagerman P, Hagerman R, Casanova EL. PMID: 34193467; PMCID: PMC8717836.
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    77. Sulforaphane improves mitochondrial metabolism in fibroblasts from patients with fragile X-associated tremor and ataxia syndrome. Neurobiol Dis. 2021 09; 157:105427. Napoli E, Flores A, Mansuri Y, Hagerman RJ, Giulivi C. PMID: 34153466; PMCID: PMC8475276.
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    78. Deficits in Prenatal Serine Biosynthesis Underlie the Mitochondrial Dysfunction Associated with the Autism-Linked FMR1 Gene. Int J Mol Sci. 2021 May 30; 22(11). Nolin SL, Napoli E, Flores A, Hagerman RJ, Giulivi C. PMID: 34070950; PMCID: PMC8198117.
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    79. Corrigendum: Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome. Front Mol Biosci. 2021; 8:695407. Holm KN, Herren AW, Taylor SL, Randol JL, Kim K, Espinal G, Martínez-Cerdeño V, Pessah IN, Hagerman RJ, Hagerman PJ. PMID: 34055898; PMCID: PMC8152804.
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    80. Cerebral Microbleeds in Fragile X-Associated Tremor/Ataxia Syndrome. Mov Disord. 2021 08; 36(8):1935-1943. Salcedo-Arellano MJ, Wang JY, McLennan YA, Doan M, Cabal-Herrera AM, Jimenez S, Wolf-Ochoa MW, Sanchez D, Juarez P, Tassone F, Durbin-Johnson B, Hagerman RJ, Martínez-Cerdeño V. PMID: 33760253; PMCID: PMC10929604.
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    81. Fragile X syndrome. Curr Biol. 2021 03 22; 31(6):R273-R275. Hagerman PJ, Hagerman R. PMID: 33756134.
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    82. Inequities in diagnosis of Fragile X syndrome in Colombia. J Appl Res Intellect Disabil. 2021 May; 34(3):830-839. Saldarriaga-Gil W, Cabal-Herrera AM, Fandiño-Losada A, Vásquez A, Hagerman R, Tassone F. PMID: 33538083.
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    83. Surveillance and prevalence of fragile X syndrome in Indonesia. Intractable Rare Dis Res. 2021 Feb; 10(1):11-16. Sihombing NRB, Winarni TI, Utari A, van Bokhoven H, Hagerman RJ, Faradz SM. PMID: 33614370; PMCID: PMC7882090.
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    84. Human Cerebral Cortex Proteome of Fragile X-Associated Tremor/Ataxia Syndrome. Front Mol Biosci. 2020; 7:600840. Holm KN, Herren AW, Taylor SL, Randol JL, Kim K, Espinal G, Martiínez-Cerdeño V, Pessah IN, Hagerman RJ, Hagerman PJ. PMID: 33585555; PMCID: PMC7879451.
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    85. Fragile X premutation and associated health conditions: A review. Clin Genet. 2021 06; 99(6):751-760. Tassanakijpanich N, Hagerman RJ, Worachotekamjorn J. PMID: 33443313.
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    86. Double Genetic Hit: Fragile X Syndrome and Partial Deletion of Protein Patched Homolog 1 Antisense as Cause of Severe Autism Spectrum Disorder. J Dev Behav Pediatr. 2020 12; 41(9):724-728. Saldarriaga W, Payán-Gómez C, González-Teshima LY, Rosa L, Tassone F, Hagerman RJ. PMID: 32947579.
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    87. Overlapping Molecular Pathways Leading to Autism Spectrum Disorders, Fragile X Syndrome, and Targeted Treatments. Neurotherapeutics. 2021 01; 18(1):265-283. Salcedo-Arellano MJ, Cabal-Herrera AM, Punatar RH, Clark CJ, Romney CA, Hagerman RJ. PMID: 33215285; PMCID: PMC8116395.
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    88. Review of Autism Profiles and Response to Sertraline in Fragile X Syndrome-Associated Autism vs. Non-syndromic Autism; Next Steps for Targeted Treatment. Front Neurol. 2020; 11:581429. Rajaratnam A, Potter LA, Biag HMB, Schneider A, Petrasic IC, Hagerman RJ. PMID: 33193037; PMCID: PMC7661746.
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    89. Characterization of the Metabolic, Clinical and Neuropsychological Phenotype of Female Carriers of the Premutation in the X-Linked FMR1 Gene. Front Mol Biosci. 2020; 7:578640. Napoli E, McLennan YA, Schneider A, Tassone F, Hagerman RJ, Giulivi C. PMID: 33195422; PMCID: PMC7642626.
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    90. Cardiovascular Problems in the Fragile X Premutation. Front Genet. 2020; 11:586910. Tassanakijpanich N, Cohen J, Cohen R, Srivatsa UN, Hagerman RJ. PMID: 33133171; PMCID: PMC7578382.
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    91. Cortical gyrification and its relationships with molecular measures and cognition in children with the FMR1 premutation. Sci Rep. 2020 09 29; 10(1):16059. Wang JY, Danial M, Soleymanzadeh C, Kim B, Xia Y, Kim K, Tassone F, Hagerman RJ, Rivera SM. PMID: 32994518; PMCID: PMC7525519.
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    92. Women with Fragile X-associated Tremor/Ataxia Syndrome. Mov Disord Clin Pract. 2020 Nov; 7(8):910-919. Schneider A, Summers S, Tassone F, Seritan A, Hessl D, Hagerman P, Hagerman R. PMID: 33163562; PMCID: PMC7604678.
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    93. Response to Placebo in Fragile X Syndrome Clinical Trials: An Initial Analysis. Brain Sci. 2020 Sep 11; 10(9). Luu S, Province H, Berry-Kravis E, Hagerman R, Hessl D, Vaidya D, Lozano R, Rosselot H, Erickson C, Kaufmann WE, Budimirovic DB. PMID: 32932789; PMCID: PMC7563217.
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    94. Cerebellar-cortical function and connectivity during sensorimotor behavior in aging FMR1 gene premutation carriers. Neuroimage Clin. 2020; 27:102332. McKinney WS, Bartolotti J, Khemani P, Wang JY, Hagerman RJ, Mosconi MW. PMID: 32711390; PMCID: PMC7381687.
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    95. Elevated FMR1-mRNA and lowered FMRP - A double-hit mechanism for psychiatric features in men with FMR1 premutations. Transl Psychiatry. 2020 06 23; 10(1):205. Schneider A, Winarni TI, Cabal-Herrera AM, Bacalman S, Gane L, Hagerman P, Tassone F, Hagerman R. PMID: 32576818; PMCID: PMC7311546.
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    96. Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Pathophysiology and Clinical Implications. Int J Mol Sci. 2020 Jun 20; 21(12). Cabal-Herrera AM, Tassanakijpanich N, Salcedo-Arellano MJ, Hagerman RJ. PMID: 32575683; PMCID: PMC7352421.
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    97. Blood-Based Biomarkers Predictive of Metformin Target Engagement in Fragile X Syndrome. Brain Sci. 2020 Jun 10; 10(6). Jasoliya M, Bowling H, Petrasic IC, Durbin-Johnson B, Klann E, Bhattacharya A, Hagerman R, Tassone F. PMID: 32531912; PMCID: PMC7349631.
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    98. Ataxia as the Major Manifestation of Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Case Series. Biomedicines. 2020 May 25; 8(5). Salcedo-Arellano MJ, Cabal-Herrera AM, Tassanakijpanich N, McLennan YA, Hagerman RJ. PMID: 32466255; PMCID: PMC7277845.
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    99. A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Fragile X Syndrome. Pediatr Neurol. 2020 09; 110:30-41. Berry-Kravis E, Horrigan JP, Tartaglia N, Hagerman R, Kolevzon A, Erickson CA, Hatti S, Snape M, Yaroshinsky A, Stoms G, FXS-001 Investigators, Glass L, Jones NE. PMID: 32660869.
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    100. Fragile X associated neuropsychiatric disorders in a male without FXTAS. Intractable Rare Dis Res. 2020 May; 9(2):113-118. Cabal-Herrera AM, Saldarriaga-Gil W, Salcedo-Arellano MJ, Hagerman RJ. PMID: 32494560; PMCID: PMC7263992.
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    101. Controlled trial of lovastatin combined with an open-label treatment of a parent-implemented language intervention in youth with fragile X syndrome. J Neurodev Disord. 2020 04 22; 12(1):12. Thurman AJ, Potter LA, Kim K, Tassone F, Banasik A, Potter SN, Bullard L, Nguyen V, McDuffie A, Hagerman R, Abbeduto L. PMID: 32316911; PMCID: PMC7175541.
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    102. Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder. Front Genet. 2020; 11:308. Alolaby RR, Jiraanont P, Durbin-Johnson B, Jasoliya M, Tang HT, Hagerman R, Tassone F. PMID: 32346385; PMCID: PMC7174723.
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    103. Editorial: Secondary vs. Idiopathic Autism. Front Psychiatry. 2020; 11:297. Casanova MF, Casanova EL, Frye RE, Baeza-Velasco C, LaSalle JM, Hagerman RJ, Scherer SW, Natowicz MR. PMID: 32346372; PMCID: PMC7171716.
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    104. Parkinsonism Versus Concomitant Parkinson's Disease in Fragile X-Associated Tremor/Ataxia Syndrome. Mov Disord Clin Pract. 2020 May; 7(4):413-418. Salcedo-Arellano MJ, Wolf-Ochoa MW, Hong T, Amina S, Tassone F, Lechpammer M, Hagerman R, Martínez-Cerdeño V. PMID: 32373658; PMCID: PMC7197312.
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    105. Placebo Response in Fragile X-associated Tremor/Ataxia Syndrome. Mov Disord Clin Pract. 2020 Apr; 7(3):298-302. Hill EJ, Goetz CG, Stebbins GT, Hagerman R, Ouyang B, Hall DA. PMID: 32258228; PMCID: PMC7111569.
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    106. Rapidly Progressing Neurocognitive Disorder in a Male with FXTAS and Alzheimer's Disease. Clin Interv Aging. 2020; 15:285-292. Aydin EY, Schneider A, Protic D, Wang JY, Martínez-Cerdeño V, Tassone F, Tang HT, Perlman S, Hagerman RJ. PMID: 32161452; PMCID: PMC7051898.
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    107. Spontaneous Coronary Artery Dissection in Females With the Fragile X FMR1 Premutation. JACC Case Rep. 2020 Jan; 2(1):40-44. McKenzie FJ, Tassankijpanich N, Epps KC, March SK, Hagerman RJ. PMID: 32154514; PMCID: PMC7062363.
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    108. Fragile X syndrome and associated disorders: Clinical aspects and pathology. Neurobiol Dis. 2020 03; 136:104740. Salcedo-Arellano MJ, Dufour B, McLennan Y, Martinez-Cerdeno V, Hagerman R. PMID: 31927143; PMCID: PMC7027994.
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    109. Developmental aspects of FXAND in a man with the FMR1 premutation. Mol Genet Genomic Med. 2020 02; 8(2):e1050. Santos E, Emeka-Nwonovo C, Wang JY, Schneider A, Tassone F, Hagerman P, Hagerman R. PMID: 31899609; PMCID: PMC7005639.
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    110. Fragile X syndrome: clinical presentation, pathology and treatment. Gac Med Mex. 2020; 156(1):60-66. Salcedo-Arellano MJ, Hagerman RJ, Martínez-Cerdeño V. PMID: 32026885.
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    111. Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions. PLoS One. 2019; 14(12):e0226811. Kim K, Hessl D, Randol JL, Espinal GM, Schneider A, Protic D, Aydin EY, Hagerman RJ, Hagerman PJ. PMID: 31891607; PMCID: PMC6938341.
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    112. A Randomized Controlled Trial of Sertraline in Young Children With Autism Spectrum Disorder. Front Psychiatry. 2019; 10:810. Potter LA, Scholze DA, Biag HMB, Schneider A, Chen Y, Nguyen DV, Rajaratnam A, Rivera SM, Dwyer PS, Tassone F, Al Olaby RR, Choudhary NS, Salcedo-Arellano MJ, Hagerman RJ. PMID: 31780970; PMCID: PMC6851992.
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    113. Interaction between ventricular expansion and structural changes in the corpus callosum and putamen in males with FMR1 normal and premutation alleles. Neurobiol Aging. 2020 02; 86:27-38. Wang JY, Hessl D, Tassone F, Kim K, Hagerman RJ, Rivera SM. PMID: 31733943; PMCID: PMC6995416.
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    114. Metformin treatment in young children with fragile X syndrome. Mol Genet Genomic Med. 2019 11; 7(11):e956. Biag HMB, Potter LA, Wilkins V, Afzal S, Rosvall A, Salcedo-Arellano MJ, Rajaratnam A, Manzano-Nunez R, Schneider A, Tassone F, Rivera SM, Hagerman RJ. PMID: 31520524; PMCID: PMC6825840.
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    115. Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome. Acta Neuropathol Commun. 2019 09 03; 7(1):143. Ma L, Herren AW, Espinal G, Randol J, McLaughlin B, Martinez-Cerdeño V, Pessah IN, Hagerman RJ, Hagerman PJ. PMID: 31481131; PMCID: PMC6720097.
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    116. General Anesthetic Use in Fragile X Spectrum Disorders. J Neurosurg Anesthesiol. 2019 Jul; 31(3):285-290. Ligsay A, El-Deeb M, Salcedo-Arellano MJ, Schloemerkemper N, Grayson JS, Hagerman R. PMID: 29734272; PMCID: PMC6215737.
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    117. EEG Abnormalities as a Neurophysiological Biomarker of Severity in Autism Spectrum Disorder: A Pilot Cohort Study. J Autism Dev Disord. 2019 Jun; 49(6):2337-2347. Nicotera AG, Hagerman RJ, Catania MV, Buono S, Di Nuovo S, Liprino EM, Stracuzzi E, Giusto S, Di Vita G, Musumeci SA. PMID: 30726535.
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    118. Fragile X- associated Neuropsychiatric Disorders: A Case Report. Future Neurol. 2019 May; 14(2). Tan MM, Dy JB, Salcedo-Arellano MJ, Tassone F, Hagerman RJ. PMID: 32089651; PMCID: PMC7034938.
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    119. Cognitive and behavioral improvement in adults with fragile X syndrome treated with metformin-two cases. Mol Genet Genomic Med. 2019 07; 7(7):e00745. Protic D, Aydin EY, Tassone F, Tan MM, Hagerman RJ, Schneider A. PMID: 31104364; PMCID: PMC6625129.
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    120. De novo and biallelic DEAF1 variants cause a phenotypic spectrum. Genet Med. 2019 09; 21(9):2059-2069. Nabais Sá MJ, Jensik PJ, McGee SR, Parker MJ, Lahiri N, McNeil EP, Kroes HY, Hagerman RJ, Harrison RE, Montgomery T, Splitt M, Palmer EE, Sachdev RK, Mefford HC, Scott AA, Martinez-Agosto JA, Lorenz R, Orenstein N, Berg JN, Amiel J, Heron D, Keren B, Cobben JM, Menke LA, Marco EJ, Graham JM, Pierson TM, Karimiani EG, Maroofian R, Manzini MC, Cauley ES, Colombo R, Odent S, Dubourg C, Phornphutkul C, de Brouwer APM, de Vries BBA, Vulto-vanSilfhout AT. PMID: 30923367.
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    121. Turning the tide on targeted treatments for neurodevelopmental disorders. Neurology. 2019 04 16; 92(16):741-742. Hagerman R, Tuchman R. PMID: 30918096.
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    122. Consensus Statement of the Indian Academy of Pediatrics on Diagnosis and Management of Fragile X Syndrome in India. Indian Pediatr. 2019 03 15; 56(3):221-228. Sachdeva A, Jain P, Gunasekaran V, Mahay SB, Mukherjee S, Hagerman R, Shankar S, Kapoor S, Kedia SN, Indian Academy of Pediatrics Consensus in Diagnosis and Management of Fragile X Syndrome Committee., Indian Academy of Pediatrics Consensus in Diagnosis and Management of Fragile X Syndrome Committee. PMID: 30954995.
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    123. Treatment of Fragile X Syndrome with Cannabidiol: A Case Series Study and Brief Review of the Literature. Cannabis Cannabinoid Res. 2019; 4(1):3-9. Tartaglia N, Bonn-Miller M, Hagerman R. PMID: 30944868; PMCID: PMC6446166.
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    124. [Fragile X associated tremor/ataxia syndrome: its clinical presentation, pathology, and treatment]. Rev Neurol. 2019 Mar 01; 68(5):199-206. Salcedo-Arellano MJ, Hagerman RJ, Martinez-Cerdeno V. PMID: 30805918; PMCID: PMC7001878.
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    125. Clinimetric Properties of the Fragile X-associated Tremor Ataxia Syndrome Rating Scale. Mov Disord Clin Pract. 2019 Feb; 6(2):120-124. Hall DA, Stebbins GT, Jacquemont S, Berry-Kravis E, Goetz CG, Hagerman R, Zhang L, Leehey MA. PMID: 30838310; PMCID: PMC6384171.
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    126. Effects of mavoglurant on visual attention and pupil reactivity while viewing photographs of faces in Fragile X Syndrome. PLoS One. 2019; 14(1):e0209984. Hessl D, Harvey D, Sansone S, Crestodina C, Chin J, Joshi R, Hagerman RJ, Berry-Kravis E. PMID: 30653533; PMCID: PMC6336311.
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    127. New Targeted Treatments for Fragile X Syndrome. Curr Pediatr Rev. 2019; 15(4):251-258. Protic D, Salcedo-Arellano MJ, Dy JB, Potter LA, Hagerman RJ. PMID: 31241016; PMCID: PMC6930353.
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    128. Widespread RNA editing dysregulation in brains from autistic individuals. Nat Neurosci. 2019 01; 22(1):25-36. Tran SS, Jun HI, Bahn JH, Azghadi A, Ramaswami G, Van Nostrand EL, Nguyen TB, Hsiao YE, Lee C, Pratt GA, Martínez-Cerdeño V, Hagerman RJ, Yeo GW, Geschwind DH, Xiao X. PMID: 30559470; PMCID: PMC6375307.
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    153. Distance delivery of a spoken language intervention for school-aged and adolescent boys with fragile X syndrome. Dev Neurorehabil. 2018 Jan; 21(1):48-63. McDuffie A, Banasik A, Bullard L, Nelson S, Feigles RT, Hagerman R, Abbeduto L. PMID: 28956679; PMCID: PMC5986725.
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    154. Metformin as targeted treatment in fragile X syndrome. Clin Genet. 2018 02; 93(2):216-222. Dy ABC, Tassone F, Eldeeb M, Salcedo-Arellano MJ, Tartaglia N, Hagerman R. PMID: 28436599; PMCID: PMC6944702.
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    156. Effect of the mGluR5-NAM Basimglurant on Behavior in Adolescents and Adults with Fragile X Syndrome in a Randomized, Double-Blind, Placebo-Controlled Trial: FragXis Phase 2 Results. Neuropsychopharmacology. 2018 02; 43(3):503-512. Youssef EA, Berry-Kravis E, Czech C, Hagerman RJ, Hessl D, Wong CY, Rabbia M, Deptula D, John A, Kinch R, Drewitt P, Lindemann L, Marcinowski M, Langland R, Horn C, Fontoura P, Santarelli L, Quiroz JA, FragXis Study Group. PMID: 28816242; PMCID: PMC5770759.
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    158. Children With Fragile X Syndrome Display Threat-Specific Biases Toward Emotion. Biol Psychiatry Cogn Neurosci Neuroimaging. 2017 09; 2(6):487-492. Burris JL, Barry-Anwar RA, Sims RN, Hagerman RJ, Tassone F, Rivera SM. PMID: 29348038.
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    159. Autism Symptoms in Fragile X Syndrome. J Child Neurol. 2017 Sep; 32(10):903-909. Niu M, Han Y, Dy ABC, Du J, Jin H, Qin J, Zhang J, Li Q, Hagerman RJ. PMID: 28617074.
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    160. Fragile X targeted pharmacotherapy: lessons learned and future directions. J Neurodev Disord. 2017; 9:7. Erickson CA, Davenport MH, Schaefer TL, Wink LK, Pedapati EV, Sweeney JA, Fitzpatrick SE, Brown WT, Budimirovic D, Hagerman RJ, Hessl D, Kaufmann WE, Berry-Kravis E. PMID: 28616096; PMCID: PMC5467059.
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    167. The Gut Microbiota and Autism Spectrum Disorders. Front Cell Neurosci. 2017; 11:120. Li Q, Han Y, Dy ABC, Hagerman RJ. PMID: 28503135; PMCID: PMC5408485.
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    172. Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome. Brain. 2017 03 01; 140(3):582-598. Boland MJ, Nazor KL, Tran HT, Szücs A, Lynch CL, Paredes R, Tassone F, Sanna PP, Hagerman RJ, Loring JF. PMID: 28137726; PMCID: PMC5837342.
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    174. Developmental profiles of infants with an FMR1 premutation. J Neurodev Disord. 2016; 8:40. Wheeler AC, Sideris J, Hagerman R, Berry-Kravis E, Tassone F, Bailey DB. PMID: 27822316; PMCID: PMC5095966.
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    178. Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers. Cerebellum. 2016 10; 15(5):578-86. Hall DA, Robertson E, Shelton AL, Losh MC, Mila M, Moreno EG, Gomez-Anson B, Martínez-Cerdeño V, Grigsby J, Lozano R, Hagerman R, Maria LS, Berry-Kravis E, O'Keefe JA. PMID: 27287737; PMCID: PMC7608648.
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    179. Altered Bioenergetics in Primary Dermal Fibroblasts from Adult Carriers of the FMR1 Premutation Before the Onset of the Neurodegenerative Disease Fragile X-Associated Tremor/Ataxia Syndrome. Cerebellum. 2016 10; 15(5):552-64. Napoli E, Song G, Wong S, Hagerman R, Giulivi C. PMID: 27089882; PMCID: PMC5014718.
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    189. Down Syndrome and Fragile X Syndrome in a Colombian Woman: Case Report. J Appl Res Intellect Disabil. 2017 Sep; 30(5):970-974. Saldarriaga W, Ruiz FA, Tassone F, Hagerman R. PMID: 27456465.
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    190. Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis. J Genet Disord Genet Rep. 2016; 5(3). Yrigollen CM, Pacini L, Nobile V, Lozano R, Hagerman RJ, Bagni C, Tassone F. PMID: 28232951; PMCID: PMC5319728.
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    191. Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicine. Mol Med. 2016 Oct; 22:548-559. Song G, Napoli E, Wong S, Hagerman R, Liu S, Tassone F, Giulivi C. PMID: 27385396; PMCID: PMC5082295.
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    194. Fragile X-associated tremor/ataxia syndrome - features, mechanisms and management. Nat Rev Neurol. 2016 07; 12(7):403-12. Hagerman RJ, Hagerman P. PMID: 27340021.
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    195. Warburg effect linked to cognitive-executive deficits in FMR1 premutation. FASEB J. 2016 10; 30(10):3334-3351. Napoli E, Song G, Schneider A, Hagerman R, Eldeeb MA, Azarang A, Tassone F, Giulivi C. PMID: 27335370; PMCID: PMC5024697.
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    196. Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome. Sci Signal. 2016 06 07; 9(431):ra58. Kashima R, Roy S, Ascano M, Martinez-Cerdeno V, Ariza-Torres J, Kim S, Louie J, Lu Y, Leyton P, Bloch KD, Kornberg TB, Hagerman PJ, Hagerman R, Lagna G, Hata A. PMID: 27273096; PMCID: PMC5274719.
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    201. Phenobarbital use and neurological problems in FMR1 premutation carriers. Neurotoxicology. 2016 Mar; 53:141-147. Saldarriaga W, Lein P, González Teshima LY, Isaza C, Rosa L, Polyak A, Hagerman R, Girirajan S, Silva M, Tassone F. PMID: 26802682; PMCID: PMC4808401.
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    202. Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials. Sci Transl Med. 2016 Jan 13; 8(321):321ra5. Berry-Kravis E, Des Portes V, Hagerman R, Jacquemont S, Charles P, Visootsak J, Brinkman M, Rerat K, Koumaras B, Zhu L, Barth GM, Jaecklin T, Apostol G, von Raison F. PMID: 26764156.
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    207. Evaluation of the neuroactive steroid ganaxolone on social and repetitive behaviors in the BTBR mouse model of autism. Psychopharmacology (Berl). 2016 Jan; 233(2):309-23. Kazdoba TM, Hagerman RJ, Zolkowska D, Rogawski MA, Crawley JN. PMID: 26525567; PMCID: PMC4703522.
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    208. The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery. Stem Cells Transl Med. 2015 Nov; 4(11):1369. Brick DJ, Nethercott HE, Montesano S, Banuelos MG, Stover AE, Schutte SS, O'Dowd DK, Hagerman RJ, Ono M, Hessl DR, Tassone F, Schwartz PH. PMID: 26508786; PMCID: PMC4622400.
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    239. The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery. Stem Cells Transl Med. 2014 Nov; 3(11):1275-86. Brick DJ, Nethercott HE, Montesano S, Banuelos MG, Stover AE, Schutte SS, O'Dowd DK, Hagerman RJ, Ono M, Hessl DR, Tassone F, Schwartz PH. PMID: 25273538; PMCID: PMC4214842.
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    244. Sentence comprehension in boys with autism spectrum disorder. Am J Speech Lang Pathol. 2014 Aug; 23(3):385-94. Kover ST, Haebig E, Oakes A, McDuffie A, Hagerman RJ, Abbeduto L. PMID: 24687049; PMCID: PMC4119529.
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    245. Prevalence of restless legs syndrome and sleep quality in carriers of the fragile X premutation. Clin Genet. 2014 Aug; 86(2):181-4. Summers SM, Cogswell J, Goodrich JE, Mu Y, Nguyen DV, Brass SD, Hagerman RJ. PMID: 25180401; PMCID: PMC4391968.
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    251. Group I metabotropic glutamate receptor mediated dynamic immune dysfunction in children with fragile X syndrome. J Neuroinflammation. 2014 Jun 19; 11:110. Careaga M, Noyon T, Basuta K, Van de Water J, Tassone F, Hagerman RJ, Ashwood P. PMID: 24942544; PMCID: PMC4107617.
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    255. Staged transthoracic approach to persistent atrial fibrillation (TOP-AF): study protocol for a randomized trial. Trials. 2014 May 26; 15:190. Pragliola C, Mastroroberto P, Gaudino M, Chello M, Covino E. PMID: 24885377; PMCID: PMC4066274.
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    270. The challenges of clinical trials in fragile X syndrome. Psychopharmacology (Berl). 2014 Mar; 231(6):1237-50. Jacquemont S, Berry-Kravis E, Hagerman R, von Raison F, Gasparini F, Apostol G, Ufer M, Des Portes V, Gomez-Mancilla B. PMID: 24173622; PMCID: PMC3932172.
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    272. Electrocortical changes associated with minocycline treatment in fragile X syndrome. J Psychopharmacol. 2013 Oct; 27(10):956-63. Schneider A, Leigh MJ, Adams P, Nanakul R, Chechi T, Olichney J, Hagerman R, Hessl D. PMID: 23981511; PMCID: PMC4962861.
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    273. Phenotypes of hypofrontality in older female fragile X premutation carriers. Ann Neurol. 2013 Aug; 74(2):275-83. Yang JC, Simon C, Niu YQ, Bogost M, Schneider A, Tassone F, Seritan A, Grigsby J, Hagerman PJ, Hagerman RJ, Olichney JM. PMID: 23686745; PMCID: PMC3906211.
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    274. Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurol. 2013 Aug; 12(8):786-98. Hagerman R, Hagerman P. PMID: 23867198; PMCID: PMC3922535.
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    275. Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles. JAMA Neurol. 2013 Aug; 70(8):1022-9. Wang JY, Hessl D, Schneider A, Tassone F, Hagerman RJ, Rivera SM. PMID: 23753897; PMCID: PMC4028037.
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    276. A family with two female siblings with compound heterozygous FMR1 premutation alleles. Clin Genet. 2014 May; 85(5):458-63. Basuta K, Lozano R, Schneider A, Yrigollen CM, Hessl D, Hagerman RJ, Tassone F. PMID: 23786467; PMCID: PMC3996450.
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    277. High MMP-9 activity levels in fragile X syndrome are lowered by minocycline. Am J Med Genet A. 2013 Aug; 161A(8):1897-903. Dziembowska M, Pretto DI, Janusz A, Kaczmarek L, Leigh MJ, Gabriel N, Durbin-Johnson B, Hagerman RJ, Tassone F. PMID: 23824974.
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    278. Investigating word learning in fragile X syndrome: a fast-mapping study. J Autism Dev Disord. 2013 Jul; 43(7):1676-91. McDuffie A, Kover ST, Hagerman R, Abbeduto L. PMID: 23179343; PMCID: PMC3620772.
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    279. Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptions. J Hum Genet. 2013 Aug; 58(8):553-9. Yrigollen CM, Mendoza-Morales G, Hagerman R, Tassone F. PMID: 23739124; PMCID: PMC4003888.
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    280. Intranuclear inclusions in a fragile X mosaic male. Transl Neurodegener. 2013 May 21; 2(1):10. Pretto DI, Hunsaker MR, Cunningham CL, Greco CM, Hagerman RJ, Noctor SC, Hall DA, Hagerman PJ, Tassone F. PMID: 23692864; PMCID: PMC3668897.
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    281. A multimodal imaging analysis of subcortical gray matter in fragile X premutation carriers. Mov Disord. 2013 Aug; 28(9):1278-84. Wang JY, Hagerman RJ, Rivera SM. PMID: 23649693; PMCID: PMC3785985.
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    282. A randomized double-blind, placebo-controlled trial of minocycline in children and adolescents with fragile x syndrome. J Dev Behav Pediatr. 2013 Apr; 34(3):147-55. Leigh MJ, Nguyen DV, Mu Y, Winarni TI, Schneider A, Chechi T, Polussa J, Doucet P, Tassone F, Rivera SM, Hessl D, Hagerman RJ. PMID: 23572165; PMCID: PMC3706260.
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    283. Prevalence and risk of migraine headaches in adult fragile X premutation carriers. Clin Genet. 2013 Dec; 84(6):546-51. Au J, Akins RS, Berkowitz-Sutherland L, Tang HT, Chen Y, Boyd A, Tassone F, Nguyen DV, Hagerman R. PMID: 23373759; PMCID: PMC4991825.
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    284. Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in Indonesia. Clin Genet. 2013 Dec; 84(6):577-80. Winarni TI, Utari A, Mundhofir FE, Hagerman RJ, Faradz SM. PMID: 23320543.
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    285. Epilepsy drives autism in neurodevelopmental disorders. Dev Med Child Neurol. 2013 Feb; 55(2):101-102. Hagerman RJ. PMID: 23320573; PMCID: PMC4051495.
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    286. FRAGILE X SYNDROME: PSYCHIATRIC MANIFESTATIONS, ASSESSMENT AND EMERGING THERAPIES. Curr Psychiatry Rev. 2013 Feb 01; 9(1):53-58. Wadell PM, Hagerman RJ, Hessl DR. PMID: 25632275; PMCID: PMC4306413.
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    287. Ages of Onset of Mood and Anxiety Disorders in Fragile X Premutation Carriers. Curr Psychiatry Rev. 2013 Feb; 9(1):65-71. Seritan AL, Bourgeois JA, Schneider A, Mu Y, Hagerman RJ, Nguyen DV. PMID: 25844075; PMCID: PMC4383251.
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    288. Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and puberty. Hum Mol Genet. 2013 Apr 15; 22(8):1516-24. Godler DE, Inaba Y, Shi EZ, Skinner C, Bui QM, Francis D, Amor DJ, Hopper JL, Loesch DZ, Hagerman RJ, Schwartz CE, Slater HR. PMID: 23307923; PMCID: PMC3605829.
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    289. PSYCHIATRIC DISORDERS ASSOCIATED WITH FXTAS. Curr Psychiatry Rev. 2013; 9(1):59-64. Seritan AL, Ortigas M, Seritan S, Bourgeois JA, Hagerman RJ. PMID: 25620899; PMCID: PMC4304643.
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    290. Fragile X syndrome: an aging perspective. Dev Disabil Res Rev. 2013; 18(1):68-74. Schneider A, Ligsay A, Hagerman RJ. PMID: 23949830; PMCID: PMC4959461.
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    291. Psychiatric features in high-functioning adult brothers with fragile x spectrum disorders. Prim Care Companion CNS Disord. 2013; 15(2). Schneider A, Seritan A, Tassone F, Rivera SM, Hagerman R, Hessl D. PMID: 23930232; PMCID: PMC3733525.
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    292. Neurodevelopmental disabilities in children with intermediate and premutation range fragile X cytosine-guanine-guanine expansions. J Child Neurol. 2014 Mar; 29(3):326-30. Renda MM, Voigt RG, Babovic-Vuksanovic D, Highsmith WE, Vinson SS, Sadowski CM, Hagerman RJ. PMID: 23266944.
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    293. FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States. Genome Med. 2012; 4(12):100. Tassone F, Iong KP, Tong TH, Lo J, Gane LW, Berry-Kravis E, Nguyen D, Mu LY, Laffin J, Bailey DB, Hagerman RJ. PMID: 23259642; PMCID: PMC4064316.
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    294. Newborn screening and cascade testing for FMR1 mutations. Am J Med Genet A. 2013 Jan; 161A(1):59-69. Sorensen PL, Gane LW, Yarborough M, Hagerman RJ, Tassone F. PMID: 23239591; PMCID: PMC3980469.
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    295. Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics. J Clin Invest. 2012 Dec; 122(12):4314-22. Bagni C, Tassone F, Neri G, Hagerman R. PMID: 23202739; PMCID: PMC3533539.
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    296. Newborn, carrier, and early childhood screening recommendations for fragile X. Pediatrics. 2012 Dec; 130(6):1126-35. Abrams L, Cronister A, Brown WT, Tassone F, Sherman SL, Finucane B, McConkie-Rosell A, Hagerman R, Kaufmann WE, Picker J, Coffey S, Skinner D, Johnson V, Miller R, Berry-Kravis E. PMID: 23129072.
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    297. Fragile X-associated tremor/ataxia syndrome (FXTAS) in grey zone carriers. Clin Genet. 2013 Jul; 84(1):74-7. Liu Y, Winarni TI, Zhang L, Tassone F, Hagerman RJ. PMID: 23009394; PMCID: PMC4991824.
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    298. Influence of the fragile X mental retardation (FMR1) gene on the brain and working memory in men with normal FMR1 alleles. Neuroimage. 2013 Jan 15; 65:288-98. Wang JY, Hessl D, Iwahashi C, Cheung K, Schneider A, Hagerman RJ, Hagerman PJ, Rivera SM. PMID: 23063447; PMCID: PMC3540208.
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    299. Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene. Genome Res. 2013 Jan; 23(1):121-8. Loomis EW, Eid JS, Peluso P, Yin J, Hickey L, Rank D, McCalmon S, Hagerman RJ, Tassone F, Hagerman PJ. PMID: 23064752; PMCID: PMC3530672.
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    300. Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study. Genet Med. 2013 Apr; 15(4):290-8. Inaba Y, Herlihy AS, Schwartz CE, Skinner C, Bui QM, Cobb J, Shi EZ, Francis D, Arvaj A, Amor DJ, Pope K, Wotton T, Cohen J, Hewitt JK, Hagerman RJ, Metcalfe SA, Hopper JL, Loesch DZ, Slater HR, Godler DE. PMID: 23060046.
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    301. Treatment of neurodevelopmental disorders in adulthood. J Neurosci. 2012 Oct 10; 32(41):14074-9. Castrén E, Elgersma Y, Maffei L, Hagerman R. PMID: 23055475; PMCID: PMC3500763.
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    302. TARGETED TREATMENTS IN AUTISM AND FRAGILE X SYNDROME. Res Autism Spectr Disord. 2012 Oct 01; 6(4):1311-1320. Gürkan CK, Hagerman RJ. PMID: 23162607; PMCID: PMC3498468.
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    303. Effects of STX209 (arbaclofen) on neurobehavioral function in children and adults with fragile X syndrome: a randomized, controlled, phase 2 trial. Sci Transl Med. 2012 Sep 19; 4(152):152ra127. Berry-Kravis EM, Hessl D, Rathmell B, Zarevics P, Cherubini M, Walton-Bowen K, Mu Y, Nguyen DV, Gonzalez-Heydrich J, Wang PP, Carpenter RL, Bear MF, Hagerman RJ. PMID: 22993294.
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    304. Neural substrates of executive dysfunction in fragile X-associated tremor/ataxia syndrome (FXTAS): a brain potential study. Cereb Cortex. 2013 Nov; 23(11):2657-66. Yang JC, Chan SH, Khan S, Schneider A, Nanakul R, Teichholtz S, Niu YQ, Seritan A, Tassone F, Grigsby J, Hagerman PJ, Hagerman RJ, Olichney JM. PMID: 22918986; PMCID: PMC3792740.
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    305. Immune-mediated disorders among women carriers of fragile X premutation alleles. Am J Med Genet A. 2012 Oct; 158A(10):2473-81. Winarni TI, Chonchaiya W, Sumekar TA, Ashwood P, Morales GM, Tassone F, Nguyen DV, Faradz SM, Van de Water J, Cook K, Hamlin A, Mu Y, Hagerman PJ, Hagerman RJ. PMID: 22903889; PMCID: PMC4105154.
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    306. The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia. Clin Genet. 2013 Mar; 83(3):263-8. Winarni TI, Mundhofir FE, Ediati A, Belladona M, Nillesen WM, Yntema HG, Hamel BC, Faradz SM, Hagerman RJ. PMID: 22568721.
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    307. Sertraline may improve language developmental trajectory in young children with fragile x syndrome: a retrospective chart review. Autism Res Treat. 2012; 2012:104317. Indah Winarni T, Chonchaiya W, Adams E, Au J, Mu Y, Rivera SM, Nguyen DV, Hagerman RJ. PMID: 22934167; PMCID: PMC3420618.
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    308. Signaling defects in iPSC-derived fragile X premutation neurons. Hum Mol Genet. 2012 Sep 01; 21(17):3795-805. Liu J, Koscielska KA, Cao Z, Hulsizer S, Grace N, Mitchell G, Nacey C, Githinji J, McGee J, Garcia-Arocena D, Hagerman RJ, Nolta J, Pessah IN, Hagerman PJ. PMID: 22641815; PMCID: PMC3412379.
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    309. Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS). Am J Med Genet A. 2012 Jun; 158A(6):1304-9. Hamlin AA, Sukharev D, Campos L, Mu Y, Tassone F, Hessl D, Nguyen DV, Loesch D, Hagerman RJ. PMID: 22528549; PMCID: PMC3983689.
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    310. AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome. Genet Med. 2012 Aug; 14(8):729-36. Yrigollen CM, Durbin-Johnson B, Gane L, Nelson DL, Hagerman R, Hagerman PJ, Tassone F. PMID: 22498846; PMCID: PMC3990283.
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    311. A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. Am J Med Genet A. 2012 May; 158A(5):1221-4. Sorensen PL, Basuta K, Mendoza-Morales G, Gane LW, Schneider A, Hagerman R, Tassone F. PMID: 22488807; PMCID: PMC3331966.
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    312. Reduced telomere length in individuals with FMR1 premutations and full mutations. Am J Med Genet A. 2012 May; 158A(5):1060-5. Jenkins EC, Tassone F, Ye L, Hoogeveen AT, Brown WT, Hagerman RJ, Hagerman PJ. PMID: 22489017; PMCID: PMC3402180.
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    313. Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS. Genes Brain Behav. 2012 Jul; 11(5):577-85. Tassone F, Greco CM, Hunsaker MR, Seritan AL, Berman RF, Gane LW, Jacquemont S, Basuta K, Jin LW, Hagerman PJ, Hagerman RJ. PMID: 22463693; PMCID: PMC3965773.
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    314. Age-dependent structural connectivity effects in fragile x premutation. Arch Neurol. 2012 Apr; 69(4):482-9. Wang JY, Hessl DH, Hagerman RJ, Tassone F, Rivera SM. PMID: 22491193; PMCID: PMC3979438.
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    315. Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone. Hum Mol Genet. 2012 Jul 01; 21(13):2923-35. Cao Z, Hulsizer S, Tassone F, Tang HT, Hagerman RJ, Rogawski MA, Hagerman PJ, Pessah IN. PMID: 22466801; PMCID: PMC3373240.
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    316. Early intervention combined with targeted treatment promotes cognitive and behavioral improvements in young children with fragile x syndrome. Case Rep Genet. 2012; 2012:280813. Winarni TI, Schneider A, Borodyanskara M, Hagerman RJ. PMID: 23074686; PMCID: PMC3447258.
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    317. Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome. Genes Brain Behav. 2012 Apr; 11(3):332-41. Hoeffer CA, Sanchez E, Hagerman RJ, Mu Y, Nguyen DV, Wong H, Whelan AM, Zukin RS, Klann E, Tassone F. PMID: 22268788; PMCID: PMC3319643.
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    318. Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study. Clin Chem. 2012 Mar; 58(3):590-8. Godler DE, Slater HR, Bui QM, Storey E, Ono MY, Gehling F, Inaba Y, Francis D, Hopper JL, Kinsella G, Amor DJ, Hagerman RJ, Loesch DZ. PMID: 22235103.
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    319. The fragile X-associated tremor ataxia syndrome. Results Probl Cell Differ. 2012; 54:337-57. Tassone F, Hagerman R. PMID: 22009361.
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    320. Unstable mutations in the FMR1 gene and the phenotypes. Adv Exp Med Biol. 2012; 769:78-114. Loesch D, Hagerman R. PMID: 23560306; PMCID: PMC4124039.
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    321. Fragile X syndrome and targeted treatment trials. Results Probl Cell Differ. 2012; 54:297-335. Hagerman R, Lauterborn J, Au J, Berry-Kravis E. PMID: 22009360; PMCID: PMC4114775.
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    322. Investigation of amygdala volume in men with the fragile X premutation. Brain Imaging Behav. 2011 Dec; 5(4):285-94. Selmeczy D, Koldewyn K, Wang JM, Lee A, Harvey D, Hessl DR, Tassone F, Adams P, Hagerman RJ, Hagerman PJ, Rivera SM. PMID: 21786216; PMCID: PMC3982607.
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    323. Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome. Case Rep Genet. 2011; 2011:143132. Sumekar TA, Ashrani AA, Winarni TI, Hagerman RJ. PMID: 23074671; PMCID: PMC3447231.
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    324. The fragile X-associated disorders: time to order fragile X DNA testing. Biol Psychiatry. 2011 Nov 01; 70(9):802-3. Hagerman RJ. PMID: 21986091.
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    325. Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder. Hum Genet. 2012 Apr; 131(4):581-9. Chonchaiya W, Au J, Schneider A, Hessl D, Harris SW, Laird M, Mu Y, Tassone F, Nguyen DV, Hagerman RJ. PMID: 22001913; PMCID: PMC4105134.
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    326. Sleep apnea in fragile X premutation carriers with and without FXTAS. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec; 156B(8):923-8. Hamlin A, Liu Y, Nguyen DV, Tassone F, Zhang L, Hagerman RJ. PMID: 21932336; PMCID: PMC4109408.
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    327. Fibromyalgia in fragile X mental retardation 1 gene premutation carriers. Rheumatology (Oxford). 2011 Dec; 50(12):2233-6. Leehey MA, Legg W, Tassone F, Hagerman R. PMID: 21926154; PMCID: PMC3222847.
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    328. Testing the FMR1 promoter for mosaicism in DNA methylation among CpG sites, strands, and cells in FMR1-expressing males with fragile X syndrome. PLoS One. 2011; 6(8):e23648. Stöger R, Genereux DP, Hagerman RJ, Hagerman PJ, Tassone F, Laird CD. PMID: 21909353; PMCID: PMC3166088.
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    329. Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice. Acta Neuropathol. 2011 Oct; 122(4):467-79. Hunsaker MR, Greco CM, Spath MA, Smits AP, Navarro CS, Tassone F, Kros JM, Severijnen LA, Berry-Kravis EM, Berman RF, Hagerman PJ, Willemsen R, Hagerman RJ, Hukema RK. PMID: 21785977; PMCID: PMC3222079.
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    330. FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles. J Mol Diagn. 2011 Sep; 13(5):528-36. Godler DE, Slater HR, Bui QM, Ono M, Gehling F, Francis D, Amor DJ, Hopper JL, Hagerman R, Loesch DZ. PMID: 21723415; PMCID: PMC3157613.
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    331. Rare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disorders. J Neuropathol Exp Neurol. 2011 Jun; 70(6):462-9. Hunsaker MR, Greco CM, Tassone F, Berman RF, Willemsen R, Hagerman RJ, Hagerman PJ. PMID: 21572337; PMCID: PMC3109086.
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    332. FMR1 premutation and full mutation molecular mechanisms related to autism. J Neurodev Disord. 2011 Sep; 3(3):211-24. Hagerman R, Au J, Hagerman P. PMID: 21617890; PMCID: PMC3261276.
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    333. Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome. Hum Mol Genet. 2011 Aug 01; 20(15):3079-92. Napoli E, Ross-Inta C, Wong S, Omanska-Klusek A, Barrow C, Iwahashi C, Garcia-Arocena D, Sakaguchi D, Berry-Kravis E, Hagerman R, Hagerman PJ, Giulivi C. PMID: 21558427; PMCID: PMC3131047.
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    334. A Quantitative Assessment of Tremor and Ataxia in Female FMR1 Premutation Carriers Using CATSYS. Curr Gerontol Geriatr Res. 2011; 2011:484713. Narcisa V, Aguilar D, Nguyen DV, Campos L, Brodovsky J, White S, Adams P, Tassone F, Hagerman PJ, Hagerman RJ. PMID: 23008705; PMCID: PMC3114433.
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    335. Fragile x syndrome. Curr Genomics. 2011 May; 12(3):216-24. McLennan Y, Polussa J, Tassone F, Hagerman R. PMID: 22043169; PMCID: PMC3137006.
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    336. Diffusion tensor imaging in male premutation carriers of the fragile X mental retardation gene. Mov Disord. 2011 Jun; 26(7):1329-36. Hashimoto R, Srivastava S, Tassone F, Hagerman RJ, Rivera SM. PMID: 21484870; PMCID: PMC3119762.
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    337. Case report: Dystonia in a fragile X carrier. Mov Disord. 2014 Jun; 29(7):E4-5. Zhang L, Sukharev D, Schneider A, Olichney JM, Seritan A, Hagerman RJ. PMID: 21469199; PMCID: PMC3136610.
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    338. A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome. Brain. 2011 Mar; 134(Pt 3):863-78. Hashimoto R, Javan AK, Tassone F, Hagerman RJ, Rivera SM. PMID: 21354978; PMCID: PMC3044831.
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    339. Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation. Am J Med Genet A. 2011 Mar; 155A(3):519-25. Basuta K, Narcisa V, Chavez A, Kumar M, Gane L, Hagerman R, Tassone F. PMID: 21344625; PMCID: PMC3568664.
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    340. Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome. Mol Autism. 2011 Feb 08; 2(1):2. Greco CM, Navarro CS, Hunsaker MR, Maezawa I, Shuler JF, Tassone F, Delany M, Au JW, Berman RF, Jin LW, Schumann C, Hagerman PJ, Hagerman RJ. PMID: 21303513; PMCID: PMC3045897.
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    341. Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056. Sci Transl Med. 2011 Jan 05; 3(64):64ra1. Jacquemont S, Curie A, des Portes V, Torrioli MG, Berry-Kravis E, Hagerman RJ, Ramos FJ, Cornish K, He Y, Paulding C, Neri G, Chen F, Hadjikhani N, Martinet D, Meyer J, Beckmann JS, Delange K, Brun A, Bussy G, Gasparini F, Hilse T, Floesser A, Branson J, Bilbe G, Johns D, Gomez-Mancilla B. PMID: 21209411.
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    342. Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization. J Neurodev Disord. 2011 Mar; 3(1):57-67. Cordeiro L, Ballinger E, Hagerman R, Hessl D. PMID: 21475730; PMCID: PMC3057014.
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    343. Assessment of patient and caregiver needs in fragile X-associated tremor/ataxia syndrome by utilizing Q-sort methodology. Aging Ment Health. 2010 Nov; 14(8):1000-7. Gane LW, Iosif AM, Flynn-Wilson L, Venturino M, Hagerman RJ, Seritan AL. PMID: 21069606; PMCID: PMC3189491.
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    344. Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome. Neurobiol Aging. 2012 Jun; 33(6):1045-53. Schneider A, Ballinger E, Chavez A, Tassone F, Hagerman RJ, Hessl D. PMID: 20961665; PMCID: PMC3044775.
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    345. Improving fragile X-associated tremor/ataxia syndrome symptoms with memantine and venlafaxine. J Clin Psychopharmacol. 2010 Oct; 30(5):642-4. Ortigas MC, Bourgeois JA, Schneider A, Olichney J, Nguyen DV, Cogswell JB, Hall DA, Hagerman RJ. PMID: 20841969; PMCID: PMC4022473.
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    346. Fragile X and autism: Intertwined at the molecular level leading to targeted treatments. Mol Autism. 2010 Sep 21; 1(1):12. Hagerman R, Hoem G, Hagerman P. PMID: 20858229; PMCID: PMC2954865.
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    347. Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome. Hum Genet. 2010 Nov; 128(5):539-48. Chonchaiya W, Tassone F, Ashwood P, Hessl D, Schneider A, Campos L, Nguyen DV, Hagerman RJ. PMID: 20809278; PMCID: PMC2955238.
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    348. Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures. Am J Intellect Dev Disabil. 2010 Sep; 115(5):433-43. Utari A, Chonchaiya W, Rivera SM, Schneider A, Hagerman RJ, Faradz SM, Ethell IM, Nguyen DV. PMID: 20687826; PMCID: PMC4031088.
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    349. Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers. J Clin Psychiatry. 2011 Feb; 72(2):175-82. Bourgeois JA, Seritan AL, Casillas EM, Hessl D, Schneider A, Yang Y, Kaur I, Cogswell JB, Nguyen DV, Hagerman RJ. PMID: 20816038; PMCID: PMC4038118.
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    350. Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome. Biochem J. 2010 Aug 01; 429(3):545-52. Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C. PMID: 20513237; PMCID: PMC4011071.
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    351. Parkinsonism and cognitive decline in a fragile X mosaic male. Mov Disord. 2010 Jul 30; 25(10):1523-4. Hall D, Pickler L, Riley K, Tassone F, Hagerman R. PMID: 20568092; PMCID: PMC4051493.
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    352. Shifting the paradigm for autism treatments. Neurotherapeutics. 2010 Jul; 7(3):230-1. Hagerman RJ, Hendren RL. PMID: 20643374; PMCID: PMC4043294.
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    353. Fragile X: leading the way for targeted treatments in autism. Neurotherapeutics. 2010 Jul; 7(3):264-74. Wang LW, Berry-Kravis E, Hagerman RJ. PMID: 20643379; PMCID: PMC4084556.
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    354. An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS). J Psychiatr Res. 2011 Jan; 45(1):36-43. Hashimoto R, Backer KC, Tassone F, Hagerman RJ, Rivera SM. PMID: 20537351; PMCID: PMC2978252.
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    355. Aging in fragile X syndrome. J Neurodev Disord. 2010 Jun; 2(2):70-76. Utari A, Adams E, Berry-Kravis E, Chavez A, Scaggs F, Ngotran L, Boyd A, Hessl D, Gane LW, Tassone F, Tartaglia N, Leehey MA, Hagerman RJ. PMID: 20585378; PMCID: PMC2882562.
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    356. Early onset of neurological symptoms in fragile X premutation carriers exposed to neurotoxins. Neurotoxicology. 2010 Aug; 31(4):399-402. Paul R, Pessah IN, Gane L, Ono M, Hagerman PJ, Brunberg JA, Tassone F, Bourgeois JA, Adams PE, Nguyen DV, Hagerman R. PMID: 20466021; PMCID: PMC3918243.
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    357. Clinical report: a male with Down syndrome, fragile X syndrome, and autism. J Dev Behav Pediatr. 2010 May; 31(4):333-7. Stevens L, Tartaglia N, Hagerman R, Riley K. PMID: 20453578; PMCID: PMC3740577.
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    358. Abnormal N400 word repetition effects in fragile X-associated tremor/ataxia syndrome. Brain. 2010 May; 133(Pt 5):1438-50. Olichney JM, Chan S, Wong LM, Schneider A, Seritan A, Niese A, Yang JC, Laird K, Teichholtz S, Khan S, Tassone F, Hagerman R. PMID: 20410144; PMCID: PMC2859155.
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    359. Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome. Clin Genet. 2010 Jul; 78(1):38-46. Chonchaiya W, Nguyen DV, Au J, Campos L, Berry-Kravis EM, Lohse K, Mu Y, Utari A, Hervey C, Wang L, Sorensen P, Cook K, Gane L, Tassone F, Hagerman RJ. PMID: 20497189; PMCID: PMC4031089.
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    360. Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers. Am J Med Genet B Neuropsychiatr Genet. 2010 Apr 05; 153B(3):775-85. Adams PE, Adams JS, Nguyen DV, Hessl D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, Decarli C, Hagerman PJ, Hagerman RJ. PMID: 19908235; PMCID: PMC2868927.
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    361. Fragile X Syndrome and Premutation-Associated Disorders. . 2010 Mar 17; 397-411. Hagerman HR. .
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    362. Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio. Hum Mol Genet. 2010 Apr 15; 19(8):1618-32. Godler DE, Tassone F, Loesch DZ, Taylor AK, Gehling F, Hagerman RJ, Burgess T, Ganesamoorthy D, Hennerich D, Gordon L, Evans A, Choo KH, Slater HR. PMID: 20118148; PMCID: PMC2846165.
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    363. Plasma cytokine profiles in Fragile X subjects: is there a role for cytokines in the pathogenesis? Brain Behav Immun. 2010 Aug; 24(6):898-902. Ashwood P, Nguyen DV, Hessl D, Hagerman RJ, Tassone F. PMID: 20102735; PMCID: PMC3626458.
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    364. Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration. Hum Mol Genet. 2010 Jan 01; 19(1):196-208. Chen Y, Tassone F, Berman RF, Hagerman PJ, Hagerman RJ, Willemsen R, Pessah IN. PMID: 19846466; PMCID: PMC2792156.
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    365. Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back. Am J Med Genet A. 2010 Jan; 152A(1):4-24. Rauen KA, Schoyer L, McCormick F, Lin AE, Allanson JE, Stevenson DA, Gripp KW, Neri G, Carey JC, Legius E, Tartaglia M, Schubbert S, Roberts AE, Gelb BD, Shannon K, Gutmann DH, McMahon M, Guerra C, Fagin JA, Yu B, Aoki Y, Neel BG, Balmain A, Drake RR, Nolan GP, Zenker M, Bollag G, Sebolt-Leopold J, Gibbs JB, Silva AJ, Patton EE, Viskochil DH, Kieran MW, Korf BR, Hagerman RJ, Packer RJ, Melese T. PMID: 20014119; PMCID: PMC4051786.
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    366. Intergenerational effects of mutations in the fragile X mental retardation 1 gene. Fragile X: A model of X-linked mental retardation and neurodegeneration. . 2010 Jan 1; 3-18. Borodyanskaya BM, Coffey CS, Ono OM, Hagerman HR. .
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    367. Treatment and Management of FXTAS. . 2010 Jan 1; 137-154. Berry-Kravis BE, Hall HD, Leehey LM, Hagerman HR. .
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    368. Clinical Neurological Phenotype of FXTAS. . 2010 Jan 1; 1-16. Leehey LM, Berry-Kravis BE, Goetz GC, Hagerman HR. .
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    369. FRAGILE X SYNDROME AND ASSOCIATED DISORDERS IN ADULTHOOD. CONTINUUM Lifelong Learning in Neurology. 2009 Dec 1; 15(6, Childhood Neurologic Disorders in Adulthood):32-49. Hagerman HR. .
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    370. Broad clinical involvement in a family affected by the fragile X premutation. J Dev Behav Pediatr. 2009 Dec; 30(6):544-51. Chonchaiya W, Utari A, Pereira GM, Tassone F, Hessl D, Hagerman RJ. PMID: 19996900; PMCID: PMC2822648.
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    371. High-risk fragile x screening in Guatemala: use of a new blood spot polymerase chain reaction technique. Genet Test Mol Biomarkers. 2009 Dec; 13(6):855-9. Yuhas J, Walichiewicz P, Pan R, Zhang W, Casillas EM, Hagerman RJ, Tassone F. PMID: 19810826; PMCID: PMC2935836.
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    372. Conversion disorder in women with the FMR1 premutation. Am J Med Genet A. 2009 Nov; 149A(11):2501-6. Seritan AL, Schneider A, Olichney JM, Leehey MA, Akins RS, Hagerman RJ. PMID: 19842197; PMCID: PMC2783547.
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    373. Fibroblast phenotype in male carriers of FMR1 premutation alleles. Hum Mol Genet. 2010 Jan 15; 19(2):299-312. Garcia-Arocena D, Yang JE, Brouwer JR, Tassone F, Iwahashi C, Berry-Kravis EM, Goetz CG, Sumis AM, Zhou L, Nguyen DV, Campos L, Howell E, Ludwig A, Greco C, Willemsen R, Hagerman RJ, Hagerman PJ. PMID: 19864489; PMCID: PMC2796892.
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    374. A voxel-based morphometry comparison of regional gray matter between fragile X syndrome and autism. Psychiatry Res. 2009 Nov 30; 174(2):138-45. Wilson LB, Tregellas JR, Hagerman RJ, Rogers SJ, Rojas DC. PMID: 19853418; PMCID: PMC2783567.
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    375. Functional status of men with the fragile X premutation, with and without the tremor/ataxia syndrome (FXTAS). Int J Geriatr Psychiatry. 2009 Oct; 24(10):1101-9. Brega AG, Reynolds A, Bennett RE, Leehey MA, Bounds LS, Cogswell JB, Hagerman RJ, Hagerman PJ, Grigsby J. PMID: 19404994; PMCID: PMC4414034.
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    376. Imitation in fragile X syndrome. Implications for autism. Autism. 2009 Nov; 13(6):599-611. Macedoni-Luksic M, Greiss-Hess L, Rogers SJ, Gosar D, Lemons-Chitwood K, Hagerman R. PMID: 19770230; PMCID: PMC4929855.
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    377. FMR1 premutation in females diagnosed with multiple sclerosis. J Neurol Neurosurg Psychiatry. 2009 Jul; 80(7):812-4. Zhang L, Coffey S, Lua LL, Greco CM, Schafer JA, Brunberg J, Borodyanskaya M, Agius MA, Apperson M, Leehey M, Tartaglia N, Tassone F, Hagerman PJ, Hagerman RJ. PMID: 19531693.
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    378. Prepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 05; 150B(4):545-53. Hessl D, Berry-Kravis E, Cordeiro L, Yuhas J, Ornitz EM, Campbell A, Chruscinski E, Hervey C, Long JM, Hagerman RJ. PMID: 18785205; PMCID: PMC2693303.
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    379. A quantitative ELISA assay for the fragile x mental retardation 1 protein. J Mol Diagn. 2009 Jul; 11(4):281-9. Iwahashi C, Tassone F, Hagerman RJ, Yasui D, Parrott G, Nguyen D, Mayeur G, Hagerman PJ. PMID: 19460937; PMCID: PMC2710703.
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    380. A review of fragile X premutation disorders: expanding the psychiatric perspective. J Clin Psychiatry. 2009 Jun; 70(6):852-62. Bourgeois JA, Coffey SM, Rivera SM, Hessl D, Gane LW, Tassone F, Greco C, Finucane B, Nelson L, Berry-Kravis E, Grigsby J, Hagerman PJ, Hagerman RJ. PMID: 19422761; PMCID: PMC2705685.
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    381. The efficacy of melatonin for sleep problems in children with autism, fragile X syndrome, or autism and fragile X syndrome. J Clin Sleep Med. 2009 Apr 15; 5(2):145-50. Wirojanan J, Jacquemont S, Diaz R, Bacalman S, Anders TF, Hagerman RJ, Goodlin-Jones BL. PMID: 19968048; PMCID: PMC2670334.
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    382. A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome. J Neurodev Disord. 2009 Mar; 1(1):33-45. Hessl D, Nguyen DV, Green C, Chavez A, Tassone F, Hagerman RJ, Senturk D, Schneider A, Lightbody A, Reiss AL, Hall S. PMID: 19865612; PMCID: PMC2768415.
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    383. Covariate adjusted correlation analysis with application to FMR1 premutation female carrier data. Biometrics. 2009 Sep; 65(3):781-92. Sentürk D, Nguyen DV, Tassone F, Hagerman RJ, Carroll RJ, Hagerman PJ. PMID: 19173699; PMCID: PMC2748149.
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    384. A pilot open label, single dose trial of fenobam in adults with fragile X syndrome. J Med Genet. 2009 Apr; 46(4):266-71. Berry-Kravis E, Hessl D, Coffey S, Hervey C, Schneider A, Yuhas J, Hutchison J, Snape M, Tranfaglia M, Nguyen DV, Hagerman R. PMID: 19126569; PMCID: PMC2658751.
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    385. Fragile X syndrome -- from genes to cognition. Dev Disabil Res Rev. 2009; 15(4):333-42. Schneider A, Hagerman RJ, Hessl D. PMID: 20014363.
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    386. Advances in the treatment of fragile X syndrome. Pediatrics. 2009 Jan; 123(1):378-90. Hagerman RJ, Berry-Kravis E, Kaufmann WE, Ono MY, Tartaglia N, Lachiewicz A, Kronk R, Delahunty C, Hessl D, Visootsak J, Picker J, Gane L, Tranfaglia M. PMID: 19117905; PMCID: PMC2888470.
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    387. Fragile X: a family of disorders. Adv Pediatr. 2009; 56:165-86. Chonchaiya W, Schneider A, Hagerman RJ. PMID: 19968948; PMCID: PMC2921504.
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    388. Lifespan changes in working memory in fragile X premutation males. Brain Cogn. 2009 Apr; 69(3):551-8. Cornish KM, Kogan CS, Li L, Turk J, Jacquemont S, Hagerman RJ. PMID: 19114290; PMCID: PMC4158922.
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    389. Testing for fragile X gene mutations throughout the life span. JAMA. 2008 Nov 26; 300(20):2419-21. Hagerman RJ, Hagerman PJ. PMID: 19033593; PMCID: PMC2766594.
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    390. Autism profiles of males with fragile X syndrome. Am J Ment Retard. 2008 Nov; 113(6):427-38. Harris SW, Hessl D, Goodlin-Jones B, Ferranti J, Bacalman S, Barbato I, Tassone F, Hagerman PJ, Herman H, Hagerman RJ. PMID: 19127654; PMCID: PMC2629645.
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    391. Dementia in fragile X-associated tremor/ataxia syndrome (FXTAS): comparison with Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 05; 147B(7):1138-44. Seritan AL, Nguyen DV, Farias ST, Hinton L, Grigsby J, Bourgeois JA, Hagerman RJ. PMID: 18384046; PMCID: PMC2898561.
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    392. Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 05; 147B(6):859-72. Kogan CS, Turk J, Hagerman RJ, Cornish KM. PMID: 18165971.
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    393. Motor abilities of children diagnosed with fragile X syndrome with and without autism. J Intellect Disabil Res. 2009 Jan; 53(1):11-8. Zingerevich C, Greiss-Hess L, Lemons-Chitwood K, Harris SW, Hessl D, Cook K, Hagerman RJ. PMID: 18771512; PMCID: PMC2614297.
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    394. Clinical and neuropathologic findings in a woman with the FMR1 premutation and multiple sclerosis. Arch Neurol. 2008 Aug; 65(8):1114-6. Greco CM, Tassone F, Garcia-Arocena D, Tartaglia N, Coffey SM, Vartanian TK, Brunberg JA, Hagerman PJ, Hagerman RJ. PMID: 18695063; PMCID: PMC3081275.
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    395. Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder. Am J Med Genet A. 2008 Aug 01; 146A(15):1911-6. García-Nonell C, Ratera ER, Harris S, Hessl D, Ono MY, Tartaglia N, Marvin E, Tassone F, Hagerman RJ. PMID: 18627038; PMCID: PMC4097171.
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    396. Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease. Parkinsonism Relat Disord. 2009 Feb; 15(2):156-9. Hall DA, Howard K, Hagerman R, Leehey MA. PMID: 18565783; PMCID: PMC2685192.
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    397. Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene. Am J Med Genet A. 2008 Jun 15; 146A(12):1543-6. Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. PMID: 18478592; PMCID: PMC2766597.
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    398. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet A. 2008 Jun 15; 146A(12):1509-22. Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. PMID: 18481271; PMCID: PMC3056496.
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    399. Contrast detection in infants with fragile X syndrome. Vision Res. 2008 Jun; 48(13):1471-8. Farzin F, Whitney D, Hagerman RJ, Rivera SM. PMID: 18457856; PMCID: PMC2486371.
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    400. Altered hypothalamus-pituitary-adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndrome. Psychoneuroendocrinology. 2008 Jul; 33(6):863-73. Brouwer JR, Severijnen E, de Jong FH, Hessl D, Hagerman RJ, Oostra BA, Willemsen R. PMID: 18472227; PMCID: PMC4408208.
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    401. The fragile X continuum: new advances and perspectives. J Intellect Disabil Res. 2008 Jun; 52(Pt 6):469-82. Cornish K, Turk J, Hagerman R. PMID: 18444988.
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    402. Expanded clinical phenotype of women with the FMR1 premutation. Am J Med Genet A. 2008 Apr 15; 146A(8):1009-16. Coffey SM, Cook K, Tartaglia N, Tassone F, Nguyen DV, Pan R, Bronsky HE, Yuhas J, Borodyanskaya M, Grigsby J, Doerflinger M, Hagerman PJ, Hagerman RJ. PMID: 18348275; PMCID: PMC2888464.
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    403. Abnormal nerve conduction features in fragile X premutation carriers. Arch Neurol. 2008 Apr; 65(4):495-8. Soontarapornchai K, Maselli R, Fenton-Farrell G, Tassone F, Hagerman PJ, Hessl D, Hagerman RJ. PMID: 18413472; PMCID: PMC2888466.
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    404. A girl with fragile X premutation from sperm donation. Am J Med Genet A. 2008 Apr 01; 146A(7):888-92. Wirojanan J, Angkustsiri K, Tassone F, Gane LW, Hagerman RJ. PMID: 18286596.
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    405. Two boys with fragile x syndrome and hepatic tumors. J Pediatr Hematol Oncol. 2008 Mar; 30(3):239-41. Wirojanan J, Kraff J, Hawkins DS, Laird C, Gane LW, Angkustsiri K, Tassone F, Hagerman RJ. PMID: 18376289.
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    406. A quantitative assessment of tremor and ataxia in FMR1 premutation carriers using CATSYS. Am J Med Genet A. 2008 Mar 01; 146A(5):629-35. Aguilar D, Sigford KE, Soontarapornchai K, Nguyen DV, Adams PE, Yuhas JM, Tassone F, Hagerman PJ, Hagerman RJ. PMID: 18241072.
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    407. The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. J Clin Exp Neuropsychol. 2008 Nov; 30(8):853-69. Brega AG, Goodrich G, Bennett RE, Hessl D, Engle K, Leehey MA, Bounds LS, Paulich MJ, Hagerman RJ, Hagerman PJ, Cogswell JB, Tassone F, Reynolds A, Kooken R, Kenny M, Grigsby J. PMID: 18608667; PMCID: PMC4098148.
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    408. Fragile X syndrome with anxiety disorder and exceptional verbal intelligence. Am J Med Genet A. 2008 Feb 01; 146A(3):376-9. Angkustsiri K, Wirojanan J, Deprey LJ, Gane LW, Hagerman RJ. PMID: 18203169.
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    409. Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation. Brain Imaging Behav. 2008 Jan 18; 2(2):105-116. Koldewyn K, Hessl D, Adams J, Tassone F, Hagerman PJ, Hagerman RJ, Rivera SM. PMID: 19430586; PMCID: PMC2678852.
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    410. Fragile X-associated tremor/ataxia syndrome: an aging face of the fragile X gene. Arch Neurol. 2008 Jan; 65(1):19-25. Amiri K, Hagerman RJ, Hagerman PJ. PMID: 18195136.
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    411. Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology. 2008 Jan; 22(1):48-60. Grigsby J, Brega AG, Engle K, Leehey MA, Hagerman RJ, Tassone F, Hessl D, Hagerman PJ, Cogswell JB, Bennett RE, Cook K, Hall DA, Bounds LS, Paulich MJ, Reynolds A. PMID: 18211155.
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    412. Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems. Clin Interv Aging. 2008; 3(2):251-62. Hagerman RJ, Hall DA, Coffey S, Leehey M, Bourgeois J, Gould J, Zhang L, Seritan A, Berry-Kravis E, Olichney J, Miller JW, Fong AL, Carpenter R, Bodine C, Gane LW, Rainin E, Hagerman H, Hagerman PJ. PMID: 18686748; PMCID: PMC2546470.
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    413. Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex. 2008 Jun; 44(6):628-36. Cornish KM, Li L, Kogan CS, Jacquemont S, Turk J, Dalton A, Hagerman RJ, Hagerman PJ. PMID: 18472033; PMCID: PMC11060834.
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    414. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. Neurology. 2008 Apr 15; 70(16 Pt 2):1397-402. Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, Hagerman PJ. PMID: 18057320; PMCID: PMC2685188.
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    415. Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines. Mov Disord. 2007 Oct 31; 22(14):2018-30, quiz 2140. Berry-Kravis E, Abrams L, Coffey SM, Hall DA, Greco C, Gane LW, Grigsby J, Bourgeois JA, Finucane B, Jacquemont S, Brunberg JA, Zhang L, Lin J, Tassone F, Hagerman PJ, Hagerman RJ, Leehey MA. PMID: 17618523.
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    416. An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals. Hum Mol Genet. 2007 Dec 15; 16(24):3174-87. Ladd PD, Smith LE, Rabaia NA, Moore JM, Georges SA, Hansen RS, Hagerman RJ, Tassone F, Tapscott SJ, Filippova GN. PMID: 17921506.
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    417. Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome. Am J Med Genet A. 2007 Oct 01; 143A(19):2256-60. Hagerman RJ, Coffey SM, Maselli R, Soontarapornchai K, Brunberg JA, Leehey MA, Zhang L, Gane LW, Fenton-Farrell G, Tassone F, Hagerman PJ. PMID: 17726686.
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    418. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS). Neurology. 2007 Aug 28; 69(9):851-9. Adams JS, Adams PE, Nguyen D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, DeCarli C, Hagerman PJ, Hagerman RJ. PMID: 17724287.
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    419. Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome. Gen Hosp Psychiatry. 2007 Jul-Aug; 29(4):349-56. Bourgeois JA, Cogswell JB, Hessl D, Zhang L, Ono MY, Tassone F, Farzin F, Brunberg JA, Grigsby J, Hagerman RJ. PMID: 17591512; PMCID: PMC3991490.
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    420. CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS). Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 05; 144B(4):566-9. Tassone F, Adams J, Berry-Kravis EM, Cohen SS, Brusco A, Leehey MA, Li L, Hagerman RJ, Hagerman PJ. PMID: 17427188.
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    421. Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders. J Genet Couns. 2007 Oct; 16(5):593-606. McConkie-Rosell A, Abrams L, Finucane B, Cronister A, Gane LW, Coffey SM, Sherman S, Nelson LM, Berry-Kravis E, Hessl D, Chiu S, Street N, Vatave A, Hagerman RJ. PMID: 17497108.
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    422. Impairment of executive cognitive functioning in males with fragile X-associated tremor/ataxia syndrome. Mov Disord. 2007 Apr 15; 22(5):645-50. Grigsby J, Brega AG, Leehey MA, Goodrich GK, Jacquemont S, Loesch DZ, Cogswell JB, Epstein J, Wilson R, Jardini T, Gould E, Bennett RE, Hessl D, Cohen S, Cook K, Tassone F, Hagerman PJ, Hagerman RJ. PMID: 17266074.
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    423. The Prader-Willi phenotype of fragile X syndrome. J Dev Behav Pediatr. 2007 Apr; 28(2):133-8. Nowicki ST, Tassone F, Ono MY, Ferranti J, Croquette MF, Goodlin-Jones B, Hagerman RJ. PMID: 17435464.
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    424. A genetic etiology of pervasive developmental disorder guides treatment. Am J Psychiatry. 2007 Apr; 164(4):575-80. Solomon M, Hessl D, Chiu S, Hagerman R, Hendren R. PMID: 17403969.
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    425. Testicular and pituitary inclusion formation in fragile X associated tremor/ataxia syndrome. J Urol. 2007 Apr; 177(4):1434-7. Greco CM, Soontrapornchai K, Wirojanan J, Gould JE, Hagerman PJ, Hagerman RJ. PMID: 17382748.
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    426. A preliminary study of screening for risk of autism in children with fragile X syndrome: testing two risk cut-offs for the Checklist for Autism in Toddlers. J Intellect Disabil Res. 2007 Apr; 51(Pt 4):269-76. Scambler DJ, Hepburn SL, Hagerman RJ, Rogers SJ. PMID: 17326808.
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    427. Brief report: aggression and stereotypic behavior in males with fragile X syndrome--moderating secondary genes in a "single gene" disorder. J Autism Dev Disord. 2008 Jan; 38(1):184-9. Hessl D, Tassone F, Cordeiro L, Koldewyn K, McCormick C, Green C, Wegelin J, Yuhas J, Hagerman RJ. PMID: 17340199.
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    428. Fragile X syndrome vs fragile X-associated tremor/ataxia syndrome. Arch Neurol. 2007 Feb; 64(2):289; author reply 289-90. Leehey MA, Hagerman RJ, Hagerman PJ. PMID: 17296852.
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    429. Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene. Nat Clin Pract Neurol. 2007 Feb; 3(2):107-12. Hagerman PJ, Hagerman RJ. PMID: 17279084.
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    430. Early acceleration of head circumference in children with fragile x syndrome and autism. J Dev Behav Pediatr. 2007 Feb; 28(1):31-5. Chiu S, Wegelin JA, Blank J, Jenkins M, Day J, Hessl D, Tassone F, Hagerman R. PMID: 17353729.
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    431. Progression of tremor and ataxia in male carriers of the FMR1 premutation. Mov Disord. 2007 Jan 15; 22(2):203-6. Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, Hagerman PJ. PMID: 17133502.
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    432. Neuropathic features in fragile X premutation carriers. Am J Med Genet A. 2007 Jan 01; 143A(1):19-26. Berry-Kravis E, Goetz CG, Leehey MA, Hagerman RJ, Zhang L, Li L, Nguyen D, Hall DA, Tartaglia N, Cogswell J, Tassone F, Hagerman PJ. PMID: 17152065.
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    433. Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1. Lancet Neurol. 2007 Jan; 6(1):45-55. Jacquemont S, Hagerman RJ, Hagerman PJ, Leehey MA. PMID: 17166801.
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    434. Amygdala dysfunction in men with the fragile X premutation. Brain. 2007 Feb; 130(Pt 2):404-16. Hessl D, Rivera S, Koldewyn K, Cordeiro L, Adams J, Tassone F, Hagerman PJ, Hagerman RJ. PMID: 17166860.
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    435. Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X. Neurosci Biobehav Rev. 2007; 31(3):315-26. Loesch DZ, Bui QM, Dissanayake C, Clifford S, Gould E, Bulhak-Paterson D, Tassone F, Taylor AK, Hessl D, Hagerman R, Huggins RM. PMID: 17097142; PMCID: PMC2145511.
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    436. The FMR1 premutation and reproduction. Fertil Steril. 2007 Mar; 87(3):456-65. Wittenberger MD, Hagerman RJ, Sherman SL, McConkie-Rosell A, Welt CK, Rebar RW, Corrigan EC, Simpson JL, Nelson LM. PMID: 17074338.
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    437. Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome. Neurology. 2006 Oct 24; 67(8):1426-31. Cohen S, Masyn K, Adams J, Hessl D, Rivera S, Tassone F, Brunberg J, DeCarli C, Zhang L, Cogswell J, Loesch D, Leehey M, Grigsby J, Hagerman PJ, Hagerman R. PMID: 17060569.
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    438. Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome. Mov Disord. 2006 Oct; 21(10):1741-4. Hall DA, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Rice CD, Leehey MA. PMID: 16773616.
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    439. Effect of CX516, an AMPA-modulating compound, on cognition and behavior in fragile X syndrome: a controlled trial. J Child Adolesc Psychopharmacol. 2006 Oct; 16(5):525-40. Berry-Kravis E, Krause SE, Block SS, Guter S, Wuu J, Leurgans S, Decle P, Potanos K, Cook E, Salt J, Maino D, Weinberg D, Lara R, Jardini T, Cogswell J, Johnson SA, Hagerman R. PMID: 17069542.
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    440. Cognitive impairment in a 65-year-old male with the fragile X-associated tremor-ataxia syndrome (FXTAS). Cogn Behav Neurol. 2006 Sep; 19(3):165-71. Grigsby J, Leehey MA, Jacquemont S, Brunberg JA, Hagerman RJ, Wilson R, Epstein JH, Greco CM, Tassone F, Hagerman PJ. PMID: 16957495.
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    441. X inactivation and cellular mosaicism. JAMA. 2006 Aug 23; 296(8):930-1; author reply 931. Hagerman RJ, Hagerman PJ. PMID: 16926349.
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    442. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. J Med Genet. 2007 Mar; 44(3):200-4. Loesch DZ, Bui QM, Huggins RM, Mitchell RJ, Hagerman RJ, Tassone F. PMID: 16905681; PMCID: PMC2598026.
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    443. Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS). J Neurol Sci. 2006 Oct 25; 248(1-2):227-33. Grigsby J, Brega AG, Jacquemont S, Loesch DZ, Leehey MA, Goodrich GK, Hagerman RJ, Epstein J, Wilson R, Cogswell JB, Jardini T, Tassone F, Hagerman PJ. PMID: 16780889.
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    444. Size bias of fragile X premutation alleles in late-onset movement disorders. J Med Genet. 2006 Oct; 43(10):804-9. Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ. PMID: 16723388; PMCID: PMC2563171.
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    445. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation. J Dev Behav Pediatr. 2006 Apr; 27(2 Suppl):S137-44. Farzin F, Perry H, Hessl D, Loesch D, Cohen J, Bacalman S, Gane L, Tassone F, Hagerman P, Hagerman R. PMID: 16685180.
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    446. Prevalence of FMR1 repeat expansions in movement disorders. A systematic review. Neuroepidemiology. 2006; 26(3):151-5. Hall DA, Hagerman RJ, Hagerman PJ, Jacquemont S, Leehey MA. PMID: 16493202.
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    447. Lessons from fragile X regarding neurobiology, autism, and neurodegeneration. J Dev Behav Pediatr. 2006 Feb; 27(1):63-74. Hagerman RJ. PMID: 16511373.
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    448. Psychiatric phenotype of the fragile X-associated tremor/ataxia syndrome (FXTAS) in males: newly described fronto-subcortical dementia. J Clin Psychiatry. 2006 Jan; 67(1):87-94. Bacalman S, Farzin F, Bourgeois JA, Cogswell J, Goodlin-Jones BL, Gane LW, Grigsby J, Leehey MA, Tassone F, Hagerman RJ. PMID: 16426093.
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    449. Dementia with mood symptoms in a fragile X premutation carrier with the fragile X-associated tremor/ataxia syndrome: clinical intervention with donepezil and venlafaxine. J Neuropsychiatry Clin Neurosci. 2006; 18(2):171-7. Bourgeois JA, Farzin F, Brunberg JA, Tassone F, Hagerman P, Zhang L, Hessl D, Hagerman R. PMID: 16720793.
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    450. Chapter 10 Fragile X Syndrome and Fragile X-Associated Tremor/Ataxia Syndrome. . 2006 Jan 1; (Am. J. Med. Genet.841999):165-174. Hagerman HR, Hagerman HP, Hagerman HP. .
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    451. Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). Brain. 2006 Jan; 129(Pt 1):243-55. Greco CM, Berman RF, Martin RM, Tassone F, Schwartz PH, Chang A, Trapp BD, Iwahashi C, Brunberg J, Grigsby J, Hessl D, Becker EJ, Papazian J, Leehey MA, Hagerman RJ, Hagerman PJ. PMID: 16332642.
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    452. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 05; 139B(1):115-21. Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, Hagerman PJ, Hagerman RJ. PMID: 16184602.
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    453. Protein composition of the intranuclear inclusions of FXTAS. Brain. 2006 Jan; 129(Pt 1):256-71. Iwahashi CK, Yasui DH, An HJ, Greco CM, Tassone F, Nannen K, Babineau B, Lebrilla CB, Hagerman RJ, Hagerman PJ. PMID: 16246864.
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    454. Recent advances in fragile X: a model for autism and neurodegeneration. Curr Opin Psychiatry. 2005 Sep; 18(5):490-6. Hagerman RJ, Ono MY, Hagerman PJ. PMID: 16639106.
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    455. Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS). Neurology. 2005 Jul 26; 65(2):299-301. Hall DA, Berry-Kravis E, Jacquemont S, Rice CD, Cogswell J, Zhang L, Hagerman RJ, Hagerman PJ, Leehey MA. PMID: 16043804.
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    456. No evidence of paternal transmission of fragile X syndrome. Am J Med Genet A. 2005 Jul 01; 136(1):107-8; author reply 109-10. Steinbach D, Steinbach P. PMID: 15887276.
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    457. Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS? J Med Genet. 2005 Feb; 42(2):e14. Jacquemont S, Orrico A, Galli L, Sahota PK, Brunberg JA, Anichini C, Leehey M, Schaeffer S, Hagerman RJ, Hagerman PJ, Tassone F. PMID: 15689437; PMCID: PMC1735999.
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    458. Neural progenitor cells from an adult patient with fragile X syndrome. BMC Med Genet. 2005 Jan 14; 6:2. Schwartz PH, Tassone F, Greco CM, Nethercott HE, Ziaeian B, Hagerman RJ, Hagerman PJ. PMID: 15649335; PMCID: PMC545950.
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    459. GRAND ROUNDS: an atypical progressive dementia in a male carrier of the fragile X premutation: an example of fragile X-associated tremor/ataxia syndrome. Appl Neuropsychol. 2005; 12(3):169-78. Mothersead PK, Conrad K, Hagerman RJ, Greco CM, Hessl D, Tassone F. PMID: 16131344.
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    460. Autistic spectrum disorder and the fragile X premutation. J Dev Behav Pediatr. 2004 Dec; 25(6):392-8. Goodlin-Jones BL, Tassone F, Gane LW, Hagerman RJ. PMID: 15613987.
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    461. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. Brain. 2004 Dec; 127(Pt 12):2672-81. Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V, Chitnis X, McGuire P, Suckling J, Davies KE, Hagerman RJ, Hagerman PJ, Murphy KC, Murphy DG. PMID: 15483045.
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    462. Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach. J Child Psychol Psychiatry. 2004 Sep; 45(6):1042-53. Cornish KM, Turk J, Wilding J, Sudhalter V, Munir F, Kooy F, Hagerman R. PMID: 15257661.
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    463. Paternal transmission of fragile X syndrome. Am J Med Genet A. 2004 Aug 30; 129A(2):184-9. Zeesman S, Zwaigenbaum L, Whelan DT, Hagerman RJ, Tassone F, Taylor SA. PMID: 15316964.
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    464. Genetic counseling for families of patients with fragile X syndrome. JAMA. 2004 Jun 23; 291(24):2945; author reply 2945-6. Barrett SK, Drazin T, Rosa D, Kupchik GS. PMID: 15213204.
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    465. Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome. Am J Ment Retard. 2004 May; 109(3):208-18. Philofsky A, Hepburn SL, Hayes A, Hagerman R, Rogers SJ. PMID: 15072521.
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    466. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. Am J Hum Genet. 2004 May; 74(5):1051-6. Hagerman RJ, Leavitt BR, Farzin F, Jacquemont S, Greco CM, Brunberg JA, Tassone F, Hessl D, Harris SW, Zhang L, Jardini T, Gane LW, Ferranti J, Ruiz L, Leehey MA, Grigsby J, Hagerman PJ. PMID: 15065016; PMCID: PMC1181968.
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    467. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome. J Med Genet. 2004 Apr; 41(4):e43. Tassone F, Hagerman RJ, Garcia-Arocena D, Khandjian EW, Greco CM, Hagerman PJ. PMID: 15060119; PMCID: PMC1735735.
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    468. The fragile-X premutation: a maturing perspective. Am J Hum Genet. 2004 May; 74(5):805-16. Hagerman PJ, Hagerman RJ. PMID: 15052536; PMCID: PMC1181976.
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    469. Aging in individuals with the FMR1 mutation. Am J Ment Retard. 2004 Mar; 109(2):154-64. Jacquemont S, Farzin F, Hall D, Leehey M, Tassone F, Gane L, Zhang L, Grigsby J, Jardini T, Lewin F, Berry-Kravis E, Hagerman PJ, Hagerman RJ. PMID: 15000674; PMCID: PMC3249442.
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    470. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population. JAMA. 2004 Jan 28; 291(4):460-9. Jacquemont S, Hagerman RJ, Leehey MA, Hall DA, Levine RA, Brunberg JA, Zhang L, Jardini T, Gane LW, Harris SW, Herman K, Grigsby J, Greco CM, Berry-Kravis E, Tassone F, Hagerman PJ. PMID: 14747503.
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    471. A neuropsychological investigation of male premutation carriers of fragile X syndrome. Neuropsychologia. 2004; 42(14):1934-47. Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG. PMID: 15381024.
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    472. Preface: fragile X syndrome: frontiers of understanding gene-brain-behavior relationships. Ment Retard Dev Disabil Res Rev. 2004; 10(1):1-2. Crnic LS, Hagerman R. PMID: 14994281.
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    473. Phenotypic variation and FMRP levels in fragile X. Ment Retard Dev Disabil Res Rev. 2004; 10(1):31-41. Loesch DZ, Huggins RM, Hagerman RJ. PMID: 14994286.
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    474. Fragile X-associated tremor/ataxia syndrome (FXTAS). Ment Retard Dev Disabil Res Rev. 2004; 10(1):25-30. Hagerman PJ, Hagerman RJ. PMID: 14994285.
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    475. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X. Neuropsychology. 2003 Oct; 17(4):646-657. Loesch DZ, Bui QM, Grigsby J, Butler E, Epstein J, Huggins RM, Taylor AK, Hagerman RJ. PMID: 14599277.
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    476. Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis. Am J Med Genet A. 2003 Sep 15; 122A(1):13-23. Loesch DZ, Huggins RM, Bui QM, Taylor AK, Pratt C, Epstein J, Hagerman RJ. PMID: 12949966.
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    477. Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment. Am J Med Genet A. 2003 Jun 01; 119A(2):111-20. Thomas JA, Johnson J, Peterson Kraai TL, Wilson R, Tartaglia N, LeRoux J, Beischel L, McGavran L, Hagerman RJ. PMID: 12749048.
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    478. Tremor and ataxia in fragile X premutation carriers: blinded videotape study. Ann Neurol. 2003 May; 53(5):616-23. Berry-Kravis E, Lewin F, Wuu J, Leehey M, Hagerman R, Hagerman P, Goetz CG. PMID: 12730995.
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    479. Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective. Am J Med Genet A. 2003 Apr 15; 118A(2):127-34. Loesch DZ, Huggins RM, Bui QM, Taylor AK, Hagerman RJ. PMID: 12655493.
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    480. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet. 2003 Apr; 72(4):869-78. Jacquemont S, Hagerman RJ, Leehey M, Grigsby J, Zhang L, Brunberg JA, Greco C, Des Portes V, Jardini T, Levine R, Berry-Kravis E, Brown WT, Schaeffer S, Kissel J, Tassone F, Hagerman PJ. PMID: 12638084; PMCID: PMC1180350.
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    481. The fragile X premutation presenting as essential tremor. Arch Neurol. 2003 Jan; 60(1):117-21. Leehey MA, Munhoz RP, Lang AE, Brunberg JA, Grigsby J, Greco C, Jacquemont S, Tassone F, Lozano AM, Hagerman PJ, Hagerman RJ. PMID: 12533098.
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    482. A cerebellar tremor/ataxia syndrome among fragile X premutation carriers. Cytogenet Genome Res. 2003; 100(1-4):206-12. Hagerman PJ, Greco CM, Hagerman RJ. PMID: 14526182.
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    483. Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis. J Dev Behav Pediatr. 2002 Dec; 23(6):416-23. Loesch DZ, Huggins RM, Bui QM, Epstein JL, Taylor AK, Hagerman RJ. PMID: 12476071.
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    484. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations. RNA. 2002 Dec; 8(12):1482-8. Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C. PMID: 12515381; PMCID: PMC1370354.
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    485. Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. AJNR Am J Neuroradiol. 2002 Nov-Dec; 23(10):1757-66. Brunberg JA, Jacquemont S, Hagerman RJ, Berry-Kravis EM, Grigsby J, Leehey MA, Tassone F, Brown WT, Greco CM, Hagerman PJ. PMID: 12427636; PMCID: PMC8185834.
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    486. Double-blind, placebo-controlled study of risperidone for the treatment of disruptive behaviors in children with subaverage intelligence. Am J Psychiatry. 2002 Aug; 159(8):1337-46. Aman MG, De Smedt G, Derivan A, Lyons B, Findling RL, Risperidone Disruptive Behavior Study Group. PMID: 12153826.
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    487. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain. 2002 Aug; 125(Pt 8):1760-71. Greco CM, Hagerman RJ, Tassone F, Chudley AE, Del Bigio MR, Jacquemont S, Leehey M, Hagerman PJ. PMID: 12135967.
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    488. Tremor/Ataxia syndrome in fragile X carrier males. Movement Disorders. 2002 Jul 1; 17(4):744-745. Leehey LM, Hagerman HR, Landau LW, Grigsby GJ, Tassone TF, Hagerman HP, Hagerman HP. .
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    489. The fragile X premutation: into the phenotypic fold. Curr Opin Genet Dev. 2002 Jun; 12(3):278-83. Hagerman RJ, Hagerman PJ. PMID: 12076670.
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    490. Influence of stimulants on electrodermal studies in Fragile X syndrome. Microsc Res Tech. 2002 May 01; 57(3):168-73. Hagerman RJ, Miller LJ, McGrath-Clarke J, Riley K, Goldson E, Harris SW, Simon J, Church K, Bonnell J, Ognibene TC, McIntosh DN. PMID: 12112453.
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    491. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr. 2001 Dec; 22(6):409-17. Rogers SJ, Wehner DE, Hagerman R. PMID: 11773805.
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    492. [Fragile X syndrome: a model of gene-brain-behaviour relationships]. Rev Neurol. 2001 Oct; 33 Suppl 1:S51-7. Hagerman RJ, Hagerman PJ. PMID: 12447820.
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    493. Fragile X syndrome: a model of gene-brain-behavior relationships. Mol Genet Metab. 2001 Sep-Oct; 74(1-2):89-97. Hagerman RJ, Hagerman PJ. PMID: 11592806.
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    494. Auditory evoked magnetic fields in adults with fragile X syndrome. Neuroreport. 2001 Aug 08; 12(11):2573-6. Rojas DC, Benkers TL, Rogers SJ, Teale PD, Reite ML, Hagerman RJ. PMID: 11496151.
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    495. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology. 2001 Jul 10; 57(1):127-30. Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J, Grigsby J, Gage B, Hagerman PJ. PMID: 11445641.
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    496. A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA. J Med Genet. 2001 Jul; 38(7):453-6. Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. PMID: 11432964; PMCID: PMC1757182.
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    497. Sensory modulation dysfunction in children with attention-deficit-hyperactivity disorder. Dev Med Child Neurol. 2001 Jun; 43(6):399-406. Mangeot SD, Miller LJ, McIntosh DN, McGrath-Clarke J, Simon J, Hagerman RJ, Goldson E. PMID: 11409829.
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    498. Profile of cognitive functioning in women with the fragile X mutation. Neuropsychology. 2001 Apr; 15(2):290-9. Bennetto L, Pennington BF, Porter D, Taylor AK, Hagerman RJ. PMID: 11324870.
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    499. Discourse processing in women with fragile x syndrome: evidence for a deficit establishing coherence. Cogn Neuropsychol. 2001 Feb 01; 18(1):1-18. Simon JA, Keenan JM, Pennington BF, Taylor AK, Hagerman RJ. PMID: 20945204.
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    500. Melatonin profiles and sleep characteristics in boys with fragile X syndrome: a preliminary study. Am J Med Genet. 2000 Dec 11; 95(4):307-15. Gould EL, Loesch DZ, Martin MJ, Hagerman RJ, Armstrong SM, Huggins RM. PMID: 11186882.
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    501. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA. Am J Med Genet. 2000 Sep 18; 94(3):232-6. Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. PMID: 10995510.
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    502. Clinical involvement and protein expression in individuals with the FMR1 premutation. Am J Med Genet. 2000 Mar 13; 91(2):144-52. Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. PMID: 10748416.
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    503. Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome. Am J Hum Genet. 2000 Jan; 66(1):6-15. Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. PMID: 10631132; PMCID: PMC1288349.
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    504. Transcription of the FMR1 gene in individuals with fragile X syndrome. Am J Med Genet. 2000; 97(3):195-203. Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. PMID: 11449488.
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    505. Sensory-modulation disruption, electrodermal responses, and functional behaviors. Dev Med Child Neurol. 1999 Sep; 41(9):608-15. McIntosh DN, Miller LJ, Shyu V, Hagerman RJ. PMID: 10503919.
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    506. Fragile X syndrome: new developments. Current Opinion in Psychiatry. 1999 Sep 1; 12(5):573-578. Harris HS, Hagerman HR. .
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    507. Epilepsy and EEG findings in males with fragile X syndrome. Epilepsia. 1999 Aug; 40(8):1092-9. Musumeci SA, Hagerman RJ, Ferri R, Bosco P, Dalla Bernardina B, Tassinari CA, De Sarro GB, Elia M. PMID: 10448821.
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    508. Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development. Am J Med Genet. 1999 Jul 30; 85(3):197-201. Freedenberg DL, Gane LW, Richards CS, Lampe M, Hills J, O'Connor R, Manchester D, Taylor A, Tassone F, Hulseberg D, Hagerman RJ, Patil SR. PMID: 10398226.
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    509. Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome. Am J Med Genet. 1999 May 28; 84(3):233-9. Taylor AK, Tassone F, Dyer PN, Hersch SM, Harris JB, Greenough WT, Hagerman RJ. PMID: 10331599.
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    510. Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutation. Am J Med Genet. 1999 May 28; 84(3):240-4. Tassone F, Hagerman RJ, Gane LW, Taylor AK. PMID: 10331600.
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    511. FMRP expression as a potential prognostic indicator in fragile X syndrome. Am J Med Genet. 1999 May 28; 84(3):250-61. Tassone F, Hagerman RJ, Iklé DN, Dyer PN, Lampe M, Willemsen R, Oostra BA, Taylor AK. PMID: 10331602.
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    512. Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997. Am J Med Genet. 1999 Apr 02; 83(4):221-36. Holden JJ, Percy M, Allingham-Hawkins D, Brown WT, Chiurazzi P, Fisch G, Gane L, Gunter C, Hagerman R, Jenkins EC, Kooy RF, Lubs HA, Murray A, Neri G, Schwartz C, Tranebjaerg L, Villard L, Willems PJ. PMID: 10208154.
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    513. Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report. Am J Med Genet. 1999 Apr 02; 83(4):268-79. Miller LJ, McIntosh DN, McGrath J, Shyu V, Lampe M, Taylor AK, Tassone F, Neitzel K, Stackhouse T, Hagerman RJ. PMID: 10208160.
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    514. Fragile X syndrome and selective mutism. Am J Med Genet. 1999 Apr 02; 83(4):313-7. Hagerman RJ, Hills J, Scharfenaker S, Lewis H. PMID: 10208168.
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    515. Compound heterozygous female with fragile X syndrome. Am J Med Genet. 1999 Apr 02; 83(4):318-21. Linden MG, Tassone F, Gane LW, Hills JL, Hagerman RJ, Taylor AK. PMID: 10208169.
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    516. Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome. Developmental Disabilities Research Reviews. 1999 Jan 1; 5(4):305-313. Hagerman HR. .
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    517. Phenotypic involvement in females with the FMR1 gene mutation. Am J Ment Retard. 1998 May; 102(6):590-601. Riddle JE, Cheema A, Sobesky WE, Gardner SC, Taylor AK, Pennington BF, Hagerman RJ. PMID: 9606468.
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    518. Fragile X: treatment of hyperactivity. Pediatrics. 1997 May; 99(5):753. Hagerman R. PMID: 9157389.
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    519. Fragile X syndrome. Molecular and clinical insights and treatment issues. West J Med. 1997 Feb; 166(2):129-37. Hagerman RJ. PMID: 9109330; PMCID: PMC1304031.
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    520. Molecular/clinical correlations in females with fragile X. Am J Med Genet. 1996 Aug 09; 64(2):340-5. Sobesky WE, Taylor AK, Pennington BF, Bennetto L, Porter D, Riddle J, Hagerman RJ. PMID: 8844077.
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    521. A controlled study of longitudinal IQ changes in females and males with fragile X syndrome. Am J Med Genet. 1996 Aug 09; 64(2):350-5. Wright-Talamante C, Cheema A, Riddle JE, Luckey DW, Taylor AK, Hagerman RJ. PMID: 8844079.
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    522. Experiences and attitudes concerning genetic testing and insurance in a Colorado population: a survey of families diagnosed with fragile X syndrome. Am J Med Genet. 1996 Aug 09; 64(2):378-81. Wingrove KJ, Norris J, Barton PL, Hagerman R. PMID: 8844087.
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    523. Expanding the role of the genetic counselor. Am J Med Genet. 1996 Aug 09; 64(2):382-7. Staley-Gane L, Flynn L, Neitzel K, Cronister A, Hagerman RJ. PMID: 8844088.
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    524. Molecular-clinical correlations in males with an expanded FMR1 mutation. Am J Med Genet. 1996 Aug 09; 64(2):388-94. Merenstein SA, Sobesky WE, Taylor AK, Riddle JE, Tran HX, Hagerman RJ. PMID: 8844089.
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    525. Seventh International Workshop on the Fragile X and X-linked Mental Retardation. Am J Med Genet. 1996 Jul 12; 64(1):1-14. Tranebjaerg L, Lubs HA, Borghgraef M, Brown WT, Fisch G, Fryns JP, Hagerman R, Jacobs PA, Mandel JL, Mulley J, Oostra B, Schwartz C, Sherman S, Willard H, Willems P. PMID: 8826442.
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    526. Trajectories and profiles of adaptive behavior in males with fragile X syndrome: multicenter studies. J Autism Dev Disord. 1996 Jun; 26(3):287-301. Dykens E, Ort S, Cohen I, Finucane B, Spiridigliozzi G, Lachiewicz A, Reiss A, Freund L, Hagerman R, O'Connor R. PMID: 8792261.
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    527. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range. Pediatrics. 1996 Jan; 97(1):122-6. Hagerman RJ, Staley LW, O'Conner R, Lugenbeel K, Nelson D, McLean SD, Taylor A. PMID: 8545206.
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    528. Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolism. Am J Med Genet. 1995 Dec 18; 60(6):480-93. Schapiro MB, Murphy DG, Hagerman RJ, Azari NP, Alexander GE, Miezejeski CM, Hinton VJ, Horwitz B, Haxby JV, Kumar A, et al. PMID: 8825884.
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    529. Fragile X syndrome in a normal IQ male with learning and emotional problems. J Am Acad Child Adolesc Psychiatry. 1994 Nov-Dec; 33(9):1316-21. Merenstein SA, Shyu V, Sobesky WE, Staley L, Berry-Kravis E, Nelson DL, Lugenbeel KA, Taylor AK, Pennington BF, Hagerman RJ. PMID: 7995799.
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    530. Social cognition skills among females with fragile X. J Autism Dev Disord. 1994 Aug; 24(4):473-85. Mazzocco MM, Pennington BF, Hagerman RJ. PMID: 7961331.
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    531. Sixth international workshop on the fragile X and X-linked mental retardation. Am J Med Genet. 1994 Jul 15; 51(4):281-93. Sutherland GR, Brown WT, Hagerman R, Jenkins E, Lubs H, Mandel JL, Nelson D, Neri G, Partington MW, Richards RI, et al. PMID: 7942989.
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    532. High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression. Am J Med Genet. 1994 Jul 15; 51(4):298-308. Hagerman RJ, Hull CE, Safanda JF, Carpenter I, Staley LW, O'Connor RA, Seydel C, Mazzocco MM, Snow K, Thibodeau SN, et al. PMID: 7942991.
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    533. Emotional and neurocognitive deficits in fragile X. Am J Med Genet. 1994 Jul 15; 51(4):378-85. Sobesky WE, Pennington BF, Porter D, Hull CE, Hagerman RJ. PMID: 7943003.
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    534. Obstetrical and gynecological complications in fragile X carriers: a multicenter study. Am J Med Genet. 1994 Jul 15; 51(4):400-2. Schwartz CE, Dean J, Howard-Peebles PN, Bugge M, Mikkelsen M, Tommerup N, Hull C, Hagerman R, Holden JJ, Stevenson RE. PMID: 7943006.
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    535. Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing. Am J Med Genet. 1994 Jul 15; 51(4):474-81. Hagerman RJ, Wilson P, Staley LW, Lang KA, Fan T, Uhlhorn C, Jewell-Smart S, Hull C, Drisko J, Flom K, et al. PMID: 7943023.
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    536. Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses. Am J Med Genet. 1994 Jul 15; 51(4):503-6. Sherman SL, Maddalena A, Howard-Peebles PN, Brown WT, Nolin S, Jenkins E, Schwartz C, Tarrelton J, Shapiro LR, Smits AP, et al. PMID: 7943029.
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    537. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome. JAMA. 1994 Feb 16; 271(7):507-14. Taylor AK, Safanda JF, Fall MZ, Quince C, Lang KA, Hull CE, Carpenter I, Staley LW, Hagerman RJ. PMID: 8301764.
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    538. Symptoms of schizotypal personality disorder in fragile X women. J Am Acad Child Adolesc Psychiatry. 1994 Feb; 33(2):247-55. Sobesky WE, Hull CE, Hagerman RJ. PMID: 8150797.
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    539. Behavioral and psychiatric disorders in adult male carriers of fragile X. J Am Acad Child Adolesc Psychiatry. 1994 Feb; 33(2):256-64. Dorn MB, Mazzocco MM, Hagerman RJ. PMID: 8150798.
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    540. Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population. Am J Hum Genet. 1993 Dec; 53(6):1217-28. Snow K, Doud LK, Hagerman R, Pergolizzi RG, Erster SH, Thibodeau SN. PMID: 7902673; PMCID: PMC1682501.
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    541. A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome. Am J Dis Child. 1993 Nov; 147(11):1236-41. Hull C, Hagerman RJ. PMID: 8237919.
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    542. The neurocognitive phenotype of female carriers of fragile X: additional evidence for specificity. J Dev Behav Pediatr. 1993 Oct; 14(5):328-35. Mazzocco MM, Pennington BF, Hagerman RJ. PMID: 8254064.
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    543. Molecular-clinical correlations in children and adults with fragile X syndrome. Am J Dis Child. 1993 Jul; 147(7):723-6. Staley LW, Hull CE, Mazzocco MM, Thibodeau SN, Snow K, Wilson VL, Taylor A, McGavran L, Weiner D, Riddle J, et al. PMID: 8322740.
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    544. Fragile X syndrome and failure to thrive. Am J Dis Child. 1993 Jun; 147(6):605-7. Goldson E, Hagerman RJ. PMID: 8506819.
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    545. Specific frontal lobe deficits among women with the fragile X gene. J Am Acad Child Adolesc Psychiatry. 1992 Nov; 31(6):1141-8. Mazzocco MM, Hagerman RJ, Cronister-Silverman A, Pennington BF. PMID: 1429419.
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    546. Annotation: fragile X syndrome: advances and controversy. J Child Psychol Psychiatry. 1992 Oct; 33(7):1127-39. Hagerman RJ. PMID: 1400696.
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    547. The fragile X syndrome. Dev Med Child Neurol. 1992 Sep; 34(9):826-32. Goldson E, Hagerman RJ. PMID: 1526353.
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    548. Standards for selected anthropometric measurements in males with the fragile X syndrome. Pediatrics. 1992 Jun; 89(6 Pt 1):1059-62. Butler MG, Brunschwig A, Miller LK, Hagerman RJ. PMID: 1594348; PMCID: PMC5459612.
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    549. Clinical conundrums in fragile X syndrome. Nat Genet. 1992 Jun; 1(3):157-8. Hagerman R. PMID: 1303227.
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    550. Verbal learning and memory among heterozygous fragile X females. Am J Med Genet. 1992 Apr 15-May 1; 43(1-2):111-5. Grigsby J, Kemper MB, Hagerman RJ. PMID: 1605177.
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    551. Analysis of mutations at the fragile X locus using the DNA probe Ox1.9. Am J Med Genet. 1992 Apr 15-May 1; 43(1-2):244-54. Snow K, Doud L, Hagerman R, Hull C, Hirst MC, Davies KE, Thibodeau SL. PMID: 1605198.
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    552. Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendation. Am J Med Genet. 1992 Apr 15-May 1; 43(1-2):61-4. Reiss AL, Cianchetti C, Cohen IL, DeVries B, Hagerman R, Hinton V, Froster U, Lachiewicz A, Mazzocco M, Sobesky W, et al. PMID: 1605236.
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    553. Problem solving limitations among cytogenetically expressing fragile X women. Am J Med Genet. 1992 Apr 15-May 1; 43(1-2):78-86. Mazzocco MM, Hagerman RJ, Pennington BF. PMID: 1605239.
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    554. Fifth international workshop on fragile X and X-linked mental retardation. Am J Med Genet. 1992 Apr 15-May 1; 43(1-2):5-27. Mandel JL, Hagerman R, Froster U, Brown WT, Jenkins EC, Jacobs P, Lubs H, Neri G. PMID: 1605233.
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    555. Girls with fragile X syndrome: physical and neurocognitive status and outcome. Pediatrics. 1992 Mar; 89(3):395-400. Hagerman RJ, Jackson C, Amiri K, Silverman AC, O'Connor R, Sobesky W. PMID: 1741210.
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    556. Attention deficit hyperactivity disorder in children: diagnosis, treatment, and follow-up. J Pediatr Health Care. 1992 Jan-Feb; 6(1):2-11. Murphy MA, Hagerman RJ. PMID: 1312153.
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    557. Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome. Arch Gen Psychiatry. 1992 Jan; 49(1):54-60. Freund LS, Reiss AL, Hagerman R, Vinogradov S. PMID: 1728251.
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    558. Heterozygous fragile X female: historical, physical, cognitive, and cytogenetic features. Am J Med Genet. 1991 Feb-Mar; 38(2-3):269-74. Cronister A, Schreiner R, Wittenberger M, Amiri K, Harris K, Hagerman RJ. PMID: 2018071.
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    559. Fragile X checklist. Am J Med Genet. 1991 Feb-Mar; 38(2-3):283-7. Hagerman RJ, Amiri K, Cronister A. PMID: 2018072.
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    560. Mental impairment in cytogenetically positive fragile X females. Am J Med Genet. 1991 Feb-Mar; 38(2-3):503-4. Cronister A, Hagerman RJ, Wittenberger M, Amiri K. PMID: 2018094.
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    561. Cognitive profiles of the carrier fragile X woman. Am J Med Genet. 1991 Feb-Mar; 38(2-3):505-8. Brainard SS, Schreiner RA, Hagerman RJ. PMID: 2018095.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    562. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. Am J Med Genet. 1991 Feb-Mar; 38(2-3):158-72. Brown WT, Jenkins E, Neri G, Lubs H, Shapiro LR, Davies KE, Sherman S, Hagerman R, Laird C. PMID: 1673296.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    563. Orthopaedic aspects of fragile-X syndrome. J Bone Joint Surg Am. 1990 Jul; 72(6):889-96. Davids JR, Hagerman RJ, Eilert RE. PMID: 2195034.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    564. Developmental implications of changing trajectories of IQ in males with fragile X syndrome. J Am Acad Child Adolesc Psychiatry. 1990 Mar; 29(2):214-9. Hodapp RM, Dykens EM, Hagerman RJ, Schreiner R, Lachiewicz AM, Leckman JF. PMID: 2324062.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    565. Neuropsychological dysfunction among affected heterozygous fragile X females. Am J Med Genet. 1990 Jan; 35(1):28-35. Grigsby JP, Kemper MB, Hagerman RJ, Myers CS. PMID: 1689106.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    566. The usefulness of cytogenetic and DNA linkage analysis in counseling families with fragile X syndrome. Birth Defects Orig Artic Ser. 1990; 26(3):238-53. Silverman AC, Thibodeau SN, Jirikowic J, Hagerman RJ. PMID: 2092851.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    567. Fragile X syndrome: a genetic etiology for developmental Gerstmann's syndrome. Arch Neurol. 1989 Dec; 46(12):1269-70. Grisby J, Haggerman R. PMID: 2590008.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    568. Parental inheritance and psychological disability in fragile X females. Am J Hum Genet. 1989 Nov; 45(5):697-705. Reiss AL, Freund L, Vinogradov S, Hagerman R, Cronister A. PMID: 2816940; PMCID: PMC1683434.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    569. Longitudinal IQ changes in fragile X males. Am J Med Genet. 1989 Aug; 33(4):513-8. Hagerman RJ, Schreiner RA, Kemper MB, Wittenberger MD, Zahn B, Habicht K. PMID: 2596514.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    570. Psychopathology in fragile X syndrome. Am J Orthopsychiatry. 1989 Jan; 59(1):142-52. Hagerman RJ, Sobesky WE. PMID: 2648854.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    571. Fragile X syndrome. J Pediatr Health Care. 1989 Jan-Feb; 3(1):9-19. Cronister AE, Hagerman RJ. PMID: 2644412.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    572. Institutional screening for the fragile X syndrome. Am J Dis Child. 1988 Nov; 142(11):1216-21. Hagerman R, Berry R, Jackson AW, Campbell J, Smith AC, McGavran L. PMID: 3177330.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    573. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome. Hum Genet. 1988 Jul; 79(3):219-27. Thibodeau SN, Dorkins HR, Faulk KR, Berry R, Smith AC, Hagerman R, King A, Davies KE. PMID: 3402993.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    574. A controlled trial of stimulant medication in children with the fragile X syndrome. Am J Med Genet. 1988 May-Jun; 30(1-2):377-92. Hagerman RJ, Murphy MA, Wittenberger MD. PMID: 3052064.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCTClinical Trials
    575. Cognitive profiles of boys with the fragile X syndrome. Am J Med Genet. 1988 May-Jun; 30(1-2):191-200. Kemper MB, Hagerman RJ, Altshul-Stark D. PMID: 3177444.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    576. Crown size asymmetry in males with fra (X) or Martin-Bell syndrome. Am J Med Genet. 1988 May-Jun; 30(1-2):185-90. Peretz B, Ever-Hadani P, Casamassimo P, Eidelman E, Shellhart C, Hagerman R. PMID: 2972204.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    577. Aortic hypoplasia and cardiac valvular abnormalities in a boy with fragile X syndrome. Am J Med Genet. 1988 May-Jun; 30(1-2):83-98. Waldstein G, Hagerman R. PMID: 2972207.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    578. Multilocus analysis of the fragile X syndrome. Hum Genet. 1988 Mar; 78(3):201-5. Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R, et al. PMID: 3162224.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    579. Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study. Am J Ment Retard. 1988 Mar; 92(5):436-46. Cohen IL, Fisch GS, Sudhalter V, Wolf-Schein EG, Hanson D, Hagerman R, Jenkins EC, Brown WT. PMID: 2965890.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    580. Psychiatric disability in female carriers of the fragile X chromosome. Arch Gen Psychiatry. 1988 Jan; 45(1):25-30. Reiss AL, Hagerman RJ, Vinogradov S, Abrams M, King RJ. PMID: 3337608.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    581. Fragile-X chromosome and learning disability. J Am Acad Child Adolesc Psychiatry. 1987 Nov; 26(6):938. Hagerman RJ. PMID: 3429417.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    582. Fragile X syndrome. Curr Probl Pediatr. 1987 Nov; 17(11):621-74. Hagerman RJ. PMID: 3325231.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    583. Cognitive variability in the fragile X syndrome. Am J Med Genet. 1987 Sep; 28(1):13-5. Chudley AE, de von Flindt R, Hagerman RJ. PMID: 3674106.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    584. Speech-language and the fragile X syndrome: initial findings. ASHA. 1987 Jul; 29(7):35-8. Wolf-Schein EG, Sudhalter V, Cohen IL, Fisch GS, Hanson D, Pfadt AG, Hagerman R, Jenkins E, Brown WT. PMID: 2956959.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    585. Fragile X syndrome. J Pediatr. 1987 Jun; 110(6):821-31. Chudley AE, Hagerman RJ. PMID: 3295158.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    586. Possible Similarities Between the Fragile X and Asperger's Syndromes-Reply. JAMA Pediatrics. 1987 Jun 1; 141(6):601-602. Hagerman HR. .
      View in: Publisher Site   Mentions:
    587. An association between recurrent otitis media in infancy and later hyperactivity. Clin Pediatr (Phila). 1987 May; 26(5):253-7. Hagerman RJ, Falkenstein AR. PMID: 3568530.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    588. Recurrent otitis media in the fragile X syndrome. Am J Dis Child. 1987 Feb; 141(2):184-7. Hagerman RJ, Altshul-Stark D, McBogg P. PMID: 3812386.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    589. Fragile X syndrome: skin elastin abnormalities. Birth Defects Orig Artic Ser. 1987; 23(1):103-14. Waldstein G, Mierau G, Ahmad R, Thibodeau SN, Hagerman RJ, Caldwell S. PMID: 3580542.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    590. Developmental Gerstmann syndrome without aphasia in Fragile X syndrome. Neuropsychologia. 1987 Jan 1; 25(6):881-891. Grigsby GJ, Kemper KM, Hagerman HR. .
      View in: Publisher Site   Mentions:
    591. Autism, mental retardation, and chromosomal abnormalities. J Autism Dev Disord. 1986 Dec; 16(4):425-40. Mariner R, Jackson AW, Levitas A, Hagerman RJ, Braden M, McBogg PM, Smith AC, Berry R. PMID: 3542957.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    592. Fragile X syndrome: a review. J Oral Med. 1986 Oct-Dec; 41(4):228-33. Casamassimo PS, Shellhart WC, Hagerman R. PMID: 3537237.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    593. Oral folic acid versus placebo in the treatment of males with the fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):241-62. Hagerman RJ, Jackson AW, Levitas A, Braden M, McBogg P, Kemper M, McGavran L, Berry R, Matus I, Hagerman PJ. PMID: 3513567.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCTClinical Trials
    594. Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) females. Am J Med Genet. 1986 Jan-Feb; 23(1-2):139-56. Kemper MB, Hagerman RJ, Ahmad RS, Mariner R. PMID: 3953643.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    595. Oral findings in fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):179-87. Shellhart WC, Casamassimo PS, Hagerman RJ, Belanger GK. PMID: 3953646.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    596. Aortic root dilatation and mitral valve prolapse in the fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):189-94. Loehr JP, Synhorst DP, Wolfe RR, Hagerman RJ. PMID: 3953647.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    597. Speech disturbances (cluttering) in mildly impaired males with the Martin-Bell/fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):195-206. Hanson DM, Jackson AW, Hagerman RJ. PMID: 3953648.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    598. An analysis of autism in fifty males with the fragile X syndrome. Am J Med Genet. 1986 Jan-Feb; 23(1-2):359-74. Hagerman RJ, Jackson AW, Levitas A, Rimland B, Braden M. PMID: 3953654.
      View in: PubMed   Mentions: 67     Fields:    Translation:Humans
    599. Autism in fragile X females. Am J Med Genet. 1986 Jan-Feb; 23(1-2):375-80. Hagerman RJ, Chudley AE, Knoll JH, Jackson AW, Kemper M, Ahmad R. PMID: 3953655.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    600. Learning disabilities and attentional problems in boys with the fragile X syndrome. Am J Dis Child. 1985 Jul; 139(7):674-8. Hagerman R, Kemper M, Hudson M. PMID: 4014089.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    601. General anesthesia and fragile X syndrome: report of a case. Anesth Prog. 1985 May-Jun; 32(3):104-6. Casamassimo PS, Mcllvaine WB, Hagerman R, Shellhart WC. PMID: 2934007; PMCID: PMC2148507.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    602. Autism or fragile X syndrome? J Am Acad Child Psychiatry. 1985 Mar; 24(2):239-40. Hagerman RJ, Jackson AW. PMID: 3989170.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    603. Pediatric assessment of the learning-disabled child. J Dev Behav Pediatr. 1984 Oct; 5(5):274-84. Hagerman RJ. PMID: 6149234.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    604. Consideration of connective tissue dysfunction in the fragile X syndrome. Am J Med Genet. 1984 Jan; 17(1):111-21. Hagerman RJ, Van Housen K, Smith AC, McGavran L. PMID: 6711590.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    605. Mitral valve prolapse and aortic dilatation in the fragile X syndrome. Am J Med Genet. 1984 Jan; 17(1):123-31. Hagerman RJ, Synhorst DP. PMID: 6711591.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    606. Autism and the fragile X syndrome. J Dev Behav Pediatr. 1983 Sep; 4(3):151-8. Levitas A, Hagerman RJ, Braden M, Rimland B, McBogg P, Matus I. PMID: 6630529.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    607. Dilantin and the fragile X syndrome. N Engl J Med. 1983 Jun 09; 308(23):1424. Hagerman RJ, Levitas A. PMID: 6843639.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    608. The fragile X syndrome: history, diagnosis, and treatment. J Dev Behav Pediatr. 1983 Jun; 4(2):122-30. Hagerman RJ, McBogg P, Hagerman PJ. PMID: 6348096.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
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