Kathleen Angkustsiri

Title(s)Associate Professor, Pediatrics
SchoolSchool of Medicine
AddressMIND Institute
CA 95817
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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. Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome. Metabolomics. 2024 Feb 28; 20(2):31. Zafarullah M, Angkustsiri K, Quach A, Yeo S, Durbin-Johnson BP, Bowling H, Tassone F. PMID: 38418685; PMCID: PMC10901937.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Hum Brain Mapp. 2024 Jan; 45(1):e26553. Ge R, Ching CRK, Bassett AS, Kushan L, Antshel KM, van Amelsvoort T, Bakker G, Butcher NJ, Campbell LE, Chow EWC, Craig M, Crossley NA, Cunningham A, Daly E, Doherty JL, Durdle CA, Emanuel BS, Fiksinski A, Forsyth JK, Fremont W, Goodrich-Hunsaker NJ, Gudbrandsen M, Gur RE, Jalbrzikowski M, Kates WR, Lin A, Linden DEJ, McCabe KL, McDonald-McGinn D, Moss H, Murphy DG, Murphy KC, Owen MJ, Villalon-Reina JE, Repetto GM, Roalf DR, Ruparel K, Schmitt JE, Schuite-Koops S, Angkustsiri K, Sun D, Vajdi A, van den Bree M, Vorstman J, Thompson PM, Vila-Rodriguez F, Bearden CE. PMID: 38224541; PMCID: PMC10785196.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ Genom Med. 2023 Jul 18; 8(1):17. Zhao Y, Wang Y, Shi L, McDonald-McGinn DM, Crowley TB, McGinn DE, Tran OT, Miller D, Lin JR, Zackai E, Johnston HR, Chow EWC, Vorstman JAS, Vingerhoets C, van Amelsvoort T, Gothelf D, Swillen A, Breckpot J, Vermeesch JR, Eliez S, Schneider M, van den Bree MBM, Owen MJ, Kates WR, Repetto GM, Shashi V, Schoch K, Bearden CE, Digilio MC, Unolt M, Putotto C, Marino B, Pontillo M, Armando M, Vicari S, Angkustsiri K, Campbell L, Busa T, Heine-Suñer D, Murphy KC, Murphy D, García-Miñaúr S, Fernández L, International 22q11.2 Brain and Behavior Consortium (IBBC), Zhang ZD, Goldmuntz E, Gur RE, Emanuel BS, Zheng D, Marshall CR, Bassett AS, Wang T, Morrow BE. PMID: 37463940; PMCID: PMC10354062.
      View in: PubMed   Mentions: 1  
    4. Atypical presentation of Angelman syndrome with intact expressive language due to low-level mosaicism. Mol Genet Genomic Med. 2022 10; 10(10):e2018. Punatar R, Egense A, Mao R, Procter M, Bosworth M, Quigley DI, Angkustsiri K, Shankar SP. PMID: 35929060; PMCID: PMC9544204.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    5. Pilot Study of Maternal Autoantibody-Related Autism. J Dev Behav Pediatr. 2022 Oct-Nov 01; 43(8):465-471. Angkustsiri K, Fussell JJ, Bennett A, Schauer J, Ramirez-Celis A, Hansen RL, Van de Water J. PMID: 35943360; PMCID: PMC9561005.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. Comparison of Attention-Deficit Hyperactivity Disorder in Typically Developing Children and Children with Down Syndrome. J Dev Behav Pediatr. 2022 01 01; 43(1):1-8. Esbensen AJ, Epstein JN, Vincent LB, Kamimura-Nishimura K, Wiley S, Angkustsiri K, Abbeduto L, Fidler D, Froehlich TE. PMID: 34001744; PMCID: PMC8590700.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    7. Longitudinal Psychiatric and Developmental Outcomes in 22q11.2 Deletion Syndrome: A Systematic Review. J Dev Behav Pediatr. 2021 Jun-Jul 01; 42(5):415-427. Jhawar N, Brown MJ, Cutler-Landsman D, Kates WR, Angkustsiri K, Antshel KM. PMID: 34110308.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    8. Developmental-behavioral profiles in children with autism spectrum disorder and co-occurring gastrointestinal symptoms. Autism Res. 2020 10; 13(10):1778-1789. Restrepo B, Angkustsiri K, Taylor SL, Rogers SJ, Cabral J, Heath B, Hechtman A, Solomon M, Ashwood P, Amaral DG, Nordahl CW. PMID: 32767543; PMCID: PMC7689713.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    9. Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis. Am J Med Genet C Semin Med Genet. 2020 06; 184(2):456-468. Wigby K, Cordeiro L, Wilson R, Angkustsiri K, Simon TJ, Tartaglia N. PMID: 32548885; PMCID: PMC8363475.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    10. Seeing Eye to Eye With Threat: Atypical Threat Bias in Children With 22q11.2 Deletion Syndrome. Am J Intellect Dev Disabil. 2019 11; 124(6):549-567. Popa AM, Cruz JR, Wong LM, Harvey DJ, Angkustsiri K, Leckliter IN, Perez-Edgar K, Simon TJ. PMID: 31756146; PMCID: PMC6927396.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    11. Interrelationship Between Cognitive Control, Anxiety, and Restricted and Repetitive Behaviors in Children with 22q11.2 Deletion Syndrome. Autism Res. 2019 12; 12(12):1737-1744. Uljarevic M, McCabe KL, Angkustsiri K, Simon TJ, Hardan AY. PMID: 31433576; PMCID: PMC6927400.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    12. Pilot study of probiotic/colostrum supplementation on gut function in children with autism and gastrointestinal symptoms. PLoS One. 2019; 14(1):e0210064. Sanctuary MR, Kain JN, Chen SY, Kalanetra K, Lemay DG, Rose DR, Yang HT, Tancredi DJ, German JB, Slupsky CM, Ashwood P, Mills DA, Smilowitz JT, Angkustsiri K. PMID: 30625189; PMCID: PMC6326569.
      View in: PubMed   Mentions: 63     Fields:    Translation:HumansAnimals
    13. Extra-axial cerebrospinal fluid in high-risk and normal-risk children with autism aged 2-4 years: a case-control study. Lancet Psychiatry. 2018 11; 5(11):895-904. Shen MD, Nordahl CW, Li DD, Lee A, Angkustsiri K, Emerson RW, Rogers SJ, Ozonoff S, Amaral DG. PMID: 30270033; PMCID: PMC6223655.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    14. Comparison of maternal beliefs about causes of autism spectrum disorder and association with utilization of services and treatments. Child Care Health Dev. 2018 11; 44(6):916-925. Chaidez V, Fernandez Y Garcia E, Wang LW, Angkustsiri K, Krakowiak P, Hertz-Picciotto I, Hansen RL. PMID: 30136409; PMCID: PMC6447086.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansPHPublic Health
    15. Dietary Considerations in Autism Spectrum Disorders: The Potential Role of Protein Digestion and Microbial Putrefaction in the Gut-Brain Axis. Front Nutr. 2018; 5:40. Sanctuary MR, Kain JN, Angkustsiri K, German JB. PMID: 29868601; PMCID: PMC5968124.
      View in: PubMed   Mentions: 30  
    16. Effects of Yoga on Attention, Impulsivity, and Hyperactivity in Preschool-Aged Children with Attention-Deficit Hyperactivity Disorder Symptoms. J Dev Behav Pediatr. 2018 04; 39(3):200-209. Cohen SCL, Harvey DJ, Shields RH, Shields GS, Rashedi RN, Tancredi DJ, Angkustsiri K, Hansen RL, Schweitzer JB. PMID: 29538185; PMCID: PMC5871620.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    17. Differential immune responses and microbiota profiles in children with autism spectrum disorders and co-morbid gastrointestinal symptoms. Brain Behav Immun. 2018 05; 70:354-368. Rose DR, Yang H, Serena G, Sturgeon C, Ma B, Careaga M, Hughes HK, Angkustsiri K, Rose M, Hertz-Picciotto I, Van de Water J, Hansen RL, Ravel J, Fasano A, Ashwood P. PMID: 29571898; PMCID: PMC5953830.
      View in: PubMed   Mentions: 85     Fields:    Translation:HumansCells
    18. Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome. Hum Brain Mapp. 2018 01; 39(1):232-248. Zhan L, Jenkins LM, Zhang A, Conte G, Forbes A, Harvey D, Angkustsiri K, Goodrich-Hunsaker NJ, Durdle C, Lee A, Schumann C, Carmichael O, Kalish K, Leow AD, Simon TJ. PMID: 28990258; PMCID: PMC5757536.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    19. Erratum to: Safety and tolerability of Bifidobacterium longum subspecies infantis EVC001 supplementation in healthy term breastfed infants: a phase I clinical trial. BMC Pediatr. 2017 08 15; 17(1):180. Smilowitz JT, Moya J, Breck MA, Cook C, Fineberg A, Angkustsiri K, Underwood MA. PMID: 28810848; PMCID: PMC5558702.
      View in: PubMed   Mentions: 3     Fields:    
    20. A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome. J Neurodev Disord. 2017 Aug 02; 9(1):26. Ligsay A, Van Dijck A, Nguyen DV, Lozano R, Chen Y, Bickel ES, Hessl D, Schneider A, Angkustsiri K, Tassone F, Ceulemans B, Kooy RF, Hagerman RJ. PMID: 28764646; PMCID: PMC5540519.
      View in: PubMed   Mentions: 31     Fields:    
    21. Safety and tolerability of Bifidobacterium longum subspecies infantis EVC001 supplementation in healthy term breastfed infants: a phase I clinical trial. BMC Pediatr. 2017 May 30; 17(1):133. Smilowitz JT, Moya J, Breck MA, Cook C, Fineberg A, Angkustsiri K, Underwood MA. PMID: 28558732; PMCID: PMC5450358.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCellsCTClinical Trials
    22. Sociodemographic Disparities in Intervention Service Utilization in Families of Children with Autism Spectrum Disorder. J Autism Dev Disord. 2016 Dec; 46(12):3729-3738. Nguyen CT, Krakowiak P, Hansen R, Hertz-Picciotto I, Angkustsiri K. PMID: 27639855; PMCID: PMC5112120.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    23. Functional Connectivity of the Amygdala Is Disrupted in Preschool-Aged Children With Autism Spectrum Disorder. J Am Acad Child Adolesc Psychiatry. 2016 09; 55(9):817-24. Shen MD, Li DD, Keown CL, Lee A, Johnson RT, Angkustsiri K, Rogers SJ, Müller RA, Amaral DG, Nordahl CW. PMID: 27566123; PMCID: PMC5003422.
      View in: PubMed   Mentions: 47     Fields:    Translation:Humans
    24. Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder During Adolescence in the Primary Care Setting: A Concise Review. J Adolesc Health. 2016 08; 59(2):135-43. Brahmbhatt K, Hilty DM, Hah M, Han J, Angkustsiri K, Schweitzer JB. PMID: 27209327; PMCID: PMC5576000.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    25. Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. J Biol Chem. 2015 Sep 18; 290(38):23240-53. Napoli E, Tassone F, Wong S, Angkustsiri K, Simon TJ, Song G, Giulivi C. PMID: 26221035; PMCID: PMC4645608.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    26. Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR. BMC Med Genet. 2014 Oct 14; 15:106. Hwang VJ, Maar D, Regan J, Angkustsiri K, Simon TJ, Tassone F. PMID: 25312060; PMCID: PMC4258952.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    27. Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome. PLoS One. 2014; 9(8):e103884. Sellier C, Hwang VJ, Dandekar R, Durbin-Johnson B, Charlet-Berguerand N, Ander BP, Sharp FR, Angkustsiri K, Simon TJ, Tassone F. PMID: 25084529; PMCID: PMC4118991.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    28. Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications. Behav Brain Res. 2015 Jan 01; 276:190-8. Stephenson DD, Beaton EA, Weems CF, Angkustsiri K, Simon TJ. PMID: 24906195; PMCID: PMC4254311.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    29. Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype? J Autism Dev Disord. 2014 Apr; 44(4):739-46. Angkustsiri K, Goodlin-Jones B, Deprey L, Brahmbhatt K, Harris S, Simon TJ. PMID: 24045981; PMCID: PMC4327991.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    30. Utilization patterns of conventional and complementary/alternative treatments in children with autism spectrum disorders and developmental disabilities in a population-based study. J Dev Behav Pediatr. 2014 Jan; 35(1):1-10. Akins RS, Krakowiak P, Angkustsiri K, Hertz-Picciotto I, Hansen RL. PMID: 24399100; PMCID: PMC3896860.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansPHPublic Health
    31. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome. J Dev Behav Pediatr. 2012 Nov-Dec; 33(9):713-20. Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon TJ. PMID: 23117596; PMCID: PMC3523689.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    32. Minor physical anomalies in children with autism spectrum disorders. Autism. 2011 Nov; 15(6):746-60. Angkustsiri K, Krakowiak P, Moghaddam B, Wardinsky T, Gardner J, Kalamkarian N, Hertz-Picciotto I, Hansen RL. PMID: 21610186; PMCID: PMC4245022.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    33. Complementary and alternative medicine in autism: an evidence-based approach to negotiating safe and efficacious interventions with families. Neurotherapeutics. 2010 Jul; 7(3):307-19. Akins RS, Angkustsiri K, Hansen RL. PMID: 20643384; PMCID: PMC5084235.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    34. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    35. 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.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    36. 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.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    37. Regression in autism: prevalence and associated factors in the CHARGE Study. Ambul Pediatr. 2008 Jan-Feb; 8(1):25-31. Hansen RL, Ozonoff S, Krakowiak P, Angkustsiri K, Jones C, Deprey LJ, Le DN, Croen LA, Hertz-Picciotto I. PMID: 18191778.
      View in: PubMed   Mentions: 58     Fields:    Translation:Humans