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Alexander Nord

Title(s)Assistant Professor, Neurobiology, Physiology and Behavior
SchoolUniversity of California, Davis
Address1515 Newton Court
CA 95618
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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. Correction for Rodriguez-Medina et al., "Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments". Microbiol Resour Announc. 2020 Apr 09; 9(15). Rodriguez-Medina J, Kim HG, Castro J, Contreras CM, Glon CL, Goyal A, Guo BY, Knowles S, Lin JC, McGuiness CL, Sorkin E, Stefani J, Yegireddi SJ, Chaganti S, Cui D, Deck SL, Deokule Y, Douglas H, Kenaston M, O'Brien A, Patterson E, Schoppa N, Vo DT, Tran K, Tran TL, Pérez-Irizarry V, Carrasquillo-Nieves K, Montalvo-Rodriguez R, Yao AI, Albeck JG, Facciotti MT, Nord AS, Furrow RE. PMID: 32273364.
      View in: PubMed   Mentions:
    2. Draft Genome Sequences of 16 Halophilic Prokaryotes Isolated from Diverse Environments. Microbiol Resour Announc. 2020 Feb 20; 9(8). Rodriguez-Medina J, Kim HG, Castro J, Contreras CM, Glon CL, Goyal A, Guo BY, Knowles S, Lin JC, McGuiness CL, Sorkin E, Stefani J, Yegireddi SJ, Chaganti S, Cui D, Deck SL, Deokule Y, Douglas H, Kenaston M, O'Brien A, Patterson E, Schoppa N, Tran Vo D, Tran K, Tran TL, Pérez-Irizarry V, Carrasquillo-Nieves K, Montalvo-Rodriguez R, Yao AI, Albeck JG, Facciotti MT, Nord AS, Furrow RE. PMID: 32079635.
      View in: PubMed   Mentions:
    3. Neurobiological functions of transcriptional enhancers. Nat Neurosci. 2020 01; 23(1):5-14. Nord AS, West AE. PMID: 31740812.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    4. Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons. Cell Rep. 2019 08 20; 28(8):2048-2063.e8. Lindtner S, Catta-Preta R, Tian H, Su-Feher L, Price JD, Dickel DE, Greiner V, Silberberg SN, McKinsey GL, McManus MT, Pennacchio LA, Visel A, Nord AS, Rubenstein JLR. PMID: 31433982.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    5. Noncoding deletions reveal a gene that is critical for intestinal function. Nature. 2019 07; 571(7763):107-111. Oz-Levi D, Olender T, Bar-Joseph I, Zhu Y, Marek-Yagel D, Barozzi I, Osterwalder M, Alkelai A, Ruzzo EK, Han Y, Vos ESM, Reznik-Wolf H, Hartman C, Shamir R, Weiss B, Shapiro R, Pode-Shakked B, Tatarskyy P, Milgrom R, Schvimer M, Barshack I, Imai DM, Coleman-Derr D, Dickel DE, Nord AS, Afzal V, van Bueren KL, Barnes RM, Black BL, Mayhew CN, Kuhar MF, Pitstick A, Tekman M, Stanescu HC, Wells JM, Kleta R, de Laat W, Goldstein DB, Pras E, Visel A, Lancet D, Anikster Y, Pennacchio LA. PMID: 31217582.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    6. Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency. Front Mol Neurosci. 2018; 11:481. Wade AA, Lim K, Catta-Preta R, Nord AS. PMID: 30692911.
      View in: PubMed   Mentions:
    7. 15 years of PhosphoSitePlus®: integrating post-translationally modified sites, disease variants and isoforms. Nucleic Acids Res. 2019 01 08; 47(D1):D433-D441. Hornbeck PV, Kornhauser JM, Latham V, Murray B, Nandhikonda V, Nord A, Skrzypek E, Wheeler T, Zhang B, Gnad F. PMID: 30445427.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimalsCells
    8. Dlx1 and Dlx2 Promote Interneuron GABA Synthesis, Synaptogenesis, and Dendritogenesis. Cereb Cortex. 2018 11 01; 28(11):3797-3815. Pla R, Stanco A, Howard MA, Rubin AN, Vogt D, Mortimer N, Cobos I, Potter GB, Lindtner S, Price JD, Nord AS, Visel A, Schreiner CE, Baraban SC, Rowitch DH, Rubenstein JLR. PMID: 29028947.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    9. Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity. Neuron. 2018 11 21; 100(4):831-845.e7. Fazel Darbandi S, Robinson Schwartz SE, Qi Q, Catta-Preta R, Pai EL, Mandell JD, Everitt A, Rubin A, Krasnoff RA, Katzman S, Tastad D, Nord AS, Willsey AJ, Chen B, State MW, Sohal VS, Rubenstein JLR. PMID: 30318412.
      View in: PubMed   Mentions: 8     Fields:    Translation:AnimalsCells
    10. Genomic analysis of transcriptional networks directing progression of cell states during MGE development. Neural Dev. 2018 09 14; 13(1):21. Sandberg M, Taher L, Hu J, Black BL, Nord AS, Rubenstein JLR. PMID: 30217225.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
    11. Germline Chd8 haploinsufficiency alters brain development in mouse. Nat Neurosci. 2017 Aug; 20(8):1062-1073. Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, Afzal V, Visel A, Pennacchio LA, Dickel DE, Lerch JP, Crawley JN, Zarbalis KS, Silverman JL, Nord AS. PMID: 28671691.
      View in: PubMed   Mentions: 33     Fields:    Translation:AnimalsCells
    12. Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate. Neuron. 2016 Oct 05; 92(1):59-74. Silberberg SN, Taher L, Lindtner S, Sandberg M, Nord AS, Vogt D, Mckinsey GL, Hoch R, Pattabiraman K, Zhang D, Ferran JL, Rajkovic A, Golonzhka O, Kim C, Zeng H, Puelles L, Visel A, Rubenstein JLR. PMID: 27710791.
      View in: PubMed   Mentions: 17     Fields:    Translation:AnimalsCells
    13. 52 Genetic Loci Influencing Myocardial Mass. J Am Coll Cardiol. 2016 09 27; 68(13):1435-1448. van der Harst P, van Setten J, Verweij N, Vogler G, Franke L, Maurano MT, Wang X, Mateo Leach I, Eijgelsheim M, Sotoodehnia N, Hayward C, Sorice R, Meirelles O, Lyytikäinen LP, Polašek O, Tanaka T, Arking DE, Ulivi S, Trompet S, Müller-Nurasyid M, Smith AV, Dörr M, Kerr KF, Magnani JW, Del Greco M F, Zhang W, Nolte IM, Silva CT, Padmanabhan S, Tragante V, Esko T, Abecasis GR, Adriaens ME, Andersen K, Barnett P, Bis JC, Bodmer R, Buckley BM, Campbell H, Cannon MV, Chakravarti A, Chen LY, Delitala A, Devereux RB, Doevendans PA, Dominiczak AF, Ferrucci L, Ford I, Gieger C, Harris TB, Haugen E, Heinig M, Hernandez DG, Hillege HL, Hirschhorn JN, Hofman A, Hubner N, Hwang SJ, Iorio A, Kähönen M, Kellis M, Kolcic I, Kooner IK, Kooner JS, Kors JA, Lakatta EG, Lage K, Launer LJ, Levy D, Lundby A, Macfarlane PW, May D, Meitinger T, Metspalu A, Nappo S, Naitza S, Neph S, Nord AS, Nutile T, Okin PM, Olsen JV, Oostra BA, Penninger JM, Pennacchio LA, Pers TH, Perz S, Peters A, Pinto YM, Pfeufer A, Pilia MG, Pramstaller PP, Prins BP, Raitakari OT, Raychaudhuri S, Rice KM, Rossin EJ, Rotter JI, Schafer S, Schlessinger D, Schmidt CO, Sehmi J, Silljé HHW, Sinagra G, Sinner MF, Slowikowski K, Soliman EZ, Spector TD, Spiering W, Stamatoyannopoulos JA, Stolk RP, Strauch K, Tan ST, Tarasov KV, Trinh B, Uitterlinden AG, van den Boogaard M, van Duijn CM, van Gilst WH, Viikari JS, Visscher PM, Vitart V, Völker U, Waldenberger M, Weichenberger CX, Westra HJ, Wijmenga C, Wolffenbuttel BH, Yang J, Bezzina CR, Munroe PB, Snieder H, Wright AF, Rudan I, Boyer LA, Asselbergs FW, van Veldhuisen DJ, Stricker BH, Psaty BM, Ciullo M, Sanna S, Lehtimäki T, Wilson JF, Bandinelli S, Alonso A, Gasparini P, Jukema JW, Kääb S, Gudnason V, Felix SB, Heckbert SR, de Boer RA, Newton-Cheh C, Hicks AA, Chambers JC, Jamshidi Y, Visel A, Christoffels VM, Isaacs A, Samani NJ, de Bakker PIW. PMID: 27659466.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansAnimals
    14. Transcriptional Networks Controlled by NKX2-1 in the Development of Forebrain GABAergic Neurons. Neuron. 2016 Sep 21; 91(6):1260-1275. Sandberg M, Flandin P, Silberberg S, Su-Feher L, Price JD, Hu JS, Kim C, Visel A, Nord AS, Rubenstein JLR. PMID: 27657450.
      View in: PubMed   Mentions: 24     Fields:    Translation:AnimalsCells
    15. Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. Hum Genet. 2016 08; 135(8):953-61. Yan D, Tekin D, Bademci G, Foster J, Cengiz FB, Kannan-Sundhari A, Guo S, Mittal R, Zou B, Grati M, Kabahuma RI, Kameswaran M, Lasisi TJ, Adedeji WA, Lasisi AO, Menendez I, Herrera M, Carranza C, Maroofian R, Crosby AH, Bensaid M, Masmoudi S, Behnam M, Mojarrad M, Feng Y, Duman D, Mawla AM, Nord AS, Blanton SH, Liu XZ, Tekin M. PMID: 27344577.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    16. Pbx Regulates Patterning of the Cerebral Cortex in Progenitors and Postmitotic Neurons. Neuron. 2015 Dec 16; 88(6):1192-1207. Golonzhka O, Nord A, Tang PLF, Lindtner S, Ypsilanti AR, Ferretti E, Visel A, Selleri L, Rubenstein JLR. PMID: 26671461.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    17. Genomic Views of Transcriptional Enhancers: Essential Determinants of Cellular Identity and Activity-Dependent Responses in the CNS. J Neurosci. 2015 Oct 14; 35(41):13819-26. Gray JM, Kim TK, West AE, Nord AS, Markenscoff-Papadimitriou E, Lomvardas S. PMID: 26468181.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    18. Learning about mammalian gene regulation from functional enhancer assays in the mouse. Genomics. 2015 Sep; 106(3):178-184. Nord AS. PMID: 26079655.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsCells
    19. Genomic perspectives of transcriptional regulation in forebrain development. Neuron. 2015 Jan 07; 85(1):27-47. Nord AS, Pattabiraman K, Visel A, Rubenstein JLR. PMID: 25569346.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansAnimalsCells
    20. Tissue-specific RNA expression marks distant-acting developmental enhancers. PLoS Genet. 2014 Sep; 10(9):e1004610. Wu H, Nord AS, Akiyama JA, Shoukry M, Afzal V, Rubin EM, Pennacchio LA, Visel A. PMID: 25188404.
      View in: PubMed   Mentions: 43     Fields:    Translation:AnimalsCells
    21. Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortex. Neuron. 2014 Jun 04; 82(5):989-1003. Pattabiraman K, Golonzhka O, Lindtner S, Nord AS, Taher L, Hoch R, Silberberg SN, Zhang D, Chen B, Zeng H, Pennacchio LA, Puelles L, Visel A, Rubenstein JL. PMID: 24814534.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansAnimalsCells
    22. Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis. Genome Res. 2014 Jun; 24(6):920-9. Attanasio C, Nord AS, Zhu Y, Blow MJ, Biddie SC, Mendenhall EM, Dixon J, Wright C, Hosseini R, Akiyama JA, Holt A, Plajzer-Frick I, Shoukry M, Afzal V, Ren B, Bernstein BE, Rubin EM, Visel A, Pennacchio LA. PMID: 24752179.
      View in: PubMed   Mentions: 28     Fields:    Translation:AnimalsCells
    23. Function-based identification of mammalian enhancers using site-specific integration. Nat Methods. 2014 May; 11(5):566-71. Dickel DE, Zhu Y, Nord AS, Wylie JN, Akiyama JA, Afzal V, Plajzer-Frick I, Kirkpatrick A, Göttgens B, Bruneau BG, Visel A, Pennacchio LA. PMID: 24658141.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimalsCells
    24. Rapid and pervasive changes in genome-wide enhancer usage during mammalian development. Cell. 2013 Dec 19; 155(7):1521-31. Nord AS, Blow MJ, Attanasio C, Akiyama JA, Holt A, Hosseini R, Phouanenavong S, Plajzer-Frick I, Shoukry M, Afzal V, Rubenstein JL, Rubin EM, Pennacchio LA, Visel A. PMID: 24360275.
      View in: PubMed   Mentions: 122     Fields:    Translation:AnimalsCells
    25. Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas. Clin Cancer Res. 2014 Feb 01; 20(3):764-75. Pennington KP, Walsh T, Harrell MI, Lee MK, Pennil CC, Rendi MH, Thornton A, Norquist BM, Casadei S, Nord AS, Agnew KJ, Pritchard CC, Scroggins S, Garcia RL, King MC, Swisher EM. PMID: 24240112.
      View in: PubMed   Mentions: 180     Fields:    Translation:Humans
    26. Fine tuning of craniofacial morphology by distant-acting enhancers. Science. 2013 Oct 25; 342(6157):1241006. Attanasio C, Nord AS, Zhu Y, Blow MJ, Li Z, Liberton DK, Morrison H, Plajzer-Frick I, Holt A, Hosseini R, Phouanenavong S, Akiyama JA, Shoukry M, Afzal V, Rubin EM, FitzPatrick DR, Ren B, Hallgrímsson B, Pennacchio LA, Visel A. PMID: 24159046.
      View in: PubMed   Mentions: 80     Fields:    Translation:AnimalsCells
    27. Congenital heart defects in patients with deletions upstream of SOX9. Hum Mutat. 2013 Dec; 34(12):1628-31. Sanchez-Castro M, Gordon CT, Petit F, Nord AS, Callier P, Andrieux J, Guérin P, Pichon O, David A, Abadie V, Bonnet D, Visel A, Pennacchio LA, Amiel J, Lyonnet S, Le Caignec C. PMID: 24115316.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    28. Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia. Am J Hum Genet. 2013 Oct 03; 93(4):697-710. Rippey C, Walsh T, Gulsuner S, Brodsky M, Nord AS, Gasperini M, Pierce S, Spurrell C, Coe BP, Krumm N, Lee MK, Sebat J, McClellan JM, King MC. PMID: 24094746.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    29. Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy. Epilepsia. 2013 Jul; 54(7):1262-9. Kodera H, Kato M, Nord AS, Walsh T, Lee M, Yamanaka G, Tohyama J, Nakamura K, Nakagawa E, Ikeda T, Ben-Zeev B, Lev D, Lerman-Sagie T, Straussberg R, Tanabe S, Ueda K, Amamoto M, Ohta S, Nonoda Y, Nishiyama K, Tsurusaki Y, Nakashima M, Miyake N, Hayasaka K, King MC, Matsumoto N, Saitsu H. PMID: 23662938.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    30. A high-resolution enhancer atlas of the developing telencephalon. Cell. 2013 Feb 14; 152(4):895-908. Visel A, Taher L, Girgis H, May D, Golonzhka O, Hoch RV, McKinsey GL, Pattabiraman K, Silberberg SN, Blow MJ, Hansen DV, Nord AS, Akiyama JA, Holt A, Hosseini R, Phouanenavong S, Plajzer-Frick I, Shoukry M, Afzal V, Kaplan T, Kriegstein AR, Rubin EM, Ovcharenko I, Pennacchio LA, Rubenstein JL. PMID: 23375746.
      View in: PubMed   Mentions: 96     Fields:    Translation:HumansAnimalsCells
    31. ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing. J Mol Diagn. 2012 Jul; 14(4):357-66. Pritchard CC, Smith C, Salipante SJ, Lee MK, Thornton AM, Nord AS, Gulden C, Kupfer SS, Swisher EM, Bennett RL, Novetsky AP, Jarvik GP, Olopade OI, Goodfellow PJ, King MC, Tait JF, Walsh T. PMID: 22658618.
      View in: PubMed   Mentions: 83     Fields:    Translation:Humans
    32. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proc Natl Acad Sci U S A. 2011 Nov 01; 108(44):18032-7. Walsh T, Casadei S, Lee MK, Pennil CC, Nord AS, Thornton AM, Roeb W, Agnew KJ, Stray SM, Wickramanayake A, Norquist B, Pennington KP, Garcia RL, King MC, Swisher EM. PMID: 22006311.
      View in: PubMed   Mentions: 257     Fields:    Translation:Humans
    33. Accurate and exact CNV identification from targeted high-throughput sequence data. BMC Genomics. 2011 Apr 12; 12:184. Nord AS, Lee M, King MC, Walsh T. PMID: 21486468.
      View in: PubMed   Mentions: 69     Fields:    
    34. Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. Eur J Hum Genet. 2011 Jun; 19(6):727-31. Nord AS, Roeb W, Dickel DE, Walsh T, Kusenda M, O'Connor KL, Malhotra D, McCarthy SE, Stray SM, Taylor SM, Sebat J, King B, King MC, McClellan JM. PMID: 21448237.
      View in: PubMed   Mentions: 45     Fields:    Translation:HumansCells
    35. Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk. Stroke. 2011 Jan; 42(1):2-9. Ronald J, Rajagopalan R, Cerrato F, Nord AS, Hatsukami T, Kohler T, Marcovina S, Heagerty P, Jarvik GP. PMID: 21127300.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    36. Is cardiac diagnosis a predictor of neurodevelopmental outcome after cardiac surgery in infancy? J Thorac Cardiovasc Surg. 2010 Dec; 140(6):1230-7. Gaynor JW, Gerdes M, Nord AS, Bernbaum J, Zackai E, Wernovsky G, Clancy RR, Heagerty PJ, Solot CB, McDonald-McGinn D, Jarvik GP. PMID: 20951391.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    37. Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Proc Natl Acad Sci U S A. 2010 Jul 13; 107(28):12629-33. Walsh T, Lee MK, Casadei S, Thornton AM, Stray SM, Pennil C, Nord AS, Mandell JB, Swisher EM, King MC. PMID: 20616022.
      View in: PubMed   Mentions: 175     Fields:    Translation:HumansCells
    38. Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51. Am J Hum Genet. 2010 Jul 09; 87(1):101-9. Walsh T, Pierce SB, Lenz DR, Brownstein Z, Dagan-Rosenfeld O, Shahin H, Roeb W, McCarthy S, Nord AS, Gordon CR, Ben-Neriah Z, Sebat J, Kanaan M, Lee MK, Frydman M, King MC, Avraham KB. PMID: 20602916.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    39. Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. Eur J Hum Genet. 2010 Apr; 18(4):407-13. Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M. PMID: 19888295.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    40. Perioperative stroke in infants undergoing open heart operations for congenital heart disease. Ann Thorac Surg. 2009 Sep; 88(3):823-9. Chen J, Zimmerman RA, Jarvik GP, Nord AS, Clancy RR, Wernovsky G, Montenegro LM, Hartman DM, Nicolson SC, Spray TL, Gaynor JW, Ichord R. PMID: 19699905.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    41. Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgery. Pediatrics. 2009 Jul; 124(1):241-50. Gaynor JW, Nord AS, Wernovsky G, Bernbaum J, Solot CB, Burnham N, Zackai E, Heagerty PJ, Clancy RR, Nicolson SC, Jarvik GP, Gerdes M. PMID: 19564306.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    42. Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery. Eur J Cardiothorac Surg. 2009 Jul; 36(1):40-7. Fuller S, Nord AS, Gerdes M, Wernovsky G, Jarvik GP, Bernbaum J, Zackai E, Gaynor JW. PMID: 19394849.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    43. Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. J Lipid Res. 2009 May; 50(5):798-806. Ober C, Nord AS, Thompson EE, Pan L, Tan Z, Cusanovich D, Sun Y, Nicolae R, Edelstein C, Schneider DH, Billstrand C, Pfaffinger D, Phillips N, Anderson RL, Philips B, Rajagopalan R, Hatsukami TS, Rieder MJ, Heagerty PJ, Nickerson DA, Abney M, Marcovina S, Jarvik GP, Scanu AM, Nicolae DL. PMID: 19124843.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansAnimalsCells
    44. Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation. Arterioscler Thromb Vasc Biol. 2008 Jul; 28(7):1407-12. Reiner AP, Wurfel MM, Lange LA, Carlson CS, Nord AS, Carty CL, Rieder MJ, Desmarais C, Jenny NS, Iribarren C, Walston JD, Williams OD, Nickerson DA, Jarvik GP. PMID: 18451331.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    45. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science. 2008 Apr 25; 320(5875):539-43. Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J. PMID: 18369103.
      View in: PubMed   Mentions: 701     Fields:    Translation:HumansCells
    46. Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndrome. Pediatrics. 2008 Mar; 121(3):476-83. Tabbutt S, Nord AS, Jarvik GP, Bernbaum J, Wernovsky G, Gerdes M, Zackai E, Clancy RR, Nicolson SC, Spray TL, Gaynor JW. PMID: 18310195.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    47. Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot. J Thorac Cardiovasc Surg. 2008 Jan; 135(1):91-7. Zeltser I, Jarvik GP, Bernbaum J, Wernovsky G, Nord AS, Gerdes M, Zackai E, Clancy R, Nicolson SC, Spray TL, Gaynor JW. PMID: 18179924.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    48. Comparison of tagging single-nucleotide polymorphism methods in association analyses. BMC Proc. 2007; 1 Suppl 1:S6. Goode EL, Fridley BL, Sun Z, Atkinson EJ, Nord AS, McDonnell SK, Jarvik GP, de Andrade M, Slager SL. PMID: 18466560.
      View in: PubMed   Mentions:
    49. A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk. J Lipid Res. 2008 Mar; 49(3):588-96. Crawford DC, Nord AS, Badzioch MD, Ranchalis J, McKinstry LA, Ahearn M, Bertucci C, Shephard C, Wong M, Rieder MJ, Schellenberg GD, Nickerson DA, Heagerty PJ, Wijsman EM, Jarvik GP. PMID: 18056683.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    50. Modeling insertional mutagenesis using gene length and expression in murine embryonic stem cells. PLoS One. 2007 Jul 18; 2(7):e617. Nord AS, Vranizan K, Tingley W, Zambon AC, Hanspers K, Fong LG, Hu Y, Bacchetti P, Ferrin TE, Babbitt PC, Doniger SW, Skarnes WC, Young SG, Conklin BR. PMID: 17637833.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    51. Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery. J Thorac Cardiovasc Surg. 2007 May; 133(5):1344-53, 1353.e1-3. Gaynor JW, Wernovsky G, Jarvik GP, Bernbaum J, Gerdes M, Zackai E, Nord AS, Clancy RR, Nicolson SC, Spray TL. PMID: 17467455.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    52. TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects. Hum Genet. 2007 Mar; 121(1):65-75. Carlson CS, Heagerty PJ, Nord AS, Pritchard DK, Ranchalis J, Boguch JM, Duan H, Hatsukami TS, Schwartz SM, Rieder MJ, Nickerson DA, Jarvik GP. PMID: 17115186.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    53. The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse. Nucleic Acids Res. 2006 Jan 01; 34(Database issue):D642-8. Nord AS, Chang PJ, Conklin BR, Cox AV, Harper CA, Hicks GG, Huang CC, Johns SJ, Kawamoto M, Liu S, Meng EC, Morris JH, Rossant J, Ruiz P, Skarnes WC, Soriano P, Stanford WL, Stryke D, von Melchner H, Wurst W, Yamamura K, Young SG, Babbitt PC, Ferrin TE. PMID: 16381950.
      View in: PubMed   Mentions: 59     Fields:    Translation:AnimalsCells
    54. A public gene trap resource for mouse functional genomics. Nat Genet. 2004 Jun; 36(6):543-4. Skarnes WC, von Melchner H, Wurst W, Hicks G, Nord AS, Cox T, Young SG, Ruiz P, Soriano P, Tessier-Lavigne M, Conklin BR, Stanford WL, Rossant J. PMID: 15167922.
      View in: PubMed   Mentions: 94     Fields:    Translation:AnimalsCells