These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

677 related items for PubMed ID: 30392412

  • 1. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE, Ploner A, Howrigan D, CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics ConsortiumFrom the Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm; the Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Mass.; the Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston; the MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom; the Department of Psychiatry, Harvard Medical School, and Massachusetts General Hospital, Boston; the Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetics Research, Massachusetts General Hospital, Boston; the Departments of Genetics and Psychiatry, University of North Carolina, Chapel Hill; the Departments of Psychiatry and Cellular and Molecular Medicine, University of California, San Diego; and the Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond., O'Donovan MC, Smoller JW, Sullivan PF, Sebat J, Neale B, Kendler KS.
    Am J Psychiatry; 2019 Jan 01; 176(1):29-35. PubMed ID: 30392412
    [Abstract] [Full Text] [Related]

  • 2. Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
    Saarentaus EC, Havulinna AS, Mars N, Ahola-Olli A, Kiiskinen TTJ, Partanen J, Ruotsalainen S, Kurki M, Urpa LM, Chen L, Perola M, Salomaa V, Veijola J, Männikkö M, Hall IM, Pietiläinen O, Kaprio J, Ripatti S, Daly M, Palotie A.
    Mol Psychiatry; 2021 Sep 01; 26(9):4884-4895. PubMed ID: 33526825
    [Abstract] [Full Text] [Related]

  • 3. A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number Variations.
    Chang X, Qu H, Liu Y, Glessner J, Hakonarson H.
    Biol Psychiatry; 2024 May 01; 95(9):881-887. PubMed ID: 37865391
    [Abstract] [Full Text] [Related]

  • 4. A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
    Rudd DS, Axelsen M, Epping EA, Andreasen NC, Wassink TH.
    Am J Med Genet B Neuropsychiatr Genet; 2014 Dec 01; 165B(8):619-26. PubMed ID: 25228354
    [Abstract] [Full Text] [Related]

  • 5. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
    Charney AW, Stahl EA, Green EK, Chen CY, Moran JL, Chambert K, Belliveau RA, Forty L, Gordon-Smith K, Lee PH, Bromet EJ, Buckley PF, Escamilla MA, Fanous AH, Fochtmann LJ, Lehrer DS, Malaspina D, Marder SR, Morley CP, Nicolini H, Perkins DO, Rakofsky JJ, Rapaport MH, Medeiros H, Sobell JL, Backlund L, Bergen SE, Juréus A, Schalling M, Lichtenstein P, Knowles JA, Burdick KE, Jones I, Jones LA, Hultman CM, Perlis R, Purcell SM, McCarroll SA, Pato CN, Pato MT, Di Florio A, Craddock N, Landén M, Smoller JW, Ruderfer DM, Sklar P.
    Biol Psychiatry; 2019 Jul 15; 86(2):110-119. PubMed ID: 30686506
    [Abstract] [Full Text] [Related]

  • 6. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M, Wasserman J, Wasserman D.
    PLoS One; 2016 Jul 15; 11(12):e0168531. PubMed ID: 28030616
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide association study of multiplex schizophrenia pedigrees.
    Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S, Schizophrenia Psychiatric GWAS Consortium, Dudbridge F, Holmans PA.
    Am J Psychiatry; 2012 Sep 15; 169(9):963-73. PubMed ID: 22885689
    [Abstract] [Full Text] [Related]

  • 8. Polygenic risk scores in schizophrenia with clinically significant copy number variants.
    Taniguchi S, Ninomiya K, Kushima I, Saito T, Shimasaki A, Sakusabe T, Momozawa Y, Kubo M, Kamatani Y, Ozaki N, Ikeda M, Iwata N.
    Psychiatry Clin Neurosci; 2020 Jan 15; 74(1):35-39. PubMed ID: 31461559
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.
    Martin AK, Robinson G, Reutens D, Mowry B.
    Am J Med Genet B Neuropsychiatr Genet; 2015 Jul 15; 168B(5):374-82. PubMed ID: 25943776
    [Abstract] [Full Text] [Related]

  • 14. The relative contribution of common and rare genetic variants to ADHD.
    Martin J, O'Donovan MC, Thapar A, Langley K, Williams N.
    Transl Psychiatry; 2015 Feb 10; 5(2):e506. PubMed ID: 25668434
    [Abstract] [Full Text] [Related]

  • 15. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
    Guyatt AL, Stergiakouli E, Martin J, Walters J, O'Donovan M, Owen M, Thapar A, Kirov G, Rodriguez S, Rai D, Zammit S, Gaunt TR.
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jul 10; 177(5):489-502. PubMed ID: 29687944
    [Abstract] [Full Text] [Related]

  • 16. Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
    Rees E, Kendall K, Pardiñas AF, Legge SE, Pocklington A, Escott-Price V, MacCabe JH, Collier DA, Holmans P, O'Donovan MC, Owen MJ, Walters JTR, Kirov G.
    JAMA Psychiatry; 2016 Sep 01; 73(9):963-969. PubMed ID: 27602560
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K, Magnusson P, Gudmundsson OO, Gustafsson O, Holmans P, Owen MJ, O'Donovan M, Thapar A.
    Lancet; 2010 Oct 23; 376(9750):1401-8. PubMed ID: 20888040
    [Abstract] [Full Text] [Related]

  • 19. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
    Liu J, Zhou Y, Liu S, Song X, Yang XZ, Fan Y, Chen W, Akdemir ZC, Yan Z, Zuo Y, Du R, Liu Z, Yuan B, Zhao S, Liu G, Chen Y, Zhao Y, Lin M, Zhu Q, Niu Y, Liu P, Ikegawa S, Song YQ, Posey JE, Qiu G, DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) Study, Zhang F, Wu Z, Lupski JR, Wu N.
    Hum Genet; 2018 Jul 23; 137(6-7):553-567. PubMed ID: 30019117
    [Abstract] [Full Text] [Related]

  • 20. Schizophrenia genetic variants are not associated with intelligence.
    van Scheltinga AF, Bakker SC, van Haren NE, Derks EM, Buizer-Voskamp JE, Cahn W, Ripke S, Psychiatric Genome-Wide Association Study (GWAS) Consortium, Ophoff RA, Kahn RS.
    Psychol Med; 2013 Dec 23; 43(12):2563-70. PubMed ID: 23410598
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 34.