BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

992 related articles for article (PubMed ID: 28030616)

  • 1. 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; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polygenic associations of neurodevelopmental genes in suicide attempt.
    Sokolowski M; Wasserman J; Wasserman D
    Mol Psychiatry; 2016 Oct; 21(10):1381-90. PubMed ID: 26666204
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder.
    Rao S; Shi M; Han X; Lam MHB; Chien WT; Zhou K; Liu G; Wing YK; So HC; Waye MMY
    Gene; 2020 Sep; 755():144901. PubMed ID: 32554045
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.
    Bae JS; Cheong HS; Chun JY; Park TJ; Kim JO; Kim EM; Park M; Kim DJ; Lee EJ; Kim EK; Lee JY; Shin HD
    Ophthalmology; 2010 Jul; 117(7):1306-12.e4. PubMed ID: 20202685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
    Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 73(9):963-969. PubMed ID: 27602560
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The effect of algorithms on copy number variant detection.
    Tsuang DW; Millard SP; Ely B; Chi P; Wang K; Raskind WH; Kim S; Brkanac Z; Yu CE
    PLoS One; 2010 Dec; 5(12):e14456. PubMed ID: 21209939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Family-Based Benchmarking of Copy Number Variation Detection Software.
    Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
    PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number variation in schizophrenia in Sweden.
    Szatkiewicz JP; O'Dushlaine C; Chen G; Chambert K; Moran JL; Neale BM; Fromer M; Ruderfer D; Akterin S; Bergen SE; Kähler A; Magnusson PK; Kim Y; Crowley JJ; Rees E; Kirov G; O'Donovan MC; Owen MJ; Walters J; Scolnick E; Sklar P; Purcell S; Hultman CM; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2014 Jul; 19(7):762-73. PubMed ID: 24776740
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide algorithm for detecting CNV associations with diseases.
    Xu Y; Peng B; Fu Y; Amos CI
    BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 165B(8):619-26. PubMed ID: 25228354
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders.
    Ye T; Lipska BK; Tao R; Hyde TM; Wang L; Li C; Choi KH; Straub RE; Kleinman JE; Weinberger DR
    Biol Psychiatry; 2012 Oct; 72(8):651-4. PubMed ID: 22795968
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Accuracy of CNV Detection from GWAS Data.
    Zhang D; Qian Y; Akula N; Alliey-Rodriguez N; Tang J; ; Gershon ES; Liu C
    PLoS One; 2011 Jan; 6(1):e14511. PubMed ID: 21249187
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A genome-wide copy number variant study of suicidal behavior.
    Gross JA; Bureau A; Croteau J; Galfalvy H; Oquendo MA; Haghighi F; Mérette C; Giegling I; Hodgkinson C; Goldman D; Rujescu D; Mann JJ; Turecki G
    PLoS One; 2015; 10(5):e0128369. PubMed ID: 26010658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reduced burden of very large and rare CNVs in bipolar affective disorder.
    Grozeva D; Kirov G; Conrad DF; Barnes CP; Hurles M; Owen MJ; O'Donovan MC; Craddock N
    Bipolar Disord; 2013 Dec; 15(8):893-8. PubMed ID: 24127788
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; ; Zhang F; Wu Z; Lupski JR; Wu N
    Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene-level associations in suicide attempter families show overrepresentation of synaptic genes and genes differentially expressed in brain development.
    Sokolowski M; Wasserman J; Wasserman D
    Am J Med Genet B Neuropsychiatr Genet; 2018 Dec; 177(8):774-784. PubMed ID: 30381879
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
    Hosak L; Silhan P; Hosakova J
    Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 50.