329 related articles for article (PubMed ID: 34895138)
21. Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.
Ulloa AE; Chen J; Vergara VM; Calhoun V; Liu J
Alcohol Clin Exp Res; 2014 May; 38(5):1266-74. PubMed ID: 24512105
[TBL] [Abstract][Full Text] [Related]
22. A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.
Chen C; Qiao R; Wei R; Guo Y; Ai H; Ma J; Ren J; Huang L
BMC Genomics; 2012 Dec; 13():733. PubMed ID: 23270433
[TBL] [Abstract][Full Text] [Related]
23. Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.
Vysotskiy M; ; ; ; Weiss LA
PLoS Genet; 2023 Jun; 19(6):e1010780. PubMed ID: 37267418
[TBL] [Abstract][Full Text] [Related]
24. Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array.
Molin AM; Berglund J; Webster MT; Lindblad-Toh K
BMC Genomics; 2014 Mar; 15():210. PubMed ID: 24640994
[TBL] [Abstract][Full Text] [Related]
25. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.
Buizer-Voskamp JE; Muntjewerff JW; ; Strengman E; Sabatti C; Stefansson H; Vorstman JA; Ophoff RA
Biol Psychiatry; 2011 Oct; 70(7):655-62. PubMed ID: 21489405
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. The individual and global impact of copy-number variants on complex human traits.
Auwerx C; Lepamets M; Sadler MC; Patxot M; Stojanov M; Baud D; Mägi R; ; Porcu E; Reymond A; Kutalik Z
Am J Hum Genet; 2022 Apr; 109(4):647-668. PubMed ID: 35240056
[TBL] [Abstract][Full Text] [Related]
28. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.
Xu L; Cole JB; Bickhart DM; Hou Y; Song J; VanRaden PM; Sonstegard TS; Van Tassell CP; Liu GE
BMC Genomics; 2014 Aug; 15(1):683. PubMed ID: 25128478
[TBL] [Abstract][Full Text] [Related]
32. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
Raychaudhuri S; Korn JM; McCarroll SA; ; Altshuler D; Sklar P; Purcell S; Daly MJ
PLoS Genet; 2010 Sep; 6(9):e1001097. PubMed ID: 20838587
[TBL] [Abstract][Full Text] [Related]
33. Noise cancellation using total variation for copy number variation detection.
Zare F; Hosny A; Nabavi S
BMC Bioinformatics; 2018 Oct; 19(Suppl 11):361. PubMed ID: 30343665
[TBL] [Abstract][Full Text] [Related]
34. Copy number variations of
Wen Y; Wang E; Wang X; Qing S; Chaogetu B; Wang C; Xu Z; Zhang Z; Huang Y
Anim Biotechnol; 2023 Dec; 34(7):3008-3015. PubMed ID: 36170043
[TBL] [Abstract][Full Text] [Related]
35. Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.
Hiroi N; Takahashi T; Hishimoto A; Izumi T; Boku S; Hiramoto T
Mol Psychiatry; 2013 Nov; 18(11):1153-65. PubMed ID: 23917946
[TBL] [Abstract][Full Text] [Related]
36. Gender differences in CNV burden do not confound schizophrenia CNV associations.
Han J; Walters JT; Kirov G; Pocklington A; Escott-Price V; Owen MJ; Holmans P; O'Donovan MC; Rees E
Sci Rep; 2016 May; 6():25986. PubMed ID: 27185616
[TBL] [Abstract][Full Text] [Related]
37. Copy number variations and cognitive phenotypes in unselected populations.
Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
[TBL] [Abstract][Full Text] [Related]
38. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.
Nygaard M; Debrabant B; Tan Q; Deelen J; Andersen-Ranberg K; de Craen AJ; Beekman M; Jeune B; Slagboom PE; Christensen K; Christiansen L
Aging Cell; 2016 Feb; 15(1):49-55. PubMed ID: 26446717
[TBL] [Abstract][Full Text] [Related]
39. JAX-CNV: A Whole-genome Sequencing-based Algorithm for Copy Number Detection at Clinical Grade Level.
Lee WP; Zhu Q; Yang X; Liu S; Cerveira E; Ryan M; Mil-Homens A; Bellfy L; Ye K; Lee C; Zhang C
Genomics Proteomics Bioinformatics; 2022 Dec; 20(6):1197-1206. PubMed ID: 35085778
[TBL] [Abstract][Full Text] [Related]
40. Genome-wide association study between CNVs and milk production traits in Valle del Belice sheep.
Di Gerlando R; Sutera AM; Mastrangelo S; Tolone M; Portolano B; Sottile G; Bagnato A; Strillacci MG; Sardina MT
PLoS One; 2019; 14(4):e0215204. PubMed ID: 31013280
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]