229 related articles for article (PubMed ID: 25887117)
21. 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]
22. 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]
23. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
[TBL] [Abstract][Full Text] [Related]
24. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
Badner JA; Koller D; Foroud T; Edenberg H; Nurnberger JI; Zandi PP; Willour VL; McMahon FJ; Potash JB; Hamshere M; Grozeva D; Green E; Kirov G; Jones I; Jones L; Craddock N; Morris D; Segurado R; Gill M; Sadovnick D; Remick R; Keck P; Kelsoe J; Ayub M; MacLean A; Blackwood D; Liu CY; Gershon ES; McMahon W; Lyon GJ; Robinson R; Ross J; Byerley W
Mol Psychiatry; 2012 Jul; 17(8):818-26. PubMed ID: 21769101
[TBL] [Abstract][Full Text] [Related]
25. Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals.
Fullerton JM; Koller DL; Edenberg HJ; Foroud T; Liu H; Glowinski AL; McInnis MG; Wilcox HC; Frankland A; Roberts G; Schofield PR; Mitchell PB; Nurnberger JI;
Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):617-29. PubMed ID: 26178159
[TBL] [Abstract][Full Text] [Related]
26. Copy Number Variation in
Wang Y; Li L; Yang Y; Feng J; Wang L; Zhang H
Genet Test Mol Biomarkers; 2020 Apr; 24(4):173-180. PubMed ID: 32208937
[No Abstract] [Full Text] [Related]
27. Copy number variants in siblings of Mexican origin concordant for schizophrenia or bipolar disorder.
Vega-Sevey JG; Martínez-Magaña JJ; Genis-Mendoza AD; Escamilla M; Lanzagorta N; Tovilla-Zarate CA; Nicolini H
Psychiatry Res; 2020 Sep; 291():113018. PubMed ID: 32540681
[TBL] [Abstract][Full Text] [Related]
28. Novel association strategy with copy number variation for identifying new risk Loci of human diseases.
Chen X; Li X; Wang P; Liu Y; Zhang Z; Zhao G; Xu H; Zhu J; Qin X; Chen S; Hu L; Kong X
PLoS One; 2010 Aug; 5(8):e12185. PubMed ID: 20808825
[TBL] [Abstract][Full Text] [Related]
29. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
Toma C; Pierce KD; Shaw AD; Heath A; Mitchell PB; Schofield PR; Fullerton JM
PLoS Genet; 2018 Dec; 14(12):e1007535. PubMed ID: 30586385
[TBL] [Abstract][Full Text] [Related]
30. Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Simpson NH; Ceroni F; Reader RH; Covill LE; Knight JC; ; Hennessy ER; Bolton PF; Conti-Ramsden G; O'Hare A; Baird G; Fisher SE; Newbury DF
Eur J Hum Genet; 2015 Oct; 23(10):1370-7. PubMed ID: 25585696
[TBL] [Abstract][Full Text] [Related]
31. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.
Shrine N; Tobin MD; Schurmann C; Soler Artigas M; Hui J; Lehtimäki T; Raitakari OT; Pennell CE; Ang QW; Strachan DP; Homuth G; Gläser S; Felix SB; Evans DM; Henderson J; Granell R; Palmer LJ; Huffman J; Hayward C; Scotland G; Malarstig A; Musk B; James AL; ; Wain LV
BMC Genet; 2016 Aug; 17(1):116. PubMed ID: 27514831
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
[TBL] [Abstract][Full Text] [Related]
34. A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish.
Ginns EI; Ott J; Egeland JA; Allen CR; Fann CS; Pauls DL; Weissenbachoff J; Carulli JP; Falls KM; Keith TP; Paul SM
Nat Genet; 1996 Apr; 12(4):431-5. PubMed ID: 8630500
[TBL] [Abstract][Full Text] [Related]
35. Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder.
Kushima I; Nakatochi M; Aleksic B; Okada T; Kimura H; Kato H; Morikawa M; Inada T; Ishizuka K; Torii Y; Nakamura Y; Tanaka S; Imaeda M; Takahashi N; Yamamoto M; Iwamoto K; Nawa Y; Ogawa N; Iritani S; Hayashi Y; Lo T; Otgonbayar G; Furuta S; Iwata N; Ikeda M; Saito T; Ninomiya K; Okochi T; Hashimoto R; Yamamori H; Yasuda Y; Fujimoto M; Miura K; Itokawa M; Arai M; Miyashita M; Toriumi K; Ohi K; Shioiri T; Kitaichi K; Someya T; Watanabe Y; Egawa J; Takahashi T; Suzuki M; Sasaki T; Tochigi M; Nishimura F; Yamasue H; Kuwabara H; Wakuda T; Kato TA; Kanba S; Horikawa H; Usami M; Kodaira M; Watanabe K; Yoshikawa T; Toyota T; Yokoyama S; Munesue T; Kimura R; Funabiki Y; Kosaka H; Jung M; Kasai K; Ikegame T; Jinde S; Numata S; Kinoshita M; Kato T; Kakiuchi C; Yamakawa K; Suzuki T; Hashimoto N; Ishikawa S; Yamagata B; Nio S; Murai T; Son S; Kunii Y; Yabe H; Inagaki M; Goto YI; Okumura Y; Ito T; Arioka Y; Mori D; Ozaki N
Biol Psychiatry; 2022 Sep; 92(5):362-374. PubMed ID: 35667888
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
[TBL] [Abstract][Full Text] [Related]
38. 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; 177(5):489-502. PubMed ID: 29687944
[TBL] [Abstract][Full Text] [Related]
39. Copy Number Variations in Neuropsychiatric Disorders.
Büki G; Hadzsiev K; Bene J
Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37761973
[TBL] [Abstract][Full Text] [Related]
40. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
