368 related articles for article (PubMed ID: 31185018)
1. Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.
Frenkel S; Bernstein CN; Sargent M; Kuang Q; Jiang W; Wei J; Thiruvahindrapuram B; Spriggs E; Scherer SW; Hu P
PLoS One; 2019; 14(6):e0217846. PubMed ID: 31185018
[TBL] [Abstract][Full Text] [Related]
2. Copy number variation-based gene set analysis reveals cytokine signalling pathways associated with psychiatric comorbidity in patients with inflammatory bowel disease.
Frenkel S; Bernstein CN; Sargent M; Jiang W; Kuang Q; Xu W; Hu P
Genomics; 2020 Jan; 112(1):683-693. PubMed ID: 31075388
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
[TBL] [Abstract][Full Text] [Related]
6. Copy number variations in the genome of the Qatari population.
Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
[TBL] [Abstract][Full Text] [Related]
7. The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.
Wain LV; Pedroso I; Landers JE; Breen G; Shaw CE; Leigh PN; Brown RH; Tobin MD; Al-Chalabi A
PLoS One; 2009 Dec; 4(12):e8175. PubMed ID: 19997636
[TBL] [Abstract][Full Text] [Related]
8. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Rare copy number variation in posttraumatic stress disorder.
Maihofer AX; Engchuan W; Huguet G; Klein M; MacDonald JR; Shanta O; Thiruvahindrapuram B; Jean-Louis M; Saci Z; Jacquemont S; Scherer SW; Ketema E; Aiello AE; Amstadter AB; Avdibegović E; Babic D; Baker DG; Bisson JI; Boks MP; Bolger EA; Bryant RA; Bustamante AC; Caldas-de-Almeida JM; Cardoso G; Deckert J; Delahanty DL; Domschke K; Dunlop BW; Dzubur-Kulenovic A; Evans A; Feeny NC; Franz CE; Gautam A; Geuze E; Goci A; Hammamieh R; Jakovljevic M; Jett M; Jones I; Kaufman ML; Kessler RC; King AP; Kremen WS; Lawford BR; Lebois LAM; Lewis C; Liberzon I; Linnstaedt SD; Lugonja B; Luykx JJ; Lyons MJ; Mavissakalian MR; McLaughlin KA; McLean SA; Mehta D; Mellor R; Morris CP; Muhie S; Orcutt HK; Peverill M; Ratanatharathorn A; Risbrough VB; Rizzo A; Roberts AL; Rothbaum AO; Rothbaum BO; Roy-Byrne P; Ruggiero KJ; Rutten BPF; Schijven D; Seng JS; Sheerin CM; Sorenson MA; Teicher MH; Uddin M; Ursano RJ; Vinkers CH; Voisey J; Weber H; Winternitz S; Xavier M; Yang R; McD Young R; Zoellner LA; ; ; Salem RM; Shaffer RA; Wu T; Ressler KJ; Stein MB; Koenen KC; Sebat J; Nievergelt CM
Mol Psychiatry; 2022 Dec; 27(12):5062-5069. PubMed ID: 36131047
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.
Poniah P; Mohd Zain S; Abdul Razack AH; Kuppusamy S; Karuppayah S; Sian Eng H; Mohamed Z
Urol Oncol; 2017 Sep; 35(9):545.e1-545.e11. PubMed ID: 28527622
[TBL] [Abstract][Full Text] [Related]
13. A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.
Low JS; Chin YM; Mushiroda T; Kubo M; Govindasamy GK; Pua KC; Yap YY; Yap LF; Subramaniam SK; Ong CA; Tan TY; Khoo AS; ; Ng CC
PLoS One; 2016; 11(1):e0145774. PubMed ID: 26730743
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
Costain G; Lionel AC; Ogura L; Marshall CR; Scherer SW; Silversides CK; Bassett AS
Int J Cardiol; 2016 Feb; 204():115-21. PubMed ID: 26655555
[TBL] [Abstract][Full Text] [Related]
15. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Silversides CK; Lionel AC; Costain G; Merico D; Migita O; Liu B; Yuen T; Rickaby J; Thiruvahindrapuram B; Marshall CR; Scherer SW; Bassett AS
PLoS Genet; 2012; 8(8):e1002843. PubMed ID: 22912587
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.
Walker LC; Pearson JF; Wiggins GA; Giles GG; Hopper JL; Southey MC
Breast Cancer Res; 2017 Mar; 19(1):30. PubMed ID: 28302160
[TBL] [Abstract][Full Text] [Related]
18. Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD.
Hu S; Vich Vila A; Gacesa R; Collij V; Stevens C; Fu JM; Wong I; Talkowski ME; Rivas MA; Imhann F; Bolte L; van Dullemen H; Dijkstra G; Visschedijk MC; Festen EA; Xavier RJ; Fu J; Daly MJ; Wijmenga C; Zhernakova A; Kurilshikov A; Weersma RK
Gut; 2021 Feb; 70(2):285-296. PubMed ID: 32651235
[TBL] [Abstract][Full Text] [Related]
19. Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease.
Meddens CA; Harakalova M; van den Dungen NA; Foroughi Asl H; Hijma HJ; Cuppen EP; Björkegren JL; Asselbergs FW; Nieuwenhuis EE; Mokry M
Genome Biol; 2016 Nov; 17(1):247. PubMed ID: 27903283
[TBL] [Abstract][Full Text] [Related]
20. Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
Yamasaki M; Makino T; Khor SS; Toyoda H; Miyagawa T; Liu X; Kuwabara H; Kano Y; Shimada T; Sugiyama T; Nishida H; Sugaya N; Tochigi M; Otowa T; Okazaki Y; Kaiya H; Kawamura Y; Miyashita A; Kuwano R; Kasai K; Tanii H; Sasaki T; Honda M; Tokunaga K
BMC Med Genomics; 2020 Mar; 13(1):55. PubMed ID: 32223758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]