141 related articles for article (PubMed ID: 24073418)
1. Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews.
Liu X; Cheng R; Ye X; Verbitsky M; Kisselev S; Mejia-Santana H; Louis E; Cote L; Andrews H; Waters C; Ford B; Fahn S; Marder K; Lee J; Clark L
Mol Genet Genomic Med; 2013 Sep; 1(3):142-154. PubMed ID: 24073418
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
Liu X; Cheng R; Verbitsky M; Kisselev S; Browne A; Mejia-Sanatana H; Louis ED; Cote LJ; Andrews H; Waters C; Ford B; Frucht S; Fahn S; Marder K; Clark LN; Lee JH
BMC Med Genet; 2011 Aug; 12():104. PubMed ID: 21812969
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics.
Ghani M; Pinto D; Lee JH; Grinberg Y; Sato C; Moreno D; Scherer SW; Mayeux R; St George-Hyslop P; Rogaeva E
G3 (Bethesda); 2012 Jan; 2(1):71-8. PubMed ID: 22384383
[TBL] [Abstract][Full Text] [Related]
5. A genome-wide assessment of rare copy number variants in colorectal cancer.
Li Z; Yu D; Gan M; Shan Q; Yin X; Tang S; Zhang S; Shi Y; Zhu Y; Lai M; Zhang D
Oncotarget; 2015 Sep; 6(28):26411-23. PubMed ID: 26315111
[TBL] [Abstract][Full Text] [Related]
6. Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Soemedi R; Wilson IJ; Bentham J; Darlay R; Töpf A; Zelenika D; Cosgrove C; Setchfield K; Thornborough C; Granados-Riveron J; Blue GM; Breckpot J; Hellens S; Zwolinkski S; Glen E; Mamasoula C; Rahman TJ; Hall D; Rauch A; Devriendt K; Gewillig M; O' Sullivan J; Winlaw DS; Bu'Lock F; Brook JD; Bhattacharya S; Lathrop M; Santibanez-Koref M; Cordell HJ; Goodship JA; Keavney BD
Am J Hum Genet; 2012 Sep; 91(3):489-501. PubMed ID: 22939634
[TBL] [Abstract][Full Text] [Related]
7. A genome-wide CNV association study on panic disorder in a Japanese population.
Kawamura Y; Otowa T; Koike A; Sugaya N; Yoshida E; Yasuda S; Inoue K; Takei K; Konishi Y; Tanii H; Shimada T; Tochigi M; Kakiuchi C; Umekage T; Liu X; Nishida N; Tokunaga K; Kuwano R; Okazaki Y; Kaiya H; Sasaki T
J Hum Genet; 2011 Dec; 56(12):852-6. PubMed ID: 22011818
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.
Kim DS; Kim JH; Burt AA; Crosslin DR; Burnham N; Kim CE; McDonald-McGinn DM; Zackai EH; Nicolson SC; Spray TL; Stanaway IB; Nickerson DA; Heagerty PJ; Hakonarson H; Gaynor JW; Jarvik GP
J Thorac Cardiovasc Surg; 2016 Apr; 151(4):1147-51.e4. PubMed ID: 26704054
[TBL] [Abstract][Full Text] [Related]
10. A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder.
Halvorsen M; de Schipper E; Boberg J; Strom N; Hagen K; Lindblad-Toh K; Karlsson E; Pedersen N; Bulik C; Fundín B; Landén M; Kvale G; Hansen B; Haavik J; Mattheisen M; Rück C; Mataix-Cols D; Crowley J
Res Sq; 2024 Jan; ():. PubMed ID: 38260575
[TBL] [Abstract][Full Text] [Related]
11. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
Szatkiewicz JP; Neale BM; O'Dushlaine C; Fromer M; Goldstein JI; Moran JL; Chambert K; Kähler A; Magnusson PK; Hultman CM; Sklar P; Purcell S; McCarroll SA; Sullivan PF
Mol Psychiatry; 2013 Nov; 18(11):1178-84. PubMed ID: 23938935
[TBL] [Abstract][Full Text] [Related]
12. Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve.
Carlisle SG; Albasha H; Michelena H; Sabate-Rotes A; Bianco L; De Backer J; Mosquera LM; Yetman AT; Bissell MM; Andreassi MG; Foffa I; Hui DS; Caffarelli A; Kim YY; Guo DC; Citro R; De Marco M; Tretter JT; McBride KL; ; ; Milewicz DM; Body SC; Prakash SK
medRxiv; 2023 Oct; ():. PubMed ID: 37961530
[TBL] [Abstract][Full Text] [Related]
13. Genetic landscape of Parkinson's disease and related diseases in Luxembourg.
Landoulsi Z; Pachchek S; Bobbili DR; Pavelka L; May P; Krüger R;
Front Aging Neurosci; 2023; 15():1282174. PubMed ID: 38173558
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genome-wide Association Study (GWAS) of Germline Copy Number Variations (CNVs) Reveal Genetic Risks of Prostate Cancer in Chinese population.
Wu Y; Chen H; Jiang G; Mo Z; Ye D; Wang M; Qi J; Lin X; Zheng SL; Zhang N; Na R; Ding Q; Xu J; Sun Y
J Cancer; 2018; 9(5):923-928. PubMed ID: 29581771
[No Abstract] [Full Text] [Related]
16. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Niestroj LM; Perez-Palma E; Howrigan DP; Zhou Y; Cheng F; Saarentaus E; Nürnberg P; Stevelink R; Daly MJ; Palotie A; Lal D;
Brain; 2020 Jul; 143(7):2106-2118. PubMed ID: 32568404
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]