194 related articles for article (PubMed ID: 22384383)
1. 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]
2. Genome-wide association study of Alzheimer's disease.
Kamboh MI; Demirci FY; Wang X; Minster RL; Carrasquillo MM; Pankratz VS; Younkin SG; Saykin AJ; ; Jun G; Baldwin C; Logue MW; Buros J; Farrer L; Pericak-Vance MA; Haines JL; Sweet RA; Ganguli M; Feingold E; Dekosky ST; Lopez OL; Barmada MM
Transl Psychiatry; 2012 May; 2(5):e117. PubMed ID: 22832961
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts.
Zhang X; Abdellaoui A; Rucker J; de Jong S; Potash JB; Weissman MM; Shi J; Knowles JA; Pato C; Pato M; Sobell J; Smit JH; Hottenga JJ; de Geus EJC; Lewis CM; Buttenschøn HN; Craddock N; Jones I; Jones L; McGuffin P; Mors O; Owen MJ; Preisig M; Rietschel M; Rice JP; Rivera M; Uher R; Gejman PV; Sanders AR; Boomsma D; Penninx BWJH; Breen G; Levinson DF
Biol Psychiatry; 2019 Jun; 85(12):1065-1073. PubMed ID: 31003785
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study.
Swaminathan S; Shen L; Kim S; Inlow M; West JD; Faber KM; Foroud T; Mayeux R; Saykin AJ; ;
Curr Alzheimer Res; 2012 Sep; 9(7):801-14. PubMed ID: 22486522
[TBL] [Abstract][Full Text] [Related]
7. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
Chapman J; Rees E; Harold D; Ivanov D; Gerrish A; Sims R; Hollingworth P; Stretton A; ; Holmans P; Owen MJ; O'Donovan MC; Williams J; Kirov G
Hum Mol Genet; 2013 Feb; 22(4):816-24. PubMed ID: 23148125
[TBL] [Abstract][Full Text] [Related]
8. Late-Onset Alzheimer's Disease Genes and the Potentially Implicated Pathways.
Rosenthal SL; Kamboh MI
Curr Genet Med Rep; 2014; 2(2):85-101. PubMed ID: 24829845
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
Vardarajan BN; Ghani M; Kahn A; Sheikh S; Sato C; Barral S; Lee JH; Cheng R; Reitz C; Lantigua R; Reyes-Dumeyer D; Medrano M; Jimenez-Velazquez IZ; Rogaeva E; St George-Hyslop P; Mayeux R
Ann Neurol; 2015 Sep; 78(3):487-98. PubMed ID: 26101835
[TBL] [Abstract][Full Text] [Related]
11. Genetics of Alzheimer's disease.
Chouraki V; Seshadri S
Adv Genet; 2014; 87():245-94. PubMed ID: 25311924
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Expression of novel Alzheimer's disease risk genes in control and Alzheimer's disease brains.
Karch CM; Jeng AT; Nowotny P; Cady J; Cruchaga C; Goate AM
PLoS One; 2012; 7(11):e50976. PubMed ID: 23226438
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample.
Guffanti G; Torri F; Rasmussen J; Clark AP; Lakatos A; Turner JA; Fallon JH; Saykin AJ; Weiner M; ; Vawter MP; Knowles JA; Potkin SG; Macciardi F
Genomics; 2013 Aug; 102(2):112-22. PubMed ID: 23583670
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.
Szigeti K; Lal D; Li Y; Doody RS; Wilhelmsen K; Yan L; Liu S; Ma C;
J Alzheimers Dis; 2013; 33(2):517-23. PubMed ID: 23202439
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. CR1, ABCA7, and APOE genes affect the features of cognitive impairment in Alzheimer's disease.
Chung SJ; Kim MJ; Kim YJ; Kim J; You S; Jang EH; Kim SY; Lee JH
J Neurol Sci; 2014 Apr; 339(1-2):91-6. PubMed ID: 24530172
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]