424 related articles for article (PubMed ID: 19997636)
1. 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]
2. Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
Blauw HM; Veldink JH; van Es MA; van Vught PW; Saris CG; van der Zwaag B; Franke L; Burbach JP; Wokke JH; Ophoff RA; van den Berg LH
Lancet Neurol; 2008 Apr; 7(4):319-26. PubMed ID: 18313986
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Blauw HM; Al-Chalabi A; Andersen PM; van Vught PW; Diekstra FP; van Es MA; Saris CG; Groen EJ; van Rheenen W; Koppers M; Van't Slot R; Strengman E; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Kiemeney LA; Vermeulen SH; Birve A; Waibel S; Meyer T; Cronin S; McLaughlin RL; Hardiman O; Sapp PC; Tobin MD; Wain LV; Tomik B; Slowik A; Lemmens R; Rujescu D; Schulte C; Gasser T; Brown RH; Landers JE; Robberecht W; Ludolph AC; Ophoff RA; Veldink JH; van den Berg LH
Hum Mol Genet; 2010 Oct; 19(20):4091-9. PubMed ID: 20685689
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.
Morello G; Guarnaccia M; Spampinato AG; La Cognata V; D'Agata V; Cavallaro S
Mol Neurobiol; 2018 Feb; 55(2):1299-1322. PubMed ID: 28120152
[TBL] [Abstract][Full Text] [Related]
7. Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
Laaksovirta H; Peuralinna T; Schymick JC; Scholz SW; Lai SL; Myllykangas L; Sulkava R; Jansson L; Hernandez DG; Gibbs JR; Nalls MA; Heckerman D; Tienari PJ; Traynor BJ
Lancet Neurol; 2010 Oct; 9(10):978-85. PubMed ID: 20801718
[TBL] [Abstract][Full Text] [Related]
8. Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.
Cronin S; Blauw HM; Veldink JH; van Es MA; Ophoff RA; Bradley DG; van den Berg LH; Hardiman O
Hum Mol Genet; 2008 Nov; 17(21):3392-8. PubMed ID: 18689356
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.
Moon S; Keam B; Hwang MY; Lee Y; Park S; Oh JH; Kim YJ; Lee HS; Kim NH; Kim YJ; Kim DH; Han BG; Kim BJ; Lee J
BMC Musculoskelet Disord; 2015 Apr; 16():76. PubMed ID: 25880085
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.
Uyan Ö; Ömür Ö; Ağım ZS; Özoğuz A; Li H; Parman Y; Deymeer F; Oflazer P; Koç F; Tan E; Özçelik H; Başak AN
PLoS One; 2013; 8(8):e72381. PubMed ID: 23991104
[TBL] [Abstract][Full Text] [Related]
16. Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis.
Pamphlett R; Morahan JM; Luquin N; Yu B
Muscle Nerve; 2011 Oct; 44(4):492-8. PubMed ID: 21826678
[TBL] [Abstract][Full Text] [Related]
17. Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis.
Meltz Steinberg K; Nicholas TJ; Koboldt DC; Yu B; Mardis E; Pamphlett R
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(5-6):385-92. PubMed ID: 25960086
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
; Craddock N; Hurles ME; Cardin N; Pearson RD; Plagnol V; Robson S; Vukcevic D; Barnes C; Conrad DF; Giannoulatou E; Holmes C; Marchini JL; Stirrups K; Tobin MD; Wain LV; Yau C; Aerts J; Ahmad T; Andrews TD; Arbury H; Attwood A; Auton A; Ball SG; Balmforth AJ; Barrett JC; Barroso I; Barton A; Bennett AJ; Bhaskar S; Blaszczyk K; Bowes J; Brand OJ; Braund PS; Bredin F; Breen G; Brown MJ; Bruce IN; Bull J; Burren OS; Burton J; Byrnes J; Caesar S; Clee CM; Coffey AJ; Connell JM; Cooper JD; Dominiczak AF; Downes K; Drummond HE; Dudakia D; Dunham A; Ebbs B; Eccles D; Edkins S; Edwards C; Elliot A; Emery P; Evans DM; Evans G; Eyre S; Farmer A; Ferrier IN; Feuk L; Fitzgerald T; Flynn E; Forbes A; Forty L; Franklyn JA; Freathy RM; Gibbs P; Gilbert P; Gokumen O; Gordon-Smith K; Gray E; Green E; Groves CJ; Grozeva D; Gwilliam R; Hall A; Hammond N; Hardy M; Harrison P; Hassanali N; Hebaishi H; Hines S; Hinks A; Hitman GA; Hocking L; Howard E; Howard P; Howson JM; Hughes D; Hunt S; Isaacs JD; Jain M; Jewell DP; Johnson T; Jolley JD; Jones IR; Jones LA; Kirov G; Langford CF; Lango-Allen H; Lathrop GM; Lee J; Lee KL; Lees C; Lewis K; Lindgren CM; Maisuria-Armer M; Maller J; Mansfield J; Martin P; Massey DC; McArdle WL; McGuffin P; McLay KE; Mentzer A; Mimmack ML; Morgan AE; Morris AP; Mowat C; Myers S; Newman W; Nimmo ER; O'Donovan MC; Onipinla A; Onyiah I; Ovington NR; Owen MJ; Palin K; Parnell K; Pernet D; Perry JR; Phillips A; Pinto D; Prescott NJ; Prokopenko I; Quail MA; Rafelt S; Rayner NW; Redon R; Reid DM; Renwick ; Ring SM; Robertson N; Russell E; St Clair D; Sambrook JG; Sanderson JD; Schuilenburg H; Scott CE; Scott R; Seal S; Shaw-Hawkins S; Shields BM; Simmonds MJ; Smyth DJ; Somaskantharajah E; Spanova K; Steer S; Stephens J; Stevens HE; Stone MA; Su Z; Symmons DP; Thompson JR; Thomson W; Travers ME; Turnbull C; Valsesia A; Walker M; Walker NM; Wallace C; Warren-Perry M; Watkins NA; Webster J; Weedon MN; Wilson AG; Woodburn M; Wordsworth BP; Young AH; Zeggini E; Carter NP; Frayling TM; Lee C; McVean G; Munroe PB; Palotie A; Sawcer SJ; Scherer SW; Strachan DP; Tyler-Smith C; Brown MA; Burton PR; Caulfield MJ; Compston A; Farrall M; Gough SC; Hall AS; Hattersley AT; Hill AV; Mathew CG; Pembrey M; Satsangi J; Stratton MR; Worthington J; Deloukas P; Duncanson A; Kwiatkowski DP; McCarthy MI; Ouwehand W; Parkes M; Rahman N; Todd JA; Samani NJ; Donnelly P
Nature; 2010 Apr; 464(7289):713-20. PubMed ID: 20360734
[TBL] [Abstract][Full Text] [Related]
19. Analysis of copy number variations at 15 schizophrenia-associated loci.
Rees E; Walters JT; Georgieva L; Isles AR; Chambert KD; Richards AL; Mahoney-Davies G; Legge SE; Moran JL; McCarroll SA; O'Donovan MC; Owen MJ; Kirov G
Br J Psychiatry; 2014 Feb; 204(2):108-14. PubMed ID: 24311552
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
