190 related articles for article (PubMed ID: 21304891)
1. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.
Gamazon ER; Nicolae DL; Cox NJ
PLoS Genet; 2011 Feb; 7(2):e1001292. PubMed ID: 21304891
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Copy number polymorphisms and anticancer pharmacogenomics.
Gamazon ER; Huang RS; Dolan ME; Cox NJ
Genome Biol; 2011; 12(5):R46. PubMed ID: 21609475
[TBL] [Abstract][Full Text] [Related]
4. Origins and functional impact of copy number variation in the human genome.
Conrad DF; Pinto D; Redon R; Feuk L; Gokcumen O; Zhang Y; Aerts J; Andrews TD; Barnes C; Campbell P; Fitzgerald T; Hu M; Ihm CH; Kristiansson K; Macarthur DG; Macdonald JR; Onyiah I; Pang AW; Robson S; Stirrups K; Valsesia A; Walter K; Wei J; ; Tyler-Smith C; Carter NP; Lee C; Scherer SW; Hurles ME
Nature; 2010 Apr; 464(7289):704-12. PubMed ID: 19812545
[TBL] [Abstract][Full Text] [Related]
5. Cis and trans effects of human genomic variants on gene expression.
Bryois J; Buil A; Evans DM; Kemp JP; Montgomery SB; Conrad DF; Ho KM; Ring S; Hurles M; Deloukas P; Davey Smith G; Dermitzakis ET
PLoS Genet; 2014 Jul; 10(7):e1004461. PubMed ID: 25010687
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.
Xu L; Cole JB; Bickhart DM; Hou Y; Song J; VanRaden PM; Sonstegard TS; Van Tassell CP; Liu GE
BMC Genomics; 2014 Aug; 15(1):683. PubMed ID: 25128478
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.
Falque M; Jebreen K; Paux E; Knaak C; Mezmouk S; Martin OC
Genetics; 2020 Mar; 214(3):561-576. PubMed ID: 31882400
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer.
Yu Y; Werdyani S; Carey M; Parfrey P; Yilmaz YE; Savas S
Mol Oncol; 2021 Dec; 15(12):3329-3347. PubMed ID: 34309201
[TBL] [Abstract][Full Text] [Related]
12. Polymorphisms involving gain or loss of CpG sites are significantly enriched in trait-associated SNPs.
Zhou D; Li Z; Yu D; Wan L; Zhu Y; Lai M; Zhang D
Oncotarget; 2015 Nov; 6(37):39995-40004. PubMed ID: 26503467
[TBL] [Abstract][Full Text] [Related]
13. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.
Gamazon ER; Badner JA; Cheng L; Zhang C; Zhang D; Cox NJ; Gershon ES; Kelsoe JR; Greenwood TA; Nievergelt CM; Chen C; McKinney R; Shilling PD; Schork NJ; Smith EN; Bloss CS; Nurnberger JI; Edenberg HJ; Foroud T; Koller DL; Scheftner WA; Coryell W; Rice J; Lawson WB; Nwulia EA; Hipolito M; Byerley W; McMahon FJ; Schulze TG; Berrettini WH; Potash JB; Zandi PP; Mahon PB; McInnis MG; Zöllner S; Zhang P; Craig DW; Szelinger S; Barrett TB; Liu C
Mol Psychiatry; 2013 Mar; 18(3):340-6. PubMed ID: 22212596
[TBL] [Abstract][Full Text] [Related]
14. Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs.
Seroussi E; Glick G; Shirak A; Yakobson E; Weller JI; Ezra E; Zeron Y
BMC Genomics; 2010 Nov; 11():673. PubMed ID: 21114805
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Tissue-Specific eQTL in Zebrafish.
Dobrinski KP
Methods Mol Biol; 2020; 2082():239-249. PubMed ID: 31849020
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Priebe L; Degenhardt FA; Herms S; Haenisch B; Mattheisen M; Nieratschker V; Weingarten M; Witt S; Breuer R; Paul T; Alblas M; Moebus S; Lathrop M; Leboyer M; Schreiber S; Grigoroiu-Serbanescu M; Maier W; Propping P; Rietschel M; Nöthen MM; Cichon S; Mühleisen TW
Mol Psychiatry; 2012 Apr; 17(4):421-32. PubMed ID: 21358712
[TBL] [Abstract][Full Text] [Related]
18. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.
Glessner JT; Li J; Desai A; Palmer M; Kim D; Lucas AM; Chang X; Connolly JJ; Almoguera B; Harley JB; Jarvik GP; Ritchie MD; Sleiman PMA; Roden DM; Crosslin D; Hakonarson H
Int J Cardiol; 2020 Jan; 298():107-113. PubMed ID: 31447229
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
[TBL] [Abstract][Full Text] [Related]
20. Genetic-variant hotspots and hotspot clusters in the human genome facilitating adaptation while increasing instability.
Long X; Xue H
Hum Genomics; 2021 Mar; 15(1):19. PubMed ID: 33741065
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
