-
1
-
-
0034121235
-
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins
-
A.J. MacGregor, H. Snieder, A.S. Rigby, M. Koskenvuo, J. Kaprio, K. Aho, and A.J. Silman Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins Arthritis Rheum. 43 2000 30 37
-
(2000)
Arthritis Rheum.
, vol.43
, pp. 30-37
-
-
MacGregor, A.J.1
Snieder, H.2
Rigby, A.S.3
Koskenvuo, M.4
Kaprio, J.5
Aho, K.6
Silman, A.J.7
-
2
-
-
77952888454
-
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
-
BIRAC Consortium YEAR Consortium
-
E.A. Stahl, S. Raychaudhuri, E.F. Remmers, G. Xie, S. Eyre, B.P. Thomson, Y. Li, F.A. Kurreeman, A. Zhernakova, A. Hinks BIRAC Consortium YEAR Consortium Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci Nat. Genet. 42 2010 508 514
-
(2010)
Nat. Genet.
, vol.42
, pp. 508-514
-
-
Stahl, E.A.1
Raychaudhuri, S.2
Remmers, E.F.3
Xie, G.4
Eyre, S.5
Thomson, B.P.6
Li, Y.7
Kurreeman, F.A.8
Zhernakova, A.9
Hinks, A.10
-
3
-
-
79952262073
-
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci
-
A. Zhernakova, E.A. Stahl, G. Trynka, S. Raychaudhuri, E.A. Festen, L. Franke, H.J. Westra, R.S. Fehrmann, F.A. Kurreeman, and B. Thomson Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci PLoS Genet. 7 2011 e1002004
-
(2011)
PLoS Genet.
, vol.7
, pp. 1002004
-
-
Zhernakova, A.1
Stahl, E.A.2
Trynka, G.3
Raychaudhuri, S.4
Festen, E.A.5
Franke, L.6
Westra, H.J.7
Fehrmann, R.S.8
Kurreeman, F.A.9
Thomson, B.10
-
4
-
-
79958006547
-
Fine mapping the TAGAP risk locus in rheumatoid arthritis
-
R. Chen, E.A. Stahl, F.A. Kurreeman, P.K. Gregersen, K.A. Siminovitch, J. Worthington, L. Padyukov, S. Raychaudhuri, and R.M. Plenge Fine mapping the TAGAP risk locus in rheumatoid arthritis Genes Immun. 12 2011 314 318
-
(2011)
Genes Immun.
, vol.12
, pp. 314-318
-
-
Chen, R.1
Stahl, E.A.2
Kurreeman, F.A.3
Gregersen, P.K.4
Siminovitch, K.A.5
Worthington, J.6
Padyukov, L.7
Raychaudhuri, S.8
Plenge, R.M.9
-
5
-
-
52949111858
-
Common variants at CD40 and other loci confer risk of rheumatoid arthritis
-
S. Raychaudhuri, E.F. Remmers, A.T. Lee, R. Hackett, C. Guiducci, N.P. Burtt, L. Gianniny, B.D. Korman, L. Padyukov, and F.A. Kurreeman Common variants at CD40 and other loci confer risk of rheumatoid arthritis Nat. Genet. 40 2008 1216 1223
-
(2008)
Nat. Genet.
, vol.40
, pp. 1216-1223
-
-
Raychaudhuri, S.1
Remmers, E.F.2
Lee, A.T.3
Hackett, R.4
Guiducci, C.5
Burtt, N.P.6
Gianniny, L.7
Korman, B.D.8
Padyukov, L.9
Kurreeman, F.A.10
-
6
-
-
70649086092
-
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk
-
BIRAC Consortium YEAR Consortium
-
S. Raychaudhuri, B.P. Thomson, E.F. Remmers, S. Eyre, A. Hinks, C. Guiducci, J.J. Catanese, G. Xie, E.A. Stahl, R. Chen BIRAC Consortium YEAR Consortium Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk Nat. Genet. 41 2009 1313 1318
-
(2009)
Nat. Genet.
, vol.41
, pp. 1313-1318
-
-
Raychaudhuri, S.1
Thomson, B.P.2
Remmers, E.F.3
Eyre, S.4
Hinks, A.5
Guiducci, C.6
Catanese, J.J.7
Xie, G.8
Stahl, E.A.9
Chen, R.10
-
7
-
-
77952885768
-
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
-
Y. Kochi, Y. Okada, A. Suzuki, K. Ikari, C. Terao, A. Takahashi, K. Yamazaki, N. Hosono, K. Myouzen, and T. Tsunoda A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility Nat. Genet. 42 2010 515 519
-
(2010)
Nat. Genet.
, vol.42
, pp. 515-519
-
-
Kochi, Y.1
Okada, Y.2
Suzuki, A.3
Ikari, K.4
Terao, C.5
Takahashi, A.6
Yamazaki, K.7
Hosono, N.8
Myouzen, K.9
Tsunoda, T.10
-
8
-
-
78650860672
-
Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records
-
F. Kurreeman, K. Liao, L. Chibnik, B. Hickey, E. Stahl, V. Gainer, G. Li, L. Bry, S. Mahan, and K. Ardlie Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records Am. J. Hum. Genet. 88 2011 57 69
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 57-69
-
-
Kurreeman, F.1
Liao, K.2
Chibnik, L.3
Hickey, B.4
Stahl, E.5
Gainer, V.6
Li, G.7
Bry, L.8
Mahan, S.9
Ardlie, K.10
-
9
-
-
79953705986
-
Genome-wide association study of rheumatoid arthritis in Koreans: Population-specific loci as well as overlap with European susceptibility loci
-
J. Freudenberg, H.S. Lee, B.G. Han, H.D. Shin, Y.M. Kang, Y.K. Sung, S.C. Shim, C.B. Choi, A.T. Lee, P.K. Gregersen, and S.C. Bae Genome-wide association study of rheumatoid arthritis in Koreans: Population-specific loci as well as overlap with European susceptibility loci Arthritis Rheum. 63 2011 884 893
-
(2011)
Arthritis Rheum.
, vol.63
, pp. 884-893
-
-
Freudenberg, J.1
Lee, H.S.2
Han, B.G.3
Shin, H.D.4
Kang, Y.M.5
Sung, Y.K.6
Shim, S.C.7
Choi, C.B.8
Lee, A.T.9
Gregersen, P.K.10
Bae, S.C.11
-
10
-
-
78649831816
-
Most common single-nucleotide polymorphisms associated with rheumatoid arthritis in persons of European ancestry confer risk of rheumatoid arthritis in African Americans
-
L.B. Hughes, R.J. Reynolds, E.E. Brown, J.M. Kelley, B. Thomson, D.L. Conn, B.L. Jonas, A.O. Westfall, M.A. Padilla, and L.F. Callahan Most common single-nucleotide polymorphisms associated with rheumatoid arthritis in persons of European ancestry confer risk of rheumatoid arthritis in African Americans Arthritis Rheum. 62 2010 3547 3553
-
(2010)
Arthritis Rheum.
, vol.62
, pp. 3547-3553
-
-
Hughes, L.B.1
Reynolds, R.J.2
Brown, E.E.3
Kelley, J.M.4
Thomson, B.5
Conn, D.L.6
Jonas, B.L.7
Westfall, A.O.8
Padilla, M.A.9
Callahan, L.F.10
-
11
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
S.P. Dickson, K. Wang, I. Krantz, H. Hakonarson, and D.B. Goldstein Rare variants create synthetic genome-wide associations PLoS Biol. 8 2010 e1000294
-
(2010)
PLoS Biol.
, vol.8
, pp. 1000294
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
13
-
-
79959859184
-
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
-
Y. Okada, T. Hirota, Y. Kamatani, A. Takahashi, H. Ohmiya, N. Kumasaka, K. Higasa, Y. Yamaguchi-Kabata, N. Hosono, and M.A. Nalls Identification of nine novel loci associated with white blood cell subtypes in a Japanese population PLoS Genet. 7 2011 e1002067
-
(2011)
PLoS Genet.
, vol.7
, pp. 1002067
-
-
Okada, Y.1
Hirota, T.2
Kamatani, Y.3
Takahashi, A.4
Ohmiya, H.5
Kumasaka, N.6
Higasa, K.7
Yamaguchi-Kabata, Y.8
Hosono, N.9
Nalls, M.A.10
-
14
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
B.L. Browning, and S.R. Browning A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals Am. J. Hum. Genet. 84 2009 210 223
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
15
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
J. Marchini, B. Howie, S. Myers, G. McVean, and P. Donnelly A new multipoint method for genome-wide association studies by imputation of genotypes Nat. Genet. 39 2007 906 913
-
(2007)
Nat. Genet.
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
16
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
S. Purcell, B. Neale, K. Todd-Brown, L. Thomas, M.A. Ferreira, D. Bender, J. Maller, P. Sklar, P.I. de Bakker, M.J. Daly, and P.C. Sham PLINK: A tool set for whole-genome association and population-based linkage analyses Am. J. Hum. Genet. 81 2007 559 575
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
17
-
-
58149345887
-
Practical aspects of imputation-driven meta-analysis of genome-wide association studies
-
P.I. de Bakker, M.A. Ferreira, X. Jia, B.M. Neale, S. Raychaudhuri, and B.F. Voight Practical aspects of imputation-driven meta-analysis of genome-wide association studies Hum. Mol. Genet. 17 R2 2008 R122 R128
-
(2008)
Hum. Mol. Genet.
, vol.17
, Issue.R2
-
-
De Bakker, P.I.1
Ferreira, M.A.2
Jia, X.3
Neale, B.M.4
Raychaudhuri, S.5
Voight, B.F.6
-
18
-
-
79952195585
-
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
-
C.A. Anderson, G. Boucher, C.W. Lees, A. Franke, M. D'Amato, K.D. Taylor, J.C. Lee, P. Goyette, M. Imielinski, and A. Latiano Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 Nat. Genet. 43 2011 246 252
-
(2011)
Nat. Genet.
, vol.43
, pp. 246-252
-
-
Anderson, C.A.1
Boucher, G.2
Lees, C.W.3
Franke, A.4
D'Amato, M.5
Taylor, K.D.6
Lee, J.C.7
Goyette, P.8
Imielinski, M.9
Latiano, A.10
-
19
-
-
77950243833
-
Multiple common variants for celiac disease influencing immune gene expression
-
P.C. Dubois, G. Trynka, L. Franke, K.A. Hunt, J. Romanos, A. Curtotti, A. Zhernakova, G.A. Heap, R. Adány, and A. Aromaa Multiple common variants for celiac disease influencing immune gene expression Nat. Genet. 42 2010 295 302
-
(2010)
Nat. Genet.
, vol.42
, pp. 295-302
-
-
Dubois, P.C.1
Trynka, G.2
Franke, L.3
Hunt, K.A.4
Romanos, J.5
Curtotti, A.6
Zhernakova, A.7
Heap, G.A.8
Adány, R.9
Aromaa, A.10
-
20
-
-
48349136889
-
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
-
NIDDK IBD Genetics Consortium Belgian-French IBD Consortium Wellcome Trust Case Control Consortium
-
J.C. Barrett, S. Hansoul, D.L. Nicolae, J.H. Cho, R.H. Duerr, J.D. Rioux, S.R. Brant, M.S. Silverberg, K.D. Taylor, M.M. Barmada NIDDK IBD Genetics Consortium Belgian-French IBD Consortium Wellcome Trust Case Control Consortium Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease Nat. Genet. 40 2008 955 962
-
(2008)
Nat. Genet.
, vol.40
, pp. 955-962
-
-
Barrett, J.C.1
Hansoul, S.2
Nicolae, D.L.3
Cho, J.H.4
Duerr, R.H.5
Rioux, J.D.6
Brant, S.R.7
Silverberg, M.S.8
Taylor, K.D.9
Barmada, M.M.10
-
21
-
-
77950298959
-
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
-
NIDDK IBD Genetics Consortium
-
D.P. McGovern, A. Gardet, L. Törkvist, P. Goyette, J. Essers, K.D. Taylor, B.M. Neale, R.T. Ong, C. Lagacé, C. Li NIDDK IBD Genetics Consortium Genome-wide association identifies multiple ulcerative colitis susceptibility loci Nat. Genet. 42 2010 332 337
-
(2010)
Nat. Genet.
, vol.42
, pp. 332-337
-
-
McGovern, D.P.1
Gardet, A.2
Törkvist, L.3
Goyette, P.4
Essers, J.5
Taylor, K.D.6
Neale, B.M.7
Ong, R.T.8
Lagacé, C.9
Li, C.10
-
22
-
-
67349199566
-
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
-
Type 1 Diabetes Genetics Consortium
-
J.C. Barrett, D.G. Clayton, P. Concannon, B. Akolkar, J.D. Cooper, H.A. Erlich, C. Julier, G. Morahan, J. Nerup, C. Nierras Type 1 Diabetes Genetics Consortium Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Nat. Genet. 41 2009 703 707
-
(2009)
Nat. Genet.
, vol.41
, pp. 703-707
-
-
Barrett, J.C.1
Clayton, D.G.2
Concannon, P.3
Akolkar, B.4
Cooper, J.D.5
Erlich, H.A.6
Julier, C.7
Morahan, G.8
Nerup, J.9
Nierras, C.10
-
23
-
-
77957113600
-
A large-scale, consortium-based genomewide association study of asthma
-
GABRIEL Consortium
-
M.F. Moffatt, I.G. Gut, F. Demenais, D.P. Strachan, E. Bouzigon, S. Heath, E. von Mutius, M. Farrall, M. Lathrop, W.O. Cookson GABRIEL Consortium A large-scale, consortium-based genomewide association study of asthma N. Engl. J. Med. 363 2010 1211 1221
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 1211-1221
-
-
Moffatt, M.F.1
Gut, I.G.2
Demenais, F.3
Strachan, D.P.4
Bouzigon, E.5
Heath, S.6
Von Mutius, E.7
Farrall, M.8
Lathrop, M.9
Cookson, W.O.10
-
24
-
-
77955088582
-
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
-
X. Liu, P. Invernizzi, Y. Lu, R. Kosoy, Y. Lu, I. Bianchi, M. Podda, C. Xu, G. Xie, and F. Macciardi Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis Nat. Genet. 42 2010 658 660
-
(2010)
Nat. Genet.
, vol.42
, pp. 658-660
-
-
Liu, X.1
Invernizzi, P.2
Lu, Y.3
Kosoy, R.4
Lu, Y.5
Bianchi, I.6
Podda, M.7
Xu, C.8
Xie, G.9
MacCiardi, F.10
-
25
-
-
34548367511
-
Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes
-
C.E. Lowe, J.D. Cooper, T. Brusko, N.M. Walker, D.J. Smyth, R. Bailey, K. Bourget, V. Plagnol, S. Field, and M. Atkinson Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes Nat. Genet. 39 2007 1074 1082
-
(2007)
Nat. Genet.
, vol.39
, pp. 1074-1082
-
-
Lowe, C.E.1
Cooper, J.D.2
Brusko, T.3
Walker, N.M.4
Smyth, D.J.5
Bailey, R.6
Bourget, K.7
Plagnol, V.8
Field, S.9
Atkinson, M.10
-
26
-
-
41349103493
-
Newly identified genetic risk variants for celiac disease related to the immune response
-
K.A. Hunt, A. Zhernakova, G. Turner, G.A. Heap, L. Franke, M. Bruinenberg, J. Romanos, L.C. Dinesen, A.W. Ryan, and D. Panesar Newly identified genetic risk variants for celiac disease related to the immune response Nat. Genet. 40 2008 395 402
-
(2008)
Nat. Genet.
, vol.40
, pp. 395-402
-
-
Hunt, K.A.1
Zhernakova, A.2
Turner, G.3
Heap, G.A.4
Franke, L.5
Bruinenberg, M.6
Romanos, J.7
Dinesen, L.C.8
Ryan, A.W.9
Panesar, D.10
-
27
-
-
34347341846
-
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
-
Genetics of Type 1 Diabetes in Finland Wellcome Trust Case Control Consortium
-
J.A. Todd, N.M. Walker, J.D. Cooper, D.J. Smyth, K. Downes, V. Plagnol, R. Bailey, S. Nejentsev, S.F. Field, F. Payne Genetics of Type 1 Diabetes in Finland Wellcome Trust Case Control Consortium Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Nat. Genet. 39 2007 857 864
-
(2007)
Nat. Genet.
, vol.39
, pp. 857-864
-
-
Todd, J.A.1
Walker, N.M.2
Cooper, J.D.3
Smyth, D.J.4
Downes, K.5
Plagnol, V.6
Bailey, R.7
Nejentsev, S.8
Field, S.F.9
Payne, F.10
-
28
-
-
67651205715
-
Identifying relationships among genomic disease regions: Predicting genes at pathogenic SNP associations and rare deletions
-
International Schizophrenia Consortium
-
S. Raychaudhuri, R.M. Plenge, E.J. Rossin, A.C. Ng, S.M. Purcell, P. Sklar, E.M. Scolnick, R.J. Xavier, D. Altshuler, M.J. Daly International Schizophrenia Consortium Identifying relationships among genomic disease regions: Predicting genes at pathogenic SNP associations and rare deletions PLoS Genet. 5 2009 e1000534
-
(2009)
PLoS Genet.
, vol.5
, pp. 1000534
-
-
Raychaudhuri, S.1
Plenge, R.M.2
Rossin, E.J.3
Ng, A.C.4
Purcell, S.M.5
Sklar, P.6
Scolnick, E.M.7
Xavier, R.J.8
Altshuler, D.9
Daly, M.J.10
-
29
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
E.T. Cirulli, and D.B. Goldstein Uncovering the roles of rare variants in common disease through whole-genome sequencing Nat. Rev. Genet. 11 2010 415 425
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
30
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
I.A. Adzhubei, S. Schmidt, L. Peshkin, V.E. Ramensky, A. Gerasimova, P. Bork, A.S. Kondrashov, and S.R. Sunyaev A method and server for predicting damaging missense mutations Nat. Methods 7 2010 248 249
-
(2010)
Nat. Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
31
-
-
0036016931
-
Aiolos and Ikaros: Regulators of lymphocyte development, homeostasis and lymphoproliferation
-
C. Schmitt, C. Tonnelle, A. Dalloul, C. Chabannon, P. Debré, and A. Rebollo Aiolos and Ikaros: Regulators of lymphocyte development, homeostasis and lymphoproliferation Apoptosis 7 2002 277 284
-
(2002)
Apoptosis
, vol.7
, pp. 277-284
-
-
Schmitt, C.1
Tonnelle, C.2
Dalloul, A.3
Chabannon, C.4
Debré, P.5
Rebollo, A.6
-
32
-
-
0037442214
-
Lack of the transcriptional coactivator OBF-1 prevents the development of systemic lupus erythematosus-like phenotypes in Aiolos mutant mice
-
J. Sun, G. Matthias, M.J. Mihatsch, K. Georgopoulos, and P. Matthias Lack of the transcriptional coactivator OBF-1 prevents the development of systemic lupus erythematosus-like phenotypes in Aiolos mutant mice J. Immunol. 170 2003 1699 1706
-
(2003)
J. Immunol.
, vol.170
, pp. 1699-1706
-
-
Sun, J.1
Matthias, G.2
Mihatsch, M.J.3
Georgopoulos, K.4
Matthias, P.5
-
33
-
-
69449101386
-
Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease
-
D.J. Verlaan, S. Berlivet, G.M. Hunninghake, A.M. Madore, M. Larivire, S. Moussette, E. Grundberg, T. Kwan, M. Ouimet, and B. Ge Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease Am. J. Hum. Genet. 85 2009 377 393
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 377-393
-
-
Verlaan, D.J.1
Berlivet, S.2
Hunninghake, G.M.3
Madore, A.M.4
Larivire, M.5
Moussette, S.6
Grundberg, E.7
Kwan, T.8
Ouimet, M.9
Ge, B.10
-
34
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
International Schizophrenia Consortium
-
S.M. Purcell, N.R. Wray, J.L. Stone, P.M. Visscher, M.C. O'Donovan, P.F. Sullivan, P. Sklar International Schizophrenia Consortium Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature 460 2009 748 752
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
35
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
J. Yang, T.A. Manolio, L.R. Pasquale, E. Boerwinkle, N. Caporaso, J.M. Cunningham, M. de Andrade, B. Feenstra, E. Feingold, and M.G. Hayes Genome partitioning of genetic variation for complex traits using common SNPs Nat. Genet. 43 2011 519 525
-
(2011)
Nat. Genet.
, vol.43
, pp. 519-525
-
-
Yang, J.1
Manolio, T.A.2
Pasquale, L.R.3
Boerwinkle, E.4
Caporaso, N.5
Cunningham, J.M.6
De Andrade, M.7
Feenstra, B.8
Feingold, E.9
Hayes, M.G.10
|