-
1
-
-
0034121235
-
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins
-
MacGregor AJ, Snieder H, Rigby AS, Koskenvuo M, Kaprio J, Aho K, Silman AJ: Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins. Arthritis Rheum 2000, 43:30-37.
-
(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
-
3
-
-
77952888454
-
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
-
Stahl EA, Raychaudhuri S, Remmers EF, Xie G, Eyre S, Thomson BP, Li Y, Kurreeman FAS, Zhernakova A, Hinks A, Guiducci C, Chen R, Alfredsson L, Amos CI, Ardlie KG, Barton A, Bowes J, Brouwer E, Burtt NP, Catanese JJ, Coblyn J, Coenen MJH, Costenbader KH, Criswell LA, Crusius JBA, Cui J, de Bakker PIW, De Jager PL, Ding B, Emery P, et al: Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet 2010, 42:508-514.
-
(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.S.8
Zhernakova, A.9
Hinks, A.10
Guiducci, C.11
Chen, R.12
Alfredsson, L.13
Amos, C.I.14
Ardlie, K.G.15
Barton, A.16
Bowes, J.17
Brouwer, E.18
Burtt, N.P.19
Catanese, J.J.20
Coblyn, J.21
Coenen, M.J.H.22
Costenbader, K.H.23
Criswell, L.A.24
Crusius, J.B.A.25
Cui, J.26
de Bakker, P.I.W.27
De Jager, P.L.28
Ding, B.29
Emery, P.30
more..
-
4
-
-
79953705986
-
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci
-
Freudenberg J, Lee HS, Han BG, Shin HD, Kang YM, Sung YK, Shim SC, Choi CB, Lee AT, Gregersen PK, Bae SC: Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. Arthritis Rheum 2011, 63:884-893.
-
(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
-
5
-
-
79952262073
-
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci
-
Zhernakova A, Stahl EA, Trynka G, Raychaudhuri S, Festen EA, Franke L, Westra HJ, Fehrmann RS, Kurreeman FA, Thomson B, Gupta N, Romanos J, McManus R, Ryan AW, Turner G, Brouwer E, Posthumus MD, Remmers EF, Tucci F, Toes R, Grandone E, Mazzilli MC, Rybak A, Cukrowska B, Coenen MJ, Radstake TR, van Riel PL, Li Y, de Bakker PI, Gregersen PK, et al: Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. PLoS Genet 2011, 7:e1002004.
-
(2011)
PLoS Genet
, vol.7
-
-
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
Gupta, N.11
Romanos, J.12
McManus, R.13
Ryan, A.W.14
Turner, G.15
Brouwer, E.16
Posthumus, M.D.17
Remmers, E.F.18
Tucci, F.19
Toes, R.20
Grandone, E.21
Mazzilli, M.C.22
Rybak, A.23
Cukrowska, B.24
Coenen, M.J.25
Radstake, T.R.26
van Riel, P.L.27
Li, Y.28
de Bakker, P.I.29
Gregersen, P.K.30
more..
-
7
-
-
84870531924
-
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
-
Eyre S, Bowes J, Diogo D, Lee A, Barton A, Martin P, Zhernakova A, Stahl E, Viatte S, McAllister K, Amos CI, Padyukov L, Toes RE, Huizinga TW, Wijmenga C, Trynka G, Franke L, Westra HJ, Alfredsson L, Hu X, Sandor C, de Bakker PI, Davila S, Khor CC, Heng KK, Andrews R, Edkins S, Hunt SE, Langford C, Symmons D, et al: High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nat Genet 2012, 44:1336-1340.
-
(2012)
Nat Genet
, vol.44
, pp. 1336-1340
-
-
Eyre, S.1
Bowes, J.2
Diogo, D.3
Lee, A.4
Barton, A.5
Martin, P.6
Zhernakova, A.7
Stahl, E.8
Viatte, S.9
McAllister, K.10
Amos, C.I.11
Padyukov, L.12
Toes, R.E.13
Huizinga, T.W.14
Wijmenga, C.15
Trynka, G.16
Franke, L.17
Westra, H.J.18
Alfredsson, L.19
Hu, X.20
Sandor, C.21
de Bakker, P.I.22
Davila, S.23
Khor, C.C.24
Heng, K.K.25
Andrews, R.26
Edkins, S.27
Hunt, S.E.28
Langford, C.29
Symmons, D.30
more..
-
8
-
-
84988846671
-
High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci
-
[Epub ahead of print].
-
Kim K, Bang SY, Lee HS, Cho SK, Choi CB, Sung YK, Kim TH, Jun JB, Yoo DH, Kang YM, Kim SK, Suh CH, Shim SC, Lee SS, Lee J, Chung WT, Choe JY, Shin HD, Lee JY, Han BG, Nath SK, Eyre S, Bowes J, Pappas DA, Kremer JM, Gonzalez-Gay MA, Rodriguez-Rodriguez L, Arlestig L, Okada Y, Diogo D, et al: High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. Ann Rheum Dis 2014, [Epub ahead of print].
-
(2014)
Ann Rheum Dis
-
-
Kim, K.1
Bang, S.Y.2
Lee, H.S.3
Cho, S.K.4
Choi, C.B.5
Sung, Y.K.6
Kim, T.H.7
Jun, J.B.8
Yoo, D.H.9
Kang, Y.M.10
Kim, S.K.11
Suh, C.H.12
Shim, S.C.13
Lee, S.S.14
Lee, J.15
Chung, W.T.16
Choe, J.Y.17
Shin, H.D.18
Lee, J.Y.19
Han, B.G.20
Nath, S.K.21
Eyre, S.22
Bowes, J.23
Pappas, D.A.24
Kremer, J.M.25
Gonzalez-Gay, M.A.26
Rodriguez-Rodriguez, L.27
Arlestig, L.28
Okada, Y.29
Diogo, D.30
more..
-
9
-
-
75749099775
-
Recent advances in the genetics of rheumatoid arthritis
-
Raychaudhuri S: Recent advances in the genetics of rheumatoid arthritis. Curr Opin Rheumatol 2010, 22:109-118.
-
(2010)
Curr Opin Rheumatol
, vol.22
, pp. 109-118
-
-
Raychaudhuri, S.1
-
10
-
-
84862776511
-
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis
-
Raychaudhuri S, Sandor C, Stahl EA, Freudenberg J, Lee H-S, Jia X, Alfredsson L, Padyukov L, Klareskog L, Worthington J, Siminovitch KA, Bae S-C, Plenge RM, Gregersen PK, de Bakker PIW: Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis. Nat Genet 2012, 44:291-296.
-
(2012)
Nat Genet
, vol.44
, pp. 291-296
-
-
Raychaudhuri, S.1
Sandor, C.2
Stahl, E.A.3
Freudenberg, J.4
Lee, H.-S.5
Jia, X.6
Alfredsson, L.7
Padyukov, L.8
Klareskog, L.9
Worthington, J.10
Siminovitch, K.A.11
Bae, S.-C.12
Plenge, R.M.13
Gregersen, P.K.14
de Bakker, P.I.W.15
-
11
-
-
84860333083
-
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
-
Stahl EA, Wegmann D, Trynka G, Gutierrez-Achury J, Do R, Voight BF, Kraft P, Chen R, Kallberg HJ, Kurreeman FA, Diabetes Genetics R, Meta-analysis C, Myocardial Infarction Genetics C, Kathiresan S, Wijmenga C, Gregersen PK, Alfredsson L, Siminovitch KA, Worthington J, de Bakker PI, Raychaudhuri S, Plenge RM: Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat Genet 2012, 44:483-489.
-
(2012)
Nat Genet
, vol.44
, pp. 483-489
-
-
Stahl, E.A.1
Wegmann, D.2
Trynka, G.3
Gutierrez-Achury, J.4
Do, R.5
Voight, B.F.6
Kraft, P.7
Chen, R.8
Kallberg, H.J.9
Kurreeman, F.A.10
Diabetes Genetics, R.11
Meta-analysis, C.12
Myocardial Infarction Genetics, C.13
Kathiresan, S.14
Wijmenga, C.15
Gregersen, P.K.16
Alfredsson, L.17
Siminovitch, K.A.18
Worthington, J.19
de Bakker, P.I.20
Raychaudhuri, S.21
Plenge, R.M.22
more..
-
13
-
-
80054975975
-
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
-
Rivas MA, Beaudoin M, Gardet A, Stevens C, Sharma Y, Zhang CK, Boucher G, Ripke S, Ellinghaus D, Burtt N, Fennell T, Kirby A, Latiano A, Goyette P, Green T, Halfvarson J, Haritunians T, Korn JM, Kuruvilla F, Lagace C, Neale B, Lo KS, Schumm P, Torkvist L, Dubinsky MC, Brant SR, Silverberg MS, Duerr RH, Altshuler D, Gabriel S, et al: Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nat Genet 2011, 43:1066-1073.
-
(2011)
Nat Genet
, vol.43
, pp. 1066-1073
-
-
Rivas, M.A.1
Beaudoin, M.2
Gardet, A.3
Stevens, C.4
Sharma, Y.5
Zhang, C.K.6
Boucher, G.7
Ripke, S.8
Ellinghaus, D.9
Burtt, N.10
Fennell, T.11
Kirby, A.12
Latiano, A.13
Goyette, P.14
Green, T.15
Halfvarson, J.16
Haritunians, T.17
Korn, J.M.18
Kuruvilla, F.19
Lagace, C.20
Neale, B.21
Lo, K.S.22
Schumm, P.23
Torkvist, L.24
Dubinsky, M.C.25
Brant, S.R.26
Silverberg, M.S.27
Duerr, R.H.28
Altshuler, D.29
Gabriel, S.30
more..
-
14
-
-
65249131713
-
Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev S, Walker N, Riches D, Egholm M, Todd JA: Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science 2009, 324:387-389.
-
(2009)
Science
, vol.324
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
15
-
-
78651225855
-
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease
-
Momozawa Y, Mni M, Nakamura K, Coppieters W, Almer S, Amininejad L, Cleynen I, Colombel JF, de Rijk P, Dewit O, Finkel Y, Gassull MA, Goossens D, Laukens D, Lemann M, Libioulle C, O'Morain C, Reenaers C, Rutgeerts P, Tysk C, Zelenika D, Lathrop M, Del-Favero J, Hugot JP, de Vos M, Franchimont D, Vermeire S, Louis E, Georges M: Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease. Nat Genet 2011, 43:43-47.
-
(2011)
Nat Genet
, vol.43
, pp. 43-47
-
-
Momozawa, Y.1
Mni, M.2
Nakamura, K.3
Coppieters, W.4
Almer, S.5
Amininejad, L.6
Cleynen, I.7
Colombel, J.F.8
de Rijk, P.9
Dewit, O.10
Finkel, Y.11
Gassull, M.A.12
Goossens, D.13
Laukens, D.14
Lemann, M.15
Libioulle, C.16
O'Morain, C.17
Reenaers, C.18
Rutgeerts, P.19
Tysk, C.20
Zelenika, D.21
Lathrop, M.22
Del-Favero, J.23
Hugot, J.P.24
de Vos, M.25
Franchimont, D.26
Vermeire, S.27
Louis, E.28
Georges, M.29
more..
-
16
-
-
84857654651
-
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes
-
Bonnefond A, Clement N, Fawcett K, Yengo L, Vaillant E, Guillaume JL, Dechaume A, Payne F, Roussel R, Czernichow S, Hercberg S, Hadjadj S, Balkau B, Marre M, Lantieri O, Langenberg C, Bouatia-Naji N, Charpentier G, Vaxillaire M, Rocheleau G, Wareham NJ, Sladek R, McCarthy MI, Dina C, Barroso I, Jockers R, Froguel P: Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nat Genet 2012, 44:1297-1301.
-
(2012)
Nat Genet
, vol.44
, pp. 1297-1301
-
-
Bonnefond, A.1
Clement, N.2
Fawcett, K.3
Yengo, L.4
Vaillant, E.5
Guillaume, J.L.6
Dechaume, A.7
Payne, F.8
Roussel, R.9
Czernichow, S.10
Hercberg, S.11
Hadjadj, S.12
Balkau, B.13
Marre, M.14
Lantieri, O.15
Langenberg, C.16
Bouatia-Naji, N.17
Charpentier, G.18
Vaxillaire, M.19
Rocheleau, G.20
Wareham, N.J.21
Sladek, R.22
McCarthy, M.I.23
Dina, C.24
Barroso, I.25
Jockers, R.26
Froguel, P.27
more..
-
17
-
-
84872323563
-
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis
-
Diogo D, Kurreeman F, Stahl Eli A, Liao Katherine P, Gupta N, Greenberg Jeffrey D, Rivas Manuel A, Hickey B, Flannick J, Thomson B, Guiducci C, Ripke S, Adzhubey I, Barton A, Kremer Joel M, Alfredsson L, Sunyaev S, Martin J, Zhernakova A, Bowes J, Eyre S, Siminovitch Katherine A, Gregersen Peter K, Worthington J, Klareskog L, Padyukov L, Raychaudhuri S, Plenge Robert M: Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis. Am J Hum Genet 2013, 92:15-27.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 15-27
-
-
Diogo, D.1
Kurreeman, F.2
Stahl Eli, A.3
Liao Katherine, P.4
Gupta, N.5
Greenberg Jeffrey, D.6
Rivas Manuel, A.7
Hickey, B.8
Flannick, J.9
Thomson, B.10
Guiducci, C.11
Ripke, S.12
Adzhubey, I.13
Barton, A.14
Kremer Joel, M.15
Alfredsson, L.16
Sunyaev, S.17
Martin, J.18
Zhernakova, A.19
Bowes, J.20
Eyre, S.21
Siminovitch Katherine, A.22
Gregersen Peter, K.23
Worthington, J.24
Klareskog, L.25
Padyukov, L.26
Raychaudhuri, S.27
Plenge Robert, M.28
more..
-
18
-
-
0023945481
-
The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis
-
Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS: The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum 1988, 31:315-324.
-
(1988)
Arthritis Rheum
, vol.31
, pp. 315-324
-
-
Arnett, F.C.1
Edworthy, S.M.2
Bloch, D.A.3
McShane, D.J.4
Fries, J.F.5
Cooper, N.S.6
Healey, L.A.7
Kaplan, S.R.8
Liang, M.H.9
Luthra, H.S.10
-
19
-
-
84862809846
-
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
-
Okada Y, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Kawaguchi T, Stahl EA, Kurreeman FA, Nishida N, Ohmiya H, Myouzen K, Takahashi M, Sawada T, Nishioka Y, Yukioka M, Matsubara T, Wakitani S, Teshima R, Tohma S, Takasugi K, Shimada K, Murasawa A, Honjo S, Matsuo K, Tanaka H, Tajima K, Suzuki T, Iwamoto T, Kawamura Y, et al: Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Nat Genet 2012, 44:511-516.
-
(2012)
Nat Genet
, vol.44
, pp. 511-516
-
-
Okada, Y.1
Terao, C.2
Ikari, K.3
Kochi, Y.4
Ohmura, K.5
Suzuki, A.6
Kawaguchi, T.7
Stahl, E.A.8
Kurreeman, F.A.9
Nishida, N.10
Ohmiya, H.11
Myouzen, K.12
Takahashi, M.13
Sawada, T.14
Nishioka, Y.15
Yukioka, M.16
Matsubara, T.17
Wakitani, S.18
Teshima, R.19
Tohma, S.20
Takasugi, K.21
Shimada, K.22
Murasawa, A.23
Honjo, S.24
Matsuo, K.25
Tanaka, H.26
Tajima, K.27
Suzuki, T.28
Iwamoto, T.29
Kawamura, Y.30
more..
-
20
-
-
84899969998
-
Ethnic specificity of lupus-associated loci identified in a genome-wide association study in Korean women
-
Lee HS, Kim T, Bang SY, Na YJ, Kim I, Kim K, Kim JH, Chung YJ, Shin HD, Kang YM, Shim SC, Suh CH, Park YB, Kim JS, Kang C, Bae SC: Ethnic specificity of lupus-associated loci identified in a genome-wide association study in Korean women. Ann Rheum Dis 2014, 73:1240-1245.
-
(2014)
Ann Rheum Dis
, vol.73
, pp. 1240-1245
-
-
Lee, H.S.1
Kim, T.2
Bang, S.Y.3
Na, Y.J.4
Kim, I.5
Kim, K.6
Kim, J.H.7
Chung, Y.J.8
Shin, H.D.9
Kang, Y.M.10
Shim, S.C.11
Suh, C.H.12
Park, Y.B.13
Kim, J.S.14
Kang, C.15
Bae, S.C.16
-
21
-
-
38549174065
-
The Mouse Genome Database (MGD): mouse biology and model systems
-
Bult CJ, Eppig JT, Kadin JA, Richardson JE, Blake JA: The Mouse Genome Database (MGD): mouse biology and model systems. Nucleic Acids Res 2008, 36:D724-D728.
-
(2008)
Nucleic Acids Res
, vol.36
, pp. D724-D728
-
-
Bult, C.J.1
Eppig, J.T.2
Kadin, J.A.3
Richardson, J.E.4
Blake, J.A.5
-
22
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
Li H, Durbin R: Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 2010, 26:589-595.
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
23
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R: The sequence alignment/map format and SAMtools. Bioinformatics 2009, 25:2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
Marth, G.7
Abecasis, G.8
Durbin, R.9
-
24
-
-
84867130076
-
Exome sequencing and complex disease: practical aspects of rare variant association studies
-
Do R, Kathiresan S, Abecasis GR: Exome sequencing and complex disease: practical aspects of rare variant association studies. Hum Mol Genet 2012, 21:R1-R9.
-
(2012)
Hum Mol Genet
, vol.21
, pp. R1-R9
-
-
Do, R.1
Kathiresan, S.2
Abecasis, G.R.3
-
25
-
-
34548292504
-
PLINK: a tool set for wholegenome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for wholegenome association and population-based linkage analyses. Am J Hum Genet 2007, 81:559-575.
-
(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
-
26
-
-
84864942403
-
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
-
Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, Nickerson DA, Christiani DC, Wurfel Mark M, Lin X: Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet 2012, 91:224-237.
-
(2012)
Am J Hum Genet
, vol.91
, pp. 224-237
-
-
Lee, S.1
Emond, M.J.2
Bamshad, M.J.3
Barnes, K.C.4
Rieder, M.J.5
Nickerson, D.A.6
Christiani, D.C.7
Wurfel Mark, M.8
Lin, X.9
-
27
-
-
79953752624
-
Testing for an unusual distribution of rare variants
-
Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ: Testing for an unusual distribution of rare variants. PLoS Genet 2011, 7:e1001322.
-
(2011)
PLoS Genet
, vol.7
-
-
Neale, B.M.1
Rivas, M.A.2
Voight, B.F.3
Altshuler, D.4
Devlin, B.5
Orho-Melander, M.6
Kathiresan, S.7
Purcell, S.M.8
Roeder, K.9
Daly, M.J.10
-
28
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin D-Y, Tang ZZ: A general framework for detecting disease associations with rare variants in sequencing studies. Am J Hum Genet 2011, 89:354-367.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 354-367
-
-
Lin, D.-Y.1
Tang, Z.Z.2
-
29
-
-
84864430562
-
SIFT web server: predicting effects of amino acid substitutions on proteins
-
Sim NL, Kumar P, Hu J, Henikoff S, Schneider G, Ng PC: SIFT web server: predicting effects of amino acid substitutions on proteins. Nucleic Acids Res 2012, 40:W452-W457.
-
(2012)
Nucleic Acids Res
, vol.40
, pp. W452-W457
-
-
Sim, N.L.1
Kumar, P.2
Hu, J.3
Henikoff, S.4
Schneider, G.5
Ng, P.C.6
-
30
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR: A method and server for predicting damaging missense mutations. Nat Methods 2010, 7:248-249.
-
(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
-
-
84855896680
-
A combined functional annotation score for non-synonymous variants
-
Lopes MC, Joyce C, Ritchie GR, John SL, Cunningham F, Asimit J, Zeggini E: A combined functional annotation score for non-synonymous variants. Hum Hered 2012, 73:47-51.
-
(2012)
Hum Hered
, vol.73
, pp. 47-51
-
-
Lopes, M.C.1
Joyce, C.2
Ritchie, G.R.3
John, S.L.4
Cunningham, F.5
Asimit, J.6
Zeggini, E.7
-
32
-
-
84874896774
-
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data
-
Liu Q, Guo Y, Li J, Long J, Zhang B, Shyr Y: Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data. BMC Genomics 2012, 13:S8.
-
(2012)
BMC Genomics
, vol.13
, pp. S8
-
-
Liu, Q.1
Guo, Y.2
Li, J.3
Long, J.4
Zhang, B.5
Shyr, Y.6
-
33
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ: A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 2011, 43:491-498.
-
(2011)
Nat Genet
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
del Angel, G.8
Rivas, M.A.9
Hanna, M.10
McKenna, A.11
Fennell, T.J.12
Kernytsky, A.M.13
Sivachenko, A.Y.14
Cibulskis, K.15
Gabriel, S.B.16
Altshuler, D.17
Daly, M.J.18
-
34
-
-
84878994629
-
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
-
Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, Barker JN, Barrett JC, Blackburn H, Brand O, Burren O, Capon F, Compston A, Gough SCL, Jostins L, Kong Y, Lee JC, Lek M, MacArthur DG, Mansfield JC, Mathew CG, Mein CA, Mirza M, Nutland S, Onengut-Gumuscu S, Papouli E, Parkes M, Rich SS, Sawcer S, Satsangi J, Simmonds MJ, et al: Negligible impact of rare autoimmune-locus coding-region variants on missing heritability. Nature 2013, 498:232-235.
-
(2013)
Nature
, vol.498
, pp. 232-235
-
-
Hunt, K.A.1
Mistry, V.2
Bockett, N.A.3
Ahmad, T.4
Ban, M.5
Barker, J.N.6
Barrett, J.C.7
Blackburn, H.8
Brand, O.9
Burren, O.10
Capon, F.11
Compston, A.12
Gough, S.C.L.13
Jostins, L.14
Kong, Y.15
Lee, J.C.16
Lek, M.17
MacArthur, D.G.18
Mansfield, J.C.19
Mathew, C.G.20
Mein, C.A.21
Mirza, M.22
Nutland, S.23
Onengut-Gumuscu, S.24
Papouli, E.25
Parkes, M.26
Rich, S.S.27
Sawcer, S.28
Satsangi, J.29
Simmonds, M.J.30
more..
-
35
-
-
84868281214
-
VSTM1-v2, a novel soluble glycoprotein, promotes the differentiation and activation of Th17 cells
-
Guo X, Zhang Y, Wang P, Li T, Fu W, Mo X, Shi T, Zhang Z, Chen Y, Ma D, Han W: VSTM1-v2, a novel soluble glycoprotein, promotes the differentiation and activation of Th17 cells. Cell Immunol 2012, 278:136-142.
-
(2012)
Cell Immunol
, vol.278
, pp. 136-142
-
-
Guo, X.1
Zhang, Y.2
Wang, P.3
Li, T.4
Fu, W.5
Mo, X.6
Shi, T.7
Zhang, Z.8
Chen, Y.9
Ma, D.10
Han, W.11
|