-
2
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E, Scott LJ, Saxena R, Voight BF, Marchini JL, Hu T, de Bakker PI, Abecasis GR, Almgren P, Andersen G, Ardlie K, Bostrom KB, Bergman RN, Bonnycastle LL, Borch-Johnsen K, Burtt NP, Chen H, Chines PS, Daly MJ, Deodhar P, Ding C-J, Doney ASF, Duren WL, Elliott KS, Erdos MR, Frayling TM, Freathy RM, Gianniny L, Grallert H, Grarup N, Groves CJ, Guiducci C, Hansen T, Herder C, Hitman GA, Hughes TE, Isomaa B, Jackson AU, Jorgensen T, Kong A, Kubalanza K, Kuruvilla FG, Kuusisto J, Langenberg C, Lango H, Lauritzen T, Li Y, Lindgren CM, Lyssenko V, Marvelle AF, Meisinger C, Midthjell K, Mohlke KL, Morken MA, Morris AD, Narisu N, Nilsson P, Owen KR, Palmer CNA, Payne F, Perry, JRB, Pettersen E, Platou C, Prokopenko I, Qi L, Qin L, Rayner NW, Rees M, Roix JJ, Sandbaek A, Shields B, Sjogren M, Steinthorsdottir V, Stringham HM, Swift AJ, Thorleifsson G, Thorsteinsdottir U, Timpson NJ, Tuomi T, Tuomilehto J, Walker M, Watanabe RM, Weedon MN, Willer CJ, Illig T, Hveem K, Hu FB, Laakso M, Stefansson K, Pedersen O, Wareham NJ, Barroso I, Hattersley AT, Collins FS, Groop L, McCarthy MI, Boehnke M, Altshuler D. 2008. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 40:638-645.
-
(2008)
Nat Genet
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
Voight, B.F.4
Marchini, J.L.5
Hu, T.6
de Bakker, P.I.7
Abecasis, G.R.8
Almgren, P.9
Andersen, G.10
Ardlie, K.11
Bostrom, K.B.12
Bergman, R.N.13
Bonnycastle, L.L.14
Borch-Johnsen, K.15
Burtt, N.P.16
Chen, H.17
Chines, P.S.18
Daly, M.J.19
Deodhar, P.20
Ding, C.-J.21
Doney, A.S.F.22
Duren, W.L.23
Elliott, K.S.24
Erdos, M.R.25
Frayling, T.M.26
Freathy, R.M.27
Gianniny, L.28
Grallert, H.29
Grarup, N.30
Groves, C.J.31
Guiducci, C.32
Hansen, T.33
Herder, C.34
Hitman, G.A.35
Hughes, T.E.36
Isomaa, B.37
Jackson, A.U.38
Jorgensen, T.39
Kong, A.40
Kubalanza, K.41
Kuruvilla, F.G.42
Kuusisto, J.43
Langenberg, C.44
Lango, H.45
Lauritzen, T.46
Li, Y.47
Lindgren, C.M.48
Lyssenko, V.49
Marvelle, A.F.50
Meisinger, C.51
Midthjell, K.52
Mohlke, K.L.53
Morken, M.A.54
Morris, A.D.55
Narisu, N.56
Nilsson, P.57
Owen, K.R.58
Palmer, C.N.A.59
Payne, F.60
Perry, J.R.B.61
Pettersen, E.62
Platou, C.63
Prokopenko, I.64
Qi, L.65
Qin, L.66
Rayner, N.W.67
Rees, M.68
Roix, J.J.69
Sandbaek, A.70
Shields, B.71
Sjogren, M.72
Steinthorsdottir, V.73
Stringham, H.M.74
Swift, A.J.75
Thorleifsson, G.76
Thorsteinsdottir, U.77
Timpson, N.J.78
Tuomi, T.79
Tuomilehto, J.80
Walker, M.81
Watanabe, R.M.82
Weedon, M.N.83
Willer, C.J.84
Illig, T.85
Hveem, K.86
Hu, F.B.87
Laakso, M.88
Stefansson, K.89
Pedersen, O.90
Wareham, N.J.91
Barroso, I.92
Hattersley, A.T.93
Collins, F.S.94
Groop, L.95
McCarthy, M.I.96
Boehnke, M.97
Altshuler, D.98
more..
-
3
-
-
34447336409
-
Cholesterol fractions and apolipoproteins as risk factors for heart disease mortality in older men
-
Clarke R. 2007. Cholesterol fractions and apolipoproteins as risk factors for heart disease mortality in older men. Arch Intern Med 167:1373-1378.
-
(2007)
Arch Intern Med
, vol.167
, pp. 1373-1378
-
-
Clarke, R.1
-
4
-
-
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, Flynn E, Harrison P, Hocking LJ, Huizinga TWJ, Kastner DL, Ke X, Lee AT, Liu X, Martin P, Morgan AW, Padyukov L, Posthumus MD, Radstake TRDJ, Reid DM, Seielstad M, Seldin MF, Shadick NA, Steer S, Tak PP, Thomson W, van der Helm-van Mil AHM, van der-Horst Bruinsma IE, van der Schoot CE, van Riel PLCM, Weinblatt ME, Wilson AG, Wolbink GJ, Wordsworth BP, Wijmenga C, Karlson EW, Toes REM, de Vries N, Begovich AB, Worthington J, Siminovitch KA, Gregersen PK, Klareskog L, Plenge R. 2010. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet 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
Flynn, E.31
Harrison, P.32
Hocking, L.J.33
Huizinga, T.W.J.34
Kastner, D.L.35
Ke, X.36
Lee, A.T.37
Liu, X.38
Martin, P.39
Morgan, A.W.40
Padyukov, L.41
Posthumus, M.D.42
Radstake, T.R.D.J.43
Reid, D.M.44
Seielstad, M.45
Seldin, M.F.46
Shadick, N.A.47
Steer, S.48
Tak, P.P.49
Thomson, W.50
van der Helm-van Mil, A.H.M.51
van der-Horst Bruinsma, I.E.52
van der Schoot, C.E.53
van Riel, P.L.C.M.54
Weinblatt, M.E.55
Wilson, A.G.56
Wolbink, G.J.57
Wordsworth, B.P.58
Wijmenga, C.59
Karlson, E.W.60
Toes, R.E.M.61
de Vries, N.62
Begovich, A.B.63
Worthington, J.64
Siminovitch, K.A.65
Gregersen, P.K.66
Klareskog, L.67
Plenge, R.68
more..
-
5
-
-
67649876123
-
Meta-analysis of genome scans and replication identify cd6, irf8 and tnfrsf1a as new multiple sclerosis susceptibility loci
-
De Jager PL, Jia X, Wang J, de Bakker PIW, Ottoboni L, Aggarwal NT, Piccio L, Raychaudhuri S, Tran D, Aubin C, Briskin R, Romano S, Baranzini SE, McCauley JL, Pericak-Vance MA, Haines JL, Gibson RA, Naeglin Y, Uitdehaag B, Matthews PM, Kappos L, Polman C, McArdle WL, Strachan DP, Evans D, Cross AH, Daly MJ, Compston A, Sawcer SJ, Weiner HL, Hauser SL, Hafler DA, Oksenberg JR. 2009. Meta-analysis of genome scans and replication identify cd6, irf8 and tnfrsf1a as new multiple sclerosis susceptibility loci. Nat Genet 41:776-782.
-
(2009)
Nat Genet
, vol.41
, pp. 776-782
-
-
De Jager, P.L.1
Jia, X.2
Wang, J.3
de Bakker, P.I.W.4
Ottoboni, L.5
Aggarwal, N.T.6
Piccio, L.7
Raychaudhuri, S.8
Tran, D.9
Aubin, C.10
Briskin, R.11
Romano, S.12
Baranzini, S.E.13
McCauley, J.L.14
Pericak-Vance, M.A.15
Haines, J.L.16
Gibson, R.A.17
Naeglin, Y.18
Uitdehaag, B.19
Matthews, P.M.20
Kappos, L.21
Polman, C.22
McArdle, W.L.23
Strachan, D.P.24
Evans, D.25
Cross, A.H.26
Daly, M.J.27
Compston, A.28
Sawcer, S.J.29
Weiner, H.L.30
Hauser, S.L.31
Hafler, D.A.32
Oksenberg, J.R.33
more..
-
6
-
-
77957947562
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height
-
Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Visscher PM, Chatterjee N, Loos RJF, Boehnke M, McCarthy MI, Ingelsson E, Lindgren CM, Abecasis GR, Stefansson K, Frayling TM, Hirschhorn JN. 2010. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467:832-838.
-
(2010)
Nature
, vol.467
, pp. 832-838
-
-
Lango, A.H.1
Estrada, K.2
Lettre, G.3
Berndt, S.I.4
Weedon, M.N.5
Rivadeneira, F.6
Willer, C.J.7
Jackson, A.U.8
Visscher, P.M.9
Chatterjee, N.10
Loos, R.J.F.11
Boehnke, M.12
McCarthy, M.I.13
Ingelsson, E.14
Lindgren, C.M.15
Abecasis, G.R.16
Stefansson, K.17
Frayling, T.M.18
Hirschhorn, J.N.19
-
7
-
-
71249120778
-
Assessment of genotype imputation methods
-
BMC Proceedings
-
Biernacka J, Tang R, Li J, McDonnell S, Rabe K, Sinnwell J, Rider D, de Andrade M, Goode E, Fridley B. 2009. Assessment of genotype imputation methods. BMC Proceedings 3:S5.
-
(2009)
, vol.3
-
-
Biernacka, J.1
Tang, R.2
Li, J.3
McDonnell, S.4
Rabe, K.5
Sinnwell, J.6
Rider, D.7
de Andrade, M.8
Goode, E.9
Fridley, B.10
-
9
-
-
56149105085
-
Analyses and comparison of accuracy of different genotype imputation methods
-
Pei Y, Li J, Zhang L, Papasian C, Deng H. 2008. Analyses and comparison of accuracy of different genotype imputation methods. PLoS ONE 3:e3551.
-
(2008)
PLoS ONE
, vol.3
-
-
Pei, Y.1
Li, J.2
Zhang, L.3
Papasian, C.4
Deng, H.5
-
10
-
-
34547622688
-
Imputation-based analysis of association studies: candidate regions and quantitative traits
-
Servin B, Stephens M. 2007. Imputation-based analysis of association studies: candidate regions and quantitative traits. PLoS Genet 3:e114.
-
(2007)
PLoS Genet
, vol.3
-
-
Servin, B.1
Stephens, M.2
-
11
-
-
60549106036
-
Imputation of missing genotypes: an empirical evaluation of impute
-
Zhao Z. 2008. Imputation of missing genotypes: an empirical evaluation of impute. BMC Genet 9:85.
-
(2008)
BMC Genet
, vol.9
, pp. 85
-
-
Zhao, Z.1
-
12
-
-
33644974019
-
A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase
-
Scheet P, Stephens M. 2006. A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet 78:629-644.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 629-644
-
-
Scheet, P.1
Stephens, M.2
-
13
-
-
78649508578
-
Mach: using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR. 2010. Mach: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 34:816-834.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
Scheet, P.4
Abecasis, G.R.5
-
14
-
-
0347361674
-
Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data
-
Li N, Stephens, M. 2003. Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. Genetics 165:2213-2233.
-
(2003)
Genetics
, vol.165
, pp. 2213-2233
-
-
Li, N.1
Stephens, M.2
-
15
-
-
0034619331
-
A method for fine mapping quantitative trait loci in outbred animal stocks
-
Mott R, Talbot CJ, Turri MG, Collins AC, Flint J. 2000. A method for fine mapping quantitative trait loci in outbred animal stocks. Proc Natl Acad Sci USA 97:12649-12654.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 12649-12654
-
-
Mott, R.1
Talbot, C.J.2
Turri, M.G.3
Collins, A.C.4
Flint, J.5
-
16
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. 2009. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5:e1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
17
-
-
67651049769
-
Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies
-
Hao K, Chudin E, McElwee J, Schadt E. 2009. Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies. BMC Genet 10:27.
-
(2009)
BMC Genet
, vol.10
, pp. 27
-
-
Hao, K.1
Chudin, E.2
McElwee, J.3
Schadt, E.4
-
18
-
-
33646869900
-
Multilocus association mapping using variable-length markov chains
-
Browning SR. 2006. Multilocus association mapping using variable-length markov chains. Am J Hum Genet 78:903-913.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 903-913
-
-
Browning, S.R.1
-
19
-
-
46149121706
-
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms
-
Anderson C. 2008. Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms. Am J Hum Genet 83:112-119.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 112-119
-
-
Anderson, C.1
-
20
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES. 2001. High-resolution haplotype structure in the human genome. Nat Genet 29:229-232.
-
(2001)
Nat Genet
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.F.3
Hudson, T.J.4
Lander, E.S.5
-
21
-
-
34548292504
-
Plink: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira M, Bender D, Maller J, Sklar P, de Bakker P, Daly M, Sham PC. 2007. Plink: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 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.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.9
Daly, M.10
Sham, P.C.11
-
22
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000Genomes
-
1000Genomes, 2010. A map of human genome variation from population-scale sequencing. Nature 467:1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
23
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Consortium TIH. 2010. Integrating common and rare genetic variation in diverse human populations. Nature 467:52-58.
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
Consortium, T.I.H.1
-
24
-
-
72849144434
-
Sequencing technologies---the next generation
-
Metzker ML. 2010. Sequencing technologies---the next generation. Nat Rev Genet 11:31-46.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
25
-
-
78650037203
-
Deep resequencing reveals excess rare recent variants consistent with explosive population growth
-
Coventry A, Bull-Otterson LM, Liu X, Clark AG, Maxwell TJ, Crosby J, Hixson JE, Rea TJ, Muzny DM, Lewis LR, Wheeler DA, Sabo A, Lusk C, Weiss KG, Akbar H, Cree A, Hawes AC, Newsham I, Varghese RT, Villasana D, Gross S, Joshi V, Santibanez J, Morgan M, Chang K, Walker IV H, Templeton AR, Boerwinkle E, Gibbs R, Sing CF. 2010. Deep resequencing reveals excess rare recent variants consistent with explosive population growth. Nat Commun 1:131.
-
(2010)
Nat Commun
, vol.1
, pp. 131
-
-
Coventry, A.1
Bull-Otterson, L.M.2
Liu, X.3
Clark, A.G.4
Maxwell, T.J.5
Crosby, J.6
Hixson, J.E.7
Rea, T.J.8
Muzny, D.M.9
Lewis, L.R.10
Wheeler, D.A.11
Sabo, A.12
Lusk, C.13
Weiss, K.G.14
Akbar, H.15
Cree, A.16
Hawes, A.C.17
Newsham, I.18
Varghese, R.T.19
Villasana, D.20
Gross, S.21
Joshi, V.22
Santibanez, J.23
Morgan, M.24
Chang, K.25
Walker IV, H.26
Templeton, A.R.27
Boerwinkle, E.28
Gibbs, R.29
Sing, C.F.30
more..
-
26
-
-
79953738130
-
Quantifying the underestimation of relative risks from genome-wide association studies
-
Spencer C, Hechter E, Vukcevic D, Donnelly P. 2011. Quantifying the underestimation of relative risks from genome-wide association studies. PLoS Genet 7:e1001337.
-
(2011)
PLoS Genet
, vol.7
-
-
Spencer, C.1
Hechter, E.2
Vukcevic, D.3
Donnelly, P.4
-
28
-
-
77956197018
-
Utilizing genotype imputation for the augmentation of sequence data
-
Fridley BL, Jenkins G, Deyo-Svendsen ME, Hebbring S, Freimuth R. 2010. Utilizing genotype imputation for the augmentation of sequence data. PLoS ONE 5:e11018.
-
(2010)
PLoS ONE
, vol.5
-
-
Fridley, B.L.1
Jenkins, G.2
Deyo-Svendsen, M.E.3
Hebbring, S.4
Freimuth, R.5
-
29
-
-
79953212557
-
A rare variant in myh6 is associated with high risk of sick sinus syndrome
-
Holm H, Gudbjartsson DF, Sulem P, Masson G, Helgadottir HT, Zanon C, Magnusson OT, Helgason A, Saemundsdottir J, Gylfason A, Stefansdottir H, Gretarsdottir S, Matthiasson SE, Thorgeirsson G, Jonasdottir A, Sigurdsson A, Stefansson H, Werge T, Rafnar T, Kiemeney LA, Parvez B, Muhammad R, Roden DM, Darbar D, Thorleifsson G, Walters GB, Kong A, Thorsteinsdottir U, Arnar DO, Stefansson K. 2011. A rare variant in myh6 is associated with high risk of sick sinus syndrome. Nat Genet 43:316-320.
-
(2011)
Nat Genet
, vol.43
, pp. 316-320
-
-
Holm, H.1
Gudbjartsson, D.F.2
Sulem, P.3
Masson, G.4
Helgadottir, H.T.5
Zanon, C.6
Magnusson, O.T.7
Helgason, A.8
Saemundsdottir, J.9
Gylfason, A.10
Stefansdottir, H.11
Gretarsdottir, S.12
Matthiasson, S.E.13
Thorgeirsson, G.14
Jonasdottir, A.15
Sigurdsson, A.16
Stefansson, H.17
Werge, T.18
Rafnar, T.19
Kiemeney, L.A.20
Parvez, B.21
Muhammad, R.22
Roden, D.M.23
Darbar, D.24
Thorleifsson, G.25
Walters, G.B.26
Kong, A.27
Thorsteinsdottir, U.28
Arnar, D.O.29
Stefansson, K.30
more..
-
30
-
-
79953213008
-
Next-generation association studies for complex traits
-
Zeggini E. 2011. Next-generation association studies for complex traits. Nat Genet 43:287-288.
-
(2011)
Nat Genet
, vol.43
, pp. 287-288
-
-
Zeggini, E.1
-
31
-
-
0028818968
-
Effects of alpha-tocopherol and beta-carotene supplements on cancer incidence in the alpha-tocopherol beta-carotene cancer prevention study
-
Albanes D, Heinonen O, Huttunen J, Taylor P, Virtamo J, Edwards B, Haapakoski J, Rautalahti M, Hartman A, Palmgren J. 1995. Effects of alpha-tocopherol and beta-carotene supplements on cancer incidence in the alpha-tocopherol beta-carotene cancer prevention study. Am J Clin Nutr 62:1427S-1430S.
-
(1995)
Am J Clin Nutr
, vol.62
-
-
Albanes, D.1
Heinonen, O.2
Huttunen, J.3
Taylor, P.4
Virtamo, J.5
Edwards, B.6
Haapakoski, J.7
Rautalahti, M.8
Hartman, A.9
Palmgren, J.10
-
32
-
-
39749118602
-
Multiple loci identified in a genome-wide association study of prostate cancer
-
Thomas G, Jacobs KB, Yeager M, Kraft P, Wacholder S, Orr N, Yu K, Chatterjee N, Welch R, Hutchinson A, Crenshaw A, Cancel-Tassin G, Staats BJ, Wang Z, Gonzalez-Bosquet J, Fang J, Deng X, Berndt SI, Calle EE, Feigelson HS, Thun MJ, Rodriguez C, Albanes D, Virtamo J, Weinstein S, Schumacher FR, Giovannucci E, Willett WC, Cussenot O, Valeri A, Andriole GL, Crawford ED, Tucker M, Gerhard DS, Fraumeni JF, Hoover R, Hayes RB, Hunter DJ, Chanock SJ. 2008. Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet 40:310-315.
-
(2008)
Nat Genet
, vol.40
, pp. 310-315
-
-
Thomas, G.1
Jacobs, K.B.2
Yeager, M.3
Kraft, P.4
Wacholder, S.5
Orr, N.6
Yu, K.7
Chatterjee, N.8
Welch, R.9
Hutchinson, A.10
Crenshaw, A.11
Cancel-Tassin, G.12
Staats, B.J.13
Wang, Z.14
Gonzalez-Bosquet, J.15
Fang, J.16
Deng, X.17
Berndt, S.I.18
Calle, E.E.19
Feigelson, H.S.20
Thun, M.J.21
Rodriguez, C.22
Albanes, D.23
Virtamo, J.24
Weinstein, S.25
Schumacher, F.R.26
Giovannucci, E.27
Willett, W.C.28
Cussenot, O.29
Valeri, A.30
Andriole, G.L.31
Crawford, E.D.32
Tucker, M.33
Gerhard, D.S.34
Fraumeni, J.F.35
Hoover, R.36
Hayes, R.B.37
Hunter, D.J.38
Chanock, S.J.39
more..
-
33
-
-
0036569572
-
The American Cancer Society cancer prevention study ii nutrition cohort
-
Calle EE, Rodriguez C, Jacobs EJ, Almon ML, Chao A, McCullough ML, Feigelson HS, Thun MJ. 2002. The American Cancer Society cancer prevention study ii nutrition cohort. Cancer 94:2490-2501.
-
(2002)
Cancer
, vol.94
, pp. 2490-2501
-
-
Calle, E.E.1
Rodriguez, C.2
Jacobs, E.J.3
Almon, M.L.4
Chao, A.5
McCullough, M.L.6
Feigelson, H.S.7
Thun, M.J.8
-
34
-
-
84860352047
-
Improved imputation of common and uncommon single nucleotide polymorphisms (snps) with a new reference set
-
Wang Z, Jacobs K, Yeager M, Hutchinson A, Sampson J, Chatterjee N, Albanes D, Berndt SI, Diver RW, Gapstur S, Teras L, Haiman CA, Henderson BE, Stram D, Hsing AS, Purdue M, Taylor P, Tucker M, Chanock S. 2011. Improved imputation of common and uncommon single nucleotide polymorphisms (snps) with a new reference set. Nature Precedings 44.
-
(2011)
Nature Precedings
, vol.44
-
-
Wang, Z.1
Jacobs, K.2
Yeager, M.3
Hutchinson, A.4
Sampson, J.5
Chatterjee, N.6
Albanes, D.7
Berndt, S.I.8
Diver, R.W.9
Gapstur, S.10
Teras, L.11
Haiman, C.A.12
Henderson, B.E.13
Stram, D.14
Hsing, A.S.15
Purdue, M.16
Taylor, P.17
Tucker, M.18
Chanock, S.19
-
35
-
-
33645775067
-
An utter refutation of the 'fundamental theorem of the hapmap
-
Terwilliger JD, Hiekkalinna T. 2006. An utter refutation of the 'fundamental theorem of the hapmap'. Eur J Hum Genet 14:426-437.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 426-437
-
-
Terwilliger, J.D.1
Hiekkalinna, T.2
-
36
-
-
33748804424
-
A tutorial on statistical methods for population association studies
-
Balding D. 2006. A tutorial on statistical methods for population association studies. Nat Rev Genet 7:781-91.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 781-791
-
-
Balding, D.1
-
37
-
-
18044402499
-
Design of the prostate, lung, colorectal and ovarian (plco) cancer screening trial
-
Prorok PC, Andriole GL, Bresalier RS, Buys SS, Chia D, Crawford ED, Fogel R, Gelmann EP, Gilbert F, Hasson MA, Hayes RB, Johnson CC, Mandel JS, Oberman A, O'Brien B, Oken MM, Rafia S, Reding D, Rutt W, Weissfeld JL, Yokochi L, Gohagan JK. 2000. Design of the prostate, lung, colorectal and ovarian (plco) cancer screening trial. Controlled Clinical Trials 21:273S-309S.
-
(2000)
Controlled Clinical Trials
, vol.21
-
-
Prorok, P.C.1
Andriole, G.L.2
Bresalier, R.S.3
Buys, S.S.4
Chia, D.5
Crawford, E.D.6
Fogel, R.7
Gelmann, E.P.8
Gilbert, F.9
Hasson, M.A.10
Hayes, R.B.11
Johnson, C.C.12
Mandel, J.S.13
Oberman, A.14
O'Brien, B.15
Oken, M.M.16
Rafia, S.17
Reding, D.18
Rutt, W.19
Weissfeld, J.L.20
Yokochi, L.21
Gohagan, J.K.22
more..
-
38
-
-
0034572611
-
The prostate, lung, colorectal and ovarian (plco) cancer screening trial of the national cancer institute: history, organization, and status
-
Gohagan JK, Prorok PC, Hayes RB, Kramer B-S. 2000. The prostate, lung, colorectal and ovarian (plco) cancer screening trial of the national cancer institute: history, organization, and status. Control Clin Trials 21:251S-272S.
-
(2000)
Control Clin Trials
, vol.21
-
-
Gohagan, J.K.1
Prorok, P.C.2
Hayes, R.B.3
Kramer, B.-S.4
-
39
-
-
77954133026
-
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
-
Park J-H, Wacholder S, Gail MH, Peters U, Jacobs KB, Chanock SJ, Chatterjee N. 2010. Estimation of effect size distribution from genome-wide association studies and implications for future discoveries. Nat Genet 42:570-575.
-
(2010)
Nat Genet
, vol.42
, pp. 570-575
-
-
Park, J.-H.1
Wacholder, S.2
Gail, M.H.3
Peters, U.4
Jacobs, K.B.5
Chanock, S.J.6
Chatterjee, N.7
-
40
-
-
67149117126
-
Discovery of rare variants via sequencing: implications for the design of complex trait association studies
-
Li B, Leal SM. 2009. Discovery of rare variants via sequencing: implications for the design of complex trait association studies. PLoS Genet 5:e1000481.
-
(2009)
PLoS Genet
, vol.5
-
-
Li, B.1
Leal, S.M.2
|