-
2
-
-
35648937584
-
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
-
Broderick P, Carvajal-Carmona L, Pittman AM, Webb E, Howarth K, Rowan A, Lubbe S, Spain S, Sullivan K, Fielding S and others. 2007. A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet 39:1315-1317.
-
(2007)
Nat Genet
, vol.39
, pp. 1315-1317
-
-
Broderick, P.1
Carvajal-Carmona, L.2
Pittman, A.M.3
Webb, E.4
Howarth, K.5
Rowan, A.6
Lubbe, S.7
Spain, S.8
Sullivan, K.9
Fielding, S.10
-
3
-
-
84866356984
-
Identifying genetic marker sets associated with phenotypes via an efficient adaptive score test
-
Cai T, Lin X, Carroll RJ. 2012. Identifying genetic marker sets associated with phenotypes via an efficient adaptive score test. Biostatistics (Oxford, England) 13:776-790.
-
(2012)
Biostatistics (Oxford, England)
, vol.13
, pp. 776-790
-
-
Cai, T.1
Lin, X.2
Carroll, R.J.3
-
4
-
-
12744255341
-
Semiparametric maximum likelihood estimation exploiting gene-environment independence in case-control studies
-
Chatterjee N, Carroll RJ. 2005. Semiparametric maximum likelihood estimation exploiting gene-environment independence in case-control studies. Biometrika 92:399-418.
-
(2005)
Biometrika
, vol.92
, pp. 399-418
-
-
Chatterjee, N.1
Carroll, R.J.2
-
5
-
-
33845284533
-
Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions
-
Chatterjee N, Kalaylioglu Z, Moslehi R, Peters U, Wacholder S. 2006. Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions. Am J Hum Genet 79:1002-1016.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 1002-1016
-
-
Chatterjee, N.1
Kalaylioglu, Z.2
Moslehi, R.3
Peters, U.4
Wacholder, S.5
-
6
-
-
84856155219
-
Gene-environment interactions in genome-wide association studies: a comparative study of tests applied to empirical studies of type 2 diabetes
-
Cornelis MC, Tchetgen EJT, Liang L, Qi L, Chatterjee N, Hu FB, Kraft P. 2012. Gene-environment interactions in genome-wide association studies: a comparative study of tests applied to empirical studies of type 2 diabetes. Am J Epidemiol 175:191-202.
-
(2012)
Am J Epidemiol
, vol.175
, pp. 191-202
-
-
Cornelis, M.C.1
Tchetgen, E.J.T.2
Liang, L.3
Qi, L.4
Chatterjee, N.5
Hu, F.B.6
Kraft, P.7
-
7
-
-
84869473073
-
Two-stage testing procedures with independent filtering for genome-wide gene-environment interaction
-
Dai JY, Kooperberg C, Leblanc M, Prentice RL. 2012. Two-stage testing procedures with independent filtering for genome-wide gene-environment interaction. Biometrika 99:929-944.
-
(2012)
Biometrika
, vol.99
, pp. 929-944
-
-
Dai, J.Y.1
Kooperberg, C.2
Leblanc, M.3
Prentice, R.L.4
-
8
-
-
38049072575
-
Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis
-
Dempfle A, Hein R, Beckmann L, Scherag A, Nguyen TT, Schäfer H, Chang-Claude J. 2007. Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis. BMC Proc 1(Suppl. 1):S73.
-
(2007)
BMC Proc
, vol.1
, Issue.SUPPL. 1
-
-
Dempfle, A.1
Hein, R.2
Beckmann, L.3
Scherag, A.4
Nguyen, T.T.5
Schäfer, H.6
Chang-Claude, J.7
-
9
-
-
84863005628
-
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk
-
Dunlop MG, Dobbins SE, Farrington SM, Jones AM, Palles C, Whiffin N, Tenesa A, Spain S, Broderick P, Ooi L-Y and others. 2012. Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. Nat Genet 44:770-776.
-
(2012)
Nat Genet
, vol.44
, pp. 770-776
-
-
Dunlop, M.G.1
Dobbins, S.E.2
Farrington, S.M.3
Jones, A.M.4
Palles, C.5
Whiffin, N.6
Tenesa, A.7
Spain, S.8
Broderick, P.9
Ooi, L.-Y.10
-
10
-
-
43249090541
-
A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms
-
Gao X, Starmer J, Martin ER. 2008. A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms. Genet Epidemiol 32:361-369.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 361-369
-
-
Gao, X.1
Starmer, J.2
Martin, E.R.3
-
11
-
-
23844512858
-
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses
-
García-Closas M, Malats N, Silverman D, Dosemeci M, Kogevinas M, Hein DW, Tardón A, Serra C, Carrato A, García-Closas R and others. 2005. NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses. Lancet 366:649-659.
-
(2005)
Lancet
, vol.366
, pp. 649-659
-
-
García-Closas, M.1
Malats, N.2
Silverman, D.3
Dosemeci, M.4
Kogevinas, M.5
Hein, D.W.6
Tardón, A.7
Serra, C.8
Carrato, A.9
García-Closas, R.10
-
12
-
-
84879131990
-
Finding GWAS signals in the lower Manhattan by testing GxE interactions
-
In International Genetic Epidemiology Society Annual Conference. Stevenson, WA.
-
Gauderman JW, Zhang P, Lewinger PJ. 2012. Finding GWAS signals in the lower Manhattan by testing GxE interactions. In International Genetic Epidemiology Society Annual Conference. Stevenson, WA.
-
(2012)
-
-
Gauderman, J.W.1
Zhang, P.2
Lewinger, P.J.3
-
13
-
-
34447315844
-
Testing association between disease and multiple SNPs in a candidate gene
-
Gauderman WJ, Murcray C, Gilliland F, Conti DV. 2007. Testing association between disease and multiple SNPs in a candidate gene. Genet Epidemiol 31:383-395.
-
(2007)
Genet Epidemiol
, vol.31
, pp. 383-395
-
-
Gauderman, W.J.1
Murcray, C.2
Gilliland, F.3
Conti, D.V.4
-
14
-
-
0345832338
-
A global test for groups of genes: testing association with a clinical outcome
-
Goeman JJ, Van de Geer SA, De Kort F, Van Houwelingen HC. 2004. A global test for groups of genes: testing association with a clinical outcome. Bioinformatics (Oxford, England) 20:93-99.
-
(2004)
Bioinformatics (Oxford, England)
, vol.20
, pp. 93-99
-
-
Goeman, J.J.1
Van de Geer, S.A.2
De Kort, F.3
Van Houwelingen, H.C.4
-
15
-
-
80052328932
-
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
-
Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, Tenesa A, Kusel VI, Sheehan P, Eaaswarkhanth M and others. 2011. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. PLoS Genet 7:e1002237.
-
(2011)
PLoS Genet
, vol.7
-
-
Hamza, T.H.1
Chen, H.2
Hill-Burns, E.M.3
Rhodes, S.L.4
Montimurro, J.5
Kay, D.M.6
Tenesa, A.7
Kusel, V.8
Sheehan, P.9
Eaaswarkhanth, M.10
-
16
-
-
77951028197
-
A data-adaptive sum test for disease association with multiple common or rare variants
-
Han F, Pan W. 2010. A data-adaptive sum test for disease association with multiple common or rare variants. Hum Hered 70:42-54.
-
(2010)
Hum Hered
, vol.70
, pp. 42-54
-
-
Han, F.1
Pan, W.2
-
17
-
-
44349179705
-
Multiple ADH genes are associated with upper aerodigestive cancers
-
Hashibe M, McKay JD, Curado MP, Oliveira JC, Koifman S, Koifman R, Zaridze D, Shangina O, Wünsch-Filho V, Eluf-Neto J and others. 2008. Multiple ADH genes are associated with upper aerodigestive cancers. Nat Genet 40:707-709.
-
(2008)
Nat Genet
, vol.40
, pp. 707-709
-
-
Hashibe, M.1
McKay, J.D.2
Curado, M.P.3
Oliveira, J.C.4
Koifman, S.5
Koifman, R.6
Zaridze, D.7
Shangina, O.8
Wünsch-Filho, V.9
Eluf-Neto, J.10
-
18
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362-9367.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
19
-
-
56749176944
-
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
-
Houlston RS, Webb E, Broderick P, Pittman AM, Di Bernardo MC, Lubbe S, Chandler I, Vijayakrishnan J, Sullivan K, Penegar S and others. 2008. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet 40:1426-1435.
-
(2008)
Nat Genet
, vol.40
, pp. 1426-1435
-
-
Houlston, R.S.1
Webb, E.2
Broderick, P.3
Pittman, A.M.4
Di Bernardo, M.C.5
Lubbe, S.6
Chandler, I.7
Vijayakrishnan, J.8
Sullivan, K.9
Penegar, S.10
-
20
-
-
78049353079
-
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
-
Houlston RS, Cheadle J, Dobbins SE, Tenesa A, Jones AM, Howarth K, Spain SL, Broderick P, Domingo E, Farrington S and others. 2010. Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat Genet 42:973-977.
-
(2010)
Nat Genet
, vol.42
, pp. 973-977
-
-
Houlston, R.S.1
Cheadle, J.2
Dobbins, S.E.3
Tenesa, A.4
Jones, A.M.5
Howarth, K.6
Spain, S.L.7
Broderick, P.8
Domingo, E.9
Farrington, S.10
-
21
-
-
84867614472
-
Powerful cocktail methods for detecting genome-wide gene-environment interaction
-
Hsu L, Jiao S, Dai JY, Hutter C, Peters U, Kooperberg C. 2012. Powerful cocktail methods for detecting genome-wide gene-environment interaction. Genet Epidemiol 36:183-194.
-
(2012)
Genet Epidemiol
, vol.36
, pp. 183-194
-
-
Hsu, L.1
Jiao, S.2
Dai, J.Y.3
Hutter, C.4
Peters, U.5
Kooperberg, C.6
-
22
-
-
84856052210
-
Gene-based tests of association
-
Huang H, Chanda P, Alonso A, Bader JS, Arking DE. 2011. Gene-based tests of association. PLoS Genet 7:e1002177.
-
(2011)
PLoS Genet
, vol.7
-
-
Huang, H.1
Chanda, P.2
Alonso, A.3
Bader, J.S.4
Arking, D.E.5
-
23
-
-
37549072226
-
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk
-
Jaeger E, Webb E, Howarth K, Carvajal-Carmona L, Rowan A, Broderick P, Walther A, Spain S, Pittman A, Kemp Z and others. 2008. Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nat Genet 40:26-28.
-
(2008)
Nat Genet
, vol.40
, pp. 26-28
-
-
Jaeger, E.1
Webb, E.2
Howarth, K.3
Carvajal-Carmona, L.4
Rowan, A.5
Broderick, P.6
Walther, A.7
Spain, S.8
Pittman, A.9
Kemp, Z.10
-
24
-
-
42249099044
-
Increasing the power of identifying gene x gene interactions in genome-wide association studies
-
Kooperberg C, Leblanc M. 2008. Increasing the power of identifying gene x gene interactions in genome-wide association studies. Genet Epidemiol 32:255-263.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 255-263
-
-
Kooperberg, C.1
Leblanc, M.2
-
25
-
-
40749104728
-
A powerful and flexible multilocus association test for quantitative traits
-
Kwee LC, Liu D, Lin X, Ghosh D, Epstein MP. 2008. A powerful and flexible multilocus association test for quantitative traits. Am J Hum Genet 82:386-397.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 386-397
-
-
Kwee, L.C.1
Liu, D.2
Lin, X.3
Ghosh, D.4
Epstein, M.P.5
-
26
-
-
72149129508
-
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
-
Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M and others. 2009. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet 85:679-691.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 679-691
-
-
Landi, M.T.1
Chatterjee, N.2
Yu, K.3
Goldin, L.R.4
Goldstein, A.M.5
Rotunno, M.6
Mirabello, L.7
Jacobs, K.8
Wheeler, W.9
Yeager, M.10
-
27
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
-
Li B, Leal SM. 2008. Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet 83:311-321.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
28
-
-
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
-
29
-
-
60149103126
-
Detecting gene-environment interactions using a combined case-only and case-control approach
-
Li D, Conti DV. 2009. Detecting gene-environment interactions using a combined case-only and case-control approach. Am J Epidemiol 169:497-504.
-
(2009)
Am J Epidemiol
, vol.169
, pp. 497-504
-
-
Li, D.1
Conti, D.V.2
-
30
-
-
60149093075
-
ATOM: a powerful gene-based association test by combining optimally weighted markers
-
Li M, Wang K, Grant SFA, Hakonarson H, Li C. 2009. ATOM: a powerful gene-based association test by combining optimally weighted markers. Bioinformatics (Oxford, England) 25:497-503.
-
(2009)
Bioinformatics (Oxford, England)
, vol.25
, pp. 497-503
-
-
Li, M.1
Wang, K.2
Grant, S.F.A.3
Hakonarson, H.4
Li, C.5
-
31
-
-
80052731371
-
A general framework for detecting disease associations with rare variants in sequencing studies
-
Lin D.-Y, Tang Z.-Z. 2011. A general framework for detecting disease associations with rare variants in sequencing studies. Am J Hum Genet 89:354-367.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 354-367
-
-
Lin, D.-Y.1
Tang, Z.-Z.2
-
32
-
-
77955064853
-
A versatile gene-based test for genome-wide association studies
-
Liu JZ, McRae AF, Nyholt DR, Medland SE, Wray NR, Brown KM, Hayward NK, Montgomery GW, Visscher PM, Martin NG and others. 2010. A versatile gene-based test for genome-wide association studies. Am J Hum Genet 87:139-145.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 139-145
-
-
Liu, J.Z.1
McRae, A.F.2
Nyholt, D.R.3
Medland, S.E.4
Wray, N.R.5
Brown, K.M.6
Hayward, N.K.7
Montgomery, G.W.8
Visscher, P.M.9
Martin, N.G.10
-
33
-
-
37249033229
-
Group additive regression models for genomic data analysis
-
Luan Y, Li H. 2008. Group additive regression models for genomic data analysis. Biostatistics (Oxford, England) 9:100-113.
-
(2008)
Biostatistics (Oxford, England)
, vol.9
, pp. 100-113
-
-
Luan, Y.1
Li, H.2
-
34
-
-
84555209145
-
Comprehensive evaluation of the impact of 14 genetic variants on colorectal cancer phenotype and risk
-
Lubbe SJ, Di Bernardo MC, Broderick P, Chandler I, Houlston RS. 2012. Comprehensive evaluation of the impact of 14 genetic variants on colorectal cancer phenotype and risk. Am J Epidemiol 175:1-10.
-
(2012)
Am J Epidemiol
, vol.175
, pp. 1-10
-
-
Lubbe, S.J.1
Di Bernardo, M.C.2
Broderick, P.3
Chandler, I.4
Houlston, R.S.5
-
35
-
-
61449168010
-
A groupwise association test for rare mutations using a weighted sum statistic
-
Madsen BE, Browning SR. 2009. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet 5:e1000384.
-
(2009)
PLoS Genet
, vol.5
-
-
Madsen, B.E.1
Browning, S.R.2
-
36
-
-
33846014328
-
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST)
-
Morgenthaler S, Thilly WG. 2007. A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). Mutat Res 615:28-56.
-
(2007)
Mutat Res
, vol.615
, pp. 28-56
-
-
Morgenthaler, S.1
Thilly, W.G.2
-
37
-
-
76649136928
-
An evaluation of statistical approaches to rare variant analysis in genetic association studies
-
Morris AP, Zeggini E. 2010. An evaluation of statistical approaches to rare variant analysis in genetic association studies. Genet Epidemiol 34:188-193.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 188-193
-
-
Morris, A.P.1
Zeggini, E.2
-
38
-
-
50249187303
-
On multiple-testing correction in genome-wide association studies
-
Moskvina V, Schmidt KM. 2008. On multiple-testing correction in genome-wide association studies. Genet Epidemiol 32:567-573.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 567-573
-
-
Moskvina, V.1
Schmidt, K.M.2
-
39
-
-
49749089301
-
Exploiting gene-environment independence for analysis of case-control studies: an empirical Bayes-type shrinkage estimator to trade-off between bias and efficiency
-
Mukherjee B, Chatterjee N. 2008. Exploiting gene-environment independence for analysis of case-control studies: an empirical Bayes-type shrinkage estimator to trade-off between bias and efficiency. Biometrics 64:685-694.
-
(2008)
Biometrics
, vol.64
, pp. 685-694
-
-
Mukherjee, B.1
Chatterjee, N.2
-
40
-
-
77949776227
-
Association tests using kernel-based measures of multi-locus genotype similarity between individuals
-
Mukhopadhyay I, Feingold E, Weeks DE, Thalamuthu A. 2010. Association tests using kernel-based measures of multi-locus genotype similarity between individuals. Genet Epidemiol 34:213-221.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 213-221
-
-
Mukhopadhyay, I.1
Feingold, E.2
Weeks, D.E.3
Thalamuthu, A.4
-
41
-
-
58449107994
-
Gene-environment interaction in genome-wide association studies
-
Murcray CE, Lewinger JP, Gauderman WJ. 2009. Gene-environment interaction in genome-wide association studies. Am J Epidemiol 169:219-226.
-
(2009)
Am J Epidemiol
, vol.169
, pp. 219-226
-
-
Murcray, C.E.1
Lewinger, J.P.2
Gauderman, W.J.3
-
42
-
-
79952494521
-
Sample size requirements to detect gene-environment interactions in genome-wide association studies
-
Murcray CE, Lewinger JP, Conti DV, Thomas DC, Gauderman WJ. 2011. Sample size requirements to detect gene-environment interactions in genome-wide association studies. Genet Epidemiol 35:201-210.
-
(2011)
Genet Epidemiol
, vol.35
, pp. 201-210
-
-
Murcray, C.E.1
Lewinger, J.P.2
Conti, D.V.3
Thomas, D.C.4
Gauderman, W.J.5
-
43
-
-
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. 2011. Testing for an unusual distribution of rare variants. PLoS Genet 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
-
44
-
-
84856703651
-
Meta-analysis of new genome-wide association studies of colorectal cancer risk
-
Peters U, Hutter CM, Hsu L, Schumacher FR, Conti DV, Carlson CS, Edlund CK, Haile RW, Gallinger S, Zanke BW and others. 2011. Meta-analysis of new genome-wide association studies of colorectal cancer risk. Hum Genet 131:217-234.
-
(2011)
Hum Genet
, vol.131
, pp. 217-234
-
-
Peters, U.1
Hutter, C.M.2
Hsu, L.3
Schumacher, F.R.4
Conti, D.V.5
Carlson, C.S.6
Edlund, C.K.7
Haile, R.W.8
Gallinger, S.9
Zanke, B.W.10
-
45
-
-
84875253066
-
Identification of genetic susceptibility loci for colorectal tumors in a genome-wide meta-analysis
-
Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bézieau S, Brenner H, Butterbach K and others. 2013. Identification of genetic susceptibility loci for colorectal tumors in a genome-wide meta-analysis. Gastroenterology 144:799-807.
-
(2013)
Gastroenterology
, vol.144
, pp. 799-807
-
-
Peters, U.1
Jiao, S.2
Schumacher, F.R.3
Hutter, C.M.4
Aragaki, A.K.5
Baron, J.A.6
Berndt, S.I.7
Bézieau, S.8
Brenner, H.9
Butterbach, K.10
-
46
-
-
0028089404
-
Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies
-
Piegorsch WW, Weinberg CR, Taylor JA. 1994. Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies. Stat Med 13:153-162.
-
(1994)
Stat Med
, vol.13
, pp. 153-162
-
-
Piegorsch, W.W.1
Weinberg, C.R.2
Taylor, J.A.3
-
47
-
-
77953121877
-
Pooled association tests for rare variants in exon-resequencing studies
-
Price AL, Kryukov GV, De Bakker PIW, Purcell SM, Staples J, Wei L-J, Sunyaev SR. 2010. Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet 86:832-838.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 832-838
-
-
Price, A.L.1
Kryukov, G.V.2
De Bakker, P.I.W.3
Purcell, S.M.4
Staples, J.5
Wei, L.-J.6
Sunyaev, S.R.7
-
48
-
-
84947899485
-
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
-
Rothman N, Garcia-Closas M, Chatterjee N, Malats N, Wu X, Figueroa JD, Real FX, Van Den Berg D, Matullo G, Baris D and others. 2010. A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet 42:978-984.
-
(2010)
Nat Genet
, vol.42
, pp. 978-984
-
-
Rothman, N.1
Garcia-Closas, M.2
Chatterjee, N.3
Malats, N.4
Wu, X.5
Figueroa, J.D.6
Real, F.X.7
Van Den Berg, D.8
Matullo, G.9
Baris, D.10
-
49
-
-
77954207265
-
Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations
-
Schaid DJ. 2010. Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations. Hum Hered 70:109-131.
-
(2010)
Hum Hered
, vol.70
, pp. 109-131
-
-
Schaid, D.J.1
-
50
-
-
17644378739
-
Nonparametric tests of association of multiple genes with human disease
-
Schaid DJ, McDonnell SK, Hebbring SJ, Cunningham JM, Thibodeau SN. 2005. Nonparametric tests of association of multiple genes with human disease. Am J Hum Genet 76:780-793.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 780-793
-
-
Schaid, D.J.1
McDonnell, S.K.2
Hebbring, S.J.3
Cunningham, J.M.4
Thibodeau, S.N.5
-
51
-
-
0021137170
-
The design of case-control studies: the influence of confounding and interaction effects
-
Smith PG, Day NE. 1984. The design of case-control studies: the influence of confounding and interaction effects. Int J Epidemiol 13:356-365.
-
(1984)
Int J Epidemiol
, vol.13
, pp. 356-365
-
-
Smith, P.G.1
Day, N.E.2
-
52
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
Tenesa A, Farrington SM, Prendergast JGD, Porteous ME, Walker M, Haq N, Barnetson RA, Theodoratou E, Cetnarskyj R, Cartwright N and others. 2008. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet 40:631-637.
-
(2008)
Nat Genet
, vol.40
, pp. 631-637
-
-
Tenesa, A.1
Farrington, S.M.2
Prendergast, J.G.D.3
Porteous, M.E.4
Walker, M.5
Haq, N.6
Barnetson, R.A.7
Theodoratou, E.8
Cetnarskyj, R.9
Cartwright, N.10
-
53
-
-
79959503826
-
-
The International HapMap Project
-
The International HapMap Project. 2003. Nature 426:789-796.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
54
-
-
34547498546
-
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
-
Tomlinson I, Webb E, Carvajal-Carmona L, Broderick P, Kemp Z, Spain S, Penegar S, Chandler I, Gorman M, Wood W and others. 2007. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet 39:984-988.
-
(2007)
Nat Genet
, vol.39
, pp. 984-988
-
-
Tomlinson, I.1
Webb, E.2
Carvajal-Carmona, L.3
Broderick, P.4
Kemp, Z.5
Spain, S.6
Penegar, S.7
Chandler, I.8
Gorman, M.9
Wood, W.10
-
55
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
Tomlinson IPM, Webb E, Carvajal-Carmona L, Broderick P, Howarth K, Pittman AM, Penegar S, Chandler I, Gorman M, Wood W and others. 2008. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet 40:623-630.
-
(2008)
Nat Genet
, vol.40
, pp. 623-630
-
-
Tomlinson, I.P.M.1
Webb, E.2
Carvajal-Carmona, L.3
Broderick, P.4
Howarth, K.5
Pittman, A.M.6
Penegar, S.7
Chandler, I.8
Gorman, M.9
Wood, W.10
-
56
-
-
79959851441
-
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer
-
Tomlinson IPM, Carvajal-Carmona LG, Dobbins SE, Tenesa A, Jones AM, Howarth K, Howarth K, Palles C, Broderick P, Jaeger EEM, Farrington S and others. 2011. Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS Genet 7:e1002105.
-
(2011)
PLoS Genet
, vol.7
-
-
Tomlinson, I.P.M.1
Carvajal-Carmona, L.G.2
Dobbins, S.E.3
Tenesa, A.4
Jones, A.M.5
Howarth, K.6
Howarth, K.7
Palles, C.8
Broderick, P.9
Jaeger, E.E.M.10
Farrington, S.11
-
57
-
-
35348887757
-
Haplotype-based association analysis via variance-components score test
-
Tzeng J-Y, Zhang D. 2007. Haplotype-based association analysis via variance-components score test. Am J Hum Genet 81:927-938.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 927-938
-
-
Tzeng, J.-Y.1
Zhang, D.2
-
58
-
-
0345269986
-
On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit
-
Tzeng J-Y, Devlin B, Wasserman L, Roeder K. 2003. On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. Am J Hum Genet 72:891-902.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 891-902
-
-
Tzeng, J.-Y.1
Devlin, B.2
Wasserman, L.3
Roeder, K.4
-
59
-
-
68549128324
-
Gene-trait similarity regression for multimarker-based association analysis
-
Tzeng J-Y, Zhang D, Chang S.-M, Thomas DC, Davidian M. 2009. Gene-trait similarity regression for multimarker-based association analysis. Biometrics 65:822-832.
-
(2009)
Biometrics
, vol.65
, pp. 822-832
-
-
Tzeng, J.-Y.1
Zhang, D.2
Chang, S.-M.3
Thomas, D.C.4
Davidian, M.5
-
60
-
-
80051636106
-
Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression
-
Tzeng J-Y, Zhang D, Pongpanich M, Smith C, McCarthy MI, Sale MM, Worrall BB, Hsu F-C, Thomas DC, Sullivan PF. 2011. Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression. Am J Hum Genet 89:277-288.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 277-288
-
-
Tzeng, J.-Y.1
Zhang, D.2
Pongpanich, M.3
Smith, C.4
McCarthy, M.I.5
Sale, M.M.6
Worrall, B.B.7
Hsu, F.-C.8
Thomas, D.C.9
Sullivan, P.F.10
-
61
-
-
39649125434
-
A principal components regression approach to multilocus genetic association studies
-
Wang K, Abbott D. 2008. A principal components regression approach to multilocus genetic association studies. Genet Epidemiol 32:108-118.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 108-118
-
-
Wang, K.1
Abbott, D.2
-
62
-
-
33846565755
-
Improved power by use of a weighted score test for linkage disequilibrium mapping
-
Wang T, Elston RC. 2007. Improved power by use of a weighted score test for linkage disequilibrium mapping. Am J Hum Genet 80:353-360.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 353-360
-
-
Wang, T.1
Elston, R.C.2
-
63
-
-
54049114308
-
U-statistics-based tests for multiple genes in genetic association studies
-
Wei Z, Li M, Rebbeck T, Li H. 2008. U-statistics-based tests for multiple genes in genetic association studies. Ann Hum Genet 72:821-833.
-
(2008)
Ann Hum Genet
, vol.72
, pp. 821-833
-
-
Wei, Z.1
Li, M.2
Rebbeck, T.3
Li, H.4
-
64
-
-
33751114975
-
Generalized genomic distance-based regression methodology for multilocus association analysis
-
Wessel J, Schork NJ. 2006. Generalized genomic distance-based regression methodology for multilocus association analysis. Am J Hum Genet 79:792-806.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 792-806
-
-
Wessel, J.1
Schork, N.J.2
-
65
-
-
77953121307
-
Powerful SNP-set analysis for case-control genome-wide association studies
-
Wu MC, Kraft P, Epstein MP, Taylor DM, Chanock SJ, Hunter DJ, Lin X. 2010. Powerful SNP-set analysis for case-control genome-wide association studies. Am J Hum Genet 86:929-942.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 929-942
-
-
Wu, M.C.1
Kraft, P.2
Epstein, M.P.3
Taylor, D.M.4
Chanock, S.J.5
Hunter, D.J.6
Lin, X.7
-
66
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu MC, Lee S, Cai T, Li Y, Boehnke M, Lin X. 2011. Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet 89:82-93.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.3
Li, Y.4
Boehnke, M.5
Lin, X.6
-
67
-
-
34547092701
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
-
Zanke BW, Greenwood CMT, Rangrej J, Kustra R, Tenesa A, Farrington SM, Prendergast J, Olschwang S, Chiang T, Crowdy E and others. 2007. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet 39:989-994.
-
(2007)
Nat Genet
, vol.39
, pp. 989-994
-
-
Zanke, B.W.1
Greenwood, C.M.T.2
Rangrej, J.3
Kustra, R.4
Tenesa, A.5
Farrington, S.M.6
Prendergast, J.7
Olschwang, S.8
Chiang, T.9
Crowdy, E.10
-
68
-
-
20544440135
-
An entropy-based statistic for genomewide association studies
-
Zhao J, Boerwinkle E, Xiong M. 2005. An entropy-based statistic for genomewide association studies. Am J Hum Genet 77:27-40.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 27-40
-
-
Zhao, J.1
Boerwinkle, E.2
Xiong, M.3
|