-
2
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
DOI 10.1126/science.1069424
-
Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., Liu-Cordero, S. N., Rotimi, C., Adeyemo, A., Cooper, R., Ward, R., Lander, E. S., Daly, M. J., Altshuler, D. The structure of haplotype blocks in the human genome. Science 296, 2225-2229 (2002). (Pubitemid 34680308)
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
Defelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
3
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer, K. A., Ballinger, D. G., Cox, D. R., Hinds, D. A., Stuve, L. L., Gibbs, R. A., Belmont, J. W., Boudreau, A., Hardenbol, P., Leal, S. M., Pasternak, S., Wheeler, D. A., Willis, T. D., Yu, F., Yang, H., Zeng, C., Gao, Y., Hu, H., Hu, W., Li, C., Lin, W., Liu, S., Pan, H., Tang, X., Wang, J., Wang, W., Yu, J., Zhang, B., Zhang, Q., Zhao, H., Zhou, J., Gabriel, S. B., Barry, R., Blumenstiel, B., Camargo, A., Defelice, M., Faggart, M., Goyette, M., Gupta, S., Moore, J., Nguyen, H., Onofrio, R. C., Parkin, M., Roy, J., Stahl, E., Winchester, E., Ziaugra, L., Altshuler, D., Shen, Y., Yao, Z., Huang, W., Chu, X., He, Y., Jin, L., Liu, Y., Sun, W., Wang, H., Wang, Y., Xiong, X., Xu, L., Waye, M. M., Tsui, S. K., Xue, H., Wong, J. T., Galver, L. M., Fan, J. B., Gunderson, K., Murray, S. S., Oliphant, A. R., Chee, M. S., Montpetit, A., Chagnon, F., Ferretti, V., Leboeuf, M., Olivier, J. F., Phillips, M. S., Roumy, S., Sallee, C., Verner, A., Hudson, T. J., Kwok, P. Y., Cai, D., Koboldt, D. C., Miller, R. D., Pawlikowska, L., Taillon-Miller, P., Xiao, M., Tsui, L. C., Mak, W., Song, Y. Q., Tam, P. K., Nakamura, Y., Kawaguchi, T., Kitamoto, T., Morizono, T., Nagashima, A., Ohnishi, Y., Sekine, A., Tanaka, T., Tsunoda, T., Deloukas, P., Bird, C. P., Delgado, M., Dermitzakis, E. T., Gwilliam, R., Hunt, S., Morrison, J., Powell, D., Stranger, B. E., Whittaker, P., Bentley, D. R., Daly, M. J., de Bakker, P. I., Barrett, J., Chretien, Y. R., Maller, J., McCarroll, S., Patterson, N., Pe'er, I., Price, A., Purcell, S., Richter, D. J., Sabeti, P., Saxena, R., Schaffner, S. F., Sham, P. C., Varilly, P., Stein, L. D., Krishnan, L., Smith, A. V., Tello-Ruiz, M. K., Thorisson, G. A., Chakravarti, A., Chen, P. E., Cutler, D. J., Kashuk, C. S., Lin, S., Abecasis, G. R., Guan, W., Li, Y., Munro, H. M., Qin, Z. S., Thomas, D. J., McVean, G., Auton, A., Bottolo, L., Cardin, N., Eyheramendy, S., Freeman, C., Marchini, J., Myers, S., Spencer, C., Stephens, M., Donnelly, P., Cardon, L. R., Clarke, G., Evans, D. M., Morris, A. P., Weir, B. S., Mullikin, J. C., Sherry, S. T., Feolo, M., Skol, A., Zhang, H., Matsuda, I., Fukushima, Y., Macer, D. R., Suda, E., Rotimi, C. N., Adebamowo, C. A., Ajayi, I., Aniagwu, T., Marshall, P. A., Nkwodimmah, C., Royal, C. D., Leppert, M. F., Dixon, M., Peiffer, A., Qiu, R., Kent, A., Kato, K., Niikawa, N., Adewole, I. F., Knoppers, B. M., Foster, M. W., Clayton, E. W., Watkin, J., Muzny, D., Nazareth, L., Sodergren, E., Weinstock, G. M., Yakub, I., Birren, B. W., Wilson, R.K., Fulton, L. L., Rogers, J., Burton, J., Carter, N. P., Clee, C. M., Griffiths, M., Jones, M. C., McLay, K., Plumb, R. W., Ross, M. T., Sims, S. K., Willey, D. L., Chen, Z., Han, H., Kang, L., Godbout, M., Wallenburg, J. C., L'Archeveque, P., Bellemare, G., Saeki, K., An, D., Fu, H., Li, Q., Wang, Z., Wang, R., Holden, A. L., Brooks, L. D., McEwen, J. E., Guyer, M. S., Wang, V. O., Peterson, J. L., Shi, M., Spiegel, J., Sung, L. M., Zacharia, L. F., Collins, F. S., Kennedy, K., Jamieson, R., Stewart, J. A second generation human haplotype map of over 3.1 million SNPs. Nature 449, 851-861 (2007).
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
Pasternak, S.11
Wheeler, D.A.12
Willis, T.D.13
Yu, F.14
Yang, H.15
Zeng, C.16
Gao, Y.17
Hu, H.18
Hu, W.19
Li, C.20
Lin, W.21
Liu, S.22
Pan, H.23
Tang, X.24
Wang, J.25
Wang, W.26
Yu, J.27
Zhang, B.28
Zhang, Q.29
Zhao, H.30
Zhou, J.31
Gabriel, S.B.32
Barry, R.33
Blumenstiel, B.34
Camargo, A.35
Defelice, M.36
Faggart, M.37
Goyette, M.38
Gupta, S.39
Moore, J.40
Nguyen, H.41
Onofrio, R.C.42
Parkin, M.43
Roy, J.44
Stahl, E.45
Winchester, E.46
Ziaugra, L.47
Altshuler, D.48
Shen, Y.49
Yao, Z.50
Huang, W.51
Chu, X.52
He, Y.53
Jin, L.54
Liu, Y.55
Sun, W.56
Wang, H.57
Wang, Y.58
Xiong, X.59
Xu, L.60
Waye, M.M.61
Tsui, S.K.62
Xue, H.63
Wong, J.T.64
Galver, L.M.65
Fan, J.B.66
Gunderson, K.67
Murray, S.S.68
Oliphant, A.R.69
Chee, M.S.70
Montpetit, A.71
Chagnon, F.72
Ferretti, V.73
Leboeuf, M.74
Olivier, J.F.75
Phillips, M.S.76
Roumy, S.77
Sallee, C.78
Verner, A.79
Hudson, T.J.80
Kwok, P.Y.81
Cai, D.82
Koboldt, D.C.83
Miller, R.D.84
Pawlikowska, L.85
Taillon-Miller, P.86
Xiao, M.87
Tsui, L.C.88
Mak, W.89
Song, Y.Q.90
Tam, P.K.91
Nakamura, Y.92
Kawaguchi, T.93
Kitamoto, T.94
Morizono, T.95
Nagashima, A.96
Ohnishi, Y.97
Sekine, A.98
Tanaka, T.99
more..
-
4
-
-
79959524146
-
A haplotype map of the human genome
-
A haplotype map of the human genome. Nature 437, 1299-1320 (2005).
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
5
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
DOI 10.1126/science.1109557
-
Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J. Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., Bracken, M. B., Ferris, F. L., Ott, J., Barnstable, C., Hoh, J. Complement factor H polymorphism in age-related macular degeneration. Science 308, 385-389 (2005). (Pubitemid 40530070)
-
(2005)
Science
, vol.308
, Issue.5720
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
Tsai, J.-Y.4
Sackler, R.S.5
Haynes, C.6
Henning, A.K.7
Sangiovanni, J.P.8
Mane, S.M.9
Mayne, S.T.10
Bracken, M.B.11
Ferris, F.L.12
Ott, J.13
Barnstable, C.14
Hoh, J.15
-
6
-
-
13144306071
-
Genome-wide association studies for common diseases and complex traits
-
Hirschhorn, J. N., Daly, M. J. Genome-wide association studies for common diseases and complex traits. Nat Rev Genet 6, 95-108 (2005).
-
(2005)
Nat Rev Genet
, vol.6
, pp. 95-108
-
-
Hirschhorn, J.N.1
Daly, M.J.2
-
7
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki, Y., Swensen, J., Shattuck-Eidens, D., Futreal, P. A., Harshman, K., Tavtigian, S., Liu, Q., Cochran, C., Bennett, L. M., Ding, W., et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266, 66-71 (1994). (Pubitemid 24345325)
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
8
-
-
18544376723
-
Predictive testing for BRCA1/2: Attributes, risk perception and management in a multi-centre clinical cohort
-
Foster, C., Evans, D. G., Eeles, R., Eccles, D., Ashley, S., Brooks, L., Davidson, R., Mackay, J., Morrison, P. J., Watson, M. Predictive testing for BRCA1/2: attributes, risk perception and management in a multi-centre clinical cohort. Br J Cancer 86, 1209-1216 (2002).
-
(2002)
Br J Cancer
, vol.86
, pp. 1209-1216
-
-
Foster, C.1
Evans, D.G.2
Eeles, R.3
Eccles, D.4
Ashley, S.5
Brooks, L.6
Davidson, R.7
Mackay, J.8
Morrison, P.J.9
Watson, M.10
-
9
-
-
0038744296
-
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
-
DOI 10.1086/375033
-
Antoniou, A., Pharoah, P. D., Narod, S., Risch, H. A., Eyfjord, J. E., Hopper, J. L., Loman, N., Olsson, H., Johannsson, O., Borg, A., Pasini, B., Radice, P., Manoukian, S., Eccles, D. M., Tang, N., Olah, E., Anton-Culver, H., Warner, E., Lubinski, J., Gronwald, J., Gorski, B., Tulinius, H., Thorlacius, S., Eerola, H., Nevanlinna, H., Syrjakoski, K., Kallioniemi, O. P., Thompson, D., Evans, C., Peto, J., Lalloo, F., Evans, D. G., Easton, D. F. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet 72, 1117-1130 (2003). (Pubitemid 36530000)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.5
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.D.P.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
Hopper, J.L.6
Loman, N.7
Olsson, H.8
Johannsson, O.9
Borg, A.10
Pasini, B.11
Radice, P.12
Manoukian, S.13
Eccles, D.M.14
Tang, N.15
Olah, E.16
Anton-Culver, H.17
Warner, E.18
Lubinski, J.19
Gronwald, J.20
Gorski, B.21
Tulinius, H.22
Thorlacius, S.23
Eerola, H.24
Nevanlinna, H.25
Syrjakoski, K.26
Kallioniemi, O.-P.27
Thompson, D.28
Evans, C.29
Peto, J.30
Lalloo, F.31
Evans, D.G.32
Easton, D.F.33
more..
-
10
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster, R., Neuhausen, S.L., Mangion, J., Quirk, Y., Ford, D., Collins, N., Nguyen, K., Seal, S., Tran, T., Averill, D., et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 265, 2088-2090 (1994). (Pubitemid 24325690)
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
11
-
-
0026630266
-
APC mutations occur early during colorectal tumorigenesis
-
Powell, S. M., Zilz, N., Beazer-Barclay, Y., Bryan, T. M., Hamilton, S. R., Thibodeau, S. N., Vogelstein, B., Kinzler, K.W. APC mutations occur early during colorectal tumorigenesis. Nature 359, 235-237 (1992).
-
(1992)
Nature
, vol.359
, pp. 235-237
-
-
Powell, S.M.1
Zilz, N.2
Beazer-Barclay, Y.3
Bryan, T.M.4
Hamilton, S.R.5
Thibodeau, S.N.6
Vogelstein, B.7
Kinzler, K.W.8
-
12
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
DOI 10.1016/0092-8674(93)90330-S
-
Leach, F. S., Nicolaides, N. C., Papadopoulos, N., Liu, B., Jen, J., Parsons, R., Peltomaki, P., Sistonen, P., Aaltonen, L. A., Nystrom-Lahti, M., et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 75, 1215-1225 (1993). (Pubitemid 24006117)
-
(1993)
Cell
, vol.75
, Issue.6
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomaki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
Guan, X.-Y.11
Zhang, J.12
Meltzer, P.S.13
Yu, J.-W.14
Kao, F.-T.15
Chen, D.J.16
Cerosaletti, K.M.17
Fournier, R.E.K.18
Todd, S.19
-
13
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos, N., Nicolaides, N. C., Wei, Y. F., Ruben, S. M., Carter, K. C., Rosen, C. A., Haseltine, W. A., Fleischmann, R. D., Fraser, C. M., Adams, M. D., et al. Mutation of a mutL homolog in hereditary colon cancer. Science 263, 1625-1629 (1994). (Pubitemid 24128369)
-
(1994)
Science
, vol.263
, Issue.5153
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.-F.3
Ruben, S.M.4
Carter, K.C.5
Rosen, C.A.6
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
Venter, J.C.11
Hamilton, S.R.12
Petersen, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomaki, P.16
Mecklin, J.-P.17
De La Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
14
-
-
0027410857
-
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2
-
Mulligan, L. M., Kwok, J. B., Healey, C. S., Elsdon, M. J., Eng, C., Gardner, E., Love, D. R., Mole, S. E., Moore, J. K., Papi, L., et al. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363, 458-460 (1993). (Pubitemid 23079559)
-
(1993)
Genes Chromosomes and Cancer
, vol.6
, Issue.3
, pp. 166-177
-
-
Mulligan, L.M.1
Gardner, E.2
Smith, B.A.3
Mathew, C.G.P.4
Ponder, B.A.J.5
-
15
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian, C. J., Struewing, J. P., Goldstein, A. M., Higgins, P. A., Ally, D. S., Sheahan, M. D., Clark, W. H., Jr., Tucker, M. A., Dracopoli, N. C. Germline p16 mutations in familial melanoma. Nat Genet 8, 15-21 (1994).
-
(1994)
Nat Genet
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.4
Ally, D.S.5
Sheahan, M.D.6
Clark Jr., W.H.7
Tucker, M.A.8
Dracopoli, N.C.9
-
16
-
-
0033601346
-
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome
-
DOI 10.1126/science.286.5449.2528
-
Bell, D. W., Varley, J. M., Szydlo, T. E., Kang, D. H., Wahrer, D. C., Shannon, K. E., Lubratovich, M., Verselis, S. J., Isselbacher, K. J., Fraumeni, J. F., Birch, J. M., Li, F. P., Garber, J. E., Haber, D. A. Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome. Science 286, 2528-2531 (1999). (Pubitemid 30026346)
-
(1999)
Science
, vol.286
, Issue.5449
, pp. 2528-2531
-
-
Bell, D.W.1
Varley, J.M.2
Szydlo, T.E.3
Kang, D.H.4
Wahrer, D.C.R.5
Shannon, K.E.6
Lubratovich, M.7
Verselis, S.J.8
Isselbacher, K.J.9
Fraumeni, J.F.10
Birch, J.M.11
Li, F.P.12
Garber, J.E.13
Haber, D.A.14
-
17
-
-
23844512858
-
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: Results from the Spanish Bladder Cancer Study and meta-analyses
-
DOI 10.1016/S0140-6736(05)67137-1, PII S0140673605671371
-
Garcia-Closas, M., Malats, N., Silverman, D., Dosemeci, M., Kogevinas, M., Hein, D. W., Tardon, A., Serra, C., Carrato, A., Garcia-Closas, R., Lloreta, J., Castano-Vinyals, G., Yeager, M., Welch, R., Chanock, S., Chatterjee, N., Wacholder, S., Samanic, C., Tora, M., Fernandez, F., Real, F. X., Rothman, N. 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). (Pubitemid 41176017)
-
(2005)
Lancet
, vol.366
, Issue.9486
, pp. 649-659
-
-
Garcia-Closas, M.1
Malats, N.2
Silverman, D.3
Dosemeci, M.4
Kogevinas, M.5
Hein, D.W.6
Tardon, A.7
Serra, C.8
Carrato, A.9
Garcia-Closas, R.10
Lloreta, J.11
Castano-Vinyals, G.12
Yeager, M.13
Welch, R.14
Chanock, S.15
Chatterjee, N.16
Wacholder, S.17
Samanic, C.18
Tora, M.19
Fernandez, F.20
Real, F.X.21
Rothman, N.22
more..
-
18
-
-
33847337318
-
A common coding variant in CASP8 is associated with breast cancer risk
-
Cox, A., Dunning, A. M., Garcia-Closas, M., Balasubramanian, S., Reed, M. W., Pooley, K. A., Scollen, S., Baynes, C., Ponder, B. A., Chanock, S., Lissowska, J., Brinton, L., Peplonska, B., Southey, M. C., Hopper, J. L., McCredie, M. R., Giles, G. G., Fletcher, O., Johnson, N., dos Santos Silva, I., Gibson, L., Bojesen, S. E., Nordestgaard, B. G., Axelsson, C. K., Torres, D., Hamann, U., Justenhoven, C., Brauch, H., Chang-Claude, J., Kropp, S., Risch, A., Wang-Gohrke, S., Schurmann, P., Bogdanova, N., Dork, T., Fagerholm, R., Aaltonen, K., Blomqvist, C., Nevanlinna, H., Seal, S., Renwick, A., Stratton, M. R., Rahman, N., Sangrajrang, S., Hughes, D., Odefrey, F., Brennan, P., Spurdle, A. B., Chenevix-Trench, G., Beesley, J., Mannermaa, A., Hartikainen, J., Kataja, V., Kosma, V. M., Couch, F. J., Olson, J. E., Goode, E. L., Broeks, A., Schmidt, M. K., Hogervorst, F. B., Van't Veer, L. J., Kang, D., Yoo, K. Y., Noh, D. Y., Ahn, S. H., Wedren, S., Hall, P., Low, Y. L., Liu, J., Milne, R. L., Ribas, G., Gonzalez-Neira, A., Benitez, J., Sigurdson, A. J., Stredrick, D. L., Alexander, B. H., Struewing, J. P., Pharoah, P. D., Easton, D. F. A common coding variant in CASP8 is associated with breast cancer risk. Nat Genet 39, 352-358 (2007).
-
(2007)
Nat Genet
, vol.39
, pp. 352-358
-
-
Cox, A.1
Dunning, A.M.2
Garcia-Closas, M.3
Balasubramanian, S.4
Reed, M.W.5
Pooley, K.A.6
Scollen, S.7
Baynes, C.8
Ponder, B.A.9
Chanock, S.10
Lissowska, J.11
Brinton, L.12
Peplonska, B.13
Southey, M.C.14
Hopper, J.L.15
McCredie, M.R.16
Giles, G.G.17
Fletcher, O.18
Johnson, N.19
Dos Santos Silva, I.20
Gibson, L.21
Bojesen, S.E.22
Nordestgaard, B.G.23
Axelsson, C.K.24
Torres, D.25
Hamann, U.26
Justenhoven, C.27
Brauch, H.28
Chang-Claude, J.29
Kropp, S.30
Risch, A.31
Wang-Gohrke, S.32
Schurmann, P.33
Bogdanova, N.34
Dork, T.35
Fagerholm, R.36
Aaltonen, K.37
Blomqvist, C.38
Nevanlinna, H.39
Seal, S.40
Renwick, A.41
Stratton, M.R.42
Rahman, N.43
Sangrajrang, S.44
Hughes, D.45
Odefrey, F.46
Brennan, P.47
Spurdle, A.B.48
Chenevix-Trench, G.49
Beesley, J.50
Mannermaa, A.51
Hartikainen, J.52
Kataja, V.53
Kosma, V.M.54
Couch, F.J.55
Olson, J.E.56
Goode, E.L.57
Broeks, A.58
Schmidt, M.K.59
Hogervorst, F.B.60
Van't Veer, L.J.61
Kang, D.62
Yoo, K.Y.63
Noh, D.Y.64
Ahn, S.H.65
Wedren, S.66
Hall, P.67
Low, Y.L.68
Liu, J.69
Milne, R.L.70
Ribas, G.71
Gonzalez-Neira, A.72
Benitez, J.73
Sigurdson, A.J.74
Stredrick, D.L.75
Alexander, B.H.76
Struewing, J.P.77
Pharoah, P.D.78
Easton, D.F.79
more..
-
19
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
DOI 10.1038/nature05887, PII NATURE05887
-
Easton, D. F., Pooley, K. A., Dunning, A. M., Pharoah, P. D., Thompson, D., Ballinger, D. G., Struewing, J. P., Morrison, J., Field, H., Luben, R., Wareham, N., Ahmed, S., Healey, C. S., Bowman, R., Meyer, K. B., Haiman, C. A., Kolonel, L. K., Henderson, B. E., Le Marchand, L., Brennan, P., Sangrajrang, S., Gaborieau, V., Odefrey, F., Shen, C. Y., Wu, P. E., Wang, H. C., Eccles, D., Evans, D. G., Peto, J., Fletcher, O., Johnson, N., Seal, S., Stratton, M. R., Rahman, N., Chenevix-Trench, G., Bojesen, S. E., Nordestgaard, B. G., Axelsson, C. K., Garcia-Closas, M., Brinton, L., Chanock, S., Lissowska, J., Peplonska, B., Nevanlinna, H., Fagerholm, R., Eerola, H., Kang, D., Yoo, K. Y., Noh, D. Y., Ahn, S. H., Hunter, D. J., Hankinson, S. E., Cox, D. G., Hall, P., Wedren, S., Liu, J., Low, Y. L., Bogdanova, N., Schurmann, P., Dork, T., Tollenaar, R. A., Jacobi, C. E., Devilee, P., Klijn, J. G., Sigurdson, A. J., Doody, M. M., Alexander, B. H., Zhang, J., Cox, A., Brock, I. W., MacPherson, G., Reed, M. W., Couch, F. J., Goode, E. L., Olson, J. E., Meijers-Heijboer, H., van den Ouweland, A., Uitterlinden, A., Rivadeneira, F., Milne, R. L., Ribas, G., Gonzalez-Neira, A., Benitez, J., Hopper, J. L., McCredie, M., Southey, M., Giles, G. G., Schroen, C., Justenhoven, C., Brauch, H., Hamann, U., Ko, Y. D., Spurdle, A. B., Beesley, J., Chen, X., Mannermaa, A., Kosma, V. M., Kataja, V., Hartikainen, J., Day, N. E., Cox, D. R., Ponder, B. A. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447, 1087-1093 (2007). (Pubitemid 47014426)
-
(2007)
Nature
, vol.447
, Issue.7148
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
Pharoah, P.D.P.4
Thompson, D.5
Ballinger, D.G.6
Struewing, J.P.7
Morrison, J.8
Field, H.9
Luben, R.10
Wareham, N.11
Ahmed, S.12
Healey, C.S.13
Bowman, R.14
Meyer, K.B.15
Haiman, C.A.16
Kolonel, L.K.17
Henderson, B.E.18
Le Marchand, L.19
Brennan, P.20
Sangrajrang, S.21
Gaborieau, V.22
Odefrey, F.23
Shen, C.-Y.24
Wu, P.-E.25
Wang, H.-C.26
Eccles, D.27
Evans, D.G.28
Peto, J.29
Fletcher, O.30
Johnson, N.31
Seal, S.32
Stratton, M.R.33
Rahman, N.34
Chenevix-Trench, G.35
Bojesen, S.E.36
Nordestgaard, B.G.37
Axelsson, C.K.38
Garcia-Closas, M.39
Brinton, L.40
Chanock, S.41
Lissowska, J.42
Peplonska, B.43
Nevanlinna, H.44
Fagerholm, R.45
Eerola, H.46
Kang, D.47
Yoo, K.-Y.48
Noh, D.-Y.49
Ahn, S.-H.50
Hunter, D.J.51
Hankinson, S.E.52
Cox, D.G.53
Hall, P.54
Wedren, S.55
Liu, J.56
Low, Y.-L.57
Bogdanova, N.58
Schurmann, P.59
Dork, T.60
Tollenaar, R.A.E.M.61
Jacobi, C.E.62
Devilee, P.63
Klijn, J.G.M.64
Sigurdson, A.J.65
Doody, M.M.66
Alexander, B.H.67
Zhang, J.68
Cox, A.69
Brock, I.W.70
MacPherson, G.71
Reed, M.W.R.72
Couch, F.J.73
Goode, E.L.74
Olson, J.E.75
Meijers-Heijboer, H.76
Van Den Ouweland, A.77
Uitterlinden, A.78
Rivadeneira, F.79
Milne, R.L.80
Ribas, G.81
Gonzalez-Neira, A.82
Benitez, J.83
Hopper, J.L.84
McCredie, M.85
Southey, M.86
Giles, G.G.87
Schroen, C.88
Justenhoven, C.89
Brauch, H.90
Hamann, U.91
Ko, Y.-D.92
Spurdle, A.B.93
Beesley, J.94
Chen, X.95
Mannermaa, A.96
Kosma, V.-M.97
Kataja, V.98
Hartikainen, J.99
more..
-
20
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
DOI 10.1038/ng2075, PII NG2075
-
Hunter, D. J., Kraft, P., Jacobs, K. B., Cox, D. G., Yeager, M., Hankinson, S. E., Wacholder, S., Wang, Z., Welch, R., Hutchinson, A., Wang, J., Yu, K., Chatterjee, N., Orr, N., Willett, W. C., Colditz, G. A., Ziegler, R. G., Berg, C. D., Buys, S. S., McCarty, C. A., Feigelson, H. S., Calle, E. E., Thun, M. J., Hayes, R. B., Tucker, M., Gerhard, D. S., Fraumeni, J. F., Jr., Hoover, R. N., Thomas, G., Chanock, S. J. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 39, 870-874 (2007). (Pubitemid 47014500)
-
(2007)
Nature Genetics
, vol.39
, Issue.7
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
Hankinson, S.E.6
Wacholder, S.7
Wang, Z.8
Welch, R.9
Hutchinson, A.10
Wang, J.11
Yu, K.12
Chatterjee, N.13
Orr, N.14
Willett, W.C.15
Colditz, G.A.16
Ziegler, R.G.17
Berg, C.D.18
Buys, S.S.19
McCarty, C.A.20
Feigelson, H.S.21
Calle, E.E.22
Thun, M.J.23
Hayes, R.B.24
Tucker, M.25
Gerhard, D.S.26
Fraumeni, J.F.27
Hoover, R.N.28
Thomas, G.29
Chanock, S.J.30
more..
-
21
-
-
41949142377
-
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33
-
DOI 10.1073/pnas.0800441105
-
Gold, B., Kirchhoff, T., Stefanov, S., Lautenberger, J., Viale, A., Garber, J., Friedman, E., Narod, S., Olshen, A. B., Gregersen, P., Kosarin, K., Olsh, A., Bergeron, J., Ellis, N. A., Klein, R. J., Clark, A. G., Norton, L., Dean, M., Boyd, J., Offit, K. Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Proc Natl Acad Sci USA 105, 4340-4345 (2008). (Pubitemid 351754382)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.11
, pp. 4340-4345
-
-
Gold, B.1
Kirchhoff, T.2
Stefanov, S.3
Lautenberger, J.4
Viale, A.5
Garber, J.6
Friedman, E.7
Narod, S.8
Olshen, A.B.9
Gregersen, P.10
Kosarin, K.11
Olsh, A.12
Bergeron, J.13
Ellis, N.A.14
Klein, R.J.15
Clark, A.G.16
Norton, L.17
Dean, M.18
Boyd, J.19
Offit, K.20
more..
-
22
-
-
61349163553
-
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
-
Zheng, W., Long, J., Gao, Y. T., Li, C., Zheng, Y., Xiang, Y. B., Wen, W., Levy, S., Deming, S. L., Haines, J. L., Gu, K., Fair, A. M., Cai, Q., Lu, W., Shu, X. O. Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat Genet 41, 324-328 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 324-328
-
-
Zheng, W.1
Long, J.2
Gao, Y.T.3
Li, C.4
Zheng, Y.5
Xiang, Y.B.6
Wen, W.7
Levy, S.8
Deming, S.L.9
Haines, J.L.10
Gu, K.11
Fair, A.M.12
Cai, Q.13
Lu, W.14
Shu, X.O.15
-
23
-
-
45149099137
-
Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer
-
Meyer, K. B., Maia, A. T., O'Reilly, M., Teschendorff, A. E., Chin, S. F., Caldas, C., Ponder, B. A. Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer. PloS Biol 6, e108 (2008).
-
(2008)
PloS Biol
, vol.6
-
-
Meyer, K.B.1
Maia, A.T.2
O'Reilly, M.3
Teschendorff, A.E.4
Chin, S.F.5
Caldas, C.6
Ponder, B.A.7
-
24
-
-
41649103682
-
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
-
DOI 10.1038/nature06885, PII NATURE06885
-
Hung, R. J., McKay, J. D., Gaborieau, V., Boffetta, P., Hashibe, M., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., Chen, C., Goodman, G., Field, J. K., Liloglou, T., Xinarianos, G., Cassidy, A., McLaughlin, J., Liu, G., Narod, S., Krokan, H. E., Skorpen, F., Elvestad, M. B., Hveem, K., Vatten, L., Linseisen, J., Clavel-Chapelon, F., Vineis, P., Bueno-de-Mesquita, H. B., Lund, E., Martinez, C., Bingham, S., Rasmuson, T., Hainaut, P., Riboli, E., Ahrens, W., Benhamou, S., Lagiou, P., Trichopoulos, D., Holcatova, I., Merletti, F., Kjaerheim, K., Agudo, A., Macfarlane, G., Talamini, R., Simonato, L., Lowry, R., Conway, D. I., Znaor, A., Healy, C., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M., Brennan, P. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature 452, 633-637 (2008). (Pubitemid 351483367)
-
(2008)
Nature
, vol.452
, Issue.7187
, pp. 633-637
-
-
Hung, R.J.1
McKay, J.D.2
Gaborieau, V.3
Boffetta, P.4
Hashibe, M.5
Zaridze, D.6
Mukeria, A.7
Szeszenia-Dabrowska, N.8
Lissowska, J.9
Rudnai, P.10
Fabianova, E.11
Mates, D.12
Bencko, V.13
Foretova, L.14
Janout, V.15
Chen, C.16
Goodman, G.17
Field, J.K.18
Liloglou, T.19
Xinarianos, G.20
Cassidy, A.21
McLaughlin, J.22
Liu, G.23
Narod, S.24
Krokan, H.E.25
Skorpen, F.26
Elvestad, M.B.27
Hveem, K.28
Vatten, L.29
Linseisen, J.30
Clavel-Chapelon, F.31
Vineis, P.32
Bueno-De-Mesquita, H.B.33
Lund, E.34
Martinez, C.35
Bingham, S.36
Rasmuson, T.37
Hainaut, P.38
Riboli, E.39
Ahrens, W.40
Benhamou, S.41
Lagiou, P.42
Trichopoulos, D.43
Holcatova, I.44
Merletti, F.45
Kjaerheim, K.46
Agudo, A.47
MacFarlane, G.48
Talamini, R.49
Simonato, L.50
Lowry, R.51
Conway, D.I.52
Znaor, A.53
Healy, C.54
Zelenika, D.55
Boland, A.56
Delepine, M.57
Foglio, M.58
Lechner, D.59
Matsuda, F.60
Blanche, H.61
Gut, I.62
Heath, S.63
Lathrop, M.64
Brennan, P.65
more..
-
25
-
-
41649103052
-
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
-
DOI 10.1038/nature06846, PII NATURE06846
-
Thorgeirsson, T. E., Geller, F., Sulem, P., Rafnar, T., Wiste, A., Magnusson, K. P., Manolescu, A., Thorleifsson, G., Stefansson, H., Ingason, A., Stacey, S. N., Bergthorsson, J. T., Thorlacius, S., Gudmundsson, J., Jonsson, T., Jakobsdottir, M., Saemundsdottir, J., Olafsdottir, O., Gudmundsson, L. J., Bjornsdottir, G., Kristjansson, K., Skuladottir, H., Isaksson, H. J., Gudbjartsson, T., Jones, G. T., Mueller, T., Gottsater, A., Flex, A., Aben, K. K., de Vegt, F., Mulders, P. F., Isla, D., Vidal, M. J., Asin, L., Saez, B., Murillo, L., Blondal, T., Kolbeinsson, H., Stefansson, J. G., Hansdottir, I., Runarsdottir, V., Pola, R., Lindblad, B., van Rij, A. M., Dieplinger, B., Haltmayer, M., Mayordomo, J. I., Kiemeney, L. A., Matthiasson, S. E., Oskarsson, H., Tyrfingsson, T., Gudbjartsson, D. F., Gulcher, J. R., Jonsson, S., Thorsteinsdottir, U., Kong, A., Stefansson, K. A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. Nature 452, 638-642 (2008). (Pubitemid 351483366)
-
(2008)
Nature
, vol.452
, Issue.7187
, pp. 638-642
-
-
Thorgeirsson, T.E.1
Geller, F.2
Sulem, P.3
Rafnar, T.4
Wiste, A.5
Magnusson, K.P.6
Manolescu, A.7
Thorleifsson, G.8
Stefansson, H.9
Ingason, A.10
Stacey, S.N.11
Bergthorsson, J.T.12
Thorlacius, S.13
Gudmundsson, J.14
Jonsson, T.15
Jakobsdottir, M.16
Saemundsdottir, J.17
Olafsdottir, O.18
Gudmundsson, L.J.19
Bjornsdottir, G.20
Kristjansson, K.21
Skuladottir, H.22
Isaksson, H.J.23
Gudbjartsson, T.24
Jones, G.T.25
Mueller, T.26
Gottsater, A.27
Flex, A.28
Aben, K.K.H.29
De Vegt, F.30
Mulders, P.F.A.31
Isla, D.32
Vidal, M.J.33
Asin, L.34
Saez, B.35
Murillo, L.36
Blondal, T.37
Kolbeinsson, H.38
Stefansson, J.G.39
Hansdottir, I.40
Runarsdottir, V.41
Pola, R.42
Lindblad, B.43
Van Rij, A.M.44
Dieplinger, B.45
Haltmayer, M.46
Mayordomo, J.I.47
Kiemeney, L.A.48
Matthiasson, S.E.49
Oskarsson, H.50
Tyrfingsson, T.51
Gudbjartsson, D.F.52
Gulcher, J.R.53
Jonsson, S.54
Thorsteinsdottir, U.55
Kong, A.56
Stefansson, K.57
more..
-
26
-
-
42649091460
-
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1
-
DOI 10.1038/ng.109, PII NG109
-
Amos, C. I., Wu, X., Broderick, P., Gorlov, I. P., Gu, J., Eisen, T., Dong, Q., Zhang, Q., Gu, X., Vijayakrishnan, J., Sullivan, K., Matakidou, A., Wang, Y., Mills, G., Doheny, K., Tsai, Y. Y., Chen, W. V., Shete, S., Spitz, M. R., Houlston, R. S. Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nat Genet 40, 616-622 (2008). (Pubitemid 351601203)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 616-622
-
-
Amos, C.I.1
Wu, X.2
Broderick, P.3
Gorlov, I.P.4
Gu, J.5
Eisen, T.6
Dong, Q.7
Zhang, Q.8
Gu, X.9
Vijayakrishnan, J.10
Sullivan, K.11
Matakidou, A.12
Wang, Y.13
Mills, G.14
Doheny, K.15
Tsai, Y.-Y.16
Chen, W.V.17
Shete, S.18
Spitz, M.R.19
Houlston, R.S.20
more..
-
27
-
-
56749182096
-
Lung cancer susceptibility locus at 5p15.33
-
McKay, J. D., Hung, R. J., Gaborieau, V., Boffetta, P., Chabrier, A., Byrnes, G., Zaridze, D., Mukeria, A., Szeszenia-Dabrowska, N., Lissowska, J., Rudnai, P., Fabianova, E., Mates, D., Bencko, V., Foretova, L., Janout, V., McLaughlin, J., Shepherd, F., Montpetit, A., Narod, S., Krokan, H. E., Skorpen, F., Elvestad, M. B., Vatten, L., Njolstad, I., Axelsson, T., Chen, C., Goodman, G., Barnett, M., Loomis, M. M., Lubinski, J., Matyjasik, J., Lener, M., Oszutowska, D., Field, J., Liloglou, T., Xinarianos, G., Cassidy, A., Vineis, P., Clavel-Chapelon, F., Palli, D., Tumino, R., Krogh, V., Panico, S., Gonzalez, C. A., Ramon Quiros, J., Martinez, C., Navarro, C., Ardanaz, E., Larranaga, N., Kham, K. T., Key, T., Bueno-de-Mesquita, H. B., Peeters, P. H., Trichopoulou, A., Linseisen, J., Boeing, H., Hallmans, G., Overvad, K., Tjonneland, A., Kumle, M., Riboli, E., Zelenika, D., Boland, A., Delepine, M., Foglio, M., Lechner, D., Matsuda, F., Blanche, H., Gut, I., Heath, S., Lathrop, M., Brennan, P. Lung cancer susceptibility locus at 5p15.33. Nat Genet 40, 1404-1406 (2008).
-
(2008)
Nat Genet
, vol.40
, pp. 1404-1406
-
-
McKay, J.D.1
Hung, R.J.2
Gaborieau, V.3
Boffetta, P.4
Chabrier, A.5
Byrnes, G.6
Zaridze, D.7
Mukeria, A.8
Szeszenia-Dabrowska, N.9
Lissowska, J.10
Rudnai, P.11
Fabianova, E.12
Mates, D.13
Bencko, V.14
Foretova, L.15
Janout, V.16
McLaughlin, J.17
Shepherd, F.18
Montpetit, A.19
Narod, S.20
Krokan, H.E.21
Skorpen, F.22
Elvestad, M.B.23
Vatten, L.24
Njolstad, I.25
Axelsson, T.26
Chen, C.27
Goodman, G.28
Barnett, M.29
Loomis, M.M.30
Lubinski, J.31
Matyjasik, J.32
Lener, M.33
Oszutowska, D.34
Field, J.35
Liloglou, T.36
Xinarianos, G.37
Cassidy, A.38
Vineis, P.39
Clavel-Chapelon, F.40
Palli, D.41
Tumino, R.42
Krogh, V.43
Panico, S.44
Gonzalez, C.A.45
Ramon Quiros, J.46
Martinez, C.47
Navarro, C.48
Ardanaz, E.49
Larranaga, N.50
Kham, K.T.51
Key, T.52
Bueno-de-Mesquita, H.B.53
Peeters, P.H.54
Trichopoulou, A.55
Linseisen, J.56
Boeing, H.57
Hallmans, G.58
Overvad, K.59
Tjonneland, A.60
Kumle, M.61
Riboli, E.62
Zelenika, D.63
Boland, A.64
Delepine, M.65
Foglio, M.66
Lechner, D.67
Matsuda, F.68
Blanche, H.69
Gut, I.70
Heath, S.71
Lathrop, M.72
Brennan, P.73
more..
-
28
-
-
34247563453
-
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
-
DOI 10.1038/ng1999, PII NG1999
-
Gudmundsson, J., Sulem, P., Manolescu, A., Amundadottir, L. T., Gudbjartsson, D., Helgason, A., Rafnar, T., Bergthorsson, J. T., Agnarsson, B. A., Baker, A., Sigurdsson, A., Benediktsdottir, K. R., Jakobsdottir, M., Xu, J., Blondal, T., Kostic, J., Sun, J., Ghosh, S., Stacey, S. N., Mouy, M., Saemundsdottir, J., Backman, V. M., Kristjansson, K., Tres, A., Partin, A. W., Albers-Akkers, M. T., Godino-Ivan Marcos, J., Walsh, P. C., Swinkels, D. W., Navarrete, S., Isaacs, S. D., Aben, K. K., Graif, T., Cashy, J., Ruiz-Echarri, M., Wiley, K. E., Suarez, B. K., Witjes, J. A., Frigge, M., Ober, C., Jonsson, E., Einarsson, G. V., Mayordomo, J. I., Kiemeney, L. A., Isaacs, W. B., Catalona, W. J., Barkardottir, R. B., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Stefansson, K. Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat Genet 39, 631-637 (2007). (Pubitemid 46676102)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 631-637
-
-
Gudmundsson, J.1
Sulem, P.2
Manolescu, A.3
Amundadottir, L.T.4
Gudbjartsson, D.5
Helgason, A.6
Rafnar, T.7
Bergthorsson, J.T.8
Agnarsson, B.A.9
Baker, A.10
Sigurdsson, A.11
Benediktsdottir, K.R.12
Jakobsdottir, M.13
Xu, J.14
Blondal, T.15
Kostic, J.16
Sun, J.17
Ghosh, S.18
Stacey, S.N.19
Mouy, M.20
Saemundsdottir, J.21
Backman, V.M.22
Kristjansson, K.23
Tres, A.24
Partin, A.W.25
Albers-Akkers, M.T.26
Godino-Ivan Marcos, J.27
Walsh, P.C.28
Swinkels, D.W.29
Navarrete, S.30
Isaacs, S.D.31
Aben, K.K.32
Graif, T.33
Cashy, J.34
Ruiz-Echarri, M.35
Wiley, K.E.36
Suarez, B.K.37
Witjes, J.A.38
Frigge, M.39
Ober, C.40
Jonsson, E.41
Einarsson, G.V.42
Mayordomo, J.I.43
Kiemeney, L.A.44
Isaacs, W.B.45
Catalona, W.J.46
Barkardottir, R.B.47
Gulcher, J.R.48
Thorsteinsdottir, U.49
Kong, A.50
Stefansson, K.51
more..
-
29
-
-
34247548755
-
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
-
DOI 10.1038/ng2022, PII NG2022
-
Yeager, M., Orr, N., Hayes, R. B., Jacobs, K. B., Kraft, P., Wacholder, S., Minichiello, M. J., Fearnhead, P., Yu, K., Chatterjee, N., Wang, Z., Welch, R., Staats, B. J., Calle, E. E., Feigelson, H. S., Thun, M. J., Rodriguez, C., Albanes, D., Virtamo, J., Weinstein, S., Schumacher, F. R., Giovannucci, E., Willett, W. C., Cancel-Tassin, G., Cussenot, O., Valeri, A., Andriole, G. L., Gelmann, E. P., Tucker, M., Gerhard, D. S., Fraumeni, J. F., Jr., Hoover, R., Hunter, D. J., Chanock, S. J., Thomas, G. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat Genet 39, 645-649 (2007). (Pubitemid 46676108)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 645-649
-
-
Yeager, M.1
Orr, N.2
Hayes, R.B.3
Jacobs, K.B.4
Kraft, P.5
Wacholder, S.6
Minichiello, M.J.7
Fearnhead, P.8
Yu, K.9
Chatterjee, N.10
Wang, Z.11
Welch, R.12
Staats, B.J.13
Calle, E.E.14
Feigelson, H.S.15
Thun, M.J.16
Rodriguez, C.17
Albanes, D.18
Virtamo, J.19
Weinstein, S.20
Schumacher, F.R.21
Giovannucci, E.22
Willett, W.C.23
Cancel-Tassin, G.24
Cussenot, O.25
Valeri, A.26
Andriole, G.L.27
Gelmann, E.P.28
Tucker, M.29
Gerhard, D.S.30
Fraumeni Jr., J.F.31
Hoover, R.32
Hunter, D.J.33
Chanock, S.J.34
Thomas, G.35
more..
-
30
-
-
39749129053
-
Multiple newly identified loci associated with prostate cancer susceptibility
-
DOI 10.1038/ng.90, PII NG90
-
Eeles, R. A., Kote-Jarai, Z., Giles, G. G., Olama, A. A., Guy, M., Jugurnauth, S. K., Mulholland, S., Leongamornlert, D. A., Edwards, S. M., Morrison, J., Field, H. I., Southey, M. C., Severi, G., Donovan, J. L., Hamdy, F. C., Dearnaley, D. P., Muir, K. R., Smith, C., Bagnato, M., Ardern-Jones, A. T., Hall, A. L., O'Brien, L. T., Gehr- Swain, B. N., Wilkinson, R. A., Cox, A., Lewis, S., Brown, P. M., Jhavar, S. G., Tymrakiewicz, M., Lophatananon, A., Bryant, S. L., Horwich, A., Huddart, R. A., Khoo, V. S., Parker, C. C., Woodhouse, C. J., Thompson, A., Christmas, T., Ogden, C., Fisher, C., Jamieson, C., Cooper, C. S., English, D. R., Hopper, J. L., Neal, D. E., Easton, D. F. Multiple newly identified loci associated with prostate cancer susceptibility. Nat Genet 40, 316-321 (2008). (Pubitemid 351311772)
-
(2008)
Nature Genetics
, vol.40
, Issue.3
, pp. 316-321
-
-
Eeles, R.A.1
Kote-Jarai, Z.2
Giles, G.G.3
Olama, A.A.A.4
Guy, M.5
Jugurnauth, S.K.6
Mulholland, S.7
Leongamornlert, D.A.8
Edwards, S.M.9
Morrison, J.10
Field, H.I.11
Southey, M.C.12
Severi, G.13
Donovan, J.L.14
Hamdy, F.C.15
Dearnaley, D.P.16
Muir, K.R.17
Smith, C.18
Bagnato, M.19
Ardern-Jones, A.T.20
Hall, A.L.21
O'Brien, L.T.22
Gehr-Swain, B.N.23
Wilkinson, R.A.24
Cox, A.25
Lewis, S.26
Brown, P.M.27
Jhavar, S.G.28
Tymrakiewicz, M.29
Lophatananon, A.30
Bryant, S.L.31
Horwich, A.32
Huddart, R.A.33
Khoo, V.S.34
Parker, C.C.35
Woodhouse, C.J.36
Thompson, A.37
Christmas, T.38
Ogden, C.39
Fisher, C.40
Jamieson, C.41
Cooper, C.S.42
English, D.R.43
Hopper, J.L.44
Neal, D.E.45
Easton, D.F.46
more..
-
31
-
-
39749118602
-
Multiple loci identified in a genome-wide association study of prostate cancer
-
DOI 10.1038/ng.91, PII NG91
-
Thomas, G., Jacobs, K. B., Yeager, M., Kraft, P., Wacholder, S., Orr, N., Yu, K., Chatterjee, N., Welch, R., Hutchinson, A., Crenshaw, A., Cancel-Tassin, G., Staats, B. J., Wang, Z., Gonzalez-Bosquet, J., Fang, J., Deng, X., Berndt, S. I., Calle, E. E., Feigelson, H. S., Thun, M. J., Rodriguez, C., Albanes, D., Virtamo, J., Weinstein, S., Schumacher, F. R., Giovannucci, E., Willett, W. C., Cussenot, O., Valeri, A., Andriole, G. L., Crawford, E. D., Tucker, M., Gerhard, D. S., Fraumeni, J. F., Jr., Hoover, R., Hayes, R. B., Hunter, D. J., Chanock, S. J. Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet 40, 310-315 (2008). (Pubitemid 351311773)
-
(2008)
Nature Genetics
, vol.40
, Issue.3
, 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 Jr., J.F.35
Hoover, R.36
Hayes, R.B.37
Hunter, D.J.38
Chanock, S.J.39
more..
-
32
-
-
55049112064
-
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer
-
Kiemeney, L. A., Thorlacius, S., Sulem, P., Geller, F., Aben, K. K., Stacey, S. N., Gudmundsson, J., Jakobsdottir, M., Bergthorsson, J. T., Sigurdsson, A., Blondal, T., Witjes, J. A., Vermeulen, S. H., Hulsbergen-van de Kaa, C. A., Swinkels, D. W., Ploeg, M., Cornel, E. B., Vergunst, H., Thorgeirsson, T. E., Gudbjartsson, D., Gudjonsson, S. A., Thorleifsson, G., Kristinsson, K. T., Mouy, M., Snorradottir, S., Placidi, D., Campagna, M., Arici, C., Koppova, K., Gurzau, E., Rudnai, P., Kellen, E., Polidoro, S., Guarrera, S., Sacerdote, C., Sanchez, M., Saez, B., Valdivia, G., Ryk, C., de Verdier, P., Lindblom, A., Golka, K., Bishop, D. T., Knowles, M. A., Nikulasson, S., Petursdottir, V., Jonsson, E., Geirsson, G., Kristjansson, B., Mayordomo, J. I., Steineck, G., Porru, S., Buntinx, F., Zeegers, M. P., Fletcher, T., Kumar, R., Matullo, G., Vineis, P., Kiltie, A. E., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Rafnar, T., Stefansson, K. Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nat Genet 40, 1307-1312 (2008).
-
(2008)
Nat Genet
, vol.40
, pp. 1307-1312
-
-
Kiemeney, L.A.1
Thorlacius, S.2
Sulem, P.3
Geller, F.4
Aben, K.K.5
Stacey, S.N.6
Gudmundsson, J.7
Jakobsdottir, M.8
Bergthorsson, J.T.9
Sigurdsson, A.10
Blondal, T.11
Witjes, J.A.12
Vermeulen, S.H.13
Hulsbergen-van De Kaa, C.A.14
Swinkels, D.W.15
Ploeg, M.16
Cornel, E.B.17
Vergunst, H.18
Thorgeirsson, T.E.19
Gudbjartsson, D.20
Gudjonsson, S.A.21
Thorleifsson, G.22
Kristinsson, K.T.23
Mouy, M.24
Snorradottir, S.25
Placidi, D.26
Campagna, M.27
Arici, C.28
Koppova, K.29
Gurzau, E.30
Rudnai, P.31
Kellen, E.32
Polidoro, S.33
Guarrera, S.34
Sacerdote, C.35
Sanchez, M.36
Saez, B.37
Valdivia, G.38
Ryk, C.39
De Verdier, P.40
Lindblom, A.41
Golka, K.42
Bishop, D.T.43
Knowles, M.A.44
Nikulasson, S.45
Petursdottir, V.46
Jonsson, E.47
Geirsson, G.48
Kristjansson, B.49
Mayordomo, J.I.50
Steineck, G.51
Porru, S.52
Buntinx, F.53
Zeegers, M.P.54
Fletcher, T.55
Kumar, R.56
Matullo, G.57
Vineis, P.58
Kiltie, A.E.59
Gulcher, J.R.60
Thorsteinsdottir, U.61
Kong, A.62
Rafnar, T.63
Stefansson, K.64
more..
-
33
-
-
34247548755
-
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
-
DOI 10.1038/ng2022, PII NG2022
-
Zanke, B. W., Greenwood, C. M., Rangrej, J., Kustra, R., Tenesa, A., Farrington, S. M., Prendergast, J., Olschwang, S., Chiang, T., Crowdy, E., Ferretti, V., Laflamme, P., Sundararajan, S., Roumy, S., Olivier, J. F., Robidoux, F., Sladek, R., Montpetit, A., Campbell, P., Bezieau, S., O'Shea, A. M., Zogopoulos, G., Cotterchio, M., Newcomb, P., McLaughlin, J., Younghusband, B., Green, R., Green, J., Porteous, M. E., Campbell, H., Blanche, H., Sahbatou, M., Tubacher, E., Bonaiti-Pellie, C., Buecher, B., Riboli, E., Kury, S., Chanock, S. J., Potter, J., Thomas, G., Gallinger, S., Hudson, T. J., Dunlop, M. G. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet 39, 989-994 (2007). (Pubitemid 46676108)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 645-649
-
-
Yeager, M.1
Orr, N.2
Hayes, R.B.3
Jacobs, K.B.4
Kraft, P.5
Wacholder, S.6
Minichiello, M.J.7
Fearnhead, P.8
Yu, K.9
Chatterjee, N.10
Wang, Z.11
Welch, R.12
Staats, B.J.13
Calle, E.E.14
Feigelson, H.S.15
Thun, M.J.16
Rodriguez, C.17
Albanes, D.18
Virtamo, J.19
Weinstein, S.20
Schumacher, F.R.21
Giovannucci, E.22
Willett, W.C.23
Cancel-Tassin, G.24
Cussenot, O.25
Valeri, A.26
Andriole, G.L.27
Gelmann, E.P.28
Tucker, M.29
Gerhard, D.S.30
Fraumeni Jr., J.F.31
Hoover, R.32
Hunter, D.J.33
Chanock, S.J.34
Thomas, G.35
more..
-
34
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
DOI 10.1038/ng.133, PII NG133
-
Tenesa, A., Farrington, S. M., Prendergast, J. G., Porteous, M. E., Walker, M., Haq, N., Barnetson, R. A., Theodoratou, E., Cetnarskyj, R., Cartwright, N., Semple, C., Clark, A. J., Reid, F. J., Smith, L. A., Kavoussanakis, K., Koessler, T., Pharoah, P. D., Buch, S., Schafmayer, C., Tepel, J., Schreiber, S., Volzke, H., Schmidt, C. O., Hampe, J., Chang-Claude, J., Hoffmeister, M., Brenner, H., Wilkening, S., Canzian, F., Capella, G., Moreno, V., Deary, I.J., Starr, J. M., Tomlinson, I. P., Kemp, Z., Howarth, K., Carvajal-Carmona, L., Webb, E., Broderick, P., Vijayakrishnan, J., Houlston, R. S., Rennert, G., Ballinger, D., Rozek, L., Gruber, S. B., Matsuda, K., Kidokoro, T., Nakamura, Y., Zanke, B. W., Greenwood, C. M., Rangrej, J., Kustra, R., Montpetit, A., Hudson, T. J., Gallinger, S., Campbell, H., Dunlop, M.G. 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). (Pubitemid 351601219)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, 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
Semple, C.11
Clark, A.J.12
Reid, F.J.L.13
Smith, L.A.14
Kavoussanakis, K.15
Koessler, T.16
Pharoah, P.D.P.17
Buch, S.18
Schafmayer, C.19
Tepel, J.20
Schreiber, S.21
Volzke, H.22
Schmidt, C.O.23
Hampe, J.24
Chang-Claude, J.25
Hoffmeister, M.26
Brenner, H.27
Wilkening, S.28
Canzian, F.29
Capella, G.30
Moreno, V.31
Deary, I.J.32
Starr, J.M.33
Tomlinson, I.P.M.34
Kemp, Z.35
Howarth, K.36
Carvajal-Carmona, L.37
Webb, E.38
Broderick, P.39
Vijayakrishnan, J.40
Houlston, R.S.41
Rennert, G.42
Ballinger, D.43
Rozek, L.44
Gruber, S.B.45
Matsuda, K.46
Kidokoro, T.47
Nakamura, Y.48
Zanke, B.W.49
Greenwood, C.M.T.50
Rangrej, J.51
Kustra, R.52
Montpetit, A.53
Hudson, T.J.54
Gallinger, S.55
Campbell, H.56
Dunlop, M.G.57
more..
-
35
-
-
68149180890
-
Genome-wide association study identifies five susceptibility loci for glioma
-
Shete, S., Hosking, F. J., Robertson, L. B., Dobbins, S. E., Sanson, M., Malmer, B., Simon, M., Marie, Y., Boisselier, B., Delattre, J. Y., Hoang-Xuan, K., El Hallani, S., Idbaih, A., Zelenika, D., Andersson, U., Henriksson, R., Bergenheim, A. T., Feychting, M., Lonn, S., Ahlbom, A., Schramm, J., Linnebank, M., Hemminki, K., Kumar, R., Hepworth, S. J., Price, A., Armstrong, G., Liu, Y., Gu, X., Yu, R., Lau, C., Schoemaker, M., Muir, K., Swerdlow, A., Lathrop, M., Bondy, M., Houlston, R. S. Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet 41, 899-904 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 899-904
-
-
Shete, S.1
Hosking, F.J.2
Robertson, L.B.3
Dobbins, S.E.4
Sanson, M.5
Malmer, B.6
Simon, M.7
Marie, Y.8
Boisselier, B.9
Delattre, J.Y.10
Hoang-Xuan, K.11
El Hallani, S.12
Idbaih, A.13
Zelenika, D.14
Andersson, U.15
Henriksson, R.16
Bergenheim, A.T.17
Feychting, M.18
Lonn, S.19
Ahlbom, A.20
Schramm, J.21
Linnebank, M.22
Hemminki, K.23
Kumar, R.24
Hepworth, S.J.25
Price, A.26
Armstrong, G.27
Liu, Y.28
Gu, X.29
Yu, R.30
Lau, C.31
Schoemaker, M.32
Muir, K.33
Swerdlow, A.34
Lathrop, M.35
Bondy, M.36
Houlston, R.S.37
more..
-
36
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
DOI 10.1038/ng.111, PII NG111
-
Tomlinson, I. P., Webb, E., Carvajal-Carmona, L., Broderick, P., Howarth, K., Pittman, A. M., Spain, S., Lubbe, S., Walther, A., Sullivan, K., Jaeger, E., Fielding, S., Rowan, A., Vijayakrishnan, J., Domingo, E., Chandler, I., Kemp, Z., Qureshi, M., Farrington, S. M., Tenesa, A., Prendergast, J. G., Barnetson, R. A., Penegar, S., Barclay, E., Wood, W., Martin, L., Gorman, M., Thomas, H., Peto, J., Bishop, D. T., Gray, R., Maher, E. R., Lucassen, A., Kerr, D., Evans, D. G., Schafmayer, C., Buch, S., Volzke, H., Hampe, J., Schreiber, S., John, U., Koessler, T., Pharoah, P., van Wezel, T., Morreau, H., Wijnen, J. T., Hopper, J. L., Southey, M. C., Giles, G. G., Severi, G., Castellvi-Bel, S., Ruiz-Ponte, C., Carracedo, A., Castells, A., Forsti, A., Hemminki, K., Vodicka, P., Naccarati, A., Lipton, L., Ho, J. W., Cheng, K. K., Sham, P. C., Luk, J., Agundez, J. A., Ladero, J. M., de la Hoya, M., Caldes, T., Niittymaki, I., Tuupanen, S., Karhu, A., Aaltonen, L., Cazier, J. B., Campbell, H., Dunlop, M. G., Houlston, R. S. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet 40, 623-630 (2008). (Pubitemid 351601204)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, 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
Spain, S.7
Lubbe, S.8
Walther, A.9
Sullivan, K.10
Jaeger, E.11
Fielding, S.12
Rowan, A.13
Vijayakrishnan, J.14
Domingo, E.15
Chandler, I.16
Kemp, Z.17
Qureshi, M.18
Farrington, S.M.19
Tenesa, A.20
Prendergast, J.G.D.21
Barnetson, R.A.22
Penegar, S.23
Barclay, E.24
Wood, W.25
Martin, L.26
Gorman, M.27
Thomas, H.28
Peto, J.29
Bishop, D.T.30
Gray, R.31
Maher, E.R.32
Lucassen, A.33
Kerr, D.34
Evans, D.G.R.35
Schafmayer, C.36
Buch, S.37
Volzke, H.38
Hampe, J.39
Schreiber, S.40
John, U.41
Koessler, T.42
Pharoah, P.43
Van Wezel, T.44
Morreau, H.45
Wijnen, J.T.46
Hopper, J.L.47
Southey, M.C.48
Giles, G.G.49
Severi, G.50
Castellvi-Bel, S.51
Ruiz-Ponte, C.52
Carracedo, A.53
Castells, A.54
Forsti, A.55
Hemminki, K.56
Vodicka, P.57
Naccarati, A.58
Lipton, L.59
Ho, J.W.C.60
Cheng, K.K.61
Sham, P.C.62
Luk, J.63
Agundez, J.A.G.64
Ladero, J.M.65
De La Hoya, M.66
Caldes, T.67
Niittymaki, I.68
Tuupanen, S.69
Karhu, A.70
Aaltonen, L.71
Cazier, J.-B.72
Campbell, H.73
Dunlop, M.G.74
Houlston, R.S.75
more..
-
37
-
-
45549097424
-
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
-
DOI 10.1038/ng.161, PII NG161
-
Gudbjartsson, D. F., Sulem, P., Stacey, S. N., Goldstein, A. M., Rafnar, T., Sigurgeirsson, B., Benediktsdottir, K. R., Thorisdottir, K., Ragnarsson, R., Sveinsdottir, S. G., Magnusson, V., Lindblom, A., Kostulas, K., Botella-Estrada, R., Soriano, V., Juberias, P., Grasa, M., Saez, B., Andres, R., Scherer, D., Rudnai, P., Gurzau, E., Koppova, K., Kiemeney, L. A., Jakobsdottir, M., Steinberg, S., Helgason, A., Gretarsdottir, S., Tucker, M. A., Mayordomo, J. I., Nagore, E., Kumar, R., Hansson, J., Olafsson, J. H., Gulcher, J., Kong, A., Thorsteinsdottir, U., Stefansson, K. ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nat Genet 40, 886-891 (2008). (Pubitemid 351913649)
-
(2008)
Nature Genetics
, vol.40
, Issue.7
, pp. 886-891
-
-
Gudbjartsson, D.F.1
Sulem, P.2
Stacey, S.N.3
Goldstein, A.M.4
Rafnar, T.5
Sigurgeirsson, B.6
Benediktsdottir, K.R.7
Thorisdottir, K.8
Ragnarsson, R.9
Sveinsdottir, S.G.10
Magnusson, V.11
Lindblom, A.12
Kostulas, K.13
Botella-Estrada, R.14
Soriano, V.15
Juberias, P.16
Grasa, M.17
Saez, B.18
Andres, R.19
Scherer, D.20
Rudnai, P.21
Gurzau, E.22
Koppova, K.23
Kiemeney, L.A.24
Jakobsdottir, M.25
Steinberg, S.26
Helgason, A.27
Gretarsdottir, S.28
Tucker, M.A.29
Mayordomo, J.I.30
Nagore, E.31
Kumar, R.32
Hansson, J.33
Olafsson, J.H.34
Gulcher, J.35
Kong, A.36
Thorsteinsdottir, U.37
Stefansson, K.38
more..
-
38
-
-
68149179663
-
Genome-wide association study identifies three loci associated with melanoma risk
-
Bishop, D. T., Demenais, F., Iles, M. M., Harland, M., Taylor, J. C., Corda, E., Randerson-Moor, J., Aitken, J. F., Avril, M. F., Azizi, E., Bakker, B., Bianchi-Scarra, G., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L. A., Chin, A. W. T., Debniak, T., Galore-Haskel, G., Ghiorzo, P., Gut, I., Hansson, J., Hocevar, M., Hoiom, V., Hopper, J. L., Ingvar, C., Kanetsky, P. A., Kefford, R. F., Landi, M. T., Lang, J., Lubinski, J., Mackie, R., Malvehy, J., Mann, G. J., Martin, N. G., Montgomery, G. W., van Nieuwpoort, F. A., Novakovic, S., Olsson, H., Puig, S., Weiss, M., van Workum, W., Zelenika, D., Brown, K. M., Goldstein, A. M., Gillanders, E. M., Boland, A., Galan, P., Elder, D. E., Gruis, N. A., Hayward, N. K., Lathrop, G. M., Barrett, J. H., Bishop, J. A. Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet 41, 920-925 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 920-925
-
-
Bishop, D.T.1
Demenais, F.2
Iles, M.M.3
Harland, M.4
Taylor, J.C.5
Corda, E.6
Randerson-Moor, J.7
Aitken, J.F.8
Avril, M.F.9
Azizi, E.10
Bakker, B.11
Bianchi-Scarra, G.12
Bressac-de Paillerets, B.13
Calista, D.14
Cannon-Albright, L.A.15
Chin, A.W.T.16
Debniak, T.17
Galore-Haskel, G.18
Ghiorzo, P.19
Gut, I.20
Hansson, J.21
Hocevar, M.22
Hoiom, V.23
Hopper, J.L.24
Ingvar, C.25
Kanetsky, P.A.26
Kefford, R.F.27
Landi, M.T.28
Lang, J.29
Lubinski, J.30
Mackie, R.31
Malvehy, J.32
Mann, G.J.33
Martin, N.G.34
Montgomery, G.W.35
Van Nieuwpoort, F.A.36
Novakovic, S.37
Olsson, H.38
Puig, S.39
Weiss, M.40
Van Workum, W.41
Zelenika, D.42
Brown, K.M.43
Goldstein, A.M.44
Gillanders, E.M.45
Boland, A.46
Galan, P.47
Elder, D.E.48
Gruis, N.A.49
Hayward, N.K.50
Lathrop, G.M.51
Barrett, J.H.52
Bishop, J.A.53
more..
-
39
-
-
56749163357
-
Common 5p15.33 and 6p21.33 variants influence lung cancer risk
-
Wang, Y., Broderick, P., Webb, E., Wu, X., Vijayakrishnan, J., Matakidou, A., Qureshi, M., Dong, Q., Gu, X., Chen, W. V., Spitz, M. R., Eisen, T., Amos, C. I., Houlston, R. S. Common 5p15.33 and 6p21.33 variants influence lung cancer risk. Nat Genet 40, 1407-1409 (2008).
-
(2008)
Nat Genet
, vol.40
, pp. 1407-1409
-
-
Wang, Y.1
Broderick, P.2
Webb, E.3
Wu, X.4
Vijayakrishnan, J.5
Matakidou, A.6
Qureshi, M.7
Dong, Q.8
Gu, X.9
Chen, W.V.10
Spitz, M.R.11
Eisen, T.12
Amos, C.I.13
Houlston, R.S.14
-
40
-
-
68249087152
-
Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3
-
Tse, K. P., Su, W. H., Chang, K. P., Tsang, N. M., Yu, C. J., Tang, P., See, L. C., Hsueh, C., Yang, M. L., Hao, S. P., Li, H. Y., Wang, M. H., Liao, L. P., Chen, L. C., Lin, S. R., Jorgensen, T. J., Chang, Y. S., Shugart, Y. Y. Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. Am J hum Genet 85, 194-203 (2009).
-
(2009)
Am J Hum Genet
, vol.85
, pp. 194-203
-
-
Tse, K.P.1
Su, W.H.2
Chang, K.P.3
Tsang, N.M.4
Yu, C.J.5
Tang, P.6
See, L.C.7
Hsueh, C.8
Yang, M.L.9
Hao, S.P.10
Li, H.Y.11
Wang, M.H.12
Liao, L.P.13
Chen, L.C.14
Lin, S.R.15
Jorgensen, T.J.16
Chang, Y.S.17
Shugart, Y.Y.18
-
41
-
-
68149179645
-
Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma
-
Skibola, C. F., Bracci, P. M., Halperin, E., Conde, L., Craig, D. W., Agana, L., Iyadurai, K., Becker, N., Brooks-Wilson, A., Curry, J. D., Spinelli, J. J., Holly, E. A., Riby, J., Zhang, L., Nieters, A., Smith, M. T., Brown, K. M. Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. Nat Genet 41, 873-875 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 873-875
-
-
Skibola, C.F.1
Bracci, P.M.2
Halperin, E.3
Conde, L.4
Craig, D.W.5
Agana, L.6
Iyadurai, K.7
Becker, N.8
Brooks-Wilson, A.9
Curry, J.D.10
Spinelli, J.J.11
Holly, E.A.12
Riby, J.13
Zhang, L.14
Nieters, A.15
Smith, M.T.16
Brown, K.M.17
-
42
-
-
69349100058
-
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
-
Wu, X., Ye, Y., Kiemeney, L. A., Sulem, P., Rafnar, T., Matullo, G., Seminara, D., Yoshida, T., Saeki, N., Andrew, A. S., Dinney, C. P., Czerniak, B., Zhang, Z. F., Kiltie, A. E., Bishop, D. T., Vineis, P., Porru, S., Buntinx, F., Kellen, E., Zeegers, M. P., Kumar, R., Rudnai, P., Gurzau, E., Koppova, K., Mayordomo, J. I., Sanchez, M., Saez, B., Lindblom, A., de Verdier, P., Steineck, G., Mills, G. B., Schned, A., Guarrera, S., Polidoro, S., Chang, S. C., Lin, J., Chang, D. W., Hale, K. S., Majewski, T., Grossman, H. B., Thorlacius, S., Thorsteinsdottir, U., Aben, K. K., Witjes, J. A., Stefansson, K., Amos, C. I., Karagas, M. R., Gu, J. Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nat Genet 41, 991-995 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 991-995
-
-
Wu, X.1
Ye, Y.2
Kiemeney, L.A.3
Sulem, P.4
Rafnar, T.5
Matullo, G.6
Seminara, D.7
Yoshida, T.8
Saeki, N.9
Andrew, A.S.10
Dinney, C.P.11
Czerniak, B.12
Zhang, Z.F.13
Kiltie, A.E.14
Bishop, D.T.15
Vineis, P.16
Porru, S.17
Buntinx, F.18
Kellen, E.19
Zeegers, M.P.20
Kumar, R.21
Rudnai, P.22
Gurzau, E.23
Koppova, K.24
Mayordomo, J.I.25
Sanchez, M.26
Saez, B.27
Lindblom, A.28
De Verdier, P.29
Steineck, G.30
Mills, G.B.31
Schned, A.32
Guarrera, S.33
Polidoro, S.34
Chang, S.C.35
Lin, J.36
Chang, D.W.37
Hale, K.S.38
Majewski, T.39
Grossman, H.B.40
Thorlacius, S.41
Thorsteinsdottir, U.42
Aben, K.K.43
Witjes, J.A.44
Stefansson, K.45
Amos, C.I.46
Karagas, M.R.47
Gu, J.48
more..
-
43
-
-
68149180891
-
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
-
Wrensch, M., Jenkins, R. B., Chang, J. S., Yeh, R. F., Xiao, Y., Decker, P. A., Ballman, K. V., Berger, M., Buckner, J. C., Chang, S., Giannini, C., Halder, C., Kollmeyer, T. M., Kosel, M. L., LaChance, D. H., McCoy, L., O'Neill, B. P., Patoka, J., Pico, A. R., Prados, M., Quesenberry, C., Rice, T., Rynearson, A. L., Smirnov, I., Tihan, T., Wiemels, J., Yang, P., Wiencke, J. K. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Nat Genet 41, 905-908 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 905-908
-
-
Wrensch, M.1
Jenkins, R.B.2
Chang, J.S.3
Yeh, R.F.4
Xiao, Y.5
Decker, P.A.6
Ballman, K.V.7
Berger, M.8
Buckner, J.C.9
Chang, S.10
Giannini, C.11
Halder, C.12
Kollmeyer, T.M.13
Kosel, M.L.14
Lachance, D.H.15
McCoy, L.16
O'Neill, B.P.17
Patoka, J.18
Pico, A.R.19
Prados, M.20
Quesenberry, C.21
Rice, T.22
Rynearson, A.L.23
Smirnov, I.24
Tihan, T.25
Wiemels, J.26
Yang, P.27
Wiencke, J.K.28
more..
-
44
-
-
58249121582
-
Sequence variants at 22q13 are associated with prostate cancer risk
-
Sun, J., Zheng, S. L., Wiklund, F., Isaacs, S. D., Li, G., Wiley, K. E., Kim, S. T., Zhu, Y., Zhang, Z., Hsu, F. C., Turner, A. R., Stattin, P., Liu, W., Kim, J. W., Duggan, D., Carpten, J., Isaacs, W., Gronberg, H., Xu, J., Chang, B. L. Sequence variants at 22q13 are associated with prostate cancer risk. Cancer Res 69, 10-15 (2009).
-
(2009)
Cancer Res
, vol.69
, pp. 10-15
-
-
Sun, J.1
Zheng, S.L.2
Wiklund, F.3
Isaacs, S.D.4
Li, G.5
Wiley, K.E.6
Kim, S.T.7
Zhu, Y.8
Zhang, Z.9
Hsu, F.C.10
Turner, A.R.11
Stattin, P.12
Liu, W.13
Kim, J.W.14
Duggan, D.15
Carpten, J.16
Isaacs, W.17
Gronberg, H.18
Xu, J.19
Chang, B.L.20
more..
-
45
-
-
34250002140
-
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
-
DOI 10.1038/ng2064, PII NG2064
-
Stacey, S. N., Manolescu, A., Sulem, P., Rafnar, T., Gudmundsson, J., Gudjonsson, S. A., Masson, G., Jakobsdottir, M., Thorlacius, S., Helgason, A., Aben, K. K., Strobbe, L. J., Albers-Akkers, M. T., Swinkels, D. W., Henderson, B. E., Kolonel, L. N., Le March-and, L., Millastre, E., Andres, R., Godino, J., Garcia-Prats, M. D., Polo, E., Tres, A., Mouy, M., Saemundsdottir, J., Backman, V. M., Gudmundsson, L., Kristjansson, K., Bergthorsson, J. T., Kostic, J., Frigge, M. L., Geller, F., Gudbjartsson, D., Sigurdsson, H., Jonsdottir, T., Hrafnkelsson, J., Johannsson, J., Sveinsson, T., Myrdal, G., Grimsson, H. N., Jonsson, T., von Holst, S., Werelius, B., Margolin, S., Lindblom, A., Mayordomo, J. I., Haiman, C. A., Kiemeney, L. A., Johannsson, O. T., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Stefansson, K. Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet 39, 865-869 (2007). (Pubitemid 47014497)
-
(2007)
Nature Genetics
, vol.39
, Issue.7
, pp. 865-869
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
Rafnar, T.4
Gudmundsson, J.5
Gudjonsson, S.A.6
Masson, G.7
Jakobsdottir, M.8
Thorlacius, S.9
Helgason, A.10
Aben, K.K.11
Strobbe, L.J.12
Albers-Akkers, M.T.13
Swinkels, D.W.14
Henderson, B.E.15
Kolonel, L.N.16
Le Marchand, L.17
Millastre, E.18
Andres, R.19
Godino, J.20
Garcia-Prats, M.D.21
Polo, E.22
Tres, A.23
Mouy, M.24
Saemundsdottir, J.25
Backman, V.M.26
Gudmundsson, L.27
Kristjansson, K.28
Bergthorsson, J.T.29
Kostic, J.30
Frigge, M.L.31
Geller, F.32
Gudbjartsson, D.33
Sigurdsson, H.34
Jonsdottir, T.35
Hrafnkelsson, J.36
Johannsson, J.37
Sveinsson, T.38
Myrdal, G.39
Grimsson, H.N.40
Jonsson, T.41
Von Holst, S.42
Werelius, B.43
Margolin, S.44
Lindblom, A.45
Mayordomo, J.I.46
Haiman, C.A.47
Kiemeney, L.A.48
Johannsson, O.T.49
Gulcher, J.R.50
Thorsteinsdottir, U.51
Kong, A.52
Stefansson, K.53
more..
-
46
-
-
67349156045
-
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
-
Capasso, M., Devoto, M., Hou, C., Asgharzadeh, S., Glessner, J. T., Attiyeh, E. F., Mosse, Y. P., Kim, C., Diskin, S. J., Cole, K. A., Bosse, K., Diamond, M., Laudenslager, M., Winter, C., Bradfield, J. P., Scott, R. H., Jagannathan, J., Garris, M., McConville, C., London, W. B., Seeger, R. C., Grant, S. F., Li, H., Rahman, N., Rappaport, E., Hakonarson, H., Maris, J. M. Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Nat Genet 41, 718-723 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 718-723
-
-
Capasso, M.1
Devoto, M.2
Hou, C.3
Asgharzadeh, S.4
Glessner, J.T.5
Attiyeh, E.F.6
Mosse, Y.P.7
Kim, C.8
Diskin, S.J.9
Cole, K.A.10
Bosse, K.11
Diamond, M.12
Laudenslager, M.13
Winter, C.14
Bradfield, J.P.15
Scott, R.H.16
Jagannathan, J.17
Garris, M.18
McConville, C.19
London, W.B.20
Seeger, R.C.21
Grant, S.F.22
Li, H.23
Rahman, N.24
Rappaport, E.25
Hakonarson, H.26
Maris, J.M.27
more..
-
47
-
-
59149091340
-
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
-
Rafnar, T., Sulem, P., Stacey, S. N., Geller, F., Gudmundsson, J., Sigurdsson, A., Jakobsdottir, M., Helgadottir, H., Thorlacius, S., Aben, K. K., Blondal, T., Thorgeirsson, T. E., Thorleifsson, G., Kristjansson, K., Thorisdottir, K., Ragnarsson, R., Sigurgeirsson, B., Skuladottir, H., Gudbjartsson, T., Isaksson, H. J., Einarsson, G. V., Benediktsdottir, K. R., Agnarsson, B. A., Olafsson, K., Salvarsdottir, A., Bjarnason, H., Asgeirsdottir, M., Kristinsson, K. T., Matthiasdottir, S., Sveinsdottir, S. G., Polidoro, S., Hoiom, V., Botella-Estrada, R., Hemminki, K., Rudnai, P., Bishop, D. T., Campagna, M., Kellen, E., Zeegers, M. P., de Verdier, P., Ferrer, A., Isla, D., Vidal, M. J., Andres, R., Saez, B., Juberias, P., Banzo, J., Navarrete, S., Tres, A., Kan, D., Lindblom, A., Gurzau, E., Koppova, K., de Vegt, F., Schalken, J. A., van der Heijden, H. F., Smit, H. J., Termeer, R. A., Oosterwijk, E., van Hooij, O., Nagore, E., Porru, S., Steineck, G., Hansson, J., Buntinx, F., Catalona, W. J., Matullo, G., Vineis, P., Kiltie, A. E., Mayordomo, J. I., Kumar, R., Kiemeney, L. A., Frigge, M. L., Jonsson, T., Saemundsson, H., Barkardottir, R. B., Jonsson, E., Jonsson, S., Olafsson, J. H., Gulcher, J. R., Masson, G., Gudbjartsson, D. F., Kong, A., Thorsteinsdottir, U., Stefansson, K. Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nat Genet 41, 221-227 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 221-227
-
-
Rafnar, T.1
Sulem, P.2
Stacey, S.N.3
Geller, F.4
Gudmundsson, J.5
Sigurdsson, A.6
Jakobsdottir, M.7
Helgadottir, H.8
Thorlacius, S.9
Aben, K.K.10
Blondal, T.11
Thorgeirsson, T.E.12
Thorleifsson, G.13
Kristjansson, K.14
Thorisdottir, K.15
Ragnarsson, R.16
Sigurgeirsson, B.17
Skuladottir, H.18
Gudbjartsson, T.19
Isaksson, H.J.20
Einarsson, G.V.21
Benediktsdottir, K.R.22
Agnarsson, B.A.23
Olafsson, K.24
Salvarsdottir, A.25
Bjarnason, H.26
Asgeirsdottir, M.27
Kristinsson, K.T.28
Matthiasdottir, S.29
Sveinsdottir, S.G.30
Polidoro, S.31
Hoiom, V.32
Botella-Estrada, R.33
Hemminki, K.34
Rudnai, P.35
Bishop, D.T.36
Campagna, M.37
Kellen, E.38
Zeegers, M.P.39
De Verdier, P.40
Ferrer, A.41
Isla, D.42
Vidal, M.J.43
Andres, R.44
Saez, B.45
Juberias, P.46
Banzo, J.47
Navarrete, S.48
Tres, A.49
Kan, D.50
Lindblom, A.51
Gurzau, E.52
Koppova, K.53
De Vegt, F.54
Schalken, J.A.55
Van Der Heijden, H.F.56
Smit, H.J.57
Termeer, R.A.58
Oosterwijk, E.59
Van Hooij, O.60
Nagore, E.61
Porru, S.62
Steineck, G.63
Hansson, J.64
Buntinx, F.65
Catalona, W.J.66
Matullo, G.67
Vineis, P.68
Kiltie, A.E.69
Mayordomo, J.I.70
Kumar, R.71
Kiemeney, L.A.72
Frigge, M.L.73
Jonsson, T.74
Saemundsson, H.75
Barkardottir, R.B.76
Jonsson, E.77
Jonsson, S.78
Olafsson, J.H.79
Gulcher, J.R.80
Masson, G.81
Gudbjartsson, D.F.82
Kong, A.83
Thorsteinsdottir, U.84
Stefansson, K.85
more..
-
48
-
-
67649867946
-
Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer
-
Kanetsky, P. A., Mitra, N., Vardhanabhuti, S., Li, M., Vaughn, D. J., Letrero, R., Ciosek, S. L., Doody, D. R., Smith, L. M., Weaver, J., Albano, A., Chen, C., Starr, J. R., Rader, D. J., Godwin, A. K., Reilly, M. P., Hakonarson, H., Schwartz, S. M., Nathanson, K. L. Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. Nat Genet 41, 811-815 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 811-815
-
-
Kanetsky, P.A.1
Mitra, N.2
Vardhanabhuti, S.3
Li, M.4
Vaughn, D.J.5
Letrero, R.6
Ciosek, S.L.7
Doody, D.R.8
Smith, L.M.9
Weaver, J.10
Albano, A.11
Chen, C.12
Starr, J.R.13
Rader, D.J.14
Godwin, A.K.15
Reilly, M.P.16
Hakonarson, H.17
Schwartz, S.M.18
Nathanson, K.L.19
-
49
-
-
67649876131
-
A genome-wide association study of testicular germ cell tumor
-
Rapley, E. A., Turnbull, C., Al Olama, A. A., Dermitzakis, E. T., Linger, R., Huddart, R. A., Renwick, A., Hughes, D., Hines, S., Seal, S., Morrison, J., Nsengimana, J., Deloukas, P., Rahman, N., Bishop, D. T., Easton, D. F., Stratton, M. R. A genome-wide association study of testicular germ cell tumor. Nat Genet 41, 807-810 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 807-810
-
-
Rapley, E.A.1
Turnbull, C.2
Al Olama, A.A.3
Dermitzakis, E.T.4
Linger, R.5
Huddart, R.A.6
Renwick, A.7
Hughes, D.8
Hines, S.9
Seal, S.10
Morrison, J.11
Nsengimana, J.12
Deloukas, P.13
Rahman, N.14
Bishop, D.T.15
Easton, D.F.16
Stratton, M.R.17
-
50
-
-
79959503826
-
The International HapMap Project
-
The International HapMap Project. Nature 426, 789-796 (2003).
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
51
-
-
77952051585
-
Human population genetic diversity as a function of SNP type from HapMap data
-
Garte, S. Human population genetic diversity as a function of SNP type from HapMap data. Am J hum Biol, (2009).
-
(2009)
Am J Hum Biol
-
-
Garte, S.1
-
52
-
-
66349121862
-
The HapMap and genome-wide association studies in diagnosis and therapy
-
Manolio, T. A., Collins, F. S. The HapMap and genome-wide association studies in diagnosis and therapy. Annu Rev med 60, 443-456 (2009).
-
(2009)
Annu Rev Med
, vol.60
, pp. 443-456
-
-
Manolio, T.A.1
Collins, F.S.2
-
53
-
-
30344466238
-
An analysis of identical single-nucleotide polymorphisms genotyped by two different platforms
-
DOI 10.1186/1471-2156-6-S1-S152
-
Suarez, B. K., Taylor, C., Bertelsen, S., Bierut, L. J., Dunn, G., Jin, C. H., Kauwe, J. S., Paterson, A. D., Hinrichs, A. L. An analysis of identical single-nucleotide polymorphisms genotyped by two different platforms. BmC Genet 6 (Suppl 1), S152 (2005). (Pubitemid 46437529)
-
(2005)
BMC Genetics
, vol.6
, Issue.SUPPL. 1
-
-
Suarez, B.K.1
Taylor, C.2
Bertelsen, S.3
Bierut, L.J.4
Dunn, G.5
Jin, C.H.6
Kauwe, J.S.K.7
Paterson, A.D.8
Hinrichs, A.L.9
-
54
-
-
10744221619
-
Large-scale genotyping of complex DNA
-
Kennedy, G. C., Matsuzaki, H., Dong, S., Liu, W. M., Huang, J., Liu, G., Su, X., Cao, M., Chen, W., Zhang, J., Liu, W., Yang, G., Di, X., Ryder, T., He, Z., Surti, U., Phillips, M. S., Boyce-Jacino, M. T., Fodor, S. P., Jones, K. W. Large-scale genotyping of complex DNA. Nat Biotechnol 21, 1233-1237 (2003).
-
(2003)
Nat Biotechnol
, vol.21
, pp. 1233-1237
-
-
Kennedy, G.C.1
Matsuzaki, H.2
Dong, S.3
Liu, W.M.4
Huang, J.5
Liu, G.6
Su, X.7
Cao, M.8
Chen, W.9
Zhang, J.10
Liu, W.11
Yang, G.12
Di, X.13
Ryder, T.14
He, Z.15
Surti, U.16
Phillips, M.S.17
Boyce-Jacino, M.T.18
Fodor, S.P.19
Jones, K.W.20
more..
-
55
-
-
33745279056
-
Evaluating coverage of genome-wide association studies
-
Barrett, J. C., Cardon, L. R. Evaluating coverage of genome-wide association studies. Nat Genet 38, 659-662 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 659-662
-
-
Barrett, J.C.1
Cardon, L.R.2
-
56
-
-
42649111672
-
Evaluation of coverage variation of SNP chips for genome-wide association studies
-
DOI 10.1038/sj.ejhg.5202007, PII 5202007
-
Li, M., Li, C., Guan, W. Evaluation of coverage variation of SNP chips for genome-wide association studies. Eur J hum Genet 16, 635-643 (2008). (Pubitemid 351594131)
-
(2008)
European Journal of Human Genetics
, vol.16
, Issue.5
, pp. 635-643
-
-
Li, M.1
Li, C.2
Guan, W.3
-
57
-
-
67149095078
-
Designing genome-wide association studies: Sample size, power, imputation, and the choice of genotyping chip
-
Spencer, C. C., Su, Z., Donnelly, P., Marchini, J. Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip. PloS Genet 5, e1000477 (2009).
-
(2009)
PloS Genet
, vol.5
-
-
Spencer, C.C.1
Su, Z.2
Donnelly, P.3
Marchini, J.4
-
58
-
-
33750356125
-
Optimal two-stage genome-wide association designs based on false discovery rate
-
DOI 10.1016/j.csda.2006.04.034, PII S0167947306001344
-
Wang, H., Thomas, D. C., Pe'er, I., Stram, D. O. Optimal two-stage genotyping designs for genome-wide association scans. Genet Epidemiol 30, 356-368 (2006). (Pubitemid 44635911)
-
(2006)
Computational Statistics and Data Analysis
, vol.51
, Issue.2
, pp. 457-465
-
-
Wang, H.1
Stram, D.O.2
-
59
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661-678 (2007).
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
60
-
-
0142063079
-
Polygenic inheritance of breast cancer: Implications for design of association studies
-
Antoniou, A. C., Easton, D. F. Polygenic inheritance of breast cancer: Implications for design of association studies. Genet Epidemiol 25, 190-202 (2003).
-
(2003)
Genet Epidemiol
, vol.25
, pp. 190-202
-
-
Antoniou, A.C.1
Easton, D.F.2
-
61
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
DOI 10.1038/ng2088, PII NG2088
-
Marchini, J., Howie, B., Myers, S., McVean, G., Donnelly, P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39, 906-913 (2007). (Pubitemid 47014502)
-
(2007)
Nature Genetics
, vol.39
, Issue.7
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
62
-
-
40949127393
-
How to interpret a genome-wide association study
-
Pearson, T. A., Manolio, T. A. How to interpret a genome-wide association study. JAMA 299, 1335-1344 (2008).
-
(2008)
JAMA
, vol.299
, pp. 1335-1344
-
-
Pearson, T.A.1
Manolio, T.A.2
-
63
-
-
61449136094
-
A pilot genome-wide association study of early-onset breast cancer
-
Kibriya, M. G., Jasmine, F., Argos, M., Andrulis, I. L., John, E. M., Chang-Claude, J., Ahsan, H. A pilot genome-wide association study of early-onset breast cancer. Breast Cancer Res Treat 114, 463-477 (2009).
-
(2009)
Breast Cancer Res Treat
, vol.114
, pp. 463-477
-
-
Kibriya, M.G.1
Jasmine, F.2
Argos, M.3
Andrulis, I.L.4
John, E.M.5
Chang-Claude, J.6
Ahsan, H.7
-
64
-
-
30344442002
-
Power and type 1 error rate of fales discovery rate approaches in genome-wide association studies
-
DOI 10.1186/1471-2156-6-S1-S134
-
Yang, Q., Cui, J., Chazaro, I., Cupples, L. A., Demissie, S. Power and type I error rate of false discovery rate approaches in genome-wide association studies. BmC Genet 6 (Suppl 1), S134 (2005). (Pubitemid 46437545)
-
(2005)
BMC Genetics
, vol.6
, Issue.SUPPL. 1
-
-
Yang, Q.1
Cui, J.2
Chazaro, I.3
Cupples, L.A.4
Demissie, S.5
-
65
-
-
34249997024
-
Replicating genotype-phenotype associations
-
Chanock, S. J., Manolio, T., Boehnke, M., Boerwinkle, E., Hunter, D. J., Thomas, G., Hirschhorn, J. N., Abecasis, G., Altshuler, D., Bailey-Wilson, J. E., Brooks, L. D., Cardon, L. R., Daly, M., Donnelly, P., Fraumeni, J. F., Jr., Freimer, N. B., Gerhard, D. S., Gunter, C., Guttmacher, A. E., Guyer, M. S., Harris, E. L., Hoh, J., Hoover, R., Kong, C. A., Merikangas, K. R., Morton, C. C., Palmer, L. J., Phimister, E. G., Rice, J. P., Roberts, J., Rotimi, C.,
-
(2007)
Nature
, vol.447
, pp. 655-660
-
-
Chanock, S.J.1
Manolio, T.2
Boehnke, M.3
Boerwinkle, E.4
Hunter, D.J.5
Thomas, G.6
Hirschhorn, J.N.7
Abecasis, G.8
Altshuler, D.9
Bailey-Wilson, J.E.10
Brooks, L.D.11
Cardon, L.R.12
Daly, M.13
Donnelly, P.14
Fraumeni Jr., J.F.15
Freimer, N.B.16
Gerhard, D.S.17
Gunter, C.18
Guttmacher, A.E.19
Guyer, M.S.20
Harris, E.L.21
Hoh, J.22
Hoover, R.23
Kong, C.A.24
Merikangas, K.R.25
Morton, C.C.26
Palmer, L.J.27
Phimister, E.G.28
Rice, J.P.29
Roberts, J.30
Rotimi, C.31
Tucker, M.A.32
Vogan, K.J.33
Wacholder, S.34
Wijsman, E.M.35
Winn, D.M.36
Collins, F.S.37
more..
-
66
-
-
40349084039
-
The promise and limitations of genome-wide association studies to elucidate the causes of breast cancer
-
Ambrosone, C. B. The promise and limitations of genome-wide association studies to elucidate the causes of breast cancer. Breast Cancer Res 9, 114 (2007).
-
(2007)
Breast Cancer Res
, vol.9
, pp. 114
-
-
Ambrosone, C.B.1
-
67
-
-
52449107055
-
Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies
-
Zhong, H., Prentice, R. L. Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies. Biostatistics 9, 621-634 (2008).
-
(2008)
Biostatistics
, vol.9
, pp. 621-634
-
-
Zhong, H.1
Prentice, R.L.2
-
68
-
-
34547788766
-
Enriching the analysis of genomewide association studies with hierarchical modeling
-
Chen, G. K., Witte, J. S. Enriching the analysis of genomewide association studies with hierarchical modeling. Am J hum Genet 81, 397-404 (2007).
-
(2007)
Am J Hum Genet
, vol.81
, pp. 397-404
-
-
Chen, G.K.1
Witte, J.S.2
-
69
-
-
70149101114
-
Using genome-wide pathway analysis to unravel the etiology of complex diseases
-
Elbers, C. C., van Eijk, K. R., Franke, L., Mulder, F., van der Schouw, Y. T., Wijmenga, C., Onland-Moret, N. C. Using genome-wide pathway analysis to unravel the etiology of complex diseases. Genet Epidemiol 33, 419-431 (2009).
-
(2009)
Genet Epidemiol
, vol.33
, pp. 419-431
-
-
Elbers, C.C.1
Van Eijk, K.R.2
Franke, L.3
Mulder, F.4
Van Der Schouw, Y.T.5
Wijmenga, C.6
Onland-Moret, N.C.7
-
70
-
-
67349237973
-
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
-
Ahmed, S., Thomas, G., Ghoussaini, M., Healey, C. S., Humphreys, M. K., Platte, R., Morrison, J., Maranian, M., Pooley, K. A., Luben, R., Eccles, D., Evans, D. G., Fletcher, O., Johnson, N., dos Santos Silva, I., Peto, J., Stratton, M. R., Rahman, N., Jacobs, K., Prentice, R., Anderson, G. L., Rajkovic, A., Curb, J. D., Ziegler, R. G., Berg, C. D., Buys, S. S., McCarty, C. A., Feigelson, H. S., Calle, E. E., Thun, M. J., Diver, W. R., Bojesen, S., Nordestgaard, B. G., Flyger, H., Dork, T., Schurmann, P., Hillemanns, P., Karstens, J. H., Bogdanova, N. V., Antonenkova, N. N., Zalutsky, I. V., Bermisheva, M., Fedorova, S., Khusnutdinova, E., Kang, D., Yoo, K. Y., Noh, D. Y., Ahn, S. H., Devilee, P., van Asperen, C. J., Tollenaar, R. A., Seynaeve, C., Garcia-Closas, M., Lissowska, J., Brinton, L., Peplonska, B., Nevanlinna, H., Heikkinen, T., Aittomaki, K., Blomqvist, C., Hopper, J. L., Southey, M. C., Smith, L., Spurdle, A. B., Schmidt, M. K., Broeks, A., van Hien, R. R., Cornelissen, S., Milne, R. L., Ribas, G., Gonzalez-Neira, A., Benitez, J., Schmutzler, R. K., Burwinkel, B., Bartram, C. R., Meindl, A., Brauch, H., Justenhoven, C., Hamann, U., Chang-Claude, J., Hein, R., Wang-Gohrke, S., Lindblom, A., Margolin, S., Mannermaa, A., Kosma, V. M., Kataja, V., Olson, J. E., Wang, X., Fredericksen, Z., Giles, G. G., Severi, G., Baglietto, L., English, D. R., Hankinson, S. E., Cox, D. G., Kraft, P., Vatten, L. J., Hveem, K., Kumle, M., Sigurdson, A., Doody, M., Bhatti, P., Alexander, B. H., Hooning, M. J., van den Ouweland, A. M., Oldenburg, R. A., Schutte, M., Hall, P., Czene, K., Liu, J., Li, Y., Cox, A., Elliott, G., Brock, I., Reed, M. W., Shen, C. Y., Yu, J. C., Hsu, G. C., Chen, S. T., Anton-Culver, H., Ziogas, A., Andrulis, I. L., Knight, J. A., Beesley, J., Goode, E. L., Couch, F., Chenevix-Trench, G., Hoover, R. N., Ponder, B. A., Hunter, D. J., Pharoah, P. D., Dunning, A. M., Chanock, S. J., Easton, D. F. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet 41, 585-590 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 585-590
-
-
Ahmed, S.1
Thomas, G.2
Ghoussaini, M.3
Healey, C.S.4
Humphreys, M.K.5
Platte, R.6
Morrison, J.7
Maranian, M.8
Pooley, K.A.9
Luben, R.10
Eccles, D.11
Evans, D.G.12
Fletcher, O.13
Johnson, N.14
Dos Santos Silva, I.15
Peto, J.16
Stratton, M.R.17
Rahman, N.18
Jacobs, K.19
Prentice, R.20
Anderson, G.L.21
Rajkovic, A.22
Curb, J.D.23
Ziegler, R.G.24
Berg, C.D.25
Buys, S.S.26
McCarty, C.A.27
Feigelson, H.S.28
Calle, E.E.29
Thun, M.J.30
Diver, W.R.31
Bojesen, S.32
Nordestgaard, B.G.33
Flyger, H.34
Dork, T.35
Schurmann, P.36
Hillemanns, P.37
Karstens, J.H.38
Bogdanova, N.V.39
Antonenkova, N.N.40
Zalutsky, I.V.41
Bermisheva, M.42
Fedorova, S.43
Khusnutdinova, E.44
Kang, D.45
Yoo, K.Y.46
Noh, D.Y.47
Ahn, S.H.48
Devilee, P.49
Van Asperen, C.J.50
Tollenaar, R.A.51
Seynaeve, C.52
Garcia-Closas, M.53
Lissowska, J.54
Brinton, L.55
Peplonska, B.56
Nevanlinna, H.57
Heikkinen, T.58
Aittomaki, K.59
Blomqvist, C.60
Hopper, J.L.61
Southey, M.C.62
Smith, L.63
Spurdle, A.B.64
Schmidt, M.K.65
Broeks, A.66
Van Hien, R.R.67
Cornelissen, S.68
Milne, R.L.69
Ribas, G.70
Gonzalez-Neira, A.71
Benitez, J.72
Schmutzler, R.K.73
Burwinkel, B.74
Bartram, C.R.75
Meindl, A.76
Brauch, H.77
Justenhoven, C.78
Hamann, U.79
Chang-Claude, J.80
Hein, R.81
Wang-Gohrke, S.82
Lindblom, A.83
Margolin, S.84
Mannermaa, A.85
Kosma, V.M.86
Kataja, V.87
Olson, J.E.88
Wang, X.89
Fredericksen, Z.90
Giles, G.G.91
Severi, G.92
Baglietto, L.93
English, D.R.94
Hankinson, S.E.95
Cox, D.G.96
Kraft, P.97
Vatten, L.J.98
Hveem, K.99
more..
-
71
-
-
67349158067
-
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
-
Thomas, G., Jacobs, K. B., Kraft, P., Yeager, M., Wacholder, S., Cox, D. G., Hankinson, S. E., Hutchinson, A., Wang, Z., Yu, K., Chatterjee, N., Garcia-Closas, M., Gonzalez-Bosquet, J., Prokunina-Olsson, L., Orr, N., Willett, W. C., Colditz, G. A., Ziegler, R. G., Berg, C. D., Buys, S. S., McCarty, C. A., Feigelson, H. S., Calle, E. E., Thun, M. J., Diver, R., Prentice, R., Jackson, R., Kooperberg, C., Chlebowski, R., Lissowska, J., Peplonska, B., Brinton, L. A., Sigurdson, A., Doody, M., Bhatti, P., Alexander, B. H., Buring, J., Lee, I. M., Vatten, L. J., Hveem, K., Kumle, M., Hayes, R. B., Tucker, M., Gerhard, D. S., Fraumeni, J. F., Jr., Hoover, R. N., Chanock, S. J., Hunter, D. J. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat Genet 41, 579-584 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 579-584
-
-
Thomas, G.1
Jacobs, K.B.2
Kraft, P.3
Yeager, M.4
Wacholder, S.5
Cox, D.G.6
Hankinson, S.E.7
Hutchinson, A.8
Wang, Z.9
Yu, K.10
Chatterjee, N.11
Garcia-Closas, M.12
Gonzalez-Bosquet, J.13
Prokunina-Olsson, L.14
Orr, N.15
Willett, W.C.16
Colditz, G.A.17
Ziegler, R.G.18
Berg, C.D.19
Buys, S.S.20
McCarty, C.A.21
Feigelson, H.S.22
Calle, E.E.23
Thun, M.J.24
Diver, R.25
Prentice, R.26
Jackson, R.27
Kooperberg, C.28
Chlebowski, R.29
Lissowska, J.30
Peplonska, B.31
Brinton, L.A.32
Sigurdson, A.33
Doody, M.34
Bhatti, P.35
Alexander, B.H.36
Buring, J.37
Lee, I.M.38
Vatten, L.J.39
Hveem, K.40
Kumle, M.41
Hayes, R.B.42
Tucker, M.43
Gerhard, D.S.44
Fraumeni Jr., J.F.45
Hoover, R.N.46
Chanock, S.J.47
Hunter, D.J.48
more..
-
72
-
-
44349087530
-
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer
-
DOI 10.1038/ng.131, PII NG131
-
Stacey, S.N., Manolescu, A., Sulem, P., Thorlacius, S., Gudjonsson, S. A., Jonsson, G. F., Jakobsdottir, M., Bergthorsson, J. T., Gudmundsson, J., Aben, K. K., Strobbe, L. J., Swinkels, D. W., van Engelenburg, K. C., Henderson, B. E., Kolonel, L. N., Le Marchand, L., Millastre, E., Andres, R., Saez, B., Lambea, J., Godino, J., Polo, E., Tres, A., Picelli, S., Rantala, J., Margolin, S., Jonsson, T., Sigurdsson, H., Jonsdottir, T., Hrafnkelsson, J., Johannsson, J., Sveinsson, T., Myrdal, G., Grimsson, H. N., Sveinsdottir, S. G., Alexiusdottir, K., Saemundsdottir, J., Sigurdsson, A., Kostic, J., Gudmundsson, L., Kristjansson, K., Masson, G., Fackenthal, J. D., Adebamowo, C., Ogundiran, T., Olopade, O. I., Haiman, C. A., Lindblom, A., Mayordomo, J. I., Kiemeney, L. A., Gulcher, J. R., Rafnar, T., Thorsteinsdottir, U., Johannsson, O. T., Kong, A., Stefansson, K. Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet 40, 703-706 (2008). (Pubitemid 351748861)
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 703-706
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
Thorlacius, S.4
Gudjonsson, S.A.5
Jonsson, G.F.6
Jakobsdottir, M.7
Bergthorsson, J.T.8
Gudmundsson, J.9
Aben, K.K.10
Strobbe, L.J.11
Swinkels, D.W.12
Van Engelenburg, K.C.A.13
Henderson, B.E.14
Kolonel, L.N.15
Le Marchand, L.16
Millastre, E.17
Andres, R.18
Saez, B.19
Lambea, J.20
Godino, J.21
Polo, E.22
Tres, A.23
Picelli, S.24
Rantala, J.25
Margolin, S.26
Jonsson, T.27
Sigurdsson, H.28
Jonsdottir, T.29
Hrafnkelsson, J.30
Johannsson, J.31
Sveinsson, T.32
Myrdal, G.33
Grimsson, H.N.34
Sveinsdottir, S.G.35
Alexiusdottir, K.36
Saemundsdottir, J.37
Sigurdsson, A.38
Kostic, J.39
Gudmundsson, L.40
Kristjansson, K.41
Masson, G.42
Fackenthal, J.D.43
Adebamowo, C.44
Ogundiran, T.45
Olopade, O.I.46
Haiman, C.A.47
Lindblom, A.48
Mayordomo, J.I.49
Kiemeney, L.A.50
Gulcher, J.R.51
Rafnar, T.52
Thorsteinsdottir, U.53
Johannsson, O.T.54
Kong, A.55
Stefansson, K.56
more..
-
73
-
-
69349102630
-
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
-
Song, H., Ramus, S. J., Tyrer, J., Bolton, K. L., Gentry-Maharaj, A., Wozniak, E., Anton-Culver, H., Chang-Claude, J., Cramer, D. W., DiCioccio, R., Dork, T., Goode, E. L., Goodman, M. T., Schildkraut, J. M., Sellers, T., Baglietto, L., Beckmann, M. W., Beesley, J., Blaakaer, J., Carney, M. E., Chanock, S., Chen, Z., Cunningham, J. M., Dicks, E., Doherty, J. A., Durst, M., Ekici, A. B., Fenstermacher, D., Fridley, B. L., Giles, G., Gore, M. E., De Vivo, I., Hillemanns, P., Hogdall, C., Hogdall, E., Iversen, E. S., Jacobs, I. J., Jakubowska, A., Li, D., Lissowska, J., Lubinski, J., Lurie, G., McGuire, V., McLaughlin, J., Medrek, K., Moorman, P. G., Moysich, K., Narod, S., Phelan, C., Pye, C., Risch, H., Runnebaum, I. B., Severi, G., Southey, M., Stram, D. O., Thiel, F. C., Terry, K. L., Tsai, Y. Y., Tworoger, S. S., Van Den Berg, D. J., Vierkant, R. A., Wang-Gohrke, S., Webb, P. M., Wilkens, L. R., Wu, A. H., Yang, H., Brewster, W., Ziogas, A., Houlston, R., Tomlinson, I., Whittemore, A. S., Rossing, M. A., Ponder, B. A., Pearce, C. L., Ness, R. B., Menon, U., Kjaer, S. K., Gronwald, J., Garcia-Closas, M., Fasching, P. A., Easton, D. F., Chenevix-Trench, G., Berchuck, A., Pharoah, P. D., Gayther, S. A. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nat Genet 41, 996-1000 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 996-1000
-
-
Song, H.1
Ramus, S.J.2
Tyrer, J.3
Bolton, K.L.4
Gentry-Maharaj, A.5
Wozniak, E.6
Anton-Culver, H.7
Chang-Claude, J.8
Cramer, D.W.9
Dicioccio, R.10
Dork, T.11
Goode, E.L.12
Goodman, M.T.13
Schildkraut, J.M.14
Sellers, T.15
Baglietto, L.16
Beckmann, M.W.17
Beesley, J.18
Blaakaer, J.19
Carney, M.E.20
Chanock, S.21
Chen, Z.22
Cunningham, J.M.23
Dicks, E.24
Doherty, J.A.25
Durst, M.26
Ekici, A.B.27
Fenstermacher, D.28
Fridley, B.L.29
Giles, G.30
Gore, M.E.31
De Vivo, I.32
Hillemanns, P.33
Hogdall, C.34
Hogdall, E.35
Iversen, E.S.36
Jacobs, I.J.37
Jakubowska, A.38
Li, D.39
Lissowska, J.40
Lubinski, J.41
Lurie, G.42
McGuire, V.43
McLaughlin, J.44
Medrek, K.45
Moorman, P.G.46
Moysich, K.47
Narod, S.48
Phelan, C.49
Pye, C.50
Risch, H.51
Runnebaum, I.B.52
Severi, G.53
Southey, M.54
Stram, D.O.55
Thiel, F.C.56
Terry, K.L.57
Tsai, Y.Y.58
Tworoger, S.S.59
Van Den Berg, D.J.60
Vierkant, R.A.61
Wang-Gohrke, S.62
Webb, P.M.63
Wilkens, L.R.64
Wu, A.H.65
Yang, H.66
Brewster, W.67
Ziogas, A.68
Houlston, R.69
Tomlinson, I.70
Whittemore, A.S.71
Rossing, M.A.72
Ponder, B.A.73
Pearce, C.L.74
Ness, R.B.75
Menon, U.76
Kjaer, S.K.77
Gronwald, J.78
Garcia-Closas, M.79
Fasching, P.A.80
Easton, D.F.81
Chenevix-Trench, G.82
Berchuck, A.83
Pharoah, P.D.84
Gayther, S.A.85
more..
-
74
-
-
34547510624
-
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
-
DOI 10.1038/ng2062, PII NG2062
-
Gudmundsson, J., Sulem, P., Steinthorsdottir, V., Bergthorsson, J. T., Thorleifsson, G., Manolescu, A., Rafnar, T., Gudbjartsson, D., Agnarsson, B. A., Baker, A., Sigurdsson, A., Benediktsdottir, K. R., Jakobsdottir, M., Blondal, T., Stacey, S. N., Helgason, A., Gunnarsdottir, S., Olafsdottir, A., Kristinsson, K. T., Birgisdottir, B., Ghosh, S., Thorlacius, S., Magnusdottir, D., Stefansdottir, G., Kristjansson, K., Bagger, Y., Wilensky, R. L., Reilly, M. P., Morris, A. D., Kimber, C. H., Adeyemo, A., Chen, Y., Zhou, J., So, W. Y., Tong, P. C., Ng, M. C., Hansen, T., Andersen, G., Borch-Johnsen, K., Jorgensen, T., Tres, A., Fuertes, F., Ruiz-Echarri, M., Asin, L., Saez, B., van Boven, E., Klaver, S., Swinkels, D. W., Aben, K. K., Graif, T., Cashy, J., Suarez, B. K., van Vierssen Trip, O., Frigge, M. L., Ober, C., Hofker, M. H., Wijmenga, C., Christiansen, C., Rader, D. J., Palmer, C. N., Rotimi, C., Chan, J. C., Pedersen, O., Sigurdsson, G., Benediktsson, R., Jonsson, E., Einarsson, G. V., Mayordomo, J. I., Catalona, W. J., Kiemeney, L. A., Barkardottir, R. B., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Stefansson, K. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. Nat Genet 39, 977-983 (2007). (Pubitemid 47185170)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 977-983
-
-
Gudmundsson, J.1
Sulem, P.2
Steinthorsdottir, V.3
Bergthorsson, J.T.4
Thorleifsson, G.5
Manolescu, A.6
Rafnar, T.7
Gudbjartsson, D.8
Agnarsson, B.A.9
Baker, A.10
Sigurdsson, A.11
Benediktsdottir, K.R.12
Jakobsdottir, M.13
Blondal, T.14
Stacey, S.N.15
Helgason, A.16
Gunnarsdottir, S.17
Olafsdottir, A.18
Kristinsson, K.T.19
Birgisdottir, B.20
Ghosh, S.21
Thorlacius, S.22
Magnusdottir, D.23
Stefansdottir, G.24
Kristjansson, K.25
Bagger, Y.26
Wilensky, R.L.27
Reilly, M.P.28
Morris, A.D.29
Kimber, C.H.30
Adeyemo, A.31
Chen, Y.32
Zhou, J.33
So, W.-Y.34
Tong, P.C.Y.35
Ng, M.C.Y.36
Hansen, T.37
Andersen, G.38
Borch-Johnsen, K.39
Jorgensen, T.40
Tres, A.41
Fuertes, F.42
Ruiz-Echarri, M.43
Asin, L.44
Saez, B.45
Van Boven, E.46
Klaver, S.47
Swinkels, D.W.48
Aben, K.K.49
Graif, T.50
Cashy, J.51
Suarez, B.K.52
Van Vierssen Trip, O.53
Frigge, M.L.54
Ober, C.55
Hofker, M.H.56
Wijmenga, C.57
Christiansen, C.58
Rader, D.J.59
Palmer, C.N.A.60
Rotimi, C.61
Chan, J.C.N.62
Pedersen, O.63
Sigurdsson, G.64
Benediktsson, R.65
Jonsson, E.66
Einarsson, G.V.67
Mayordomo, J.I.68
Catalona, W.J.69
Kiemeney, L.A.70
Barkardottir, R.B.71
Gulcher, J.R.72
Thorsteinsdottir, U.73
Kong, A.74
Stefansson, K.75
more..
-
75
-
-
39749159112
-
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
-
DOI 10.1038/ng.89, PII NG89
-
Gudmundsson, J., Sulem, P., Rafnar, T., Bergthorsson, J. T., Manolescu, A., Gudbjartsson, D., Agnarsson, B. A., Sigurdsson, A., Benediktsdottir, K. R., Blondal, T., Jakobsdottir, M., Stacey, S. N., Kostic, J., Kristinsson, K. T., Birgisdottir, B., Ghosh, S., Magnusdottir, D. N., Thorlacius, S., Thorleifsson, G., Zheng, S. L., Sun, J., Chang, B. L., Elmore, J. B., Breyer, J. P., McReynolds, K. M., Bradley, K. M., Yaspan, B. L., Wiklund, F., Stattin, P., Lindstrom, S., Adami, H. O., McDonnell, S. K., Schaid, D. J., Cunningham, J. M., Wang, L., Cerhan, J. R., St Sauver, J. L., Isaacs, S. D., Wiley, K. E., Partin, A. W., Walsh, P. C., Polo, S., Ruiz-Echarri, M., Navarrete, S., Fuertes, F., Saez, B., Godino, J., Weijerman, P. C., Swinkels, D. W., Aben, K. K., Witjes, J. A., Suarez, B. K., Helfand, B. T., Frigge, M. L., Kristjansson, K., Ober, C., Jonsson, E., Einarsson, G. V., Xu, J., Gronberg, H., Smith, J. R., Thibodeau, S. N., Isaacs, W. B., Catalona, W. J., Mayordomo, J. I., Kiemeney, L. A., Barkardottir, R. B., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Stefansson, K. Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Nat Genet 40, 281-283 (2008). (Pubitemid 351311771)
-
(2008)
Nature Genetics
, vol.40
, Issue.3
, pp. 281-283
-
-
Gudmundsson, J.1
Sulem, P.2
Rafnar, T.3
Bergthorsson, J.T.4
Manolescu, A.5
Gudbjartsson, D.6
Agnarsson, B.A.7
Sigurdsson, A.8
Benediktsdottir, K.R.9
Blondal, T.10
Jakobsdottir, M.11
Stacey, S.N.12
Kostic, J.13
Kristinsson, K.T.14
Birgisdottir, B.15
Ghosh, S.16
Magnusdottir, D.N.17
Thorlacius, S.18
Thorleifsson, G.19
Zheng, S.L.20
Sun, J.21
Chang, B.-L.22
Elmore, J.B.23
Breyer, J.P.24
McReynolds, K.M.25
Bradley, K.M.26
Yaspan, B.L.27
Wiklund, F.28
Stattin, P.29
Lindstrom, S.30
Adami, H.-O.31
McDonnell, S.K.32
Schaid, D.J.33
Cunningham, J.M.34
Wang, L.35
Cerhan, J.R.36
St Sauver, J.L.37
Isaacs, S.D.38
Wiley, K.E.39
Partin, A.W.40
Walsh, P.C.41
Polo, S.42
Ruiz-Echarri, M.43
Navarrete, S.44
Fuertes, F.45
Saez, B.46
Godino, J.47
Weijerman, P.C.48
Swinkels, D.W.49
Aben, K.K.50
Witjes, J.A.51
Suarez, B.K.52
Helfand, B.T.53
Frigge, M.L.54
Kristjansson, K.55
Ober, C.56
Jonsson, E.57
Einarsson, G.V.58
Xu, J.59
Gronberg, H.60
Smith, J.R.61
Thibodeau, S.N.62
Isaacs, W.B.63
Catalona, W.J.64
Mayordomo, J.I.65
Kiemeney, L.A.66
Barkardottir, R.B.67
Gulcher, J.R.68
Thorsteinsdottir, U.69
Kong, A.70
Stefansson, K.71
more..
-
76
-
-
38449103390
-
Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP
-
Duggan, D., Zheng, S. L., Knowlton, M., Benitez, D., Dimitrov, L., Wiklund, F., Robbins, C., Isaacs, S. D., Cheng, Y., Li, G., Sun, J., Chang, B. L., Marovich, L., Wiley, K. E., Balter, K., Stattin, P., Adami, H. O., Gielzak, M., Yan, G., Sauvageot, J., Liu, W., Kim, J. W., Bleecker, E. R., Meyers, D. A., Trock, B. J., Partin, A. W., Walsh, P. C., Isaacs, W. B., Gronberg, H., Xu, J., Carpten, J. D. Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP. J Natl Cancer Inst 99, 1836-1844 (2007).
-
(2007)
J Natl Cancer Inst
, vol.99
, pp. 1836-1844
-
-
Duggan, D.1
Zheng, S.L.2
Knowlton, M.3
Benitez, D.4
Dimitrov, L.5
Wiklund, F.6
Robbins, C.7
Isaacs, S.D.8
Cheng, Y.9
Li, G.10
Sun, J.11
Chang, B.L.12
Marovich, L.13
Wiley, K.E.14
Balter, K.15
Stattin, P.16
Adami, H.O.17
Gielzak, M.18
Yan, G.19
Sauvageot, J.20
Liu, W.21
Kim, J.W.22
Bleecker, E.R.23
Meyers, D.A.24
Trock, B.J.25
Partin, A.W.26
Walsh, P.C.27
Isaacs, W.B.28
Gronberg, H.29
Xu, J.30
Carpten, J.D.31
more..
-
77
-
-
72149129508
-
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
-
Landi, M. T., Chatterjee, N., Yu, K., Goldin, L. R., Goldstein, A. M., Rotunno, M., Mirabello, L., Jacobs, K., Wheeler, W., Yeager, M., Bergen, A. W., Li, Q., Consonni, D., Pesatori, A. C., Wacholder, S., Thun, M., Diver, R., Oken, M., Virtamo, J., Albanes, D., Wang, Z., Burdette, L., Doheny, K. F., Pugh, E. W., Laurie, C., Brennan, P., Hung, R., Gaborieau, V., McKay, J. D., Lathrop, M., McLaughlin, J., Wang, Y., Tsao, M. S., Spitz, M. R., Krokan, H., Vatten, L., Skorpen, F., Arnesen, E., Benhamou, S., Bouchard, C., Metsapalu, A., Vooder, T., Nelis, M., Valk, K., Field, J. K., Chen, C., Goodman, G., Sulem, P., Thorleifsson, G., Rafnar, T., Eisen, T., Sauter, W., Rosenberger, A., Bickeboller, H., Risch, A., Chang-Claude, J., Wichmann, H. E., Stefansson, K., Houlston, R., Amos, C. I., Fraumeni, J. F., Jr., Savage, S. A., Bertazzi, P. A., Tucker, M. A., Chanock, S., Caporaso, N. E. 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).
-
(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
Bergen, A.W.11
Li, Q.12
Consonni, D.13
Pesatori, A.C.14
Wacholder, S.15
Thun, M.16
Diver, R.17
Oken, M.18
Virtamo, J.19
Albanes, D.20
Wang, Z.21
Burdette, L.22
Doheny, K.F.23
Pugh, E.W.24
Laurie, C.25
Brennan, P.26
Hung, R.27
Gaborieau, V.28
McKay, J.D.29
Lathrop, M.30
McLaughlin, J.31
Wang, Y.32
Tsao, M.S.33
Spitz, M.R.34
Krokan, H.35
Vatten, L.36
Skorpen, F.37
Arnesen, E.38
Benhamou, S.39
Bouchard, C.40
Metsapalu, A.41
Vooder, T.42
Nelis, M.43
Valk, K.44
Field, J.K.45
Chen, C.46
Goodman, G.47
Sulem, P.48
Thorleifsson, G.49
Rafnar, T.50
Eisen, T.51
Sauter, W.52
Rosenberger, A.53
Bickeboller, H.54
Risch, A.55
Chang-Claude, J.56
Wichmann, H.E.57
Stefansson, K.58
Houlston, R.59
Amos, C.I.60
Fraumeni Jr., J.F.61
Savage, S.A.62
Bertazzi, P.A.63
Tucker, M.A.64
Chanock, S.65
Caporaso, N.E.66
more..
-
78
-
-
35648937584
-
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
-
DOI 10.1038/ng.2007.18, PII NG200718
-
Broderick, P., Carvajal-Carmona, L., Pittman, A. M., Webb, E., Howarth, K., Rowan, A., Lubbe, S., Spain, S., Sullivan, K., Fielding, S., Jaeger, E., Vijayakrishnan, J., Kemp, Z., Gorman, M., Chandler, I., Papaemmanuil, E., Penegar, S., Wood, W., Sellick, G., Qureshi, M., Teixeira, A., Domingo, E., Barclay, E., Martin, L., Sieber, O., Kerr, D., Gray, R., Peto, J., Cazier, J. B., Tomlinson, I., Houlston, R. S. A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet 39, 1315-1317 (2007). (Pubitemid 350034998)
-
(2007)
Nature Genetics
, vol.39
, Issue.11
, 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
Jaeger, E.11
Vijayakrishnan, J.12
Kemp, Z.13
Gorman, M.14
Chandler, I.15
Papaemmanuil, E.16
Penegar, S.17
Wood, W.18
Sellick, G.19
Qureshi, M.20
Teixeira, A.21
Domingo, E.22
Barclay, E.23
Martin, L.24
Sieber, O.25
Kerr, D.26
Gray, R.27
Peto, J.28
Cazier, J.-B.29
Tomlinson, I.30
Houlston, R.S.31
more..
-
79
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
DOI 10.1038/ng.111, PII NG111
-
Houlston, R. S., Webb, E., Broderick, P., Pittman, A. M., Di Bernardo, M. C., Lubbe, S., Chandler, I., Vijayakrishnan, J., Sullivan, K., Penegar, S., Carvajal-Carmona, L., Howarth, K., Jaeger, E., Spain, S. L., Walther, A., Barclay, E., Martin, L., Gorman, M., Domingo, E., Teixeira, A. S., Kerr, D., Cazier, J. B., Niittymaki, I., Tuupanen, S., Karhu, A., Aaltonen, L. A., Tomlinson, I. P., Farrington, S. M., Tenesa, A., Prendergast, J. G., Barnetson, R. A., Cetnarskyj, R., Porteous, M. E., Pharoah, P. D., Koessler, T., Hampe, J., Buch, S., Schafmayer, C., Tepel, J., Schreiber, S., Volzke, H., Chang-Claude, J., Hoffmeister, M., Brenner, H., Zanke, B. W., Montpetit, A., Hudson, T. J., Gallinger, S., Campbell, H., Dunlop, M. G. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet 40, 1426-1435 (2008). (Pubitemid 351601204)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, 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
Spain, S.7
Lubbe, S.8
Walther, A.9
Sullivan, K.10
Jaeger, E.11
Fielding, S.12
Rowan, A.13
Vijayakrishnan, J.14
Domingo, E.15
Chandler, I.16
Kemp, Z.17
Qureshi, M.18
Farrington, S.M.19
Tenesa, A.20
Prendergast, J.G.D.21
Barnetson, R.A.22
Penegar, S.23
Barclay, E.24
Wood, W.25
Martin, L.26
Gorman, M.27
Thomas, H.28
Peto, J.29
Bishop, D.T.30
Gray, R.31
Maher, E.R.32
Lucassen, A.33
Kerr, D.34
Evans, D.G.R.35
Schafmayer, C.36
Buch, S.37
Volzke, H.38
Hampe, J.39
Schreiber, S.40
John, U.41
Koessler, T.42
Pharoah, P.43
Van Wezel, T.44
Morreau, H.45
Wijnen, J.T.46
Hopper, J.L.47
Southey, M.C.48
Giles, G.G.49
Severi, G.50
Castellvi-Bel, S.51
Ruiz-Ponte, C.52
Carracedo, A.53
Castells, A.54
Forsti, A.55
Hemminki, K.56
Vodicka, P.57
Naccarati, A.58
Lipton, L.59
Ho, J.W.C.60
Cheng, K.K.61
Sham, P.C.62
Luk, J.63
Agundez, J.A.G.64
Ladero, J.M.65
De La Hoya, M.66
Caldes, T.67
Niittymaki, I.68
Tuupanen, S.69
Karhu, A.70
Aaltonen, L.71
Cazier, J.-B.72
Campbell, H.73
Dunlop, M.G.74
Houlston, R.S.75
more..
-
80
-
-
69349097813
-
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
-
Amundadottir, L., Kraft, P., Stolzenberg-Solomon, R. Z., Fuchs, C. S., Petersen, G. M., Arslan, A. A., Bueno-de-Mesquita, H. B., Gross, M., Helzlsouer, K., Jacobs, E. J., LaCroix, A., Zheng, W., Albanes, D., Bamlet, W., Berg, C. D., Berrino, F., Bingham, S., Buring, J. E., Bracci, P. M., Canzian, F., Clavel-Chapelon, F., Clipp, S., Cotterchio, M., de Andrade, M., Duell, E. J., Fox, J. W., Jr., Gallinger, S., Gaziano, J. M., Giovannucci, E. L., Goggins, M., Gonzalez, C. A., Hallmans, G., Hankinson, S. E., Hassan, M., Holly, E. A., Hunter, D. J., Hutchinson, A., Jackson, R., Jacobs, K. B., Jenab, M., Kaaks, R., Klein, A. P., Kooperberg, C., Kurtz, R. C., Li, D., Lynch, S. M., Mandelson, M., McWilliams, R. R., Mendelsohn, J. B., Michaud, D. S., Olson, S. H., Overvad, K., Patel, A. V., Peeters, P. H., Rajkovic, A., Riboli, E., Risch, H. A., Shu, X. O., Thomas, G., Tobias, G. S., Trichopoulos, D., Van Den Eeden, S. K., Virtamo, J., Wactawski-Wende, J., Wolpin, B. M., Yu, H., Yu, K., Zeleniuch-Jacquotte, A., Chanock, S. J., Hartge, P., Hoover, R. N. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet 41, 986-990 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 986-990
-
-
Amundadottir, L.1
Kraft, P.2
Stolzenberg-Solomon, R.Z.3
Fuchs, C.S.4
Petersen, G.M.5
Arslan, A.A.6
Bueno-de-Mesquita, H.B.7
Gross, M.8
Helzlsouer, K.9
Jacobs, E.J.10
LaCroix, A.11
Zheng, W.12
Albanes, D.13
Bamlet, W.14
Berg, C.D.15
Berrino, F.16
Bingham, S.17
Buring, J.E.18
Bracci, P.M.19
Canzian, F.20
Clavel-Chapelon, F.21
Clipp, S.22
Cotterchio, M.23
De Andrade, M.24
Duell, E.J.25
Fox Jr., J.W.26
Gallinger, S.27
Gaziano, J.M.28
Giovannucci, E.L.29
Goggins, M.30
Gonzalez, C.A.31
Hallmans, G.32
Hankinson, S.E.33
Hassan, M.34
Holly, E.A.35
Hunter, D.J.36
Hutchinson, A.37
Jackson, R.38
Jacobs, K.B.39
Jenab, M.40
Kaaks, R.41
Klein, A.P.42
Kooperberg, C.43
Kurtz, R.C.44
Li, D.45
Lynch, S.M.46
Mandelson, M.47
McWilliams, R.R.48
Mendelsohn, J.B.49
Michaud, D.S.50
Olson, S.H.51
Overvad, K.52
Patel, A.V.53
Peeters, P.H.54
Rajkovic, A.55
Riboli, E.56
Risch, H.A.57
Shu, X.O.58
Thomas, G.59
Tobias, G.S.60
Trichopoulos, D.61
Van Den Eeden, S.K.62
Virtamo, J.63
Wactawski-Wende, J.64
Wolpin, B.M.65
Yu, H.66
Yu, K.67
Zeleniuch-Jacquotte, A.68
Chanock, S.J.69
Hartge, P.70
Hoover, R.N.71
more..
-
81
-
-
44349178008
-
Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer
-
DOI 10.1038/ng.152, PII NG152
-
Sakamoto, H., Yoshimura, K., Saeki, N., Katai, H., Shimoda, T., Matsuno, Y., Saito, D., Sugimura, H., Tanioka, F., Kato, S., Matsukura, N., Matsuda, N., Nakamura, T., Hyodo, I., Nishina, T., Yasui, W., Hirose, H., Hayashi, M., Toshiro, E., Ohnami, S., Sekine, A., Sato, Y., Totsuka, H., Ando, M., Takemura, R., Takahashi, Y., Ohdaira, M., Aoki, K., Honmyo, I., Chiku, S., Aoyagi, K., Sasaki, H., Yanagihara, K., Yoon, K. A., Kook, M. C., Lee, Y. S., Park, S. R., Kim, C. G., Choi, I. J., Yoshida, T., Nakamura, Y., Hirohashi, S. Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. Nat Genet 40, 730-740 (2008). (Pubitemid 351748870)
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 730-740
-
-
Sakamoto, H.1
Yoshimura, K.2
Saeki, N.3
Katai, H.4
Shimoda, T.5
Matsuno, Y.6
Saito, D.7
Sugimura, H.8
Tanioka, F.9
Kato, S.10
Matsukura, N.11
Matsuda, N.12
Nakamura, T.13
Hyodo, I.14
Nishina, T.15
Yasui, W.16
Hirose, H.17
Hayashi, M.18
Toshiro, E.19
Ohnami, S.20
Sekine, A.21
Sato, Y.22
Totsuka, H.23
Ando, M.24
Takemura, R.25
Takahashi, Y.26
Ohdaira, M.27
Aoki, K.28
Honmyo, I.29
Chiku, S.30
Aoyagi, K.31
Sasaki, H.32
Ohnami, S.33
Yanagihara, K.34
Yoon, K.-A.35
Kook, M.-C.36
Lee, Y.-S.37
Park, S.R.38
Kim, C.G.39
Choi, I.J.40
Yoshida, T.41
Nakamura, Y.42
Hirohashi, S.43
more..
-
82
-
-
70350102890
-
Functional Variants in ADH1B and ALDH2 Coupled with Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk
-
Cui, R., Kamatani, Y., Takahashi, A., Usami, M., Hosono, N., Kawaguchi, T., Tsunoda, T., Kamatani, N., Kubo, M., Nakamura, Y., Matsuda, K. Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk. Gastroenterology, (2009).
-
(2009)
Gastroenterology
-
-
Cui, R.1
Kamatani, Y.2
Takahashi, A.3
Usami, M.4
Hosono, N.5
Kawaguchi, T.6
Tsunoda, T.7
Kamatani, N.8
Kubo, M.9
Nakamura, Y.10
Matsuda, K.11
-
83
-
-
63449092713
-
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
-
Gudmundsson, J., Sulem, P., Gudbjartsson, D. F., Jonasson, J. G., Sigurdsson, A., Bergthorsson, J. T., He, H., Blondal, T., Geller, F., Jakobsdottir, M., Magnusdottir, D. N., Matthiasdottir, S., Stacey, S. N., Skarphedinsson, O. B., Helgadottir, H., Li, W., Nagy, R., Aguillo, E., Faure, E., Prats, E., Saez, B., Martinez, M., Eyjolfsson, G. I., Bjornsdottir, U. S., Holm, H., Kristjansson, K., Frigge, M. L., Kristvinsson, H., Gulcher, J. R., Jonsson, T., Rafnar, T., Hjartarsson, H., Mayordomo, J. I., de la Chapelle, A., Hrafnkelsson, J., Thorsteinsdottir, U., Kong, A., Stefansson, K. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet 41, 460-464 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 460-464
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
Jonasson, J.G.4
Sigurdsson, A.5
Bergthorsson, J.T.6
He, H.7
Blondal, T.8
Geller, F.9
Jakobsdottir, M.10
Magnusdottir, D.N.11
Matthiasdottir, S.12
Stacey, S.N.13
Skarphedinsson, O.B.14
Helgadottir, H.15
Li, W.16
Nagy, R.17
Aguillo, E.18
Faure, E.19
Prats, E.20
Saez, B.21
Martinez, M.22
Eyjolfsson, G.I.23
Bjornsdottir, U.S.24
Holm, H.25
Kristjansson, K.26
Frigge, M.L.27
Kristvinsson, H.28
Gulcher, J.R.29
Jonsson, T.30
Rafnar, T.31
Hjartarsson, H.32
Mayordomo, J.I.33
De La Chapelle, A.34
Hrafnkelsson, J.35
Thorsteinsdottir, U.36
Kong, A.37
Stefansson, K.38
more..
-
84
-
-
45149123645
-
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
-
DOI 10.1056/NEJMoa0708698
-
Maris, J. M., Mosse, Y. P., Bradfield, J. P., Hou, C., Monni, S., Scott, R. H., Asgharzadeh, S., Attiyeh, E. F., Diskin, S. J., Laudenslager, M., Winter, C., Cole, K. A., Glessner, J. T., Kim, C., Frackelton, E. C., Casalunovo, T., Eckert, A. W., Capasso, M., Rappaport, E. F., McConville, C., London, W. B., Seeger, R. C., Rahman, N., Devoto, M., Grant, S.F., Li, H., Hakonarson, H. Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. N Engl J med 358, 2585-2593 (2008). (Pubitemid 351831359)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.24
, pp. 2585-2593
-
-
Maris, J.M.1
Mosse, Y.P.2
Bradfield, J.P.3
Hou, C.4
Monni, S.5
Scott, R.H.6
Asgharzadeh, S.7
Attiyeh, E.F.8
Diskin, S.J.9
Laudenslager, M.10
Winter, C.11
Cole, K.A.12
Glessner, J.T.13
Kim, C.14
Frackelton, E.C.15
Casalunovo, T.16
Eckert, A.W.17
Capasso, M.18
Rappaport, E.F.19
McConville, C.20
London, W.B.21
Seeger, R.C.22
Rahman, N.23
Devoto, M.24
Grant, S.F.A.25
Li, H.26
Hakonarson, H.27
more..
-
85
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
DOI 10.1038/ng.163, PII NG163
-
Brown, K. M., Macgregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Holland, E. A., Gillanders, E. M., Duffy, D. L., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Bishop, J. N., Kefford, R. F., Giles, G. G., Armstrong, B. K., Aitken, J. F., Hopper, J. L., Martin, N. G., Trent, J. M., Mann, G. J., Hayward, N. K. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet 40, 838-840 (2008). (Pubitemid 351913651)
-
(2008)
Nature Genetics
, vol.40
, Issue.7
, pp. 838-840
-
-
Brown, K.M.1
MacGregor, S.2
Montgomery, G.W.3
Craig, D.W.4
Zhao, Z.Z.5
Iyadurai, K.6
Henders, A.K.7
Homer, N.8
Campbell, M.J.9
Stark, M.10
Thomas, S.11
Schmid, H.12
Holland, E.A.13
Gillanders, E.M.14
Duffy, D.L.15
Maskiell, J.A.16
Jetann, J.17
Ferguson, M.18
Stephan, D.A.19
Cust, A.E.20
Whiteman, D.21
Green, A.22
Olsson, H.23
Puig, S.24
Ghiorzo, P.25
Hansson, J.26
Demenais, F.27
Goldstein, A.M.28
Gruis, N.A.29
Elder, D.E.30
Bishop, J.N.31
Kefford, R.F.32
Giles, G.G.33
Armstrong, B.K.34
Aitken, J.F.35
Hopper, J.L.36
Martin, N.G.37
Trent, J.M.38
Mann, G.J.39
Hayward, N.K.40
more..
-
86
-
-
55049127580
-
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
-
Stacey, S. N., Gudbjartsson, D. F., Sulem, P., Bergthorsson, J. T., Kumar, R., Thorleifsson, G., Sigurdsson, A., Jakobsdottir, M., Sigurgeirsson, B., Benediktsdottir, K. R., Thorisdottir, K., Ragnarsson, R., Scherer, D., Rudnai, P., Gurzau, E., Koppova, K., Hoiom, V., Botella-Estrada, R., Soriano, V., Juberias, P., Grasa, M., Carapeto, F. J., Tabuenca, P., Gilaberte, Y., Gudmundsson, J., Thorlacius, S., Helgason, A., Thorlacius, T., Jonasdottir, A., Blondal, T., Gudjonsson, S. A., Jonsson, G. F., Saemundsdottir, J., Kristjansson, K., Bjornsdottir, G., Sveinsdottir, S. G., Mouy, M., Geller, F., Nagore, E., Mayordomo, J. I., Hansson, J., Rafnar, T., Kong, A., Olafsson, J. H., Thorsteinsdottir, U., Stefansson, K. Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. Nat Genet 40, 1313-1318 (2008).
-
(2008)
Nat Genet
, vol.40
, pp. 1313-1318
-
-
Stacey, S.N.1
Gudbjartsson, D.F.2
Sulem, P.3
Bergthorsson, J.T.4
Kumar, R.5
Thorleifsson, G.6
Sigurdsson, A.7
Jakobsdottir, M.8
Sigurgeirsson, B.9
Benediktsdottir, K.R.10
Thorisdottir, K.11
Ragnarsson, R.12
Scherer, D.13
Rudnai, P.14
Gurzau, E.15
Koppova, K.16
Hoiom, V.17
Botella-Estrada, R.18
Soriano, V.19
Juberias, P.20
Grasa, M.21
Carapeto, F.J.22
Tabuenca, P.23
Gilaberte, Y.24
Gudmundsson, J.25
Thorlacius, S.26
Helgason, A.27
Thorlacius, T.28
Jonasdottir, A.29
Blondal, T.30
Gudjonsson, S.A.31
Jonsson, G.F.32
Saemundsdottir, J.33
Kristjansson, K.34
Bjornsdottir, G.35
Sveinsdottir, S.G.36
Mouy, M.37
Geller, F.38
Nagore, E.39
Mayordomo, J.I.40
Hansson, J.41
Rafnar, T.42
Kong, A.43
Olafsson, J.H.44
Thorsteinsdottir, U.45
Stefansson, K.46
more..
-
87
-
-
68449085620
-
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma
-
Ng, C. C., Yew, P. Y., Puah, S. M., Krishnan, G., Yap, L. F., Teo, S. H., Lim, P. V., Govindaraju, S., Ratnavelu, K., Sam, C. K., Takahashi, A., Kubo, M., Kamatani, N., Nakamura, Y., Mushiroda, T. A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. J hum Genet 54, 392-397 (2009).
-
(2009)
J Hum Genet
, vol.54
, pp. 392-397
-
-
Ng, C.C.1
Yew, P.Y.2
Puah, S.M.3
Krishnan, G.4
Yap, L.F.5
Teo, S.H.6
Lim, P.V.7
Govindaraju, S.8
Ratnavelu, K.9
Sam, C.K.10
Takahashi, A.11
Kubo, M.12
Kamatani, N.13
Nakamura, Y.14
Mushiroda, T.15
-
88
-
-
69349101565
-
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
-
Papaemmanuil, E., Hosking, F. J., Vijayakrishnan, J., Price, A., Olver, B., Sheridan, E., Kinsey, S. E., Lightfoot, T., Roman, E., Irving, J. A., Allan, J. M., Tomlinson, I. P., Taylor, M., Greaves, M., Houlston, R. S. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat Genet 41, 1006-1010 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 1006-1010
-
-
Papaemmanuil, E.1
Hosking, F.J.2
Vijayakrishnan, J.3
Price, A.4
Olver, B.5
Sheridan, E.6
Kinsey, S.E.7
Lightfoot, T.8
Roman, E.9
Irving, J.A.10
Allan, J.M.11
Tomlinson, I.P.12
Taylor, M.13
Greaves, M.14
Houlston, R.S.15
-
89
-
-
69349091330
-
Germline genomic variants associated with childhood acute lymphoblastic leukemia
-
Trevino, L. R., Yang, W., French, D., Hunger, S. P., Carroll, W. L., Devidas, M., Willman, C., Neale, G., Downing, J., Raimondi, S. C., Pui, C. H., Evans, W. E., Relling, M. V. Germline genomic variants associated with childhood acute lymphoblastic leukemia. Nat Genet 41, 1001-1005 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 1001-1005
-
-
Trevino, L.R.1
Yang, W.2
French, D.3
Hunger, S.P.4
Carroll, W.L.5
Devidas, M.6
Willman, C.7
Neale, G.8
Downing, J.9
Raimondi, S.C.10
Pui, C.H.11
Evans, W.E.12
Relling, M.V.13
-
90
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
DOI 10.1038/ng.111, PII NG111
-
Di Bernardo, M. C., Crowther-Swanepoel, D., Broderick, P., Webb, E., Sellick, G., Wild, R., Sullivan, K., Vijayakrishnan, J., Wang, Y., Pittman, A. M., Sunter, N. J., Hall, A. G., Dyer, M. J., Matutes, E., Dearden, C., Mainou-Fowler, T., Jackson, G. H., Summerfield, G., Harris, R. J., Pettitt, A. R., Hillmen, P., Allsup, D. J., Bailey, J. R., Pratt, G., Pepper, C., Fegan, C., Allan, J. M., Catovsky, D., Houlston, R. S. A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. Nat Genet 40, 1204-1210 (2008). (Pubitemid 351601204)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, 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
Spain, S.7
Lubbe, S.8
Walther, A.9
Sullivan, K.10
Jaeger, E.11
Fielding, S.12
Rowan, A.13
Vijayakrishnan, J.14
Domingo, E.15
Chandler, I.16
Kemp, Z.17
Qureshi, M.18
Farrington, S.M.19
Tenesa, A.20
Prendergast, J.G.D.21
Barnetson, R.A.22
Penegar, S.23
Barclay, E.24
Wood, W.25
Martin, L.26
Gorman, M.27
Thomas, H.28
Peto, J.29
Bishop, D.T.30
Gray, R.31
Maher, E.R.32
Lucassen, A.33
Kerr, D.34
Evans, D.G.R.35
Schafmayer, C.36
Buch, S.37
Volzke, H.38
Hampe, J.39
Schreiber, S.40
John, U.41
Koessler, T.42
Pharoah, P.43
Van Wezel, T.44
Morreau, H.45
Wijnen, J.T.46
Hopper, J.L.47
Southey, M.C.48
Giles, G.G.49
Severi, G.50
Castellvi-Bel, S.51
Ruiz-Ponte, C.52
Carracedo, A.53
Castells, A.54
Forsti, A.55
Hemminki, K.56
Vodicka, P.57
Naccarati, A.58
Lipton, L.59
Ho, J.W.C.60
Cheng, K.K.61
Sham, P.C.62
Luk, J.63
Agundez, J.A.G.64
Ladero, J.M.65
De La Hoya, M.66
Caldes, T.67
Niittymaki, I.68
Tuupanen, S.69
Karhu, A.70
Aaltonen, L.71
Cazier, J.-B.72
Campbell, H.73
Dunlop, M.G.74
Houlston, R.S.75
more..
|