-
2
-
-
42649115776
-
The success of the genome-wide association approach: A brief story of a long struggle
-
Ku CS, Chia KS. The success of the genome-wide association approach: a brief story of a long struggle. Eur. J. Hum. Genet. 16(5), 554-564 (2008).
-
(2008)
Eur. J. Hum. Genet.
, vol.16
, Issue.5
, pp. 554-564
-
-
Ku, C.S.1
Chia, K.S.2
-
3
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
Stankiewicz P, Lupski JR. Structural variation in the human genome and its role in disease. Annu. Rev. Med. 61, 437-455 (2010).
-
(2010)
Annu. Rev. Med.
, vol.61
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
4
-
-
67650735159
-
Genomic copy number variation, human health, and disease
-
Wain LV, Armour JA, Tobin MD. Genomic copy number variation, human health, and disease. Lancet 374(9686), 340-350 (2009).
-
(2009)
Lancet
, vol.374
, Issue.9686
, pp. 340-350
-
-
Wain, L.V.1
Armour, J.A.2
Tobin, M.D.3
-
5
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
Zhang F, Gu W, Hurles ME et al. Copy number variation in human health, disease, and evolution. Annu. Rev. Genomics Hum. Genet. 10, 451-481 (2009).
-
(2009)
Annu. Rev. Genomics Hum. Genet.
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.E.3
-
6
-
-
49649110984
-
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome
-
Shlien A, Tabori U, Marshall CR et al. Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome. Proc. Natl Acad. Sci. USA 105(32), 11264-11269 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, Issue.32
, pp. 11264-11269
-
-
Shlien, A.1
Tabori, U.2
Marshall, C.R.3
-
7
-
-
67650653451
-
Copy-number variation: The end of the human genome?
-
Dear PH. Copy-number variation: the end of the human genome? Trends Biotechnol. 27(8), 448-454 (2009).
-
(2009)
Trends Biotechnol.
, vol.27
, Issue.8
, pp. 448-454
-
-
Dear, P.H.1
-
8
-
-
76649114002
-
Genome-wide association studies of bladder cancer risk: A field synopsis of progress and potential applications
-
Wu X, Hildebrandt MA, Chang DW. Genome-wide association studies of bladder cancer risk: a field synopsis of progress and potential applications. Cancer Metastasis Rev. 28(3-4), 269-280 (2009).
-
(2009)
Cancer Metastasis Rev.
, vol.28
, Issue.3-4
, pp. 269-280
-
-
Wu, X.1
Hildebrandt, M.A.2
Chang, D.W.3
-
9
-
-
77953724090
-
A compendium of genome-wide associations for cancer: Critical synopsis and reappraisal
-
Ioannidis JP, Castaldi P, Evangelou E. A compendium of genome-wide associations for cancer: critical synopsis and reappraisal. J. Natl Cancer Inst. 102(12), 846-858 (2010).
-
(2010)
J. Natl Cancer Inst.
, vol.102
, Issue.12
, pp. 846-858
-
-
Ioannidis, J.P.1
Castaldi, P.2
Evangelou, E.3
-
10
-
-
34247548755
-
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
-
Yeager M, Orr N, Hayes RB et al. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat. Genet. 39(5), 645-649 (2007).
-
(2007)
Nat. Genet.
, vol.39
, Issue.5
, pp. 645-649
-
-
Yeager, M.1
Orr, N.2
Hayes, R.B.3
-
11
-
-
34247563453
-
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
-
Gudmundsson J, Sulem P, Manolescu A et al. Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat. Genet. 39(5), 631-637 (2007).
-
(2007)
Nat. Genet.
, vol.39
, Issue.5
, pp. 631-637
-
-
Gudmundsson, J.1
Sulem, P.2
Manolescu, A.3
-
12
-
-
39749118602
-
Multiple loci identified in a genome-wide association study of prostate cancer
-
Thomas G, Jacobs KB, Year M et al. Multiple loci identified in a genome-wide association study of prostate cancer. Nat. Genet. 40(3), 310-315 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.3
, pp. 310-315
-
-
Thomas, G.1
Jacobs, K.B.2
Year, M.3
-
13
-
-
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 et al. Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Nat. Genet. 40(3), 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..
-
14
-
-
70349547128
-
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
-
Gudmundsson J, Sulem P, Gudbjartsson DF et al. Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Nat. Genet. 41(10), 1122-1126 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.10
, pp. 1122-1126
-
-
Gudmundsson, J.1
Sulem, P.2
Gudbjartsson, D.F.3
-
15
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
Hunter DJ, Kraft P, Jacobs KB et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat. Genet. 39(7), 870-874 (2007).
-
(2007)
Nat. Genet.
, vol.39
, Issue.7
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
-
16
-
-
34250002140
-
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
-
Stacey SN, Manolescu A, Sulem P et al. Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat. Genet. 39(7), 865-869 (2007).
-
(2007)
Nat. Genet.
, vol.39
, Issue.7
, pp. 865-869
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
-
17
-
-
44349087530
-
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer
-
Stacey SN, Manolescu A, Sulem P et al. Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer. Nat. Genet. 40(6), 703-706 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.6
, pp. 703-706
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
-
18
-
-
61349163553
-
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1
-
Zheng W, Long J, Gao YT et al. Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat. Genet. 41(3), 324-328 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.3
, pp. 324-328
-
-
Zheng, W.1
Long, J.2
Gao, Y.T.3
-
19
-
-
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 KB, Kraft P et al. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Nat. Genet. 41(5), 579-584 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.5
, pp. 579-584
-
-
Thomas, G.1
Jacobs, K.B.2
Kraft, P.3
-
20
-
-
67349237973
-
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
-
Ahmed S, Thomas G, Ghoussaini M et al. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat. Genet. 41(5), 585-590 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.5
, pp. 585-590
-
-
Ahmed, S.1
Thomas, G.2
Ghoussaini, M.3
-
21
-
-
77952887426
-
Genome-wide association study identifies five new breast cancer susceptibility loci
-
Turnbull C, Ahmed S, Morrison J et al. Genome-wide association study identifies five new breast cancer susceptibility loci. Nat. Genet. 42(6), 504-507 (2010).
-
(2010)
Nat. Genet.
, vol.42
, Issue.6
, pp. 504-507
-
-
Turnbull, C.1
Ahmed, S.2
Morrison, J.3
-
22
-
-
34547498546
-
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
-
Tomlinson I, Webb E, Carvajal-Carmona L et al. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat. Genet. 39(8), 984-988 (2007).
-
(2007)
Nat. Genet.
, vol.39
, Issue.8
, pp. 984-988
-
-
Tomlinson, I.1
Webb, E.2
Carvajal-Carmona, L.3
-
23
-
-
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, Webb E, Carvajal-Carmona L et al. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat. Genet. 40(5), 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..
-
24
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
Tenesa A, Farrington SM, Prendergast JG et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat. Genet. 40(5), 631-637 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.5
, pp. 631-637
-
-
Tenesa, A.1
Farrington, S.M.2
Prendergast, J.G.3
-
25
-
-
44349178008
-
Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer
-
Study Group of Millennium Genome Project for Cancer
-
Sakamoto H, Yoshimura K, Saeki N et al.; Study Group of Millennium Genome Project for Cancer. Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer. Nat. Genet. 40(6), 730-740 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.6
, pp. 730-740
-
-
Sakamoto, H.1
Yoshimura, K.2
Saeki, N.3
-
26
-
-
69349101565
-
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
-
Papaemmanuil E, Hosking FJ, Vijayakrishnan J et al. Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Nat. Genet. 41(9), 1006-1010 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.9
, pp. 1006-1010
-
-
Papaemmanuil, E.1
Hosking, F.J.2
Vijayakrishnan, J.3
-
27
-
-
52949139429
-
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia
-
Di Bernardo MC, Crowther-Swanepoel D, Broderick P et al. A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. Nat. Genet. 40(10), 1204-1210 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.10
, pp. 1204-1210
-
-
Di Bernardo, M.C.1
Crowther-Swanepoel, D.2
Broderick, P.3
-
28
-
-
75749138023
-
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
-
Crowther-Swanepoel D, Broderick P, Di Bernardo MC et al. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. Nat. Genet. 42(2), 132-136 (2010).
-
(2010)
Nat. Genet.
, vol.42
, Issue.2
, pp. 132-136
-
-
Crowther-Swanepoel, D.1
Broderick, P.2
Di Bernardo, M.C.3
-
29
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
Brown KM, Macgregor S, Montgomery GW et al. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat. Genet. 40(7), 838-840 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.7
, pp. 838-840
-
-
Brown, K.M.1
MacGregor, S.2
Montgomery, G.W.3
-
30
-
-
68149179663
-
Genome-wide association study identifies three loci associated with melanoma risk
-
Bishop DT, Demenais F, Iles MM et al. Genome-wide association study identifies three loci associated with melanoma risk. Nat. Genet. 41(8), 920-925 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.8
, pp. 920-925
-
-
Bishop, D.T.1
Demenais, F.2
Iles, M.M.3
-
31
-
-
55049127580
-
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
-
Stacey SN, Gudbjartsson DF, Sulem P et al. Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. Nat. Genet. 40(11), 1313-1318 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.11
, pp. 1313-1318
-
-
Stacey, S.N.1
Gudbjartsson, D.F.2
Sulem, P.3
-
32
-
-
68149170036
-
New common variants affecting susceptibility to basal cell carcinoma
-
Stacey SN, Sulem P, Masson G et al. New common variants affecting susceptibility to basal cell carcinoma. Nat. Genet. 41(8), 909-914 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.8
, pp. 909-914
-
-
Stacey, S.N.1
Sulem, P.2
Masson, G.3
-
33
-
-
42649091460
-
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1
-
Amos CI, Wu X, Broderick P et al. Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Nat. Genet. 40(5), 616-622 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.5
, pp. 616-622
-
-
Amos, C.I.1
Wu, X.2
Broderick, P.3
-
34
-
-
56749182096
-
Lung cancer susceptibility locus at 5p15.33
-
McKay JD, Hung RJ, Gaborieau V et al. Lung cancer susceptibility locus at 5p15.33. Nat. Genet. 40(12), 1404-1406 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.12
, pp. 1404-1406
-
-
McKay, J.D.1
Hung, R.J.2
Gaborieau, V.3
-
35
-
-
56749163357
-
Common 5p15.33 and 6p21.33 variants influence lung cancer risk
-
Wang Y, Broderick P, Webb E et al. Common 5p15.33 and 6p21.33 variants influence lung cancer risk. Nat. Genet. 40(12), 1407-1409 (2008).
-
(2008)
Nat. Genet.
, vol.40
, Issue.12
, pp. 1407-1409
-
-
Wang, Y.1
Broderick, P.2
Webb, E.3
-
36
-
-
70350532521
-
Lung adenocarcinoma with EGFR amplification has distinct clinicopathologic and molecular features in never-smokers
-
Sholl LM, Yeap BY, Iafrate AJ et al. Lung adenocarcinoma with EGFR amplification has distinct clinicopathologic and molecular features in never-smokers. Cancer Res. 69(21), 8341-8348 (2009).
-
(2009)
Cancer Res.
, vol.69
, Issue.21
, pp. 8341-8348
-
-
Sholl, L.M.1
Yeap, B.Y.2
Iafrate, A.J.3
-
37
-
-
41749093019
-
Sequential molecular changes during multistage pathogenesis of small peripheral adenocarcinomas of the lung
-
Soh J, Toyooka S, Ichihara S et al. Sequential molecular changes during multistage pathogenesis of small peripheral adenocarcinomas of the lung. J. Thorac. Oncol. 3(4), 340-347 (2008).
-
(2008)
J. Thorac. Oncol.
, vol.3
, Issue.4
, pp. 340-347
-
-
Soh, J.1
Toyooka, S.2
Ichihara, S.3
-
38
-
-
61449259809
-
Epidermal growth factor receptor abnormalities in the pathogenesis and progression of lung adenocarcinomas
-
Tang X, Varella-Garcia M, Xavier AC et al. Epidermal growth factor receptor abnormalities in the pathogenesis and progression of lung adenocarcinomas. Cancer Prev. Res. (Phila. PA) 1(3), 192-200 (2008).
-
(2008)
Cancer Prev. Res. (Phila. PA)
, vol.1
, Issue.3
, pp. 192-200
-
-
Tang, X.1
Varella-Garcia, M.2
Xavier, A.C.3
-
39
-
-
42049094628
-
Epidermal growth factor receptor gene amplification is acquired in association with tumor progression of EGFR-mutated lung cancer
-
Yatabe Y, Takahashi T, Mitsudomi T. Epidermal growth factor receptor gene amplification is acquired in association with tumor progression of EGFR-mutated lung cancer. Cancer Res. 68(7), 2106-2111 (2008).
-
(2008)
Cancer Res.
, vol.68
, Issue.7
, pp. 2106-2111
-
-
Yatabe, Y.1
Takahashi, T.2
Mitsudomi, T.3
-
40
-
-
67349156045
-
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
-
Capasso M, Devoto M, Hou C et al. Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Nat. Genet. 41(6), 718-723 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.6
, pp. 718-723
-
-
Capasso, M.1
Devoto, M.2
Hou, C.3
-
41
-
-
68149180891
-
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
-
Wrensch M, Jenkins RB, Chang JS et al. Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Nat. Genet. 41(8), 905-908 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.8
, pp. 905-908
-
-
Wrensch, M.1
Jenkins, R.B.2
Chang, J.S.3
-
42
-
-
69349097813
-
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
-
Amundadottir L, Kraft P, Stolzenberg-Solomon RZ et al. Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat. Genet. 41(9), 986-990 (2009).
-
(2009)
Nat. Genet.
, vol.41
, Issue.9
, pp. 986-990
-
-
Amundadottir, L.1
Kraft, P.2
Stolzenberg-Solomon, R.Z.3
-
43
-
-
77649188501
-
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33
-
Petersen GM, Amundadottir L, Fuchs CS et al. A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Nat. Genet. 42(3), 224-228 (2010).
-
(2010)
Nat. Genet.
, vol.42
, Issue.3
, pp. 224-228
-
-
Petersen, G.M.1
Amundadottir, L.2
Fuchs, C.S.3
-
44
-
-
77954143076
-
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci
-
Bei JX, Li Y, Jia WH et al. A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. Nat. Genet. 42(7), 599-603 (2010).
-
(2010)
Nat. Genet.
, vol.42
, Issue.7
, pp. 599-603
-
-
Bei, J.X.1
Li, Y.2
Jia, W.H.3
-
45
-
-
77949261485
-
MicroRNAs in cancer -from research to therapy
-
Cho WC. MicroRNAs in cancer -from research to therapy. Biochim. Biophys. Acta 1805(2), 209-217 (2010).
-
(2010)
Biochim. Biophys. Acta
, vol.1805
, Issue.2
, pp. 209-217
-
-
Cho, W.C.1
-
46
-
-
77954386364
-
MicroRNAs: Potential biomarkers for cancer diagnosis, prognosis and targets for therapy
-
Cho WC. MicroRNAs: potential biomarkers for cancer diagnosis, prognosis and targets for therapy. Int. J. Biochem. Cell Biol. 42(8), 1273-1281 (2010).
-
(2010)
Int. J. Biochem. Cell Biol.
, vol.42
, Issue.8
, pp. 1273-1281
-
-
Cho, W.C.1
-
47
-
-
77950625464
-
Micromarkers: MiRNAs in cancer diagnosis and prognosis
-
Ferracin M, Veronese A, Negrini M. Micromarkers: miRNAs in cancer diagnosis and prognosis. Expert Rev. Mol. Diagn. 10(3), 297-308 (2010).
-
(2010)
Expert Rev. Mol. Diagn.
, vol.10
, Issue.3
, pp. 297-308
-
-
Ferracin, M.1
Veronese, A.2
Negrini, M.3
-
48
-
-
52949119537
-
MicroRNA target site polymorphisms and human disease
-
Sethupathy P, Collins FS. MicroRNA target site polymorphisms and human disease. Trends Genet. 24(10), 489-497 (2008).
-
(2008)
Trends Genet.
, vol.24
, Issue.10
, pp. 489-497
-
-
Sethupathy, P.1
Collins, F.S.2
-
49
-
-
70449657813
-
Role of miRNAs in lung cancer
-
Cho WC. Role of miRNAs in lung cancer. Expert Rev. Mol. Diagn. 9(8), 773-776 (2009).
-
(2009)
Expert Rev. Mol. Diagn.
, vol.9
, Issue.8
, pp. 773-776
-
-
Cho, W.C.1
-
50
-
-
54249117763
-
A SNP in a let-7 microRNA complementary site in the KRAS 3′ untranslated region increases non-small cell lung cancer risk
-
Chin LJ, Ratner E, Leng S et al. A SNP in a let-7 microRNA complementary site in the KRAS 3′ untranslated region increases non-small cell lung cancer risk. Cancer Res. 68(20), 8535-8540 (2008).
-
(2008)
Cancer Res.
, vol.68
, Issue.20
, pp. 8535-8540
-
-
Chin, L.J.1
Ratner, E.2
Leng, S.3
-
51
-
-
58949101499
-
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women
-
Tchatchou S, Jung A, Hemminki K et al. A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women. Carcinogenesis 30(1), 59-64 (2009).
-
(2009)
Carcinogenesis
, vol.30
, Issue.1
, pp. 59-64
-
-
Tchatchou, S.1
Jung, A.2
Hemminki, K.3
-
52
-
-
77954752364
-
Mature miRNA sequence polymorphism in MIR196A2 is associated with risk and prognosis of head and neck cancer
-
Christensen BC, Whiting MA, Ouellet LG et al. Mature miRNA sequence polymorphism in MIR196A2 is associated with risk and prognosis of head and neck cancer. Clin. Cancer Res. 16(14), 3713-3720 (2010).
-
(2010)
Clin. Cancer Res.
, vol.16
, Issue.14
, pp. 3713-3720
-
-
Christensen, B.C.1
Whiting, M.A.2
Ouellet, L.G.3
-
53
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ et al. Finding the missing heritability of complex diseases. Nature 461(7265), 747-753 (2009).
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
54
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli ET, Goldstein DB. Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat. Rev. Genet. 11(6), 415-425 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, Issue.6
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
55
-
-
39649117755
-
The impact of next-generation sequencing technology on genetics
-
Mardis ER. The impact of next-generation sequencing technology on genetics. Trends Genet. 24(3), 133-141 (2008).
-
(2008)
Trends Genet.
, vol.24
, Issue.3
, pp. 133-141
-
-
Mardis, E.R.1
-
56
-
-
77049105158
-
Beyond genome-wide association studies: Genetic heterogeneity and individual predisposition to cancer
-
Galvan A, Ioannidis JP, Dragani TA. Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer. Trends Genet. 26(3), 132-141 (2010).
-
(2010)
Trends Genet.
, vol.26
, Issue.3
, pp. 132-141
-
-
Galvan, A.1
Ioannidis, J.P.2
Dragani, T.A.3
-
57
-
-
77951585057
-
Architecture of inherited susceptibility to common cancer
-
Fletcher O, Houlston RS. Architecture of inherited susceptibility to common cancer. Nat. Rev. Cancer 10(5), 353-361 (2010).
-
(2010)
Nat. Rev. Cancer
, vol.10
, Issue.5
, pp. 353-361
-
-
Fletcher, O.1
Houlston, R.S.2
-
58
-
-
70449677606
-
Omics approaches in cancer research
-
Cho WC (Ed.). Springer, Berlin, Germany
-
Cho WC. Omics approaches in cancer research. In: An Omics Perspective on Cancer Research. Cho WC (Ed.). Springer, Berlin, Germany 1-9 (2010).
-
(2010)
An Omics Perspective on Cancer Research
, pp. 1-9
-
-
Cho, W.C.1
-
59
-
-
77956746299
-
Conquering cancer through discovery research
-
Cho WC. Conquering cancer through discovery research. IUBMB Life 62(9), 646-650 (2010).
-
(2010)
IUBMB Life
, vol.62
, Issue.9
, pp. 646-650
-
-
Cho, W.C.1
-
60
-
-
77956746684
-
-
1000 Genomes: a deep catalog of human genetic variation Accessed 21 August
-
1000 Genomes: a deep catalog of human genetic variation http://1000genomes.org/page.php (Accessed 21 August 2010)
-
(2010)
-
-
|