-
1
-
-
78049485263
-
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
-
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer 2010; 127: 2893-2917
-
(2010)
Int J Cancer
, vol.127
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
Forman, D.4
Mathers, C.5
Parkin, D.M.6
-
2
-
-
0034933494
-
PTEN mutations are uncommon in Proteus syndrome
-
Barker K, Martinez A, Wang R, et al. PTEN mutations are uncommon in Proteus syndrome. J Med Genet 2001; 38: 480-481
-
(2001)
J Med Genet
, vol.38
, pp. 480-481
-
-
Barker, K.1
Martinez, A.2
Wang, R.3
-
3
-
-
41649103682
-
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
-
Hung RJ, McKay JD, Gaborieau V, et al. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Nature 2008; 452: 633-637
-
(2008)
Nature
, vol.452
, pp. 633-637
-
-
Hung, R.J.1
McKay, J.D.2
Gaborieau, V.3
-
4
-
-
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 2008; 40: 616-622
-
(2008)
Nat Genet
, vol.40
, pp. 616-622
-
-
Amos, C.I.1
Wu, X.2
Broderick, P.3
-
5
-
-
41649103052
-
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
-
Thorgeirsson TE, Geller F, Sulem P, et al. A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. Nature 2008; 452: 638-642
-
(2008)
Nature
, vol.452
, pp. 638-642
-
-
Thorgeirsson, T.E.1
Geller, F.2
Sulem, P.3
-
6
-
-
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 2008; 40: 1404-1406
-
(2008)
Nat Genet
, vol.40
, pp. 1404-1406
-
-
McKay, J.D.1
Hung, R.J.2
Gaborieau, V.3
-
7
-
-
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 2008; 40: 1407-1409
-
(2008)
Nat Genet
, vol.40
, pp. 1407-1409
-
-
Wang, Y.1
Broderick, P.2
Webb, E.3
-
8
-
-
79960929526
-
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese
-
Hu Z, Wu C, Shi Y, et al. A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese. Nat Genet 2011; 43: 792-796
-
(2011)
Nat Genet
, vol.43
, pp. 792-796
-
-
Hu, Z.1
Wu, C.2
Shi, Y.3
-
9
-
-
77957588624
-
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
-
Miki D, Kubo M, Takahashi A, et al. Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. Nat Genet 2010; 42: 893-896
-
(2010)
Nat Genet
, vol.42
, pp. 893-896
-
-
Miki, D.1
Kubo, M.2
Takahashi, A.3
-
10
-
-
84870502715
-
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
-
Lan Q, Hsiung CA, Matsuo K, et al. Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia. Nat Genet 2012; 44: 1330-1335
-
(2012)
Nat Genet
, vol.44
, pp. 1330-1335
-
-
Lan, Q.1
Hsiung, C.A.2
Matsuo, K.3
-
11
-
-
79960102627
-
Variation in TP63 is associated with lung adenocarcinoma in the UK population
-
Wang Y, Broderick P, Matakidou A, Vijayakrishnan J, Eisen T, Houlston RS. Variation in TP63 is associated with lung adenocarcinoma in the UK population. Cancer Epidemiol Biomark Prev 2011; 20: 1453-1462
-
(2011)
Cancer Epidemiol Biomark Prev
, vol.20
, pp. 1453-1462
-
-
Wang, Y.1
Broderick, P.2
Matakidou, A.3
Vijayakrishnan, J.4
Eisen, T.5
Houlston, R.S.6
-
12
-
-
84903585835
-
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
-
Wang Y, McKay JD, Rafnar T, et al. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Nat Genet 2014; 46: 736-741
-
(2014)
Nat Genet
, vol.46
, pp. 736-741
-
-
Wang, Y.1
McKay, J.D.2
Rafnar, T.3
-
13
-
-
80053023874
-
International association for the study of lung cancer/American thoracic society/european respiratory society: International multidisciplinary classification of lung adenocarcinoma: Executive summary
-
Travis WD, Brambilla E, Noguchi M, et al. International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society: international multidisciplinary classification of lung adenocarcinoma: executive summary. Proc Am Thorac Soc 2011; 8: 381-385
-
(2011)
Proc Am Thorac Soc
, vol.8
, pp. 381-385
-
-
Travis, W.D.1
Brambilla, E.2
Noguchi, M.3
-
14
-
-
69249133245
-
Deciphering the impact of common genetic variation on lung cancer risk: A genome-wide association study
-
Broderick P, Wang Y, Vijayakrishnan J, et al. Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. Cancer Res 2009; 69: 6633-6641
-
(2009)
Cancer Res
, vol.69
, pp. 6633-6641
-
-
Broderick, P.1
Wang, Y.2
Vijayakrishnan, J.3
-
15
-
-
72149129508
-
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
-
Landi MT, Chatterjee N, Yu K, et al. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Am J Hum Genet 2009; 85: 679-691
-
(2009)
Am J Hum Genet
, vol.85
, pp. 679-691
-
-
Landi, M.T.1
Chatterjee, N.2
Yu, K.3
-
16
-
-
84868156549
-
Influence of common genetic variation on lung cancer risk: Meta-Analysis of 14 900 cases and 29 485 controls
-
Timofeeva MN, Hung RJ, Rafnar T, et al. Influence of common genetic variation on lung cancer risk: meta-Analysis of 14 900 cases and 29 485 controls. Hum Mol Genet 2012; 21: 4980-4995
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4980-4995
-
-
Timofeeva, M.N.1
Hung, R.J.2
Rafnar, T.3
-
17
-
-
84864185989
-
Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma
-
Shi J, Chatterjee N, Rotunno M, et al. Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma. Cancer Discov 2012; 2: 131-139
-
(2012)
Cancer Discov
, vol.2
, pp. 131-139
-
-
Shi, J.1
Chatterjee, N.2
Rotunno, M.3
-
18
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB. Rare variants create synthetic genome-wide associations. PLoS Biol 2010; 8: e1000294
-
(2010)
PLoS Biol
, vol.8
, pp. e1000294
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
19
-
-
33646179085
-
Genotypes and haplotypes of matrix metalloproteinase 1, 3 and 12 genes and the risk of lung cancer
-
Su L, Zhou W, Asomaning K, et al. Genotypes and haplotypes of matrix metalloproteinase 1, 3 and 12 genes and the risk of lung cancer. Carcinogenesis 2006; 27: 1024-1029
-
(2006)
Carcinogenesis
, vol.27
, pp. 1024-1029
-
-
Su, L.1
Zhou, W.2
Asomaning, K.3
-
20
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 2009; 5: e1000529
-
(2009)
PLoS Genet
, vol.5
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
21
-
-
78649508578
-
Mach: Using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR. MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol 2010; 34: 816-834
-
(2010)
Genet Epidemiol
, vol.34
, pp. 816-834
-
-
Li, Y.1
Willer, C.J.2
Ding, J.3
Scheet, P.4
Abecasis, G.R.5
-
22
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat Genet 2012; 44: 955-959
-
(2012)
Nat Genet
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
23
-
-
42349106044
-
Meta-Analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E, Scott LJ, Saxena R, et al. Meta-Analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008; 40: 638-645
-
(2008)
Nat Genet
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
-
24
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B. Genotype imputation for genome-wide association studies. Nat Rev Genet 2010; 11: 499-511
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
25
-
-
77951152163
-
ProbABEL package for genome-wide association analysis of imputed data
-
Aulchenko YS, Struchalin MV, van Duijn CM. ProbABEL package for genome-wide association analysis of imputed data. BMC Bioinform 2010; 11: 134
-
(2010)
BMC Bioinform
, vol.11
, pp. 134
-
-
Aulchenko, Y.S.1
Struchalin, M.V.2
Van Duijn, C.M.3
-
26
-
-
79953314023
-
HLA IMP-An integrated framework for imputing classical HLA alleles from SNP genotypes
-
Dilthey AT, Moutsianas L, Leslie S, McVean G. HLA IMP-An integrated framework for imputing classical HLA alleles from SNP genotypes. Bioinformatics 2011; 27: 968-972
-
(2011)
Bioinformatics
, vol.27
, pp. 968-972
-
-
Dilthey, A.T.1
Moutsianas, L.2
Leslie, S.3
McVean, G.4
-
27
-
-
38749115455
-
A statistical method for predicting classical HLA alleles from SNP data
-
Leslie S, Donnelly P, McVean G. A statistical method for predicting classical HLA alleles from SNP data. Am J Hum Genet 2008; 82: 48-56
-
(2008)
Am J Hum Genet
, vol.82
, pp. 48-56
-
-
Leslie, S.1
Donnelly, P.2
McVean, G.3
-
28
-
-
27644546712
-
Population structure, differential bias and genomic control in a large-scale, case-control association study
-
Clayton DG, Walker NM, Smyth DJ, et al. Population structure, differential bias and genomic control in a large-scale, case-control association study. Nat Genet 2005; 37: 1243-1246
-
(2005)
Nat Genet
, vol.37
, pp. 1243-1246
-
-
Clayton, D.G.1
Walker, N.M.2
Smyth, D.J.3
-
29
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559-575
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
-
31
-
-
84860771128
-
A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits
-
Bhattacharjee S, Rajaraman P, Jacobs KB, et al. A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits. Am J Hum Genet 2012; 90: 821-835
-
(2012)
Am J Hum Genet
, vol.90
, pp. 821-835
-
-
Bhattacharjee, S.1
Rajaraman, P.2
Jacobs, K.B.3
-
32
-
-
57249114505
-
SNAP: A web-based tool for identification and annotation of proxy SNPs using HapMap
-
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, de Bakker PI. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 2008; 24: 2938-2939
-
(2008)
Bioinformatics
, vol.24
, pp. 2938-2939
-
-
Johnson, A.D.1
Handsaker, R.E.2
Pulit, S.L.3
Nizzari, M.M.4
O'Donnell, C.J.5
De Bakker, P.I.6
-
33
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, et al. The structure of haplotype blocks in the human genome. Science 2002; 296: 2225-2229
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
-
34
-
-
84858779229
-
HaploReg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
-
Ward LD, Kellis M. HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic acids Res 2012; 40: D930-D934
-
(2012)
Nucleic Acids Res
, vol.40
, pp. D930-D934
-
-
Ward, L.D.1
Kellis, M.2
-
35
-
-
84865712382
-
Annotation of functional variation in personal genomes using RegulomeDB
-
Boyle AP, Hong EL, Hariharan M, et al. Annotation of functional variation in personal genomes using RegulomeDB. Genome Res 2012; 22: 1790-1797
-
(2012)
Genome Res
, vol.22
, pp. 1790-1797
-
-
Boyle, A.P.1
Hong, E.L.2
Hariharan, M.3
-
36
-
-
22244452677
-
Distribution and intensity of constraint in mammalian genomic sequence
-
Cooper GM, Stone EA, Asimenos G, et al. Distribution and intensity of constraint in mammalian genomic sequence. Genome Res 2005; 15: 901-913
-
(2005)
Genome Res
, vol.15
, pp. 901-913
-
-
Cooper, G.M.1
Stone, E.A.2
Asimenos, G.3
-
37
-
-
84921320301
-
Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue
-
Shi J, Marconett CN, Duan J, et al. Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue. Nat Commun 2014; 5: 3365
-
(2014)
Nat Commun
, vol.5
, pp. 3365
-
-
Shi, J.1
Marconett, C.N.2
Duan, J.3
-
38
-
-
77955894071
-
METAL: Fast and efficient meta-Analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR. METAL: fast and efficient meta-Analysis of genomewide association scans. Bioinformatics 2010; 26: 2190-2191
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
39
-
-
84880507665
-
Mutational heterogeneity in cancer and the search for new cancer-Associated genes
-
Lawrence MS, Stojanov P, Polak P, et al. Mutational heterogeneity in cancer and the search for new cancer-Associated genes. Nature 2013; 499: 214-218
-
(2013)
Nature
, vol.499
, pp. 214-218
-
-
Lawrence, M.S.1
Stojanov, P.2
Polak, P.3
-
40
-
-
77951585057
-
Architecture of inherited susceptibility to common cancer
-
Fletcher O, Houlston RS. Architecture of inherited susceptibility to common cancer. Nat Rev Cancer 2010; 10: 353-361
-
(2010)
Nat Rev Cancer
, vol.10
, pp. 353-361
-
-
Fletcher, O.1
Houlston, R.S.2
-
41
-
-
84878451270
-
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression
-
Kote-Jarai Z, Saunders EJ, Leongamornlert DA, et al. Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. Hum Mol Genet 2013; 22: 2520-2528
-
(2013)
Hum Mol Genet
, vol.22
, pp. 2520-2528
-
-
Kote-Jarai, Z.1
Saunders, E.J.2
Leongamornlert, D.A.3
-
42
-
-
84875717832
-
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
-
Bojesen SE, Pooley KA, Johnatty SE, et al. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nat Genet 2013; 45: 371-384
-
(2013)
Nat Genet
, vol.45
, pp. 371-384
-
-
Bojesen, S.E.1
Pooley, K.A.2
Johnatty, S.E.3
-
43
-
-
84904101984
-
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk
-
Walsh KM, Codd V, Smirnov IV, et al. Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat Genet 2014; 46: 731-735
-
(2014)
Nat Genet
, vol.46
, pp. 731-735
-
-
Walsh, K.M.1
Codd, V.2
Smirnov, I.V.3
-
44
-
-
4143126575
-
A major lung cancer susceptibility locus maps to chromosome 6q23-25
-
Bailey-Wilson JE, Amos CI, Pinney SM, et al. A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet 2004; 75: 460-474
-
(2004)
Am J Hum Genet
, vol.75
, pp. 460-474
-
-
Bailey-Wilson, J.E.1
Amos, C.I.2
Pinney, S.M.3
|