-
1
-
-
67650468322
-
Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma
-
Akulevich NM, Saenko VA, Rogounovitch TI et al. (2009) Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma. Endocr Relat Cancer 16:491-503
-
(2009)
Endocr Relat Cancer
, vol.16
, pp. 491-503
-
-
Akulevich, N.M.1
Saenko, V.A.2
Rogounovitch, T.I.3
-
2
-
-
81855199793
-
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
-
Amos CI, Wang LE, Lee JE et al. (2011) Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Hum Mol Genet 20:5012-23
-
(2011)
Hum Mol Genet
, vol.20
, pp. 5012-5023
-
-
Amos, C.I.1
Wang, L.E.2
Lee, J.E.3
-
3
-
-
84925546270
-
A database of genetic association studies in melanoma using network-driven data exploration tools
-
Athanasiadis E, Antonopoulou K, Chatzinasiou F et al. (2014) A database of genetic association studies in melanoma using network-driven data exploration tools. Database doi:10.1093/database/bau101
-
(2014)
Database
-
-
Athanasiadis, E.1
Antonopoulou, K.2
Chatzinasiou, F.3
-
4
-
-
80054996042
-
Genome-wide association study identifies three new melanoma susceptibility loci
-
Barrett JH, Iles MM, Harland M et al. (2011) Genome-wide association study identifies three new melanoma susceptibility loci. Nat Genet 43:1108-13
-
(2011)
Nat Genet
, vol.43
, pp. 1108-1113
-
-
Barrett, J.H.1
Iles, M.M.2
Harland, M.3
-
5
-
-
84925385611
-
A systematic appraisal of field synopses in genetic epidemiology: A HuGE review
-
in press
-
Belbasis L, Panagiotou OA, Dosis V et al. (2014) A systematic appraisal of field synopses in genetic epidemiology: a HuGE review. Am J Epidemiol (in press)
-
(2014)
Am J Epidemiol
-
-
Belbasis, L.1
Panagiotou, O.A.2
Dosis, V.3
-
6
-
-
82555205202
-
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
-
Bertolotto C, Lesueur F, Giuliano S et al. (2011) A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma. Nature 480:94-8
-
(2011)
Nature
, vol.480
, pp. 94-98
-
-
Bertolotto, C.1
Lesueur, F.2
Giuliano, S.3
-
7
-
-
68149179663
-
Genome-wide association study identifies three loci associated with melanoma risk
-
Bishop DT, Demenais F, Iles MM et al. (2009) Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet 41:920-5
-
(2009)
Nat Genet
, vol.41
, pp. 920-925
-
-
Bishop, D.T.1
Demenais, F.2
Iles, M.M.3
-
8
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
Brown KM, Macgregor S, Montgomery GW et al. (2008) Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet 40:838-40
-
(2008)
Nat Genet
, vol.40
, pp. 838-840
-
-
Brown, K.M.1
Macgregor, S.2
Montgomery, G.W.3
-
9
-
-
80051959840
-
Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma
-
Chatzinasiou F, Lill CM, Kypreou K et al. (2011) Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. J Natl Cancer Inst 103:1227-35
-
(2011)
J Natl Cancer Inst
, vol.103
, pp. 1227-1235
-
-
Chatzinasiou, F.1
Lill, C.M.2
Kypreou, K.3
-
10
-
-
84883293845
-
MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: An Australian case-control-family study
-
Cust AE, Goumas C, Vuong K et al. (2013) MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study. BMC Cancer 13:406
-
(2013)
BMC Cancer
, vol.13
, pp. 406
-
-
Cust, A.E.1
Goumas, C.2
Vuong, K.3
-
12
-
-
84878020180
-
Meta-analysis methods for genome-wide association studies and beyond
-
Evangelou E, Ioannidis JP (2013) Meta-analysis methods for genome-wide association studies and beyond. Nat Rev Genet 14:379-89
-
(2013)
Nat Rev Genet
, vol.14
, pp. 379-389
-
-
Evangelou, E.1
Ioannidis, J.P.2
-
13
-
-
68149100807
-
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
-
Falchi M, Bataille V, Hayward NK et al. (2009) Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nat Genet 41:915-9
-
(2009)
Nat Genet
, vol.41
, pp. 915-919
-
-
Falchi, M.1
Bataille, V.2
Hayward, N.K.3
-
14
-
-
84893594813
-
Joint effect of multiple common SNPs predicts melanoma susceptibility
-
Fang S, Han J, Zhang M et al. (2013) Joint effect of multiple common SNPs predicts melanoma susceptibility. PLoS One 8:e85642
-
(2013)
PLoS One
, vol.8
, pp. e85642
-
-
Fang, S.1
Han, J.2
Zhang, M.3
-
15
-
-
27244435224
-
Population-based analysis of prognostic factors and survival in familial melanoma
-
Florell SR, Boucher KM, Garibotti G et al. (2005) Population-based analysis of prognostic factors and survival in familial melanoma. J Clin Oncol 23:7168-77
-
(2005)
J Clin Oncol
, vol.23
, pp. 7168-7177
-
-
Florell, S.R.1
Boucher, K.M.2
Garibotti, G.3
-
16
-
-
77955965549
-
The association between ATM D1853N polymorphism and breast cancer susceptibility: A meta-analysis
-
Gao LB, Pan XM, Sun H et al. (2010) The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis. J Exp Clin Cancer Res 29:117
-
(2010)
J Exp Clin Cancer Res
, vol.29
, pp. 117
-
-
Gao, L.B.1
Pan, X.M.2
Sun, H.3
-
17
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
Genomes Project Consortium, Abecasis GR, Auton A et al. (2012) An integrated map of genetic variation from 1,092 human genomes. Nature 491:56-65
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
Genomes Project Consortium1
Abecasis, G.R.2
Auton, A.3
-
18
-
-
84874367669
-
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: Associations with histological subtypes and family cancer history
-
Ghiorzo P, Pastorino L, Queirolo P et al. (2013) Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. Pigment Cell Melanoma Res 26:259-62
-
(2013)
Pigment Cell Melanoma Res
, vol.26
, pp. 259-262
-
-
Ghiorzo, P.1
Pastorino, L.2
Queirolo, P.3
-
20
-
-
84875722359
-
A variant in FTO shows association with melanoma risk not due to BMI
-
Iles MM, Law MH, Stacey SN et al. (2013) A variant in FTO shows association with melanoma risk not due to BMI. Nat Genet 45:428-32. 32e1
-
(2013)
Nat Genet
, vol.45
-
-
Iles, M.M.1
Law, M.H.2
Stacey, S.N.3
-
21
-
-
38949094880
-
Assessment of cumulative evidence on genetic associations: Interim guidelines
-
Ioannidis JP, Boffetta P, Little J et al. (2008) Assessment of cumulative evidence on genetic associations: interim guidelines. Int J Epidemiol 37:120-32
-
(2008)
Int J Epidemiol
, vol.37
, pp. 120-132
-
-
Ioannidis, J.P.1
Boffetta, P.2
Little, J.3
-
22
-
-
41049087605
-
Heterogeneity in meta-analyses of genome-wide association investigations
-
Ioannidis JP, Patsopoulos NA, Evangelou E (2007) Heterogeneity in meta-analyses of genome-wide association investigations. PLoS One 2:e841
-
(2007)
PLoS One
, vol.2
, pp. e841
-
-
Ioannidis, J.P.1
Patsopoulos, N.A.2
Evangelou, E.3
-
23
-
-
67749106283
-
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases
-
Khoury MJ, Bertram L, Boffetta P et al. (2009) Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases. Am J Epidemiol 170:269-79
-
(2009)
Am J Epidemiol
, vol.170
, pp. 269-279
-
-
Khoury, M.J.1
Bertram, L.2
Boffetta, P.3
-
24
-
-
84862309036
-
Melanoma genetics: Recent findings take us beyond well-traveled pathways
-
Law MH, Macgregor S, Hayward NK (2012) Melanoma genetics: recent findings take us beyond well-traveled pathways. J Invest Dermatol 132:1763-74
-
(2012)
J Invest Dermatol
, vol.132
, pp. 1763-1774
-
-
Law, M.H.1
Macgregor, S.2
Hayward, N.K.3
-
25
-
-
57149094871
-
Genetic variants and haplotypes of the caspase-8 and caspase-10 genes contribute to susceptibility to cutaneous melanoma
-
Li C, Zhao H, Hu Z et al. (2008) Genetic variants and haplotypes of the caspase-8 and caspase-10 genes contribute to susceptibility to cutaneous melanoma. Hum Mutat 29:1443-51
-
(2008)
Hum Mutat
, vol.29
, pp. 1443-1451
-
-
Li, C.1
Zhao, H.2
Hu, Z.3
-
26
-
-
80055002815
-
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
-
Macgregor S, Montgomery GW, Liu JZ et al. (2011) Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nat Genet 43:1114-8
-
(2011)
Nat Genet
, vol.43
, pp. 1114-1118
-
-
Macgregor, S.1
Montgomery, G.W.2
Liu, J.Z.3
-
27
-
-
84865543320
-
Current opportunities and challenges: Genome-wide association studies on pigmentation and skin cancer
-
Meng S, Zhang M, Liang L et al. (2012) Current opportunities and challenges: genome-wide association studies on pigmentation and skin cancer. Pigment Cell Melanoma Res 25:612-7
-
(2012)
Pigment Cell Melanoma Res
, vol.25
, pp. 612-617
-
-
Meng, S.1
Zhang, M.2
Liang, L.3
-
28
-
-
84887847173
-
Emerging trends in the epidemiology of melanoma
-
Nikolaou V, Stratigos AJ (2014) Emerging trends in the epidemiology of melanoma. Br J Dermatol 170:11-9
-
(2014)
Br J Dermatol
, vol.170
, pp. 11-19
-
-
Nikolaou, V.1
Stratigos, A.J.2
-
29
-
-
84875332980
-
Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population
-
Pena-Chilet M, Blanquer-Maceiras M, Ibarrola-Villava M et al. (2013) Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population. BMC Cancer 13:160
-
(2013)
BMC Cancer
, vol.13
, pp. 160
-
-
Pena-Chilet, M.1
Blanquer-Maceiras, M.2
Ibarrola-Villava, M.3
-
30
-
-
70349745464
-
A population-based study of Australian twins with melanoma suggests a strong genetic contribution to liability
-
Shekar SN, Duffy DL, Youl P et al. (2009) A population-based study of Australian twins with melanoma suggests a strong genetic contribution to liability. J Invest Dermatol 129:2211-9
-
(2009)
J Invest Dermatol
, vol.129
, pp. 2211-2219
-
-
Shekar, S.N.1
Duffy, D.L.2
Youl, P.3
-
31
-
-
84873495253
-
Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study
-
Stefanaki I, Panagiotou OA, Kodela E et al. (2013) Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study. PLoS One 8:e55712
-
(2013)
PLoS One
, vol.8
, pp. e55712
-
-
Stefanaki, I.1
Panagiotou, O.A.2
Kodela, E.3
-
32
-
-
84856641278
-
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q
-
Teerlink C, Farnham J, Allen-Brady K et al. (2012) A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Hum Genet 131:77-85
-
(2012)
Hum Genet
, vol.131
, pp. 77-85
-
-
Teerlink, C.1
Farnham, J.2
Allen-Brady, K.3
-
33
-
-
84861845490
-
Melanoma: From mutations to medicine
-
Tsao H, Chin L, Garraway LA et al. (2012) Melanoma: from mutations to medicine. Genes Dev 26:1131-55
-
(2012)
Genes Dev
, vol.26
, pp. 1131-1155
-
-
Tsao, H.1
Chin, L.2
Garraway, L.A.3
-
34
-
-
84897509495
-
Variants in the ATM-CHEK2- BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma
-
Wojcicka A, Czetwertynska M, Swierniak M et al. (2014) Variants in the ATM-CHEK2- BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma. Genes Chromosomes Cancer 53:516-23
-
(2014)
Genes Chromosomes Cancer
, vol.53
, pp. 516-523
-
-
Wojcicka, A.1
Czetwertynska, M.2
Swierniak, M.3
-
35
-
-
77952315915
-
CASP8 polymorphisms contribute to cancer susceptibility: Evidence from a meta-analysis of 23 publications with 55 individual studies
-
Yin M, Yan J, Wei S et al. (2010) CASP8 polymorphisms contribute to cancer susceptibility: evidence from a meta-analysis of 23 publications with 55 individual studies. Carcinogenesis 31:850-7
-
(2010)
Carcinogenesis
, vol.31
, pp. 850-857
-
-
Yin, M.1
Yan, J.2
Wei, S.3
-
37
-
-
82555187007
-
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
-
Yokoyama S, Woods SL, Boyle GM et al. (2011) A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature 480:99-103
-
(2011)
Nature
, vol.480
, pp. 99-103
-
-
Yokoyama, S.1
Woods, S.L.2
Boyle, G.M.3
|