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Volumn 44, Issue 12, 2012, Pages 1326-1329

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

(47)  Gudmundsson, Julius a   Sulem, Patrick a   Gudbjartsson, Daniel F a   Masson, Gisli a   Agnarsson, Bjarni A b,c   Benediktsdottir, Kristrun R b,c   Sigurdsson, Asgeir a   Magnusson, Olafur Th a   Gudjonsson, Sigurjon A a   Magnusdottir, Droplaug N a   Johannsdottir, Hrefna a   Helgadottir, Hafdis Th a   Stacey, Simon N a   Jonasdottir, Adalbjorg a   Olafsdottir, Stefania B a   Thorleifsson, Gudmar a   Jonasson, Jon G b,c,d   Tryggvadottir, Laufey c,d   Navarrete, Sebastian e   Fuertes, Fernando e   more..


Author keywords

[No Author keywords available]

Indexed keywords

HOX PROTEIN; PROTEIN VARIANT;

EID: 84870531459     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2437     Document Type: Article
Times cited : (158)

References (27)
  • 2
    • 13444268381 scopus 로고    scopus 로고
    • Cancer as a complex phenotype: Pattern of cancer distribution within and beyond the nuclear family
    • Amundadottir, L.T. et al. Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family. PLoS Med. 1, e65 (2004).
    • (2004) PLoS Med , vol.1
    • Amundadottir, L.T.1
  • 3
    • 84856176782 scopus 로고    scopus 로고
    • Germline mutations in HOXB13 and prostate-cancer risk
    • Ewing, C.M. et al. Germline mutations in HOXB13 and prostate-cancer risk. N. Engl. J. Med. 366, 141-149 (2012).
    • (2012) N. Engl. J. Med , vol.366 , pp. 141-149
    • Ewing, C.M.1
  • 4
    • 50449089222 scopus 로고    scopus 로고
    • Detection of sharing by descent, long-range phasing and haplotype imputation
    • Kong, A. et al. Detection of sharing by descent, long-range phasing and haplotype imputation. Nat. Genet. 40, 1068-1075 (2008).
    • (2008) Nat. Genet , vol.40 , pp. 1068-1075
    • Kong, A.1
  • 5
    • 84862777075 scopus 로고    scopus 로고
    • Discovery of common variants associated with low TSH levels and thyroid cancer risk
    • Gudmundsson, J. et al. Discovery of common variants associated with low TSH levels and thyroid cancer risk. Nat. Genet. 44, 319-322 (2012).
    • (2012) Nat. Genet , vol.44 , pp. 319-322
    • Gudmundsson, J.1
  • 12
    • 70349547128 scopus 로고    scopus 로고
    • Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
    • Gudmundsson, J. et al. Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Nat. Genet. 41, 1122-1126 (2009).
    • (2009) Nat. Genet , vol.41 , pp. 1122-1126
    • Gudmundsson, J.1
  • 13
    • 70349540906 scopus 로고    scopus 로고
    • Identification of a new prostate cancer susceptibility locus on chromosome 8q24
    • Yeager, M. et al. Identification of a new prostate cancer susceptibility locus on chromosome 8q24. Nat. Genet. 41, 1055-1057 (2009).
    • (2009) Nat. Genet , vol.41 , pp. 1055-1057
    • Yeager, M.1
  • 14
    • 70349548806 scopus 로고    scopus 로고
    • Multiple loci on 8q24 associated with prostate cancer susceptibility
    • Al Olama, A.A. et al. Multiple loci on 8q24 associated with prostate cancer susceptibility. Nat. Genet. 41, 1058-1060 (2009).
    • (2009) Nat. Genet , vol.41 , pp. 1058-1060
    • Al Olama, A.A.1
  • 15
    • 75749138023 scopus 로고    scopus 로고
    • Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
    • Crowther-Swanepoel, D. et al. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk. Nat. Genet. 42, 132-136 (2010).
    • (2010) Nat. Genet , vol.42 , pp. 132-136
    • Crowther-Swanepoel, D.1
  • 20
    • 55049112064 scopus 로고    scopus 로고
    • Sequence variant on 8q24 confers susceptibility to urinary bladder cancer
    • Kiemeney, L.A. et al. 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
  • 21
    • 34247591993 scopus 로고    scopus 로고
    • Multiple prostate cancer risk variants on 8q24
    • DOI 10.1038/ng0507-579, PII NG0507579
    • Witte, J.S. Multiple prostate cancer risk variants on 8q24. Nat. Genet. 39, 579-580 (2007). (Pubitemid 46676095)
    • (2007) Nature Genetics , vol.39 , Issue.5 , pp. 579-580
    • Witte, J.S.1
  • 22
    • 33750985094 scopus 로고    scopus 로고
    • A novel endonuclease IV post-PCR genotyping system
    • Kutyavin, I.V. et al. A novel endonuclease IV post-PCR genotyping system. Nucleic Acids Res. 34, e128 (2006).
    • (2006) Nucleic Acids Res , vol.34
    • Kutyavin, I.V.1
  • 23
    • 78049354879 scopus 로고    scopus 로고
    • Fine-scale recombination rate differences between sexes, populations and individuals
    • Kong, A. et al. Fine-scale recombination rate differences between sexes, populations and individuals. Nature 467, 1099-1103 (2010).
    • (2010) Nature , vol.467 , pp. 1099-1103
    • Kong, A.1
  • 24
    • 80055001747 scopus 로고    scopus 로고
    • Identification of low-frequency variants associated with gout and serum uric acid levels
    • Sulem, P. et al. Identification of low-frequency variants associated with gout and serum uric acid levels. Nat. Genet. 43, 1127-1130 (2011).
    • (2011) Nat. Genet , vol.43 , pp. 1127-1130
    • Sulem, P.1
  • 25
    • 80054973810 scopus 로고    scopus 로고
    • Mutations in BRIP1 confer high risk of ovarian cancer
    • Rafnar, T. et al. Mutations in BRIP1 confer high risk of ovarian cancer. Nat. Genet. 43, 1104-1107 (2011).
    • (2011) Nat. Genet , vol.43 , pp. 1104-1107
    • Rafnar, T.1
  • 26
    • 80055009292 scopus 로고    scopus 로고
    • A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
    • Stacey, S.N. et al. A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Nat. Genet. 43, 1098-1103 (2011).
    • (2011) Nat. Genet , vol.43 , pp. 1098-1103
    • Stacey, S.N.1
  • 27
    • 34347344976 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.