Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

Low–moderate risk alleles that are relatively common in the population may explain a significant proportion of the excess familial risk of ovarian cancer (OC) not attributed to highly penetrant genes. In this study, we evaluated the risks of OC associated with common germline variants in five oncoge...

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Bibliografische gegevens
Hoofdauteurs: Quaye, L, Song, H, Ramus, S J, Gentry-Maharaj, A, Høgdall, E, DiCioccio, R A, McGuire, V, Wu, A H, Van Den Berg, D J, Pike, M C, Wozniak, E, Doherty, J A, Rossing, M A, Ness, R B, Moysich, K B, Høgdall, C, Blaakaer, J, Easton, D F, Ponder, B A J, Jacobs, I J, Menon, U, Whittemore, A S, Krüger-Kjaer, S, Pearce, C L, Pharoah, P D P, Gayther, S A
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group 2009
Onderwerpen:
Genetics and Genomics
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2661781/
https://ncbi.nlm.nih.gov/pubmed/19240718
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6604947
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