Association between putative functional variants in the PSMB9 gene and risk of melanoma - re-analysis of published melanoma genome-wide association studies

To mine possibly hidden causal single nucleotide polymorphisms (SNPs) in the etiology of melanoma, we investigated the association of SNPs in 76 M/G1 transition genes with melanoma risk using our published genome-wide association study (GWAS) dataset with 1804 melanoma cases and 1,026 cancer-free co...

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Bibliografiska uppgifter
Huvudupphovsmän: Qian, Ji, Liu, Hongliang, Wei, Sheng, Liu, Zhensheng, Li, Yangkai, Wang, Li-E, Chen, Wei V., Amos, Christopher I., Lee, Jeffrey E., Iles, Mark M, Law, Matthew H, Barrett, Jennifer H, Montgomery, Grant W, Taylor, John, Bishop, Julia A Newton, MacGregor, Stuart, Bishop, D Timothy, Mann, Graham J., Hayward, Nicholas K, Wei, Qingyi
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3721546/
https://ncbi.nlm.nih.gov/pubmed/23360169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pcmr.12069
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