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Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants

Genome-wide association studies (GWAS) have identified many common single nucleotide polymorphisms (SNPs) associated with colorectal cancer risk. These SNPs may tag correlated variants with biological importance. Fine-mapping around GWAS loci can facilitate detection of functional candidates and add...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Du, Mengmeng, Jiao, Shuo, Bien, Stephanie A., Gala, Manish, Abecasis, Goncalo, Bezieau, Stephane, Brenner, Hermann, Butterbach, Katja, Caan, Bette J., Carlson, Christopher S., Casey, Graham, Chang-Claude, Jenny, Conti, David V., Curtis, Keith R., Duggan, David, Gallinger, Steven, Haile, Robert W., Harrison, Tabitha A., Hayes, Richard B., Hoffmeister, Michael, Hopper, John L., Hudson, Thomas J., Jenkins, Mark A., Küry, Sébastien, Le Marchand, Loic, Leal, Suzanne M., Newcomb, Polly A., Nickerson, Deborah A., Potter, John D., Schoen, Robert E., Schumacher, Fredrick R., Seminara, Daniela, Slattery, Martha L., Hsu, Li, Chan, Andrew T., White, Emily, Berndt, Sonja I., Peters, Ulrike
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4933364/
https://ncbi.nlm.nih.gov/pubmed/27379672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0157521
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