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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus