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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer
Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study
Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk
rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer
