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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
GREM1 germline mutation screening in Ashkenazi Jewish patients with familial colorectal cancer
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagus
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort
Management and 5-year outcomes in 9938 women with screen-detected ductal carcinoma in situ: the UK Sloane Project
Targeted inactivation of fh1 causes proliferative renal cyst development and activation of the hypoxia pathway
