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Identification of proximal SUMO-dependent interactors using SUMO-ID
Breast cancer risk genes
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
Genome-wide association study of germline variants and breast cancer-specific mortality
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Association analysis identifies 65 new breast cancer risk loci
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer: Genetic Association Study in 18,723 Individuals
Association between CASP8 -652 6N Del Polymorphism (rs3834129) and Colorectal Cancer Risk: Results from a Multi-Centric Study (vol 9, e85538, 2014)
Association between CASP8-652 6N Del Polymorphism (rs3834129) and Colorectal Cancer Risk: Results from a Multi-Centric Study
Transcriptome and genome sequencing uncovers functional variation in humans
Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer