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Shared heritability and functional enrichment across six solid cancers
Shared heritability and functional enrichment across six solid cancers
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Ovarian and breast cancer risks associated with pathogenic variants in RAD51C and RAD51D
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer
Aurora kinases A and B and familial breast cancer risk
The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22
