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Works
31
Patterns of somatic mutation in human cancer genomes
Genome-wide association study identifies novel breast cancer susceptibility loci
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Shared heritability and functional enrichment across six solid cancers
Shared heritability and functional enrichment across six solid cancers
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
SNPs in lncRNA Regions and Breast Cancer Risk
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer
