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- Journal Article
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- open access
Large-scale meta–genome-wide association study reveals common genetic factors linked to radiation-induced acute toxicities across cancer types
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- Journal Article
- A1
- open access
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
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- Journal Article
- A1
- open access
Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores
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- Journal Article
- A1
- open access
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
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- Journal Article
- A1
- open access
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
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- Journal Article
- A1
- open access
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
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- Journal Article
- A1
- open access
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
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- Journal Article
- A1
- open access
Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
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Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness
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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
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- Journal Article
- A1
- open access
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
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- Journal Article
- A1
- open access
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
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- Journal Article
- A1
- open access
Shared heritability and functional enrichment across six solid cancers
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A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk
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BRCA2 hypomorphic missense variants confer moderate risks of breast cancer
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- Journal Article
- A1
- open access
Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
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Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores
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- Journal Article
- A1
- open access
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
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- Journal Article
- A1
- open access
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
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BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers
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- Journal Article
- A1
- open access
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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- Journal Article
- A1
- open access
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
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- Journal Article
- A1
- open access
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
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- Journal Article
- A1
- open access
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk