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- Journal Article
- A2
- 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
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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BRCA2 hypomorphic missense variants confer moderate risks of breast 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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Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients
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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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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
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- Journal Article
- A1
- open access
Reproducibility of telomere length assessment : an international collaborative study
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Is Southern blotting necessary to measure telomere length reproducibly?: authors' response to: Commentary: The reliability of telomere length measurements
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Reproducibility of telomere length assessment: authors' response to Damjan Krstajic and Ljubomir Buturovic
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- Journal Article
- A1
- open access
Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers
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Radiogenomics: radiobiology enters the era of big data and team science
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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
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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers