Selected publications
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Nature Genetics.
2016
Review
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Times cited: 49 -
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
Journal of the National Cancer Institute.
2016
Academic Article
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Times cited: 41 -
Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci.
Human Molecular Genetics.
2015
Academic Article
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Times cited: 18 -
Characterization of large structural genetic mosaicism in human autosomes.
American Journal of Human Genetics.
2015
Review
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Times cited: 42 -
Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk.
Cancer Epidemiology Biomarkers and Prevention.
2015
Academic Article
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Times cited: 13 -
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
Nature Genetics.
2015
Review
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Times cited: 129 -
The stomach cancer pooling (StoP) project: Study design and presentation.
European Journal of Cancer Prevention.
2015
Review
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Times cited: 19 -
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
Human Molecular Genetics.
2014
Academic Article
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Times cited: 59 -
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Nature Genetics.
2013
Academic Article
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Times cited: 341 -
Analysis of genetic variants in never-smokers with lung cancer facilitated by an internet-based blood collection protocol: A preliminary report.
Clinical Cancer Research.
2010
Academic Article
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Times cited: 59