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Journal of the National Cancer Institute|August 29, 2015
Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian CancerSusan J Ramus, Honglin Song, Ed Dicks, et al.
International Journal of Cancer|December 1, 2018
A comprehensive gene-environment interaction analysis in Ovarian Cancer using genome-wide significant common variantsSehee Kim, Miao Wang, Jonathan P Tyrer, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 16, 2016
Assessment of Multifactor Gene-Environment Interactions and Ovarian Cancer Risk: Candidate Genes, Obesity, and Hormone-Related Risk FactorsJoseph L Usset, Rama Raghavan, Jonathan P Tyrer, et al.
Nature Genetics|August 17, 2023
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer riskNaomi Wilcox, Martine Dumont, Anna González-Neira, et al.
NPJ Genomic Medicine|March 5, 2024
Genome-wide association analyses of ovarian cancer patients undergoing primary debulking surgery identify candidate genes for residual diseaseDhanya Ramachandran, Jonathan P Tyrer, Stefan Kommoss, et al.
Nature Communications|August 2, 2020
European polygenic risk score for prediction of breast cancer shows similar performance in Asian womenWeang-Kee Ho, Min-Min Tan, Nasim Mavaddat, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 24, 2021
Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian CancerMichael C J Quinn, Karen McCue, Wei Shi, et al.
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