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Nature Communications|February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.Nature Genetics|July 1, 2024
Understanding the genetic complexity of puberty timing across the allele frequency spectrumKatherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, et al.Genetic Epidemiology|March 3, 2020
Transcriptome-wide association study of breast cancer risk by estrogen-receptor statusHelian Feng, Alexander Gusev, Bogdan Pasaniuc, et al.Nature|August 5, 2021
Genetic insights into biological mechanisms governing human ovarian ageingKatherine S Ruth, Felix R Day, Jazib Hussain, et al.American Journal of Human Genetics|December 18, 2018
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer SubtypesNasim Mavaddat, Kyriaki Michailidou, Joe Dennis, et al.European Journal of Human Genetics : EJHG|January 14, 2022
Polygenic risk modeling for prediction of epithelial ovarian cancer riskEileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, et al.Nature Genetics|May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analysesHaoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.Nature Communications|September 25, 2019
Publisher Correction: Shared heritability and functional enrichment across six solid cancersXia Jiang, Hilary K Finucane, Fredrick R Schumacher, et al.Nature Communications|January 27, 2019
Shared heritability and functional enrichment across six solid cancersXia Jiang, Hilary K Finucane, Fredrick R Schumacher, et al.Pageof 87