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American Journal of Human Genetics|December 23, 2014
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1Dylan M Glubb, Mel J Maranian, Kyriaki Michailidou, et al.
Human Molecular Genetics|February 6, 2015
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2Nick Orr, Frank Dudbridge, Nicola Dryden, et al.
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.
British Journal of Cancer|February 22, 2019
Genome-wide association study of germline variants and breast cancer-specific mortalityMaria Escala-Garcia, Qi Guo, Thilo Dörk, et al.
Nature Genetics|March 29, 2013
Large-scale genotyping identifies 41 new loci associated with breast cancer riskKyriaki Michailidou, Per Hall, Anna Gonzalez-Neira, 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.
Nature Communications|May 15, 2021
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
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