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Journal of the National Cancer Institute|September 19, 2002
Cancer Incidence in BRCA1 mutation carriersDeborah Thompson, Douglas F Easton, American Journal of Human Genetics|August 6, 2003
A full-likelihood method for the evaluation of causality of sequence variants from family dataDeborah Thompson, Douglas F Easton, David E GoldgarJournal of the National Cancer Institute|June 2, 2005
Cancer risks and mortality in heterozygous ATM mutation carriersDeborah Thompson, Silvia Duedal, Jennifer Kirner, et al.Genetic Epidemiology|October 15, 2003
Polygenic inheritance of breast cancer: Implications for design of association studiesAntonis C Antoniou, Douglas F EastonFuture Oncology (London, England)|March 28, 2006
Risk prediction models for familial breast cancerAntonis C Antoniou, Douglas F EastonHuman Molecular Genetics|October 15, 2008
Genome-wide association studies in cancerDouglas F Easton, Rosalind A EelesCurrent Opinion in Genetics & Development|April 27, 2010
Genome-wide association studies in common cancers--what have we learnt?Jajini Susan Varghese, Douglas F EastonBreast Cancer Research : BCR|February 12, 2010
Familial relative risks for breast cancer by pathological subtype: a population-based cohort studyNasim Mavaddat, Paul D Pharoah, Fiona Blows, et al.Genetic Epidemiology|June 29, 2010
Evaluating the power to discriminate between highly correlated SNPs in genetic association studiesMiriam S Udler, Jonathan Tyrer, Douglas F EastonPageof 77