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Journal of Medical Genetics|June 1, 2025
Associations between ATM c.7271T>G and cancer risk: analysis of Breast Cancer Association Consortium and UK Biobank dataToqir K Mukhtar, Leila Dorling, Naomi Wilcox, et al.Human Mutation|October 28, 2008
Genetic evidence and integration of various data sources for classifying uncertain variants into a single modelDavid E Goldgar, Douglas F Easton, Graham B Byrnes, et al.Pharmacoeconomics|December 18, 2002
Generic clozapine: a cost-saving alternative to brand name clozapine?Gordon Tse, Deborah Thompson, Ric M ProcyshynNursing Management (Harrow, London, England : 1994)|May 28, 2015
Transforming emergency services for frail older people in hospitalDeborah Thompson, Mandy Rumley-Buss, Simon ConroyAmerican Journal of Botany|August 25, 2018
PHENOTYPES MEDIATED BY THE IOJAP GENOTYPE IN MAIZEEdward H Coe, Deborah Thompson, Virginia WalbotAmerican Journal of Human Genetics|August 4, 2004
Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2David E Goldgar, Douglas F Easton, Amie M Deffenbaugh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2021
Potential of polygenic risk scores for improving population estimates of women's breast cancer genetic risksMichael Wolfson, Steve Gribble, Nora Pashayan, et al.American Journal of Human Genetics|March 12, 2025
The contribution of coding variants to the heritability of multiple cancer types using UK Biobank whole-exome sequencing dataNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.Genetic Epidemiology|January 3, 2025
Using Family History Data to Improve the Power of Association Studies: Application to Cancer in UK BiobankNaomi Wilcox, Jonathan P Tyrer, Joe Dennis, et al.Investigative Ophthalmology & Visual Science|January 31, 2003
Contribution of germline mutations in BRCA2, P16(INK4A), P14(ARF) and P15 to uveal melanomaNicholas Hearle, Bertil E Damato, Jane Humphreys, et al.Pageof 77