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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 26, 2005
An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions foundJaana M Hartikainen, Hanna Tuhkanen, Vesa Kataja, et al.
Carcinogenesis|January 5, 2008
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British populationKristy E Driver, Honglin Song, Fabienne Lesueur, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 18, 2020
CanRisk Tool-A Web Interface for the Prediction of Breast and Ovarian Cancer Risk and the Likelihood of Carrying Genetic Pathogenic VariantsTim Carver, Simon Hartley, Andrew Lee, et al.
Magnetic Resonance Imaging|November 5, 2002
What is the recall rate of breast MRI when used for screening asymptomatic women at high risk?Ruth M L Warren, Linda Pointon, Rebecca Caines, et al.
European Geriatric Medicine|October 15, 2021
The Acute Frailty Network: experiences from a whole-systems quality improvement collaborative for acutely ill older patients in the English NHSJames David van Oppen, Deborah Thompson, Matt Tite, et al.
Human Molecular Genetics|May 25, 2002
Variants in DNA double-strand break repair genes and breast cancer susceptibilityBettina Kuschel, Annika Auranen, Simon McBride, et al.
Breast Cancer Research : BCR|April 13, 2007
Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer riskCaroline Baynes, Catherine S Healey, Karen A Pooley, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|June 12, 2023
Exploring the barriers to and facilitators of implementing CanRisk in primary care: a qualitative thematic framework analysisStephanie Archer, Francisca Stutzin Donoso, Tim Carver, et al.
Human Molecular Genetics|January 12, 2018
Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genesXingyi Guo, Jiajun Shi, Qiuyin Cai, et al.
Analytical and Quantitative Cytology and Histology|January 13, 2004
A karyometric approach to the characterization of atypical endometrial hyperplasia with and without co-occurring adenocarcinomaFrancisco A Garcia, John R Davis, David S Alberts, et al.
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