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Annals of Oncology : Official Journal of the European Society for Medical Oncology|July 31, 2013
Germline single nucleotide polymorphisms associated with response of urothelial carcinoma to platinum-based therapy: the role of the hostD J Gallagher, J Vijai, R J Hamilton, et al.
Nature Genetics|September 1, 1997
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APCS J Laken, G M Petersen, S B Gruber, et al.
Nature Genetics|June 1, 1996
Low incidence of BRCA2 mutations in breast carcinoma and other cancersD H Teng, R Bogden, J Mitchell, et al.
British Journal of Cancer|June 13, 2015
An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortalityJ Sullivan, R Kopp, K Stratton, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 25, 2022
Comprehensive assessment of germline pathogenic variant detection in tumor-only sequencingP Terraf, F Pareja, D N Brown, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 6, 2001
A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriersW W Wang, A B Spurdle, P Kolachana, et al.
JAMA|October 23, 1997
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testingD Shattuck-Eidens, A Oliphant, M McClure, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 17, 1998
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer riskT S Frank, S A Manley, O I Olopade, et al.
American Journal of Human Genetics|June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international studyS L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
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