William D. Foulkes
Program in Cancer Genetics
Departments of Oncology and Human Genetics
McGill University
Montreal
Canada
Name/email consistency: high
- Extending the phenotypes associated with DICER1 mutations. Foulkes, W.D., Bahubeshi, A., Hamel, N., Pasini, B., Asioli, S., Baynam, G., Choong, C.S., Charles, A., Frieder, R.P., Dishop, M.K., Graf, N., Ekim, M., Bouron-Dal Soglio, D., Arseneau, J., Young, R.H., Sabbaghian, N., Srivastava, A., Tischkowitz, M.D., Priest, J.R. Hum. Mutat. (2011)
- Triple-negative breast cancer. Foulkes, W.D., Smith, I.E., Reis-Filho, J.S. N. Engl. J. Med. (2010)
- Tumor size is an unreliable predictor of prognosis in basal-like breast cancers and does not correlate closely with lymph node status. Foulkes, W.D., Grainge, M.J., Rakha, E.A., Green, A.R., Ellis, I.O. Breast Cancer Res. Treat. (2009)
- BRCA1--sowing the seeds crooked in the furrow. Foulkes, W.D. Nat. Genet. (2008)
- Inherited susceptibility to common cancers. Foulkes, W.D. N. Engl. J. Med. (2008)
- Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women. Foulkes, W.D., Ghadirian, P., Akbari, M.R., Hamel, N., Giroux, S., Sabbaghian, N., Darnel, A., Royer, R., Poll, A., Fafard, E., Robidoux, A., Martin, G., Bismar, T.A., Tischkowitz, M., Rousseau, F., Narod, S.A. Breast Cancer Res. (2007)
- Clinically relevant biology of hereditary breast cancer. Foulkes, W.D. Semin. Oncol. (2007)
- BRCA1 and BRCA2: chemosensitivity, treatment outcomes and prognosis. Foulkes, W.D. Fam. Cancer (2006)
- BRCA1 functions as a breast stem cell regulator. Foulkes, W.D. J. Med. Genet. (2004)
- The prognostic implication of the basal-like (cyclin E high/p27 low/p53+/glomeruloid-microvascular-proliferation+) phenotype of BRCA1-related breast cancer. Foulkes, W.D., Brunet, J.S., Stefansson, I.M., Straume, O., Chappuis, P.O., Bégin, L.R., Hamel, N., Goffin, J.R., Wong, N., Trudel, M., Kapusta, L., Porter, P., Akslen, L.A. Cancer Res. (2004)
- Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: the influence of age, grade, and histological type. Foulkes, W.D., Metcalfe, K., Sun, P., Hanna, W.M., Lynch, H.T., Ghadirian, P., Tung, N., Olopade, O.I., Weber, B.L., McLennan, J., Olivotto, I.A., Bégin, L.R., Narod, S.A. Clin. Cancer Res. (2004)
- Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. Foulkes, W.D., Stefansson, I.M., Chappuis, P.O., Bégin, L.R., Goffin, J.R., Wong, N., Trudel, M., Akslen, L.A. J. Natl. Cancer Inst. (2003)
- Disruption of the expected positive correlation between breast tumor size and lymph node status in BRCA1-related breast carcinoma. Foulkes, W.D., Metcalfe, K., Hanna, W., Lynch, H.T., Ghadirian, P., Tung, N., Olopade, O., Weber, B., McLennan, J., Olivotto, I.A., Sun, P., Chappuis, P.O., Bégin, L.R., Brunet, J.S., Narod, S.A. Cancer (2003)
- Of mice and women. Foulkes, W.D. Cancer. Cell (2002)
- The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population. Foulkes, W.D., Thiffault, I., Gruber, S.B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C.M., Bonner, J.D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F.A., Gaff, C.L., Paillerets, B.B., Gregersen, P.K., Weitzel, J.N., Gordon, P.H., MacNamara, E., King, M.C., Hampel, H., De La Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N.A. Am. J. Hum. Genet. (2002)
- The contribution of inherited factors to the clinicopathological features and behavior of breast cancer. Foulkes, W.D., Rosenblatt, J., Chappuis, P.O. J. Mammary. Gland. Biol. Neoplasia (2001)