A significant response to neoadjuvant chemotherapy in BRCA1/2 related breast cancer von Chappuis, P O, Goffin, J, Wong, N, Perret, C, Ghadirian, P, Tonin, P N, Foulkes, W D

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Cyclin E expression in breast cancer: predicting germline BRCA1 mutations, prognosis and response to treatment von Chappuis, P. O., Donato, E., Goffin, J. R., Wong, N., Bégin, L. R., Kapusta, L. R., Brunet, J.-S., Porter, P., Foulkes, W. D.

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Impact of a positive family history on diagnosis, management, and survival of breast cancer: different effects across socio-economic groups von Verkooijen, H. M, Rapiti, E, Fioretta, G, Vinh-Hung, V, Keller, J, Benhamou, S, Vlastos, G, Chappuis, P. O, Bouchardy, C

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Impact of familial risk factors on management and survival of early-onset breast cancer: a population-based study von VERKOOIJEN, H. M, CHAPPUIS, P. O, RAPITI, E, VLASTOS, G, FIORETTA, G, SARP, S, SAPPINO, A. P, SCHUBERT, H, BOUCHARDY, C

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Hormonal therapy for oestrogen receptor-negative breast cancer is associated with higher disease-specific mortality von Merglen, A., Verkooijen, H.M., Fioretta, G., Neyroud-Caspar, I., Vinh-Hung, V., Vlastos, G., Chappuis, P.O., Castiglione, M., Rapiti, E., Bouchardy, C.

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Set-up of a population-based familial breast cancer registry in Geneva, Switzerland: validation of first results von Verkooijen, H. M., Fioretta, G., Chappuis, P. O., Vlastos, G., Sappino, A. P., Benhamou, S., Bouchardy, C.

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The influence of familial and hereditary factors on the prognosis of breast cancer von Chappuis, P. O., Rosenblatt, J., Foulkes, W. D.

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Germline BRCA1/2 mutations and p27(Kip1) protein levels independently predict outcome after breast cancer von Chappuis, P O, Kapusta, L, Bégin, L R, Wong, N, Brunet, J S, Narod, S A, Slingerland, J, Foulkes, W D

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Primary node negative breast cancer in BRCA1 mutation carriers has a poor outcome von FOULKES, W. D, CHAPPUIS, P. O, BEGIN, L. R, WONG, N, BRUNET, J.-S, VESPRINI, D, ROZEN, F, YUAN, Z. Q, POLLAK, M. N, KUPERSTEIN, G, NAROD, S. A

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A polymorphism in the ATM gene modulates the penetrance of hereditary non‐polyposis colorectal cancer von Maillet, P., Chappuis, P.O., Vaudan, G., Dobbie, Z., Müller, H., Hutter, P., Sappino, A.‐P.

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Constitutional alterations of the ATM gene in early onset sporadic breast cancer von Maillet, P, Bonnefoi, H, Vaudan-Vutskits, G, Pajk, B, Cufer, T, Foulkes, W D, Chappuis, P O, Sappino, A-P

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Glomeruloid microvascular proliferation is associated with p53 expression, germline BRCA1 mutations and an adverse outcome following breast cancer von Goffin, J R, Straume, O, Chappuis, P O, Brunet, J-S, Bégin, L R, Hamel, N, Wong, N, Akslen, L A, Foulkes, W D

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TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations : Distinctive spectrum and structural distribution von GREENBLATT, Marc S, CHAPPUIS, Pierre O, BOND, Jeffrey P, HAMEL, Nancy, FOULKES, William D

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Re: Magnetic Resonance Imaging and Mammography in Women With a Hereditary Risk of Breast Cancer von Goffin, John, Chappuis, Pierre O., Wong, Nora, Foulkes, William D.

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Prognostic significance of p53 mutation in breast cancer: Frequent detection of non‐missense mutations by yeast functional assay von Chappuis, Pierre O., Estreicher, Anne, Dieterich, Barbara, Bonnefoi, Hervé, Otter, Michèle, Sappino, André‐Pascal, Iggo, Richard

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Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer von Chappuis, PO, Hamel, N, Paradis, A-J, Deschênes, J, Robidoux, A, Potvin, C, Cantin, J, Tonin, P, Ghadirian, P, Foulkes, WD

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The Role of Genetic Factors in the Etiology of Pancreatic Adenocarcinoma: An Update von Chappuis, Pierre O., Ghadirian, Parviz, Foulkes, William D.

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Change in the penetrance of founder BRCA1/2 mutations? A retrospective cohort study von Foulkes, W D, Brunet, J-S, Wong, N, Goffin, J, Chappuis, P O

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Excess of hMLH1 germline mutations in Swiss families with hereditary non‐polyposis colorectal cancer von Hutter, Pierre, Couturier, Alexia, Membrez, Véronique, Joris, François, Sappino, André‐Pascal, Chappuis, Pierre O.

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Re: Population-Based Study of BRCA1 and BRCA2 Mutations in 1035 Unselected Finnish Breast Cancer Patients von Chappuis, Pierre O., Hamel, Nancy, Paradis, Ann-Josée, Deschênes, Jean, Tonin, Patricia N., Ghadirian, Parviz, Foulkes, William D.

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