William Foulkes - Dissemin

Papers authored by William Foulkes

This paper is available in a repository.

2015 William D. Foulkes

, Bartha Maria Knoppers, Clare Turnbull

Population genetic testing for cancer susceptibility: founder mutations to genomes

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Leanne de Kock

, Yu Chang Wang, Timothée Revil, Dunarel Badescu, Barbara Rivera

, Nelly Sabbaghian, Mona Wu, Evan Weber, Claudio Sandoval, Saskia M. J. Hopman, Johannes H. M. Merks, Johanna M. van Hagen, Antonia H. M. Bouts, David A. Plager, Aparna Ramasubramanian and 10 other authors

High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome

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John Semple, Kelly A. Metcalfe, Jan Lubinski, Tomasz Huzarski, Jacek Gronwald, Henry T. Lynch, Beth Karlan, Christian F. Singer, Susan L. Neuhausen, Javaid Iqbal, Steven A. Narod, Susan Armel, William Foulkes

, Charis Eng

Does the age of breast cancer diagnosis in first-degree relatives impact on the risk of breast cancer in BRCA1 and BRCA2 mutation carriers?

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This paper was not found in any repository, but could be made available legally by the author.

Christina Gavino, Nancy Hamel, Ji Bin Zeng, Catherine Legault, Marie-Christine Guiot, Jeffrey Chankowsky, Duncan Lejtenyi, Martine Lemire, Isabelle Alarie, Simon Dufresne, Jean-Nicolas Boursiquot, Fiona McIntosh, Mélanie Langelier, Marcel A. Behr, Donald C. Sheppard and 2 other authors

Impaired RASGRF1/ERK–mediated GM-CSF response characterizes CARD9 deficiency in French-Canadians

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Olivier Boucherat, Kim Landry-Truchon, F.-A. Berube-Simard, Félix-Antoine Bérubé-Simard, Nicolas Houde, Laurent Beuret, Guillaume Lezmi, William D. Foulkes

, Christophe Delacourt, Jean Charron, Lucie Jeannotte

Epithelial inactivation of Yy1 abrogates lung branching morphogenesis

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Steven A. Narod, Rebecca A. Dent, William D. Foulkes

CCR 20th Anniversary Commentary: Triple-Negative Breast Cancer in 2015-Still in the Ballpark

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T. Tulandi, William D. Foulkes

Hereditary leiomyomatosis and renal cell cancer syndrome

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Antonis C. Antoniou, William D. Foulkes

, Marc Tischkowitz

Breast cancer risk in women with PALB2 mutations in different populations

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A. Schiavi, J. Lavigne, R. Turcotte, L. Karsprzak, L. Kasprzak, N. Dumas, G. Chong, C. Freeman, M. Alameldin, P. Galiatsatos, L. Palma, W. D. Foulkes

Using a family history questionnaire to identify adult patients with increased genetic risk for sarcoma

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Douglas F. Easton, Paul D. P. Pharoah, Antonis C. Antoniou, Marc Tischkowitz, Sean V. Tavtigian, Katherine L. Nathanson, Peter Devilee, Alfons Meindl, Fergus J. Couch, Melissa Southey, David E. Goldgar, D. Gareth R. Evans, Georgia Chenevix-Trench, Nazneen Rahman, Mark Robson and 2 other authors

Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

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Kelly Metcalfe, Henry T. Lynch, William D. Foulkes

, Nadine Tung, Charmaine Kim-Sing, Olufunmilayo I. Olopade, Andrea Eisen, Barry Rosen, Carrie Snyder, Shelley Gershman, Ping Sun, Steven A. Narod

Effect of Oophorectomy on Survival After Breast Cancer inBRCA1andBRCA2Mutation Carriers

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Leanne de Kock

, Harriet Druker, Evan Weber, Nancy Hamel, Jeffrey Traubici, David Malkin, Jocelyne Arseneau, Colin J. R. Stewart, Dorothée Bouron-Dal Soglio, John R. Priest, William D. Foulkes

Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome

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E. Castellsagué, W. D. Foulkes

Lynch syndrome: five unanswered questions: Commentary

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E. Ebo Oost, E. Ebo Oost, Adrian Charles, Yee C. Leung, Catherine S. Choong, Stuart Salfinger, Hein Sonnendecker, Jason Tan, Sharron Townshend, Leora Witkowski, William D. Foulkes

, Colin J. R. Stewart

Ovarian Sex Cord-Stromal Tumors in Patients With Probable or Confirmed Germline DICER1 Mutations:

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Suzanna L. Arcand, Mohammed R. Akbari, Anne-Marie Mes-Masson, Diane Provencher, William D. Foulkes

, Steven A. Narod, Patricia N. Tonin

Germline TP53 mutational spectrum in French Canadians with breast cancer

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

Divya G. Sabapathy, R. Paul Guillerman, Robert C. Orth, Wei Zhang, Yoav Messinger, William Foulkes

, John R. Priest, Ananth V. Annapragada

Radiographic Screening of Infants and Young Children With Genetic Predisposition for Rare Malignancies: DICER1 Mutations and Pleuropulmonary Blastoma

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Alex Rabinovich, Leora Witkowski, Ruthy Shaco-Levi, Mihai Meirovitz, Martin Hasselblatt, William D. Foulkes

Primary rhabdoid tumor of the ovary: When large cells become small cells

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Polymnia Galiatsatos, Heidi Rothenmund, Sylvie Aubin, William D. Foulkes

Psychosocial Impact of Lynch Syndrome on Affected Individuals and Families

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Andrew Berchuck, Leora Witkowski, Martin Hasselblatt, William D. Foulkes

Prophylactic oophorectomy for hereditary small cell carcinoma of the ovary, hypercalcemic type

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Lili Li, Nancy Hamel, Kristi Baker, Michael J. McGuffin, Martin Couillard, Adrian Gologan, Victoria A. Marcus, Bernard Chodirker, Albert Chudley, Camelia Stefanovici, Anne Durandy, Robert A. Hegele, Bing-Jian Feng, David E. Goldgar, Jun Zhu and 7 other authors

A homozygousPMS2founder mutation with an attenuated constitutional mismatch repair deficiency phenotype

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Papers authored by William Foulkes