Foulkes WD - Search Results

1

Patient Experience with a Gynecologic Oncology-Initiated Genetic Testing Model for Women with Tubo-Ovarian Cancer.

Sadinsky MB, Power J, Ambrosio E, Palma L, Zeng X, Foulkes WD, Weber E. Sadinsky MB, et al. Among authors: foulkes wd. Curr Oncol. 2022 May 15;29(5):3565-3575. doi: 10.3390/curroncol29050288. Curr Oncol. 2022. PMID: 35621678 Free PMC article.

2

Hereditary breast and ovarian cancer: epidemiology, genetics, screening and predictive testing.

Foulkes WD, Narod SA. Foulkes WD, et al. Clin Invest Med. 1995 Dec;18(6):473-83. Clin Invest Med. 1995. PMID: 8714791 Review.

3

Risk assessment & genetic testing.

Chappuis PO, Foulkes WD. Chappuis PO, et al. Among authors: foulkes wd. Cancer Treat Res. 2002;107:29-59. doi: 10.1007/978-1-4757-3587-1_2. Cancer Treat Res. 2002. PMID: 11775456 Review.

4

Application of BRCA1 and BRCA2 mutation carrier prediction models in breast and/or ovarian cancer families of French Canadian descent.

Oros KK, Ghadirian P, Maugard CM, Perret C, Paredes Y, Mes-Masson AM, Foulkes WD, Provencher D, Tonin PN. Oros KK, et al. Among authors: foulkes wd. Clin Genet. 2006 Oct;70(4):320-9. doi: 10.1111/j.1399-0004.2006.00673.x. Clin Genet. 2006. PMID: 16965326

5

Synchronous occult cancers of the endometrium and fallopian tube in an MSH2 mutation carrier at time of prophylactic surgery.

Palma L, Marcus V, Gilbert L, Chong G, Foulkes WD. Palma L, et al. Among authors: foulkes wd. Gynecol Oncol. 2008 Dec;111(3):575-8. doi: 10.1016/j.ygyno.2008.08.002. Epub 2008 Sep 20. Gynecol Oncol. 2008. PMID: 18805575

6

High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.

Chong G, Jarry J, Marcus V, Thiffault I, Winocour S, Monczak Y, Drouin R, Latreille J, Australie K, Bapat B, Gordon PH, Giguère Y, Gologan A, Galiatsatos P, Jass JR, Wong N, Zaor S, Palma L, Kasprzak L, Tischkowitz M, Foulkes WD. Chong G, et al. Among authors: foulkes wd. Hum Mutat. 2009 Aug;30(8):E797-812. doi: 10.1002/humu.21056. Hum Mutat. 2009. PMID: 19459153

7

Clinical implications of next-generation sequencing for cancer medicine.

Shuen A, Foulkes WD. Shuen A, et al. Among authors: foulkes wd. Curr Oncol. 2010 Oct;17(5):39-42. doi: 10.3747/co.v17i5.630. Curr Oncol. 2010. PMID: 20975877 Free PMC article. No abstract available.

8

Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations.

Bordeleau L, Lipscombe L, Lubinski J, Ghadirian P, Foulkes WD, Neuhausen S, Ainsworth P, Pollak M, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group. Bordeleau L, et al. Among authors: foulkes wd. Cancer. 2011 May 1;117(9):1812-8. doi: 10.1002/cncr.25595. Epub 2010 Nov 10. Cancer. 2011. PMID: 21509758 Free PMC article.

9

A survey of APC mutations in Quebec.

Jarry J, Brunet JS, Laframboise R, Drouin R, Latreille J, Richard C, Gekas J, Maranda B, Monczak Y, Wong N, Pouchet C, Zaor S, Kasprzak L, Palma L, Wu MK, Tischkowitz M, Foulkes WD, Chong G. Jarry J, et al. Among authors: foulkes wd. Fam Cancer. 2011 Dec;10(4):659-65. doi: 10.1007/s10689-011-9468-4. Fam Cancer. 2011. PMID: 21779980

10

Reading between the lines: a comparison of responders and non-responders to a family history questionnaire and implications for cancer genetic counselling.

Appleby-Tagoe JH, Foulkes WD, Palma L. Appleby-Tagoe JH, et al. Among authors: foulkes wd. J Genet Couns. 2012 Apr;21(2):273-91. doi: 10.1007/s10897-011-9399-0. Epub 2011 Aug 16. J Genet Couns. 2012. PMID: 21845493

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