Steven Narod
Steven Narod
Canada Research Chair in Breast Cancer; Director, Familial Breast Cancer Research Unit, WCRI
Verified email at - Homepage
Cited by
Cited by
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
Y Miki, J Swensen, D Shattuck-Eidens, PA Futreal, K Harshman, ...
Science 266 (5182), 66-71, 1994
Triple-negative breast cancer: clinical features and patterns of recurrence
R Dent, M Trudeau, KI Pritchard, WM Hanna, HK Kahn, CA Sawka, ...
Clinical cancer research 13 (15), 4429-4434, 2007
Identification of the breast cancer susceptibility gene BRCA2
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, ...
Nature 378 (6559), 789-792, 1995
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies
A Antoniou, PDP Pharoah, S Narod, HA Risch, JE Eyfjord, JL Hopper, ...
The American Journal of Human Genetics 72 (5), 1117-1130, 2003
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
D Ford, DF Easton, M Stratton, S Narod, D Goldgar, P Devilee, DT Bishop, ...
The American Journal of Human Genetics 62 (3), 676-689, 1998
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
R Wooster, SL Neuhausen, J Mangion, Y Quirk, D Ford, N Collins, ...
Science 265 (5181), 2088-2090, 1994
Risks of cancer in BRCA1-mutation carriers
D Ford, DF Easton, DT Bishop, SA Narod, DE Goldgar
The Lancet 343 (8899), 692-695, 1994
Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations
TR Rebbeck, HT Lynch, SL Neuhausen, SA Narod, L Van't Veer, ...
New England Journal of Medicine 346 (21), 1616-1622, 2002
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
RJ Hung, JD McKay, V Gaborieau, P Boffetta, M Hashibe, D Zaridze, ...
Nature 452 (7187), 633-637, 2008
Surveillance of BRCA1 and BRCA2 mutation carriers with magnetic resonance imaging, ultrasound, mammography, and clinical breast examination
E Warner, DB Plewes, KA Hill, PA Causer, JT Zubovits, RA Jong, ...
Jama 292 (11), 1317-1325, 2004
Bilateral Prophylactic Mastectomy Reduces Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: The PROSE Study Group
TR Rebbeck, T Friebel, HT Lynch, SL Neuhausen, L van’t Veer, JE Garber, ...
Journal of Clinical Oncology 22 (6), 1055-1062, 2004
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations
CHEK2-Breast Cancer Consortium
Nature genetics 31 (1), 55, 2002
BRCA1 and BRCA2: 1994 and beyond
SA Narod, WD Foulkes
Nature Reviews Cancer 4 (9), 665-676, 2004
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
HA Risch, JR McLaughlin, DEC Cole, B Rosen, L Bradley, E Kwan, ...
The American Journal of Human Genetics 68 (3), 700-710, 2001
BRCA1 testing in families with hereditary breast-ovarian cancer: a prospective study of patient decision making and outcomes
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, ...
Jama 275 (24), 1885-1892, 1996
Twenty five year follow-up for breast cancer incidence and mortality of the Canadian National Breast Screening Study: randomised screening trial
AB Miller, C Wall, CJ Baines, P Sun, T To, SA Narod
Bmj 348, 2014
Oral contraceptives and the risk of hereditary ovarian cancer
SA Narod, H Risch, R Moslehi, A DÝrum, S Neuhausen, H Olsson, ...
New England Journal of Medicine 339 (7), 424-428, 1998
Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers
TR Rebbeck, AM Levin, A Eisen, C Snyder, P Watson, L Cannon-Albright, ...
Journal of the National Cancer Institute 91 (17), 1475-1479, 1999
Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin–cohort study in Ontario, Canada
HA Risch, JR McLaughlin, DEC Cole, B Rosen, L Bradley, I Fan, J Tang, ...
Journal of the National Cancer Institute 98 (23), 1694-1706, 2006
Familial breast-ovarian cancer locus on chromosome 17q12-q23
GM Lenoir, H Lynch, P Watson, T Conway, J Lynch, S Narod, J Feunteun
The Lancet 338 (8759), 82-83, 1991
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