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

Antonis C. Antoniou(Cancer Research UK), Paul D.P. Pharoah(University of Cambridge), Steven A. Narod(University of Toronto), Harvey A. Risch(Yale University), J.E. Eyfjörd(University of Iceland), John L. Hopper(The University of Melbourne), Niklas Loman(Lund University), Håkan Olsson(Lund University), Oskar T. Johannsson(Lund University), Åke Borg(Lund University), Barbara Pasini, Paolo Radice(IFOM), Siranoush Manoukian, Diana Eccles(Princess Anne Hospital), Nelson L.S. Tang(Chinese University of Hong Kong), Edith Oláh(National Institute of Oncology), Hoda Anton‐Culver(University of California, Irvine), Ellen Warner(University of Toronto), Jan Lubiński(International Hereditary Cancer Center), Jacek Gronwald(International Hereditary Cancer Center), Bohdan Górski(International Hereditary Cancer Center), Hrafn Tulinius(University of Iceland), Steinunn Thorlacius(University of Iceland), Hannaleena Eerola(Helsinki University Hospital), Heli Nevanlinna, Kirsi Syrjäkoski(Tampere University Hospital), Olli Kallioniemi(Tampere University Hospital), Deborah J. Thompson(Cancer Research UK), Chris Evans(Cancer Research UK), Julian Peto(Institute of Cancer Research), Fiona Lalloo(St. Mary's Hospital), D. Gareth Evans(St. Mary's Hospital), Douglas F. Easton(Cancer Research UK)
The American Journal of Human Genetics
April 23, 2003
Cited by 3,679Open Access
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