Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers
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author: Gareth Evans, Heli Nevanlinna, Dominique Stoppa-Lyonnet, Georgia Chenevix-Trench, Peter Devilee, Marie-Agnès Collonge-Rame, Daphne Gschwantler-Kaulich, Christina G Selkirk, Tuomas Heikkinen, Sylvie Mazoyer, Hans Ehrencrona, Amanda Spurdle, Nicoline Hoogerbrugge, Tomasz Byrski, Anna Jakubowska, Susan M Domchek, Diana Eccles, Jan Lubiński, Lesley McGuffog, Susan L Neuhausen, Olufunmilayo Olopade, Douglas F. Easton, Jonathan Beesley, Fergus J. Couch, Debra Frost, Xianshu Wang, Claudine Isaacs, Antonis C Antoniou, Nadine M Tung, Judy E. Garber, Tomasz Huzarski, Rosalind Eeles, Noralane Lindor, Mary B. Daly, Patricia A. Ganz, Timothy R Rebbeck, Juul T Wijnen, Marinus J Blok, Margreet G.E.M. Ausems, Maria Adelaide Caligo, Gail E Tomlinson, Joanne L Blum, Clare Teresa Oliver-Williams, Louise Izatt, Carol Chu, Christine Lasset, SWE-BRCA, Mads Thomassen, Sue Healey, Olga M Sinilnikova, Olga M Sinilnikova, Arvid Carlsson, Susan Peock, Rosemarie Davidson, Pascal Pujol, Fiona Lalloo, Bruno Buecher, Muriel Belotti, Laure Barjhoux, Matti A. Rookus, Helena Jernström, Annelie Liljegren, Christian F. Singer, Hanne Meijers-Heijboer, Kate Nathanson, Mieke Kriege, Senno Verhoef, Theo A M van Os
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