Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

Author:

Antoniou Antonis C.,Sinilnikova Olga M.,McGuffog Lesley,Healey Sue,Nevanlinna Heli,Heikkinen Tuomas,Simard Jacques,Spurdle Amanda B.,Beesley Jonathan,Chen Xiaoqing,Neuhausen Susan L.,Ding Yuan C.,Couch Fergus J.,Wang Xianshu,Fredericksen Zachary,Peterlongo Paolo,Peissel Bernard,Bonanni Bernardo,Viel Alessandra,Bernard Loris,Radice Paolo,Szabo Csilla I.,Foretova Lenka,Zikan Michal,Claes Kathleen,Greene Mark H.,Mai Phuong L.,Rennert Gad,Lejbkowicz Flavio,Andrulis Irene L.,Ozcelik Hilmi,Glendon Gord,Gerdes Anne-Marie,Thomassen Mads,Sunde Lone,Caligo Maria A.,Laitman Yael,Kontorovich Tair,Cohen Shimrit,Kaufman Bella,Dagan Efrat,Baruch Ruth Gershoni,Friedman Eitan,Harbst Katja,Barbany-Bustinza Gisela,Rantala Johanna,Ehrencrona Hans,Karlsson Per,Domchek Susan M.,Nathanson Katherine L.,Osorio Ana,Blanco Ignacio,Lasa Adriana,Benítez Javier,Hamann Ute,Hogervorst Frans B.L.,Rookus Matti A.,Collee J. Margriet,Devilee Peter,Ligtenberg Marjolijn J.,van der Luijt Rob B.,Aalfs Cora M.,Waisfisz Quinten,Wijnen Juul,van Roozendaal Cornelis E.P.,Peock Susan,Cook Margaret,Frost Debra,Oliver Clare,Platte Radka,Evans D. Gareth,Lalloo Fiona,Eeles Rosalind,Izatt Louise,Davidson Rosemarie,Chu Carol,Eccles Diana,Cole Trevor,Hodgson Shirley,Godwin Andrew K.,Stoppa-Lyonnet Dominique,Buecher Bruno,Léoné Mélanie,Bressac-de Paillerets Brigitte,Remenieras Audrey,Caron Olivier,Lenoir Gilbert M.,Sevenet Nicolas,Longy Michel,Ferrer Sandra Fert,Prieur Fabienne,Goldgar David,Miron Alexander,John Esther M.,Buys Saundra S.,Daly Mary B.,Hopper John L.,Terry Mary Beth,Yassin Yosuf,Gschwantler-Kaulich Daphne,Staudigl Christine,Hansen Thomas v. O.,Barkardottir Rosa Bjork,Kirchhoff Tomas,Pal Prodipto,Kosarin Kristi,Offit Kenneth,Piedmonte Marion,Rodriguez Gustavo C.,Wakeley Katie,Boggess John F.,Basil Jack,Schwartz Peter E.,Blank Stephanie V.,Toland Amanda E.,Montagna Marco,Casella Cinzia,Imyanitov Evgeny N.,Allavena Anna,Schmutzler Rita K.,Versmold Beatrix,Engel Christoph,Meindl Alfons,Ditsch Nina,Arnold Norbert,Niederacher Dieter,Deißler Helmut,Fiebig Britta,Suttner Christian,Schönbuchner Ines,Gadzicki Dorothea,Caldes Trinidad,de la Hoya Miguel,Pooley Karen A.,Easton Douglas F.,Chenevix-Trench Georgia

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference26 articles.

1. 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;Antoniou;Am. J. Hum. Genet.,2003

2. The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions;Antoniou;Br. J. Cancer,2008

3. Variation of breast cancer risk among BRCA1/2 carriers;Begg;JAMA,2008

4. Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study;Hopper;Cancer Epidemiol. Biomarkers Prev.,1999

5. The Average Cumulative Risks of Breast and Ovarian Cancer for Carriers of Mutations in BRCA1 and BRCA2 Attending Genetic Counseling Units in Spain;Milne;Clin. Cancer Res.,2008

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