Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of …

Yosr Hamdi,Penny Soucy,Karoline B Kuchenbaeker,Tomi Pastinen,Arnaud Droit,Audrey Lemašon,Julian Adlard, Kristiina Aittomńki,Irene L Andrulis,Adalgeir Arason,Norbert Arnold,Banu K Arun,Jacopo Azzollini,Anita Bane,Laure Barjhoux,Daniel Barrowdale,Javier Benitez,Pascaline Berthet,Marinus J Blok,Kristie Bobolis, ValÚrie Bonadona,Bernardo Bonanni,Angela R Bradbury,Carole Brewer,Bruno Buecher,Saundra S Buys,Maria A Caligo,Jocelyne Chiquette,Wendy K Chung,Kathleen BM Claes,Mary B Daly,Francesca Damiola,Rosemarie Davidson,Miguel De la Hoya,Kim De Leeneer,Orland Diez,Yuan Chun Ding,Riccardo Dolcetti,Susan M Domchek,Cecilia M Dorfling,Diana Eccles,Ros Eeles,Zakaria Einbeigi,Bent Ejlertsen,Christoph Engel,D Gareth Evans,Lidia Feliubadalo,Lenka Foretova,Florentia Fostira,William D Foulkes,George Fountzilas,Eitan Friedman,Debra Frost,Pamela Ganschow,Patricia A Ganz,Judy Garber,Simon A Gayther,Anne-Marie Gerdes,Gord Glendon,Andrew K Godwin,David E Goldgar,Mark H Greene,Jacek Gronwald,Eric Hahnen,Ute Hamann,Thomas VO Hansen,Steven Hart,John L Hays,Frans BL Hogervorst,Peter J Hulick,Evgeny N Imyanitov,Claudine Isaacs,Louise Izatt,Anna Jakubowska,Paul James,Ramunas Janavicius,Uffe Birk Jensen,Esther M John,Vijai Joseph,Walter Just,Katarzyna Kaczmarek,Beth Y Karlan,Carolien M Kets,Judy Kirk,Mieke Kriege,Yael Laitman,Conxi Lazaro,Goska Leslie,Jenny Lester,Fabienne Lesueur,Annelie Liljegren,Niklas Loman,Jennifer T Loud,Siranoush Manoukian,Milena Mariani,Sylvie Mazoyer,Lesley McGuffog,Hanne EJ Meijers-Heijboer,Alfons Meindl,Austin Miller,Marco Montagna,Anna Marie Mulligan,Katherine L Nathanson,Susan L Neuhausen,Heli Nevanlinna,Robert L Nussbaum,Edith Olah,Olufunmilayo I Olopade,Kai-ren Ong,Jan C Oosterwijk,Ana Osorio,Laura Papi,Sue Kyung Park,Inge Sokilde Pedersen,Bernard Peissel,Pedro Perez Segura,Paolo Peterlongo,Catherine M Phelan,Paolo Radice,Johanna Rantala,Christine Rappaport-Fuerhauser,Gad Rennert,Andrea Richardson,Mark Robson,Gustavo C Rodriguez,Matti A Rookus,Rita Katharina Schmutzler,Nicolas Sevenet,Payal D Shah,Christian F Singer,Thomas P Slavin,Katie Snape,Johanna Sokolowska,Melissa Southey,Amanda B Spurdle,Zsofia Stadler,Dominique Stoppa-Lyonnet,Grzegorz Sukiennicki,Christian Sutter,Yen Tan,Muy-Kheng Tea,Manuel R Teixeira,Alex TeulÚ,Soo-Hwang Teo,Mary Beth Terry,Mads Thomassen,Laima Tihomirova,Marc Tischkowitz,Silvia Tognazzo,Amanda Ewart Toland

Breast cancer research and treatment(2017)

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摘要
Purpose Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part, explain the underlying phenotypic variation associated with many complex diseases. To investigate whether common variants associated with DAE were involved in breast cancer susceptibility among BRCA1 and BRCA2 mutation carriers, a list of 175 genes was developed based of their involvement in cancer-related pathways. Methods Using data from a genome-wide map of SNPs associated with allelic expression, we assessed the association of ~320 SNPs located in the vicinity of these genes with breast and ovarian cancer risks in 15,252 BRCA1 and 8211 BRCA2 mutation carriers ascertained from 54 studies participating in the Consortium of Investigators of Modifiers of BRCA1/2. Results We identified a …
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