Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk
scientific article published on 4 July 2016
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author: Keitaro Matsuo, Dale Sandler, Georgia Chenevix-Trench, Aleksandra Gentry-Maharaj, Jolanta Lissowska, Cezary Cybulski, Hoda Anton-Culver, Argyrios Ziogas, Stacey J Winham, Allan Jensen, Jack A. Taylor, Hui-Yi Lin, Sara H Olson, Anna Jakubowska, Susan J. Ramus, Usha Menon, Paul D P Pharoah, Joellen M Schildkraut, Jan Lubiński, Alvaro Monteiro, Nicolas Wentzensen, Louise A. Brinton, Angela Brooks-Wilson, Joe Dennis, Elisa V. Bandera, Irene Orlow, Shelley S. Tworoger, Xiao-Ou Shu, Julie M. Cunningham, Mary Anne Rossing, Roberta B Ness, Jacek Gronwald, Celeste Leigh Pearce, Kirsten Moysich, Catherine M Phelan, Kathryn L Terry, Elizabeth M Poole, Linda E Kelemen, Simon A Gayther, Brooke L Fridley, Ellen L Goode, Anna H. Wu, Daniel W. Cramer, Estrid Høgdall, Edwin Severin Iversen, Jr., Thomas A Sellers, Douglas A Levine, Michael E. Carney, Penelope M. Webb, Wei Zheng, Ailith Pirie, Maria Bisogna, Zhihua Chen, Beth Karlan, Honglin Song, Soo Hwang Teo, Yin Ling Woo, Australian Ovarian Cancer Study, Ovarian Cancer Association Consortium, Madalene A Earp, Aimee A D'Aloisio, Jennifer A Doherty, Marc T Goodman, Andrew Berchuck, Tanja Pejovic, AOCS Group, Robert P Edwards, Gustavo A Mendoza-Fandino, Lynne R. Wilkens, Pamela J. Thompson, Peter Kraft
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