Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer
Nature Genetics2012Vol. 44(6), pp. 685–689
Citations Over TimeTop 11% of 2012 papers
Christopher E. Barbieri, Sylvan C. Baca, Michael S. Lawrence, Francesca Demichelis, Mirjam Blattner, Jean‐Philippe Theurillat, Thomas A. White, Petar Stojanov, Eliezer M. Van Allen, Nicolas Stransky, Elizabeth Nickerson, Sung‐Suk Chae, Gunther Boysen, Daniel Auclair, Robert C. Onofrio, Kyung Park, Naoki Kitabayashi, Theresa Y. MacDonald, Karen L. Sheikh, Terry Vuong, Candace Guiducci, Kristian Cibulskis, Andrey Sivachenko, Scott L. Carter, Gordon Saksena, Douglas Voet, Wasay M Hussain, Alex H. Ramos, Wendy Winckler, Michelle C Redman, Kristin Ardlie, Ashutosh Tewari, Juan Miguel Mosquera, Niels J. Rupp, Peter J. Wild, Holger Moch, Colm Morrissey, Peter S. Nelson, Philip W. Kantoff, Stacey Gabriel, Todd R. Golub, Matthew Meyerson, Eric S. Lander, Gad Getz, Mark A. Rubin, Levi A. Garraway
Related Papers
- → Recurrent Somatic Mutations in Human Gastric Cancers Identified by Whole Exome Sequencing(2012)2 cited
- → Breast cancer predisposing germline mutations identified by exome sequencing(2017)1 cited
- Identifying New Genes for Inherited Breast Cancer by Exome Sequencing(2014)
- → Su2129 Whole Exome Sequencing Revealed Putative Driver Mutations in Esophageal Cancer(2013)