Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm

Janice L. Farlow, Hai Lin, Laura Sauerbeck, Dongbing Lai, Daniel L. Koller, Elizabeth Pugh, Kurt Hetrick, Hua Ling, Rachel Kleinloog, Pieter Van Der Vlies, Patrick Deelen, Morris A. Swertz, Bon H. Verweij, Luca Regli, Gabriel J.E. Rinkel, Ynte M. Ruigrok, Kimberly Doheny, Yunlong Liu, Tatiana Foroud, Joseph BroderickDaniel Woo, Brett Kissela, Dawn Kleindorfer, Alex Schneider, Mario Zuccarello, Andrew Ringer, Ranjan Deka, Robert D. Brown, John Huston, Irene Mesissner, David Wiebers, Adnan I. Qureshi, Peter A. Rasmussen, E. Sander Connolly, Ralph L. Sacco, Marc Malkaff, Troy D. Payner, Gary G. Ferguson, E. Francois Aldrich, Guy Rouleau, Craig S. Anderson, Edward W. Mee, Graeme J. Hankey, Neville Knuckey, Peter L. Reilly, John D. Laidlaw, Paul D'Urso, Jeffrey V. Rosenfeld, Michael K. Morgan, Nicholas Dorsch, Michael Besser, H. Hunt Batjer, Michael T. Richard, Amin Kassam, Gary K. Steinberg, S. Claiborne Johnston, Nerissa U. Ko, Steven L. Giannotta, Neal F. Kassell, Bradford B. Worrall, Kenneth C. Lui, Aaron Dumont, David L. Tirschell, Anthony M. Kaufmann, Winfield S. Fisher, Khaled Mohamed Abdel Aziz, Arthur L. Day, Rose Du, Christopher Ogilvy, Stephen B. Lewis, Kieran P. Murphy, Martin Radvany, Dheerah Gandhi, Lynda Lisabeth, Aditya Pandey, Lewis Morgenstern, Colin Derdeyn, Carl Langefeld, Joan Bailey-Wilson

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