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Abreu, Traci Jester, Zarela Molle-Rios, Sirish Palle, Ellen Scherl, John H. Patel, Joel Pekow, Shehzad Ahmed Saeed, John F. Kuemmerle, Mark Lazarev, Ellen Li, Peter J. Kappelman, Jeffry Katz, Richard Kellermayer, John F. Denson, Tanvi Dhere, Heba Iskandar, Gerald W. Datta, Antonio Quiros, Jenifer Seminerio, Emebet Mengesha, Jonathan Steven Alexander, Robert Baldassano, Sharon Dudley-Brown, Raymond K. Somineni, Sini Nagpal, Suresh Venkateswaran, David J.
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Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Simon, Flora Tassone, Celso Arango, David Fraguas, Sixto García-Miñaur, Jaume Morey-Canyelles, Jordi Rosell, Damià H. Hooper, Kelly Schoch, Vandana Shashi, Tony J. Kates, Raoul Belzeaux, Tiffany Busa, Nicole Philip, Linda E. Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori-Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stephan Eliez, Corrado Sandini, Maude Schneider, Frédérique Béna, Kevin M. Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Prasad, Eileen Daly, Maria Gudbrandsen, Clodagh M. Duijff, Ania Fiksinski, Hayley Moss, Maria Niarchou, Kieran C. Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M. van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koen Devriendt, Elfi Vergaelen, Annick Vogels, T. Costain, Chelsea Lowther, Rens Evers, Therese van Amelsvoort, Esther D.A. Walters, Wolfram Demaerel, Erik Boot, Nancy J. Salmons, Oanh Tran, Peter Holmans, Antonio F. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R. Warren, Michael John Owen, Pankaj Chopra, David J. Chow, Marianne Bernadette van den Bree, Beverly S. Richard Johnston, Thomas Monfeuga, Donna M. Isabelle Cleynen, Worrawat Engchuan, Matthew S. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion