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Results: 1-5 |
Results: 5

Authors: Segurado, Ricardo Detera-Wadleigh, Sevilla D. Levinson, Douglas F. Lewis, Cathryn M. Gil, Michael Nurnberger, John I., Jr. Craddock, Nick DePaulo, Raymond J. Baron, Miron Gershon, Elliot S. Ekhoolm, Jenny Cichon, Sven Turecki, Gustavo Claes, Stephan Kelsoe, John R. Badenhop, Renee F. Morissette, J. Coon, Hilary Blackwood, Douglas McInnes, L.Allison Foroud, Tatiana Edenberg, Howard J. Reich, Theodore Rice, John P. Goate, Alison McInnis, Melvin G. McMahon, Francis J. Badner, Judith A. Goldin, Lynn R. Bennett, Phil Willour, Virginia L. Zandi, Peter P. Liu, Jianjun Gillam, Conrad Juo, Suh-Hang Berrettini, Wade H. Yoshikawa, Takeo Peltonen, Leena Lönnqvist, Juoko Nöthen, Markus M. Schumacher, Johannes Windemuth, Christine Rietschel, Marcella Proppin, Peter Maier, Wolfgang Alda, Martin Grof, Paul Rouleau, Guy A. Del-Favero, Jurgen Van Broeckhoven, Christine Mendlewicz, Julien Adolfsson, Rolf Spence, M. Anne Luebbert, Hermann Adams, Linda J. Donald, Jennifer A. Mitchell, Philip B. Barden, Nicholas Shink, Eric Byerley, William Muir, Walter Visscher, Peter M. Macgregor, Stuart Gurling, Hugh Kalsi, Gursharan McQuillin, Andrew Escamilla, Michael A. Reus, Victor I. Leon, Pedro Freimer, Nelson B. Ewald, Henrik Kruse, Torben A. Mors, Ole Radhakrishna, Uppala Blouin, Jean-Louis Antonarakis, Stylianos Akarsu, Nurten
Citation: Segurado, Ricardo et al., Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder, American journal of human genetics , 73(1), 2003, pp. 49-62

Authors: Valdmanis, Paul N. Meijer, Inge A. Reynolds, Annie Lei, Adrienne MacLeod, Patrick Schlesinger, David Zatz, Mayana Reid, Evan Dion, Patrick A. Drapeau, Pierre Rouleau, Guy A.
Citation: N. Valdmanis, Paul et al., Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia, American journal of human genetics , 80(1), 2007, pp. 152-161

Authors: Awadalla, Philip Gauthier, Julie Myers, Rachel A. Casals, Ferran Rouleau, Guy A.
Citation: Awadalla, Philip et al., Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts, American journal of human genetics (Online) AJHG , 87(3), 2010, pp. 316-324

Authors: Rouleau, Guy A. Seizinger, Bernd R. Wertelecki, Wladimir Haines, Jonathan L. Superneau, Duane W. Martuza, Robert L. Gusella, lames F.
Citation: A. Rouleau, Guy et al., Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22, American journal of human genetics , 46-I(2), 1990, pp. 323-328

Authors: Fontaine, Bertrand Rouleau, Guy A. Seizinger, Bernd Jewell, Ann F. Hanson, Mark P. Martuza, Robert L. Gusella, James F.
Citation: Fontaine, Bertrand et al., Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting., American journal of human genetics , 47-II(5), 1990, pp. 823-827
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