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