G
Guy A. Rouleau
Researcher at Montreal Neurological Institute and Hospital
Publications - 935
Citations - 75050
Guy A. Rouleau is an academic researcher from Montreal Neurological Institute and Hospital. The author has contributed to research in topics: Gene & Genome-wide association study. The author has an hindex of 129, co-authored 884 publications receiving 65892 citations. Previous affiliations of Guy A. Rouleau include Utrecht University & University of Helsinki.
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Journal ArticleDOI
Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study
Janos Kalman,Sergi Papiol,Sergi Papiol,Andreas J. Forstner,Andreas J. Forstner,Urs Heilbronner,Urs Heilbronner,Franziska Degenhardt,Jana Strohmaier,Mazda Adli,Kristina Adorjan,Nirmala Akula,Martin Alda,Heike Anderson-Schmidt,Heike Anderson-Schmidt,Till F. M. Andlauer,Ion Anghelescu,Raffaella Ardau,Bárbara Arias,Volker Arolt,Jean-Michel Aubry,Lena Backlund,Kim Bartholdi,Michael Bauer,Bernhard T. Baune,Thomas Becker,Frank Bellivier,Antonio Benabarre,Susanne Bengesser,Abesh Kumar Bhattacharjee,Joanna M. Biernacka,Armin Birner,Clara Brichant-Petitjean,Monika Budde,Pablo Cervantes,Caterina Chillotti,Sven Cichon,Sven Cichon,Scott R. Clark,Francesc Colom,Ashley L. Comes,Cristiana Cruceanu,Cristiana Cruceanu,Piotr M. Czerski,Udo Dannlowski,Alexandre Dayer,Maria Del Zompo,Jay Raymond DePaulo,Detlef E. Dietrich,Bruno Etain,Thomas Ethofer,Peter Falkai,Andreas J. Fallgatter,Christian Figge,Laura Flatau,Here Folkerts,Louise Frisén,Mark A. Frye,Janice M. Fullerton,Janice M. Fullerton,Katrin Gade,Katrin Gade,Sébastien Gard,Julie Garnham,Fernando S. Goes,Maria Grigoroiu-Serbanescu,Anna Gryaznova,Maria Hake,Joanna Hauser,Stefan Herms,Stefan Herms,Per Hoffmann,Per Hoffmann,Liping Hou,Markus Jäger,Stéphane Jamain,Esther Jiménez,Georg Juckel,Jean-Pierre Kahn,Layla Kassem,John R. Kelsoe,Sarah Kittel-Schneider,Sebastian Kliwicki,Farah Klohn-Sagatholislam,Manfred Koller,Barbara König,Carsten Konrad,N. Lackner,Gonzalo Laje,Mikael Landén,Mikael Landén,Fabian U. Lang,Catharina Lavebratt,Marion Leboyer,Susan G. Leckband,Mario Maj,Mirko Manchia,Mirko Manchia,Lina Martinsson,Michael McCarthy,Susan L. McElroy,Francis J. McMahon,Philip B. Mitchell,Philip B. Mitchell,Marina Mitjans,Francis M. Mondimore,Palmiero Monteleone,Vanessa Nieratschker,Caroline M. Nievergelt,Tomas Novak,Tomas Novak,Urban Ösby,Andrea Pfennig,James B. Potash,Daniela Reich-Erkelenz,Andreas Reif,Jens Reimer,Eva Z. Reininghaus,Markus Reitt,Stephan Ripke,Stephan Ripke,Guy A. Rouleau,Janusz K. Rybakowski,Martin Schalling,Harald Scherk,Max Schmauß,Peter R. Schofield,Peter R. Schofield,K Oliver Schubert,Eva C. Schulte,Sybille Schulz,Fanny Senner,Giovanni Severino,Tatyana Shekhtman,Paul D. Shilling,Christian Simhandl,Claire Slaney,Carsten Spitzer,Alessio Squassina,Thomas Stamm,Sophia Stegmaier,Sebastian Stierl,Pavla Stopkova,Andreas Thiel,Sarah K. Tighe,Alfonso Tortorella,Gustavo Turecki,Eduard Vieta,Julia Veeh,Martin von Hagen,Moritz E. Wigand,Jens Wiltfang,Stephanie H. Witt,Adam Wright,Adam Wright,Peter P. Zandi,Jörg Zimmermann,Markus M. Nöthen,Marcella Rietschel,Thomas G. Schulze +159 more
TL;DR: It is evaluated whether an increased polygenic burden of BD‐ and schizophrenia (SCZ)‐associated risk variants is associated with an earlier AAO in BD patients.
Journal ArticleDOI
Whole exome sequencing identifies novel predisposing genes in neural tube defects.
Philippe Lemay,Patrizia De Marco,M. Traverso,Elisa Merello,Alexandre Dionne-Laporte,Dan Spiegelman,Edouard Henrion,Ousmane Diallo,François Audibert,Jacques L. Michaud,Armando Cama,Guy A. Rouleau,Zoha Kibar,Valeria Capra +13 more
TL;DR: The clinical presentation is diverse and dependent on the site and severity of the original defect on the embryonic axis, and the etiology of NTD is multifactorial involving environmental factors and genetic variants that remain largely unknown.
Journal ArticleDOI
The ongoing dissection of the genetic architecture of autistic spectrum disorder.
Rob F Gillis,Guy A. Rouleau +1 more
TL;DR: Examining data from case/control studies and classic genetic epidemiological approaches are used to gain insights into the genetic architecture of ASD to elucidate the precise role de novo mutations play in disorders traditionally thought to have resulted from polygenic or common disease, common variants inheritance.
Journal ArticleDOI
Familial congenital mirror movements: report of a large 4-generation family.
Myriam Srour,Maxime Philibert,M. H. Dion,Antoine Duquette,Francois Richer,Guy A. Rouleau,Sylvain Chouinard +6 more
TL;DR: A large 4-generation family with congenital mirror movements not associated with other neurologic abnormalities is found, and transmission is autosomal dominant with high but incomplete penetrance, higher in males than in females.
Journal ArticleDOI
Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohort.
Anne Noreau,Jean-Baptiste Rivière,Sabrina Diab,Patrick A. Dion,Michel Panisset,Valérie Soland,Nicolas Jodoin,Mélanie Langlois,Sylvain Chouinard,Nicolas Dupré,Guy A. Rouleau +10 more
TL;DR: The goal of this study was to evaluate the possible involvement of the GBA mutations in a FrenchCanadian PD cohort and to suggest that haploinsufficiency of GBA may predispose to PD.