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Guy A. Rouleau

ResearcherPublications, citations & collaboration network

Guy A. Rouleau is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Guy A. Rouleau have?

ScholarIQindexed works

Guy A. Rouleau has 1,277 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Guy A. Rouleau have?

ScholarIQcitation count

Guy A. Rouleau has 96,358 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Guy A. Rouleau?

ScholarIQh-index

Guy A. Rouleau has an h-index of 147 in OpenAlex.

What is the i10-index of Guy A. Rouleau?

ScholarIQi10-index

Guy A. Rouleau has an i10-index of 766 in OpenAlex.

What is the ORCID of Guy A. Rouleau?

ScholarIQorcid

The ORCID for Guy A. Rouleau is on the source record.

What is the OpenAlex record for Guy A. Rouleau?

ScholarIQopenalex

The OpenAlex for Guy A. Rouleau is on the source record.

What are the most-cited papers on Guy A. Rouleau?

ScholarIQmost cited works
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D.R. Rosen, Teepu Siddique, David T. Patterson, Denise A. Figlewicz, Peter C. Sapp, Afif Hentati, Deirdre Donaldson, Jun Goto, J. O'Regan, Han‐Xiang Deng, Zohra Rahmani, Aldis Krizus, Diane McKenna‐Yasek, Annarueber Cayabyab, Sandra M. Gaston, Ralph Berger, Rudolph E. Tanzi, John Halperin, Brian Herzfeldt, R. van den Bergh, W.‐Y. Hung, Thomas D. Bird, Gang Deng, Donald W. Mulder, Celestine Smyth, Nigel G. Laing, Edwin Soriano, Margaret A. Pericak‐Vance, Jonathan Haines, Guy A. Rouleau, James S. Gusella, H. Robert Horvitz, Robert Brown
Nature. 19937,074 Citations
Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc, Eric Tamrazian, Charles Vanderburg, C Russ, Adam Davis, James M. Gilchrist, Edward J. Kasarskis, T. L. Munsat, Paul N. Valdmanis, Guy A. Rouleau, Betsy A. Hosler, Pietro Cortelli, Pieter J. de Jong, Yuko Yoshinaga, J. L. Haines, Margaret A. Pericak‐Vance, J Yan, Nicola Ticozzi, Teepu Siddique, D. McKenna‐Yasek, Peter C. Sapp, H. Robert Horvitz, John E. Landers, Robert H. Brown
Science. 20092,568 Citations
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
Edor Kabashi, Paul N. Valdmanis, Patrick A. Dion, Dan Spiegelman, Brendan J. McConkey, Christine Vande Velde, Jean‐Pierre Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, François Salachas, Pierre‐François Pradat, William Camu, Vincent Meininger, Nicolas Dupré, Guy A. Rouleau
Nature Genetics. 20081,541 Citations
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Peter C. Sapp, Patrick A. Dion, Claire S. Leblond, Julien Couthouis, Yifan Lu, Quanli Wang, Brian J. Krueger, Zhong Ren, Jonathan Keebler, Yujun Han, Shawn Levy, Braden Boone, Jack R. Wimbish, Lindsay L. Waite, Angela L. Jones, John P. Carulli, Kelly L. Williams, John F. Staropoli, Winnie Xin, Alessandra Chesi, Alya R. Raphael, Diane McKenna‐Yasek, Janet Cady, J.M.B.V. de Jong, Kevin P. Kenna, Bradley Smith, Simon Topp, Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein
Science. 2015990 CitationsOPEN ACCESS
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
Claire S. Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, Serge Lumbroso, Fabienne Giuliano, Coline Stordeur, Christel Depienne, Kévin Mouzat, Dalila Pinto, Jennifer Howe, Nathalie Lemière, Christelle M. Durand, Jessica Guibert, Elodie Ey, Roberto Toro, Hugo Peyre, Alexandre Mathieu, Frédérique Amsellem, Maria Råstam, I. Carina Gillberg, Gudrun Rappold, Richard Holt, Anthony P. Monaco, Elena Maestrini, Pilar Galán, Delphine Héron, Aurélia Jacquette, Alexandra Afenjar, Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron
PLoS Genetics. 2014672 CitationsOPEN ACCESS

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