| Increased exonic de novo mutation rate in individuals with schizophrenia SL Girard, J Gauthier, A Noreau, L Xiong, S Zhou, L Jouan, ... Nature genetics 43 (9), 860-863, 2011 | 474 | 2011 |
| High rate of recurrent de novo mutations in developmental and epileptic encephalopathies FF Hamdan, CT Myers, P Cossette, P Lemay, D Spiegelman, AD Laporte, ... The American Journal of Human Genetics 101 (5), 664-685, 2017 | 400 | 2017 |
| Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture LK Davis, D Yu, CL Keenan, ER Gamazon, AI Konkashbaev, EM Derks, ... PLoS genetics 9 (10), e1003864, 2013 | 318 | 2013 |
| Genome-wide association study of Tourette's syndrome JM Scharf, D Yu, CA Mathews, BM Neale, SE Stewart, JA Fagerness, ... Molecular psychiatry 18 (6), 721-728, 2013 | 218 | 2013 |
| Exome sequencing identifies FUS mutations as a cause of essential tremor ND Merner, SL Girard, H Catoire, CV Bourassa, VV Belzil, JB Rivière, ... The American Journal of Human Genetics 91 (2), 313-319, 2012 | 209 | 2012 |
| Mutations in DCC cause congenital mirror movements M Srour, JB Rivière, JMT Pham, MP Dubé, S Girard, S Morin, PA Dion, ... Science 328 (5978), 592-592, 2010 | 202 | 2010 |
| Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis HM Kaneb, AW Folkmann, VV Belzil, LE Jao, CS Leblond, SL Girard, ... Human molecular genetics 24 (5), 1363-1373, 2015 | 148 | 2015 |
| Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette’s syndrome and OCD D Yu, CA Mathews, JM Scharf, BM Neale, LK Davis, ER Gamazon, ... American Journal of Psychiatry 172 (1), 82-93, 2015 | 147 | 2015 |
| Functional variants of POC5 identified in patients with idiopathic scoliosis SA Patten, P Margaritte-Jeannin, JC Bernard, E Alix, A Labalme, ... The Journal of clinical investigation 125 (3), 1124-1128, 2015 | 113 | 2015 |
| MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels L Xiong, H Catoire, P Dion, C Gaspar, RG Lafrenière, SL Girard, ... Human molecular genetics 18 (6), 1065-1074, 2009 | 111 | 2009 |
| Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis H Catoire, PA Dion, L Xiong, M Amari, R Gaudet, SL Girard, A Noreau, ... Annals of neurology 70 (1), 170-175, 2011 | 102 | 2011 |
| Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans F Casals, A Hodgkinson, J Hussin, Y Idaghdour, V Bruat, T de Maillard, ... PLoS genetics 9 (9), e1003815, 2013 | 97 | 2013 |
| De novo variants in sporadic cases of childhood onset schizophrenia A Ambalavanan, SL Girard, K Ahn, S Zhou, A Dionne-Laporte, ... European Journal of Human Genetics 24 (6), 944-948, 2016 | 94 | 2016 |
| Genome-wide association study in essential tremor identifies three new loci SH Müller, SL Girard, F Hopfner, ND Merner, CV Bourassa, D Lorenz, ... Brain 139 (12), 3163-3169, 2016 | 92 | 2016 |
| Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ... The Lancet Neurology 17 (8), 699-708, 2018 | 89 | 2018 |
| Autosomal‐dominant locus for restless legs syndrome in French‐Canadians on chromosome 16p12. 1 A Levchenko, JY Montplaisir, G Asselin, S Provost, SL Girard, L Xiong, ... Movement disorders 24 (1), 40-50, 2009 | 68 | 2009 |
| Schizophrenia genetics: putting all the pieces together SL Girard, PA Dion, GA Rouleau Current neurology and neuroscience reports 12, 261-266, 2012 | 58 | 2012 |
| Global characterization of copy number variants in epilepsy patients from whole genome sequencing J Monlong, SL Girard, C Meloche, M Cadieux-Dion, DM Andrade, ... PLoS genetics 14 (4), e1007285, 2018 | 54 | 2018 |
| Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals SL Girard, CV Bourassa, LP Lemieux Perreault, MA Legault, A Barhdadi, ... PLoS One 11 (10), e0164212, 2016 | 51 | 2016 |
| Parkinson’s disease genetic loci in rapid eye movement sleep behavior disorder Z Gan-Or, SL Girard, A Noreau, CS Leblond, JF Gagnon, I Arnulf, ... Journal of Molecular Neuroscience 56, 617-622, 2015 | 50 | 2015 |
