| Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions J Winkelmann, B Schormair, P Lichtner, S Ripke, L Xiong, S Jalilzadeh, ... Nature genetics 39 (8), 1000-1006, 2007 | 782 | 2007 |
| LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ... Molecular psychiatry 12 (12), 1129-1139, 2007 | 489 | 2007 |
| 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 | 478 | 2011 |
| De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia J Gauthier, N Champagne, RG Lafrenière, L Xiong, D Spiegelman, ... Proceedings of the National Academy of Sciences 107 (17), 7863-7868, 2010 | 431 | 2010 |
| Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia A Piton, J Gauthier, FF Hamdan, RG Lafreniere, Y Yang, E Henrion, ... Molecular psychiatry 16 (8), 867-880, 2011 | 357 | 2011 |
| PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome B Schormair, D Kemlink, D Roeske, G Eckstein, L Xiong, P Lichtner, ... Nature genetics 40 (8), 946-948, 2008 | 314 | 2008 |
| Direct measure of the de novo mutation rate in autism and schizophrenia cohorts P Awadalla, J Gauthier, RA Myers, F Casals, FF Hamdan, AR Griffing, ... The American Journal of Human Genetics 87 (3), 316-324, 2010 | 290 | 2010 |
| Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia J Tarabeux, O Kebir, J Gauthier, FF Hamdan, L Xiong, A Piton, ... Translational psychiatry 1 (11), e55-e55, 2011 | 258 | 2011 |
| Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ... The Lancet Neurology 16 (11), 898-907, 2017 | 220 | 2017 |
| Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12. 1 J Winkelmann, D Czamara, B Schormair, F Knauf, EC Schulte, ... PLoS genetics 7 (7), e1002171, 2011 | 218 | 2011 |
| Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity A Desautels, G Turecki, J Montplaisir, L Xiong, AS Walters, BL Ehrenberg, ... Archives of neurology 62 (4), 591-596, 2005 | 167 | 2005 |
| A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13 A Levchenko, S Provost, JY Montplaisir, L Xiong, J St-Onge, P Thibodeau, ... Neurology 67 (5), 900-901, 2006 | 133 | 2006 |
| Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12 L Xiong, M Labuda, DS Li, TJ Hudson, R Desbiens, G Patry, S Verret, ... The American Journal of Human Genetics 65 (6), 1698-1710, 1999 | 121 | 1999 |
| 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 | 114 | 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 | 105 | 2011 |
| Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism L Mottron, P Duret, S Mueller, RD Moore, B Forgeot d’Arc, S Jacquemont, ... Molecular autism 6, 1-19, 2015 | 96 | 2015 |
| 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 |
| The 14q restless legs syndrome locus in the French Canadian population A Levchenko, JY Montplaisir, MP Dubé, JB Riviere, J St‐Onge, G Turecki, ... Annals of Neurology: Official Journal of the American Neurological …, 2004 | 94 | 2004 |
| Familial association of neuropsychological traits in patients with generalized and partial seizure disorders M Levav, AF Mirsky, J Herault, L Xiong, N Amir, E Andermann Journal of Clinical and Experimental Neuropsychology 24 (3), 311-326, 2002 | 93 | 2002 |
| Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12 SF Berkovic, JM Serratosa, HA Phillips, L Xiong, E Andermann, ... Epilepsia 45 (9), 1054-1060, 2004 | 90 | 2004 |
Jacques Montplaisirprofesseur titulaire, département Psychiatrie, Université de Montréal在 umontreal.ca 的电子邮件经过验证
