Simon Girard, Ph.D. - Publications

Psychology Université de Montréal, Montréal, Canada 
Perception, plasticity

35 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Charbonneau G, Bertone A, Véronneau M, Girard S, Pelland M, Mottron L, Lepore F, Collignon O. Within- and Cross-Modal Integration and Attention in the Autism Spectrum. Journal of Autism and Developmental Disorders. PMID 31538259 DOI: 10.1007/S10803-019-04221-8  1
2016 Girard SL, Bourassa CV, Lemieux Perreault LP, Legault MA, Barhdadi A, Ambalavanan A, Brendgen M, Vitaro F, Noreau A, Dionne G, Tremblay RE, Dion PA, Boivin M, Dubé MP, Rouleau GA. Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals. Plos One. 11: e0164212. PMID 27723766 DOI: 10.1371/Journal.Pone.0164212  1
2016 Gan-Or Z, Mohsin N, Girard SL, Montplaisir JY, Ambalavanan A, Strong S, Mallett V, Laurent SB, Bourassa CV, Boivin M, Langlois M, Arnulf I, Högl B, Frauscher B, Monaca C, et al. The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder. Neurobiology of Aging. PMID 27131830 DOI: 10.1016/J.Neurobiolaging.2016.03.029  1
2015 Ambalavanan A, Girard SL, Ahn K, Zhou S, Dionne-Laporte A, Spiegelman D, Bourassa CV, Gauthier J, Hamdan FF, Xiong L, Dion PA, Joober R, Rapoport J, Rouleau GA. De novo variants in sporadic cases of childhood onset schizophrenia. European Journal of Human Genetics : Ejhg. PMID 26508570 DOI: 10.1038/Ejhg.2015.218  1
2015 Girard SL, Dion PA, Bourassa CV, Geoffroy S, Lachance-Touchette P, Barhdadi A, Langlois M, Joober R, Krebs MO, Dubé MP, Rouleau GA. Mutation burden of rare variants in schizophrenia candidate genes. Plos One. 10: e0128988. PMID 26039597 DOI: 10.1371/Journal.Pone.0128988  1
2015 Grote D, Moison C, Duhamel S, Chagraoui J, Girard S, Yang J, Mayotte N, Coulombe Y, Masson JY, Brown GW, Meloche S, Sauvageau G. E4F1 is a master regulator of CHK1-mediated functions. Cell Reports. 11: 210-9. PMID 25843717 DOI: 10.1016/J.Celrep.2015.03.019  1
2015 Legault MA, Girard S, Lemieux Perreault LP, Rouleau GA, Dubé MP. Comparison of sequencing based CNV discovery methods using monozygotic twin quartets. Plos One. 10: e0122287. PMID 25812131 DOI: 10.1371/Journal.Pone.0122287  1
2015 Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Levert A, Vidal S, André-Guimont C, Camu W, et al. Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24: 1363-73. PMID 25343993 DOI: 10.1093/Hmg/Ddu545  1
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Girard SL, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306  1
2014 Bordeleau ME, Aucagne R, Chagraoui J, Girard S, Mayotte N, Bonneil E, Thibault P, Pabst C, Bergeron A, Barabé F, Hébert J, Sauvageau M, Boutonnet C, Meloche S, Sauvageau G. UBAP2L is a novel BMI1-interacting protein essential for hematopoietic stem cell activity. Blood. 124: 2362-9. PMID 25185265 DOI: 10.1182/Blood-2014-01-548651  1
2014 Girard SL, Rouleau GA. Genome-wide association study in FTD: divide to conquer. The Lancet. Neurology. 13: 643-4. PMID 24943334 DOI: 10.1016/S1474-4422(14)70070-5  1
2013 Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Girard SL, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864  1
2013 Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, de Maillard T, Grenier JC, Grenier JC, Gbeha E, Hamdan FF, Girard S, Spinella JF, Larivière M, Saillour V, Healy J, et al. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. Plos Genetics. 9: e1003815. PMID 24086152 DOI: 10.1371/Journal.Pgen.1003815  1
2013 Jouan L, Girard SL, Dobrzeniecka S, Ambalavanan A, Krebs MO, Joober R, Gauthier J, Dion PA, Rouleau GA. Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the disease. Behavioral and Brain Functions : Bbf. 9: 9. PMID 23425335 DOI: 10.1186/1744-9081-9-9  1
2013 Girard S, Pelland M, Lepore F, Collignon O. Impact of the spatial congruence of redundant targets on within-modal and cross-modal integration. Experimental Brain Research. 224: 275-85. PMID 23183636 DOI: 10.1007/S00221-012-3308-0  1
2013 Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Girard S, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69  1
2012 Phéron X, Girard S, Boukenter A, Brichard B, Delepine-Lesoille S, Bertrand J, Ouerdane Y. High γ-ray dose radiation effects on the performances of Brillouin scattering based optical fiber sensors. Optics Express. 20: 26978-85. PMID 23187553  0.52
2012 Merner ND, Girard SL, Catoire H, Bourassa CV, Belzil VV, Rivière JB, Hince P, Levert A, Dionne-Laporte A, Spiegelman D, Noreau A, Diab S, Szuto A, Fournier H, Raelson J, et al. Exome sequencing identifies FUS mutations as a cause of essential tremor. American Journal of Human Genetics. 91: 313-9. PMID 22863194 DOI: 10.1016/J.Ajhg.2012.07.002  1
2012 Girard SL, Dion PA, Rouleau GA. Schizophrenia genetics: putting all the pieces together. Current Neurology and Neuroscience Reports. 12: 261-6. PMID 22456906 DOI: 10.1007/S11910-012-0266-7  1
2011 Girard SL, Gauthier J, Noreau A, Xiong L, Zhou S, Jouan L, Dionne-Laporte A, Spiegelman D, Henrion E, Diallo O, Thibodeau P, Bachand I, Bao JY, Tong AH, Lin CH, et al. Increased exonic de novo mutation rate in individuals with schizophrenia. Nature Genetics. 43: 860-3. PMID 21743468 DOI: 10.1038/Ng.886  1
2011 Catoire H, Dion PA, Xiong L, Amari M, Gaudet R, Girard SL, Noreau A, Gaspar C, Turecki G, Montplaisir JY, Parker JA, Rouleau GA. Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis. Annals of Neurology. 70: 170-5. PMID 21710629 DOI: 10.1002/Ana.22435  1
2011 Chagraoui J, Hébert J, Girard S, Sauvageau G. An anticlastogenic function for the Polycomb Group gene Bmi1. Proceedings of the National Academy of Sciences of the United States of America. 108: 5284-9. PMID 21402923 DOI: 10.1073/Pnas.1014263108  1
2011 Girard SL, Xiong L, Dion PA, Rouleau GA. Where are the missing pieces of the schizophrenia genetics puzzle? Current Opinion in Genetics & Development. 21: 310-6. PMID 21277191 DOI: 10.1016/J.Gde.2011.01.001  1
2011 Girard S, Collignon O, Lepore F. Multisensory gain within and across hemispaces in simple and choice reaction time paradigms. Experimental Brain Research. 214: 1-8. PMID 21161190 DOI: 10.1007/S00221-010-2515-9  1
2011 Wilhelm BT, Briau M, Austin P, Faubert A, Boucher G, Chagnon P, Hope K, Girard S, Mayotte N, Landry JR, Hébert J, Sauvageau G. RNA-seq analysis of 2 closely related leukemia clones that differ in their self-renewal capacity. Blood. 117: e27-38. PMID 20980679 DOI: 10.1182/Blood-2010-07-293332  1
2010 Fortier S, Bilodeau M, Macrae T, Laverdure JP, Azcoitia V, Girard S, Chagraoui J, Ringuette N, Hébert J, Krosl J, Mayotte N, Sauvageau G. Genome-wide interrogation of Mammalian stem cell fate determinants by nested chromosome deletions. Plos Genetics. 6: e1001241. PMID 21170304 DOI: 10.1371/Journal.Pgen.1001241  1
2010 Krosl J, Mamo A, Chagraoui J, Wilhelm BT, Girard S, Louis I, Lessard J, Perreault C, Sauvageau G. A mutant allele of the Swi/Snf member BAF250a determines the pool size of fetal liver hemopoietic stem cell populations. Blood. 116: 1678-84. PMID 20522713 DOI: 10.1182/Blood-2010-03-273862  1
2010 Srour M, Rivière JB, Pham JM, Dubé MP, Girard S, Morin S, Dion PA, Asselin G, Rochefort D, Hince P, Diab S, Sharafaddinzadeh N, Chouinard S, Théoret H, Charron F, et al. Mutations in DCC cause congenital mirror movements. Science (New York, N.Y.). 328: 592. PMID 20431009 DOI: 10.1126/Science.1186463  1
2010 Collignon O, Girard S, Gosselin F, Saint-Amour D, Lepore F, Lassonde M. Women process multisensory emotion expressions more efficiently than men. Neuropsychologia. 48: 220-5. PMID 19761782 DOI: 10.1016/J.Neuropsychologia.2009.09.007  1
2009 Xiong L, Catoire H, Dion P, Gaspar C, Lafrenière RG, Girard SL, Levchenko A, Rivière JB, Fiori L, St-Onge J, Bachand I, Thibodeau P, Allen R, Earley C, Turecki G, et al. MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels. Human Molecular Genetics. 18: 1065-74. PMID 19126776 DOI: 10.1093/Hmg/Ddn443  1
2009 Levchenko A, Montplaisir JY, Asselin G, Provost S, Girard SL, Xiong L, Lemyre E, St-Onge J, Thibodeau P, Desautels A, Turecki G, Gaspar C, Dubé MP, Rouleau GA. Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 40-50. PMID 18946881 DOI: 10.1002/Mds.22263  1
2008 Collignon O, Girard S, Gosselin F, Roy S, Saint-Amour D, Lassonde M, Lepore F. Audio-visual integration of emotion expression. Brain Research. 1242: 126-35. PMID 18495094 DOI: 10.1016/J.Brainres.2008.04.023  1
2007 Bilodeau M, Girard S, Hébert J, Sauvageau G. A retroviral strategy that efficiently creates chromosomal deletions in mammalian cells. Nature Methods. 4: 263-8. PMID 17277782 DOI: 10.1038/Nmeth1011  1
2006 Chagraoui J, Niessen SL, Lessard J, Girard S, Coulombe P, Sauvageau M, Meloche S, Sauvageau G. E4F1: a novel candidate factor for mediating BMI1 function in primitive hematopoietic cells. Genes & Development. 20: 2110-20. PMID 16882984 DOI: 10.1101/Gad.1453406  1
2006 Mamo A, Krosl J, Kroon E, Bijl J, Thompson A, Mayotte N, Girard S, Bisaillon R, Beslu N, Featherstone M, Sauvageau G. Molecular dissection of Meis1 reveals 2 domains required for leukemia induction and a key role for Hoxa gene activation. Blood. 108: 622-9. PMID 16469876 DOI: 10.1182/Blood-2005-06-2244  1
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