Rouleau, Guy A.

A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

Myers, R. A., Casals, F., Gauthier, J., Hamdan, F. F., Keebler, J., Boyko, A. R., Bustamante, C. D., Piton, A. M., Spiegelman, D., Henrion, E., et al. (2011) · PLoS Genetics

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 97

H3K4 tri-methylation in synapsin genes leads to different expression patterns in bipolar disorder and major depression

Cruceanu, C., Alda, M., Nagy, C., Freemantle, E., Rouleau, G. A., & Turecki, G. (2013) · International Journal of Neuropsychopharmacology

Bipolar Disorder and TreatmentEpigenetics and DNA Methylation

Cited by 93

Genome-wide association study in essential tremor identifies three new loci

Müller, S. H., Girard, S. L., Hopfner, F., Merner, N. D., Bourassa, C. V., Lorenz, D., Clark, L. N., Tittmann, L., Soto-Ortolaza, A. I., Klebe, S., et al. (2016) · Brain

Deep Brain Stimulation and Movement DisordersGenetic Associations and Epidemiology

Cited by 88

Mechanisms Underlying the Hyperexcitability of CA3 and Dentate Gyrus Hippocampal Neurons Derived From Patients With Bipolar Disorder

Stern, S., Sarkar, A., Stern, T., Mei, A., Mendes, A. P. D., Stern, Y., Goldberg, G., Galor, D., Nguyen, T., Randolph-Moore, L., et al. (2020) · Biological Psychiatry

Bipolar Disorder and TreatmentNeuroscience and Neuropharmacology Research

Cited by 59

Association between schizophrenia and genetic variation in DCC: a case–control study

Grant, A., Fathalli, F., Rouleau, G., Joober, R., & Flores, C. (2012) · Schizophrenia Research

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 53

Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness

Perrault, I., Hamdan, F. F., Rio, M., Capo-Chichi, J.-M., Boddaert, N., Décarie, J.-C., Maranda, B., Nabbout, R., Sylvain, M., Lortie, A., et al. (2014) · The American Journal of Human Genetics

Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders

Cited by 50

A New ELOVL4 Mutation in a Case of Spinocerebellar Ataxia With Erythrokeratodermia

Bourassa, C. V., Raskin, S., Serafini, S., Teive, H. A. G., Dion, P. A., & Rouleau, G. A. (2015) · JAMA Neurology

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 42

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

Daoud, H., Suhail, H., Szuto, A., Camu, W., Salachas, F., Meininger, V., Bouchard, J.-P., Dupré, N., Dion, P. A., & Rouleau, G. A. (2012) · Neurobiology of Aging

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 42

A mutation in the RNF170 gene causes autosomal dominant sensory ataxia

Valdmanis, P. N., Dupré, N., Lachance, M., Stochmanski, S. J., Belzil, V. V., Dion, P. A., Thiffault, I., Brais, B., Weston, L., Saint-Amant, L., et al. (2011) · Brain

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 37

DNA hypomethylation of Synapsin II CpG islands associates with increased gene expression in bipolar disorder and major depression

Cruceanu, C., Kutsarova, E., Chen, E. S., Checknita, D. R., Nagy, C., Lopez, J. P., Alda, M., Rouleau, G. A., & Turecki, G. (2016) · BMC Psychiatry

Epigenetics and DNA MethylationBipolar Disorder and Treatment

Cited by 35

Kinin-dependent hypersensitivity reactions in hemodialysis: metabolic and genetic factors

Molinaro, G., Duan, Q. L., Chagnon, M., Moreau, M. E., Simon, P., Clavel, P., Lavaud, S., Boileau, G., Rouleau, G. A., Lepage, Y., et al. (2006) · Kidney International

Coagulation, Bradykinin, Polyphosphates, and AngioedemaDialysis and Renal Disease Management

Cited by 29

Mesocorticolimbic Connectivity and Volumetric Alterations in DCC Mutation Carriers

Vosberg, D. E., Zhang, Y., Menegaux, A., Chalupa, A., Manitt, C., Zehntner, S., Eng, C., DeDuck, K., Allard, D., Durand, F., et al. (2018) · The Journal of Neuroscience

Neurotransmitter Receptor Influence on BehaviorAxon Guidance and Neuronal Signaling

Cited by 25

Autism spectrum disorders associated with X chromosome markers in French-Canadian males

Gauthier, J., Joober, R., Dubé, M.-P., St-Onge, J., Bonnel, A., Gariépy, D., Laurent, S., Najafee, R., Lacasse, H., St-Charles, L., et al. (2006) · Molecular Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 23

Chromosome 11‐q24 region in Tourette syndrome: Association and linkage disequilibrium study in the French Canadian population

Díaz‐Anzaldúa, A., Rivière, J., Dubé, M., Joober, R., Saint‐Onge, J., Dion, Y., Lespérance, P., Richer, F., Chouinard, S., Rouleau, G. A., et al. (2005) · American Journal of Medical Genetics Part A

Obsessive-Compulsive Spectrum DisordersGenetic Associations and Epidemiology

Cited by 11

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2022) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Kwon, S., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2023) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8

Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre

Horowitz, K., Fotopoulos, N. H., Mistry, A. J., Simo, J., Medeiros, M., Bucco, I. D., Ginsberg, M., Dwosh, E., La Piana, R., Rouleau, G. A., et al. (2025) · Journal of Medical Genetics

Genomics and Rare DiseasesGenetic Neurodegenerative Diseases

Cited by 5

Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre

Horowitz, K., Fotopoulos, N. H., Mistry, A. J., Simo, J., Medeiros, M., Bucco, I. D., Ginsberg, M., Dwosh, E., La Piana, R., Rouleau, G. A., et al. (2024) · Journal of Medical Genetics

Genomics and Rare DiseasesGenetic Neurodegenerative Diseases

Cited by 5