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Guy A. Rouleau

Researcher at Montreal Neurological Institute and Hospital

Publications -  935
Citations -  75050

Guy A. Rouleau is an academic researcher from Montreal Neurological Institute and Hospital. The author has contributed to research in topics: Gene & Genome-wide association study. The author has an hindex of 129, co-authored 884 publications receiving 65892 citations. Previous affiliations of Guy A. Rouleau include Utrecht University & University of Helsinki.

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Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia

TL;DR: The clinical description and genetic analyses of a Greek family with four individuals affected with a complicated form of hereditary spastic paraplegia and a recessive pattern of inheritance led to the identification of a homozygous 25 bp deletion predicted to lead to a frameshift and premature stop codon in the SPG7 gene, encoding paraplegin.
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Epigenetic Regulation of Synapsin Genes in Mood Disorders

TL;DR: Evidence is found that enrichment of H3K4me3—an epigenetic mark associated with increased transcription—at the promoters of SYN1 and SYN2, but not SYN3 is correlated with increased expression of these genes in the prefrontal cortex of patients with BD and MDD compared with controls.
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HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders.

Sigrid Le Clerc, +141 more
- 08 Sep 2021 - 
TL;DR: In this article, a GWAS performed by the International Consortium on Lithium Genetics (ConLiGen) has recently identified genetic markers associated with treatment responses to Li in the human leukocyte antigens (HLA) region.
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Identification of informative strains and provisional QTL mapping of amphetamine (AMPH)-induced locomotion in recombinant congenic strains (RCS) of mice.

TL;DR: Using recombinant congenic strains of mice derived from A/J and C57BL/6J to identify potential quantitative trait loci associated with AMPH-TDIST may help to identify suitable candidate genes relevant to human disorders where mesolimbic dopamine dysregulation has been postulated.