Gauthier Julie

Centre of Excellence in Neuromics, Universite de Montreal

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 11	2011

Other Publications

Article	Year
Effects of plasma from bivalve mollusk species on the in vitro proliferation of the protistan parasite Perkinsus marinus. The Journal of experimental zoology\| PubMed ID: 11857456	2002
Nucleotide sequence of the p53 cDNA of beluga whale (Delphinapterus leucas). Gene\| PubMed ID: 12034505	2002
Catechol-O-methyltransferase Val-108/158-Met gene variants associated with performance on the Wisconsin Card Sorting Test. Archives of general psychiatry\| PubMed ID: 12090821	2002
cDNA cloning and characterization of two iron superoxide dismutases from the oyster parasite Perkinsus marinus. Molecular and biochemical parasitology\| PubMed ID: 12165391	2002
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. American journal of medical genetics. Part A\| PubMed ID: 12655497	2003
Superoxide dismutases from the oyster parasite Perkinsus marinus: purification, biochemical characterization, and development of a plate microassay for activity. Analytical biochemistry\| PubMed ID: 12782041	2003
A serosurvey of leptospirosis in Connecticut peridomestic wildlife. Vector borne and zoonotic diseases (Larchmont, N.Y.)\| PubMed ID: 14733671	2003
Flow cytometric analysis of lectin binding to in vitro-cultured Perkinsus marinus surface carbohydrates. The Journal of parasitology\| PubMed ID: 15270084	2004
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 15389766	2005
Capillary electrophoresis separation of a mixture of chitin and chitosan oligosaccharides derivatized using a modified fluorophore conjugation procedure. Journal of separation science\| PubMed ID: 16138691	2005
Clinical stringency greatly improves mutation detection in Rett syndrome. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques\| PubMed ID: 16225173	2005
Sleep and COMT polymorphism in ADHD children: preliminary actigraphic data. Journal of the American Academy of Child and Adolescent Psychiatry\| PubMed ID: 16865041	2006
Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Neuroscience research\| PubMed ID: 17897745	2007
Novel de novo SHANK3 mutation in autistic patients. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 18615476	2009
Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Human molecular genetics\| PubMed ID: 18801879	2008
Identification of drostanolone and 17-methyldrostanolone metabolites produced by cryopreserved human hepatocytes. Steroids\| PubMed ID: 19056412	2009
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation. The New England journal of medicine\| PubMed ID: 19196676	2009
No association between SRGAP3/MEGAP haploinsufficiency and mental retardation. Archives of neurology\| PubMed ID: 19433673	2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. Annals of neurology\| PubMed ID: 19557857	2009
[De novo mutations in SYNGAP1 associated with non-syndromic mental retardation]. MÃ©decine sciences : M/S\| PubMed ID: 20188038	2010
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 20385823	2010
De novo truncating mutation in Kinesin 17 associated with schizophrenia. Biological psychiatry\| PubMed ID: 20646681	2010
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. American journal of human genetics\| PubMed ID: 20797689	2010
Role of GacA in virulence of Vibrio vulnificus. Microbiology (Reading, England)\| PubMed ID: 20817642	2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Science translational medicine\| PubMed ID: 20844286	2010
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. American journal of human genetics\| PubMed ID: 20950788	2010
Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis. Archives of neurology\| PubMed ID: 21220648	2011
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism. Biological psychiatry\| PubMed ID: 21237447	2011
Intellectual disability without epilepsy associated with STXBP1 disruption. European journal of human genetics : EJHG\| PubMed ID: 21364700	2011
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. American journal of human genetics\| PubMed ID: 21376300	2011
A population genetic approach to mapping neurological disorder genes using deep resequencing. PLoS genetics\| PubMed ID: 21383861	2011
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia. Human genetics\| PubMed ID: 21424692	2011
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function. Human molecular genetics\| PubMed ID: 21441247	2011
Increased exonic de novo mutation rate in individuals with schizophrenia. Nature genetics\| PubMed ID: 21743468	2011
Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy. European journal of human genetics : EJHG\| PubMed ID: 22258530	2012