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Julie Gauthier

Showing results (11-20 of 62) with videos related to

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Journal of the American Academy of Child and Adolescent Psychiatry|July 26, 2006
Sleep and COMT polymorphism in ADHD children: preliminary actigraphic dataReut Gruber, Natalie Grizenko, George Schwartz, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Mutation screening of FOXP2 in individuals diagnosed with autistic disorderJulie Gauthier, Ridha Joober, Laurent Mottron, et al.
Frontiers in Allergy|April 7, 2022
Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot StudyFrançois Marceau, Georges-Etienne Rivard, Jacques Hébert, et al.
JIMD Reports|September 14, 2022
Intermittent neurologic decompensation: An underrecognized presentation of tyrosine hydroxylase deficiencyMarjolaine Champagne, Gabriella A Horvath, Sébastien Perreault, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individualsAmélie Piton, Loubna Jouan, Daniel Rochefort, et al.
Neuroscience Research|September 28, 2007
Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic probandIsabelle Martin, Julie Gauthier, Marcello D'Amelio, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec populationJulie Gauthier, Anna Bonnel, Judith St-Onge, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 23, 2020
The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assaysFanny Lassalle, Yohann Jourdy, Loubna Jouan, et al.
Genome|November 19, 2013
Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorderCristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, et al.
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Journal of the American Academy of Child and Adolescent Psychiatry|July 26, 2006
Sleep and COMT polymorphism in ADHD children: preliminary actigraphic dataReut Gruber, Natalie Grizenko, George Schwartz, et al.
American Journal of Medical Genetics. Part A|March 26, 2003
Mutation screening of FOXP2 in individuals diagnosed with autistic disorderJulie Gauthier, Ridha Joober, Laurent Mottron, et al.
Frontiers in Allergy|April 7, 2022
Picomolar Sensitivity Analysis of Multiple Bradykinin-Related Peptides in the Blood Plasma of Patients With Hereditary Angioedema in Remission: A Pilot StudyFrançois Marceau, Georges-Etienne Rivard, Jacques Hébert, et al.
JIMD Reports|September 14, 2022
Intermittent neurologic decompensation: An underrecognized presentation of tyrosine hydroxylase deficiencyMarjolaine Champagne, Gabriella A Horvath, Sébastien Perreault, et al.
European Journal of Human Genetics : EJHG|November 22, 2012
Analysis of the effects of rare variants on splicing identifies alterations in GABAA receptor genes in autism spectrum disorder individualsAmélie Piton, Loubna Jouan, Daniel Rochefort, et al.
Neuroscience Research|September 28, 2007
Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic probandIsabelle Martin, Julie Gauthier, Marcello D'Amelio, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec populationJulie Gauthier, Anna Bonnel, Judith St-Onge, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 23, 2020
The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assaysFanny Lassalle, Yohann Jourdy, Loubna Jouan, et al.
Genome|November 19, 2013
Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorderCristiana Cruceanu, Amirthagowri Ambalavanan, Dan Spiegelman, et al.
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Pageof 7