Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R Delorme

Showing results (31-40 of 41) with videos related to

Pageof 5
Sort By:
Molecular Psychiatry|August 10, 2005
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorderR Delorme, C Betancur, M Wagner, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Nature|May 30, 2014
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmissionT Karayannis, E Au, J C Patel, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Eclinicalmedicine|February 3, 2026
Efficacy, safety, and tolerability of arbaclofen in Autistic children and adolescents, the AIMS-2-TRIALS-CT1: a randomized, double-blind, placebo-controlled phase II trialM Parellada, A San José Cáceres, R Delorme, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2013
Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1S E Stewart, C Mayerfeld, P D Arnold, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|November 20, 2018
Updated European Consensus Statement on diagnosis and treatment of adult ADHDJ J S Kooij, D Bijlenga, L Salerno, et al.
Molecular Psychiatry|August 15, 2012
Genome-wide association study of obsessive-compulsive disorderS E Stewart, D Yu, J M Scharf, et al.
Nature|September 23, 2022
Publisher Correction: Brain charts for the human lifespanR A I Bethlehem, J Seidlitz, S R White, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Molecular Psychiatry|August 10, 2005
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorderR Delorme, C Betancur, M Wagner, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Nature|May 30, 2014
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmissionT Karayannis, E Au, J C Patel, et al.
Molecular Psychiatry|September 16, 2015
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autismM Pilorge, C Fassier, H Le Corronc, et al.
Eclinicalmedicine|February 3, 2026
Efficacy, safety, and tolerability of arbaclofen in Autistic children and adolescents, the AIMS-2-TRIALS-CT1: a randomized, double-blind, placebo-controlled phase II trialM Parellada, A San José Cáceres, R Delorme, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 23, 2013
Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1S E Stewart, C Mayerfeld, P D Arnold, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|November 20, 2018
Updated European Consensus Statement on diagnosis and treatment of adult ADHDJ J S Kooij, D Bijlenga, L Salerno, et al.
Molecular Psychiatry|August 15, 2012
Genome-wide association study of obsessive-compulsive disorderS E Stewart, D Yu, J M Scharf, et al.
Nature|September 23, 2022
Publisher Correction: Brain charts for the human lifespanR A I Bethlehem, J Seidlitz, S R White, et al.
Pageof 5