Kolexia
Husson Thomas Psychiatrie
Husson Thomas
Psychiatrie
Centre Hospitalier du Rouvray
Sotteville-lès-Rouen, France
21 Activités
0 Followers
Scientifique
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Collaborateurs

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Guillin Olivier
Guillin Olivier
Centre Hospitalier du Rouvray, Sotteville-lès-Rouen, France
Rotharmel Maud
Rotharmel Maud
Centre Hospitalier du Rouvray, Sotteville-lès-Rouen, France
Campion Dominique
Campion Dominique
Centre Hospitalier du Rouvray, Sotteville-lès-Rouen, France
Nicolas Gael
Nicolas Gael
Hôpital Charles Nicolle, Rouen, France

Industries

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Lundbeck
1 collaboration(s)
Dernière en 2021
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Dernières activités

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Esketamine-induced post-traumatic stress disorder flashbacks during treatment-resistant depression indication: is it just a side effect?
medRxiv : the preprint server for health sciences   18 janvier 2024
Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.
European journal of human genetics : EJHG   23 octobre 2023
Loss-of-function variants in cause a syndromic neurodevelopmental disorder.
medRxiv : the preprint server for health sciences   16 juin 2023
Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders.
Human mutation   21 août 2022
The priming effect of repetitive transcranial magnetic stimulation on clinical response to electroconvulsive therapy in treatment-resistant depression: a randomized, double-blind, sham-controlled study.
Psychological medicine   28 septembre 2021
STIMAGNECT: Clinical Trial on Efficacy of Repeated Transcranial Magnetic Stimulation (rTMS) to Improve Electroconvulsive Therapy (ECT) in Treatment-Resistant Depression (TRD): STIMAGNECT Study
Essai Clinique (Centre Hospitalier du Rouvray)   17 février 2021
Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's Disease.
Journal of Alzheimer's disease : JAD   27 août 2020
Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.
Translational psychiatry   24 février 2020
De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype.
American journal of medical genetics. Part A   07 février 2020
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.
Translational psychiatry   05 décembre 2018