Thomas Husson

Sotteville-sur-mer, France

Last Updated: 09/26/2026

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Found 12 publications

Trauma re-experiencing episodes during esketamine treatment in patients with treatment-resistant depression and comorbid PTSD: a retrospective case series.

Trauma re-experiencing episodes during esketamine treatment in patients with treatment-resistant depression and comorbid PTSD: a retrospective case series.

Journal: European journal of psychotraumatology

Published: April 01, 2026

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Journal: Journal of medical genetics

Published: April 02, 2024

Esketamine-induced post-traumatic stress disorder flashbacks during treatment-resistant depression indication: is it just a side effect?

Esketamine-induced post-traumatic stress disorder flashbacks during treatment-resistant depression indication: is it just a side effect?

Journal: medRxiv : the preprint server for health sciences

Published: January 31, 2024

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Journal: Annals of neurology

Published: November 16, 2023

Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder.

Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2023

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.

Journal: European journal of human genetics : EJHG

Published: May 10, 2023

Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders.

Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders.

Journal: Human mutation

Published: December 06, 2021

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.

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.

Journal: Psychological medicine

Published: September 28, 2021

Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.

Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.

Journal: Translational psychiatry

Published: December 02, 2019

De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype.

De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype.

Journal: American journal of medical genetics. Part A

Published: October 08, 2019

Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's Disease.

Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's Disease.

Journal: Journal of Alzheimer's disease : JAD

Published: March 26, 2019

Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.

Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.

Journal: Translational psychiatry

Published: February 07, 2018

Showing 1-12 of 12

Last Updated: 09/26/2026