Advanced search

Authors whose works are in public domain in at least one jurisdiction

List of works by Thomas Bourgeron

51-100 of 108 results

Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders

Genomic architecture of human neuroanatomical diversity

scientific article published on 16 September 2014

Dynamics in enzymatic protein complexes offer a novel principle for the regulation of melatonin synthesis in the human pineal gland

article

Human Pluripotent Stem Cell-derived Cortical Neurons for High Throughput Medication Screening in Autism: A Proof of Concept Study in SHANK3 Haploinsufficiency Syndrome

scientific article

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

scientific article (published 2005-12-01)

Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders

scientific article published on January 2006

Vitamin d in the general population of young adults with autism in the faroe islands

scientific article

Sequencing ASMT identifies rare mutations in Chinese Han patients with autism

scientific article

Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites.

scientific article

Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas

scientific article published on 13 May 2014

Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway

scientific article

Y chromosome haplogroups in autistic subjects

scientific article published in January 2002

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

scientific article

Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability

scientific article

Analysis of X chromosome inactivation in autism spectrum disorders

scientific article published on September 2008

Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution

scientific article published in November 2001

A high frequency of Y chromosome deletions in males with nonidiopathic infertility

scientific article published on 01 October 1999

Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations

scientific article (publication date: 4 March 2011)

Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia.

scientific article

Genetics of autism: from genome scans to candidate genes

scientific article published in November 2003

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls

scientific article

Recording Mouse Ultrasonic Vocalizations to Evaluate Social Communication

scientific article

The asymmetry of telomere replication contributes to replicative senescence heterogeneity

scientific article

An investigation of ribosomal protein L10 gene in autism spectrum disorders

scientific article

Lack of replication of previous autism spectrum disorder GWAS hits in European populations

scientific article published on 15 July 2016

Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae

scientific article published on 3 August 2010

Social communication in mice--are there optimal cage conditions?

scientific article

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability.

scientific article published on 23 September 2015

Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia

scientific article (publication date: 15 May 2001)

The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture

scientific article published on May 14, 2015

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures

scientific article published on 3 September 2015

Heterozygous FA2H mutations in autism spectrum disorders

scientific article

Autism: more evidence of a genetic cause

scientific article published in February 2009

Three-dimensional Quantification of Dendritic Spines from Pyramidal Neurons Derived from Human Induced Pluripotent Stem Cells

scientific article published on 10 October 2015

Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials

scientific article published in August 2014

High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters

scientific article

Alterations in synapsis formation and function in autism disorders

scientific article published in January 2008

Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders

scientific article

Génétique etbusiness : défendons la iberté de critique !

scientific article published on 01 May 2007

Mitochondrial function and male infertility

scientific article

Against Le Packing: A Consensus Statement

Genetic control of spermatogenesis: Y chromosome and male infertility

scientific article published on 01 May 1999

Genetic markers in psychiatric genetics

scientific article

Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele

scientific article published on March 2010

Differential neural circuitry behind autism subtypes with imbalanced social-communicative and restricted repetitive behavior symptoms

Mass-spectrometry analysis of the human pineal proteome during night and day and in autism

scientific article published on 23 December 2020

The meaning of significant mean group differences for biomarker discovery

scientific article published on 18 November 2021

Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles

scientific article published on 01 June 2020

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability

scientific article published on 07 January 2021

Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders

scientific article published on 07 January 2021