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Thomas Bourgeron

Professor, gäst

Thomas Bourgeron
Professor, gäst
thomas.bourgeron@gu.se

Postal Address: Su sahlgrenska, 41345 Göteborg
Visiting Address: Blå stråket 5 vån 5 su/sahlgrenska , 41345 Göteborg


Department of Psychiatry and Neurochemistry at Institute of Neuroscience and Physiology (More Information)
Blå stråket 15, vån 3 SU/Sahlgrenska
413 45 Göteborg
031-342 10 00
Visiting Address: Blå stråket 15, vån 3 SU/Sahlgrenska , 413 45 Göteborg

Latest publications

Both rare and common genetic variants contribute to autism in the Faroe Islands.
Claire S Leblond, Freddy Cliquet, Coralie Carton, Guillaume Huguet, Alexandre Mathieu et al.
NPJ genomic medicine, Journal article 2019
Journal article

Anatomy and cell biology of autism spectrum disorder: Lessons from human genetics
K. T. E. Kleijer, G. Huguet, J. Tastet, Thomas Bourgeron, J. P. H. Burbach
Translational Anatomy and Cell Biology of Autism Spectrum Disorder , Springer, Chapter in book 2017
Chapter in book

Behavioural phenotypes and neural circuit dysfunctions in mouse models of autism spectrum disorder
A. T. Ferhat, S. Halbedl, M. J. Schmeisser, M. J. Kas, Thomas Bourgeron et al.
Translational Anatomy and Cell Biology of Autism Spectrum Disorder , Chapter in book 2017
Chapter in book

Gender differences in autism spectrum disorders: Divergence among specific core symptoms.
Anita Beggiato, Hugo Peyre, Anna Maruani, Isabelle Scheid, Maria Rastam et al.
Autism research : official journal of the International Society for Autism Research, Journal article 2017
Journal article

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani et al.
Molecular psychiatry, Journal article 2017
Journal article

The Genetics of Autism Spectrum Disorders
G. Huguet, M. Benabou, Thomas Bourgeron
A Time for Metabolism and Hormones. Paolo Sassone-Corsi, Yves Christen (red.), Springer, Chapter in book 2016
Chapter in book

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures
Anna Maruani, Guillaume Huguet, Anita Beggiato, Monique Elmaleh, Roberto Toro et al.
American Journal of Medical Genetics. Part A, Journal article 2015
Journal article

Vitamin D in the General Population of Young Adults with Autism in the Faroe Islands.
Eva Kočovská, Guðrið Andorsdóttir, Pál Weihe, Jónrit Halling, Elisabeth Fernell et al.
Journal of autism and developmental disorders, Journal article 2014
Journal article

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
Claire S Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet et al.
PLoS genetics, Journal article 2014
Journal article

Showing 11 - 20 of 37

2014

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas et al.
American journal of human genetics, Journal article 2014
Journal article

Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders.
Guillaume Huguet, Caroline Nava, Nathalie Lemière, Etienne Patin, Guillaume Laval et al.
PloS one, Journal article 2014
Journal article

2013

Heterozygous FA2H mutations in autism spectrum disorders.
Isabelle Scheid, Anna Maruani, Guillaume Huguet, Claire S Leblond, Gudrun Nygren et al.
BMC medical genetics, Journal article 2013
Journal article

Progress toward treatments for synaptic defects in autism.
Richard Delorme, Elodie Ey, Roberto Toro, Marion Leboyer, Christopher Gillberg et al.
Nature Medicine, Journal article 2013
Journal article

2012

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur et al.
PLoS Genetics, Journal article 2012
Journal article

Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE.
C Nava, F Lamari, D Héron, C Mignot, A Rastetter et al.
Translational psychiatry, Journal article 2012
Journal article

Individual common variants exert weak effects on the risk for autism spectrum disorders.
Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli et al.
Human Molecular Genetics, Journal article 2012
Journal article

SHANK1 Deletions in Males with Autism Spectrum Disorder.
Daisuke Sato, Anath C Lionel, Claire S Leblond, Aparna Prasad, Dalila Pinto et al.
American Journal of Human Genetics, Journal article 2012
Journal article

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, Regina Regan, Naisha Shah et al.
Human Genetics, Journal article 2012
Journal article

Showing 11 - 20 of 37

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