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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 31 - 37 of 37

2007

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian et al.
Nature Genetics, Journal article 2007
Journal article

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle. M. Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste et al.
Nature Genetics, Journal article 2007
Journal article

2006

Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.
Christelle M Durand, Caroline Kappeler, Catalina Betancur, Richard Delorme, Hélène Quach et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication of the International Society of Psychiatric Genetics, Journal article 2006
Journal article

No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.
Richard Delorme, Christelle M Durand, Catalina Betancur, Michael Wagner, Stephan Ruhrmann et al.
Biological Psychiatry, Journal article 2006
Journal article

2005

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.
Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood et al.
Molecular Psychiatry, Journal article 2005
Journal article

2003

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux et al.
Nature genetics, Journal article 2003
Journal article

2002

Linkage and association of the glutamate receptor 6 gene with autism
Stéphane Jamain, Catalina Betancur, Hélène Quach, Anne Philippe, Marc Fellous et al.
Molecular Psychiatry, Journal article 2002
Journal article

Showing 31 - 37 of 37

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