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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 21 - 30 of 37

2011

Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Pauline Chaste, Nathalie Clement, Hany Goubran Botros, Jean-Luc Guillaume, Marina Konyukh et al.
Journal of Pineal Research, Journal article 2011
Journal article

Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
Marina Konyukh, Richard Delorme, Pauline Chaste, Claire Leblond, Nathalie Lemière et al.
PLoS One, Journal article 2011
Journal article

2010

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico et al.
Nature, Journal article 2010
Journal article

Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Roberto Toro, Marina Konyukh, Richard Delorme, Claire Leblond, Pauline Chaste et al.
Trends in Genetics, Review article 2010
Review article

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.
Richard Delorme, Catalina Betancur, Isabelle Scheid, Henrik Anckarsäter, Pauline Chaste et al.
BMC Medical Genetics, Journal article 2010
Journal article

Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population.
Pauline Chaste, Nathalie Clement, Oriane Mercati, Jean-Luc Guillaume, Richard Delorme et al.
PloS One, Journal article 2010
Journal article

A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy et al.
Human Molecular Genetics, Journal article 2010
Journal article

2009

An investigation of ribosomal protein L10 gene in autism spectrum disorders.
Xiaohong Gong, Richard Delorme, Fabien Fauchereau, Christelle M Durand, Pauline Chaste et al.
BMC Medical Genetics, Journal article 2009
Journal article

2008

Analysis of X chromosome inactivation in autism spectrum disorders.
Xiaohong Gong, Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, Journal article 2008
Journal article

Abnormal melatonin synthesis in autism spectrum disorders.
Jonas Melke, Hany Goubran-Botros, Pauline Chaste, Catalina Betancur, Gudrun Nygren et al.
Molecular Psychiatry, Journal article 2008
Journal article

Showing 21 - 30 of 37

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Denna text är utskriven från följande webbsida:
http://neurophys.gu.se/english/departments/psychiatry_and_neurochemistry/about-us/staff/?publicationPageNumber=3&selectedTab=2&languageId=100001&userId=xbouth
Utskriftsdatum: 2019-09-19