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Thomas Bourgeron

Affiliation : Centre National de la Recherche Scientifique · Institut Pasteur · Gènes, synapses et cognition · Université Paris Diderot

• 4Publications (affiliation in France)
• 460Total publications
• 31480Citations
• 84h-index

ORCIDOpenAlex

Research areas

• Autism Spectrum Disorder Research
• Genetics and Neurodevelopmental Disorders
• Genetic Associations and Epidemiology
• Genomic variations and chromosomal abnormalities
• Neuroscience and Neuropharmacology Research

Publications (4)

• Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
  2018 · Journal of Applied Genetics · cited 14 times
• Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing
  2017 · Progress in Preventive Medicine · cited 6 times
• A High Frequency of Y Chromosome Deletions in Males With Nonidiopathic Infertility
  2000 · Obstetrical & Gynecological Survey · cited 19 times
• A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility1
  1999 · The Journal of Clinical Endocrinology & Metabolism · cited 95 times

Publication venues

• Journal of Applied Genetics × 1
• Progress in Preventive Medicine × 1
• Obstetrical & Gynecological Survey × 1
• The Journal of Clinical Endocrinology & Metabolism × 1

Publications per year

• 20181
• 20171
• 20001
• 19991

Collaborations

Partner institutions : Inserm · Hôpital Tenon · Centre Hospitalier Universitaire de Caen Normandie · Centre Hospitalier de Mulhouse · Institut Pasteur du Maroc

Co-authors’ countries : Hungary · Morocco · United States · Tunisia

Co-authors

• Jean‐Pierre Dadoune
• Jean-Marie Antoine
• Marc Fellous
• Hassan Rouba
• Éric Jeandidier
• Sandrine Barbaux
• Csilla Gabriella Krausz
• Ken McElreavey
• Ghislaine Plessis
• Jean‐Pierre Siffroi
• Lluís Quintana‐Murci
• Edit Erdei

Bibliographic data from OpenAlex (open database).