Contact

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Yann HERAULT

Researcher
yann.herault@igbmc.fr

HAL

Research team(s)

Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities
Team Leader : Yann HERAULT
Department : Translational medecine and neurogenetics

Research subgroup(s)

Aging, Down's syndrome and Alzheimer's disease
Leader : Yann HERAULT
Teams : Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities
Modeling of "genotype-phenotype" relationships and therapeutic approach in Down syndrome
Leader : Yann HERAULT
Teams : Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities
neurobiology of 16p11.2 and 17q21.31syndromes and other genetic diseases with ID or ASD
Leader : Yann HERAULT
Teams : Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities

Publications

2010
- Controlled somatic and germline copy number variation in the mouse model
  - Yann Hérault
  - Arnaud Duchon
  - Damien Maréchal
  - Matthieu Raveau
  - Patricia L. Pereira
  - Emilie Dalloneau
  - Véronique Brault
  Current Genomics ; Volume: 11 ; Page: 470-480
  HAL DOI
2007
- ProMetIS 2.0: proteomics and metabolomics data analysis and integration, applied to the characterization of the Lat and Mx2 knock-out phenotypes
  - Oneeb Nasir
  - Alyssa Imbert
  - Sylvain Dechaumet
  - Pierrick Roger
  - Thomas Burger
  - Yves Vandenbrouck
  - Marion Brandolini
  - Florence Castelli
  - Franck Giacomoni
  - Magali Rompais
  - Mohammed Selloum
  - Emmanuelle Mouton-Barbosa
  - Emeline Chu-Van
  - Charlotte Joly
  - Aurélie Hirschler
  - Sophie Leblanc
  - Tania Sorg
  - Sadia Ouzia
  - Claudine Médigue
  - Christophe Junot
  - ...
  HAL
2005
- Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1.
  - Vanessa Besson
  - Valérie Nalesso
  - Alexandre Herpin
  - Jean-Charles Bizot
  - Nadia Messaddeq
  - Raymond Romand
  - Anne Puech
  - Véronique Blanquet
  - Yann Hérault
  Biology of the Cell ; Volume: 97 ; Page: 787-98
  HAL DOI

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