# Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/epigenetic-modification-of-the-i-fmr1-i-gene-in-fragile-x-syndrome-is-associated/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Sébastien Jacquemont,Aurore Curie,Vincent des Portes,Maria Giulia Torrioli,Elizabeth Berry‐Kravis,Randi J. Hagerman,Feliciano J. Ramos,Kim Cornish,Yunsheng He,Charles Paulding,Giovanni Neri,Fei Chen,Nouchine Hadjikhani,Danielle Martinet,Joanne Meyer,J. Beckmann,Delange Karine,Brun Amandine,Gérald Bussy,F. Gasparini,Talita Hilse,Annette Floesser,Janice Branson,Graeme Bilbe,Donald R. Johns,Baltazar Gomez‐Mancilla |
| Citations | 611 |
| DOI | 10.1126/scitranslmed.3001708 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | true |
| OA Status | green |
| OA URL | http://infoscience.epfl.ch/record/171156 |
| OpenAlex ID | https://openalex.org/W2103709346 |
| PMID | 21209411 |
| Type | article |
| Year | 2011 |

## Paper authors

- [Vincent des Portes](https://scholariq.org/researchers/vincent-des-portes/)

## Paper primary topic

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Paper topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.