# Thomas Bourgeron

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/thomas-bourgeron/

## Facts

| Field | Value |
| --- | --- |
| Citations | 32,282 |
| Field | Autism Spectrum Disorder Research |
| h-index | 83 |
| i10-index | 224 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5084411567 |
| ORCID iD | https://orcid.org/0000-0001-8164-9220 |
| Works | 819 |

## Researcher papers

- [Functional impact of global rare copy number variation in autism spectrum disorders](https://scholariq.org/papers/functional-impact-of-global-rare-copy-number-variation-in-autism-spectrum/)
- [Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders](https://scholariq.org/papers/mutations-in-the-gene-encoding-the-synaptic-scaffolding-protein-shank3-are/)
- [Mapping autism risk loci using genetic linkage and chromosomal rearrangements](https://scholariq.org/papers/mapping-autism-risk-loci-using-genetic-linkage-and-chromosomal-rearrangements/)
- [Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders](https://scholariq.org/papers/convergence-of-genes-and-cellular-pathways-dysregulated-in-autism-spectrum/)
- [Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments](https://scholariq.org/papers/meta-analysis-of-shank-mutations-in-autism-spectrum-disorders-a-gradient-of/)
- [A genome-wide scan for common alleles affecting risk for autism](https://scholariq.org/papers/a-genome-wide-scan-for-common-alleles-affecting-risk-for-autism/)
- [Abnormal melatonin synthesis in autism spectrum disorders](https://scholariq.org/papers/abnormal-melatonin-synthesis-in-autism-spectrum-disorders/)
- [Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders](https://scholariq.org/papers/genetic-and-functional-analyses-of-shank2-mutations-suggest-a-multiple-hit-model/)
- [Individual common variants exert weak effects on the risk for autism spectrum disorders](https://scholariq.org/papers/individual-common-variants-exert-weak-effects-on-the-risk-for-autism-spectrum/)
- [Gender differences in autism spectrum disorders: Divergence among specific core symptoms](https://scholariq.org/papers/gender-differences-in-autism-spectrum-disorders-divergence-among-specific-core/)
- [A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder](https://scholariq.org/papers/a-novel-approach-of-homozygous-haplotype-sharing-identifies-candidate-genes-in/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Metabolism and Genetic Disorders](https://scholariq.org/topics/metabolism-and-genetic-disorders/)

## Researcher university

- [Centre National de la Recherche Scientifique](https://scholariq.org/institutions/centre-national-de-la-recherche-scientifique/)

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