# Catalina Betancur

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/catalina-betancur/

## Facts

| Field | Value |
| --- | --- |
| Citations | 29,474 |
| Field | Autism Spectrum Disorder Research |
| h-index | 57 |
| i10-index | 114 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5078043271 |
| ORCID iD | https://orcid.org/0000-0002-3327-4804 |
| Works | 150 |

## Researcher papers

- [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/)
- [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/)
- [Rare coding variation provides insight into the genetic architecture and phenotypic context of autism](https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/)
- [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/)
- [Mutation screening of the <i>PTEN</i> gene in patients with autism spectrum disorders and macrocephaly](https://scholariq.org/papers/mutation-screening-of-the-i-pten-i-gene-in-patients-with-autism-spectrum/)

## 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/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Researcher university

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

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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.