# Michel Vekemans

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michel-vekemans/

## Facts

| Field | Value |
| --- | --- |
| Citations | 17,251 |
| Field | Prenatal Screening and Diagnostics |
| h-index | 65 |
| i10-index | 211 |
| Last Known Institution | Université Paris Cité |
| OpenAlex ID | https://openalex.org/A5000103412 |
| ORCID iD | https://orcid.org/0000-0003-2564-1296 |
| Works | 365 |

## Researcher papers

- [The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome](https://scholariq.org/papers/the-ciliary-gene-rpgrip1l-is-mutated-in-cerebello-oculo-renal-syndrome-joubert/)
- [SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)](https://scholariq.org/papers/shox-mutations-in-dyschondrosteosis-leri-weill-syndrome/)
- [Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome](https://scholariq.org/papers/mutational-functional-and-expression-studies-of-the-i-tcf4-i-gene-in-pitt/)

## Researcher topics

- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Hedgehog Signaling Pathway Studies](https://scholariq.org/topics/hedgehog-signaling-pathway-studies/)

## Researcher university

- [Université Paris Cité](https://scholariq.org/institutions/universite-paris-cite/)

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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.