# Tania Attié‐Bitach

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/tania-attie-bitach/

## Facts

| Field | Value |
| --- | --- |
| Citations | 17,556 |
| Field | Genetic and Kidney Cyst Diseases |
| h-index | 76 |
| i10-index | 183 |
| Last Known Institution | Hôpital Necker-Enfants Malades |
| OpenAlex ID | https://openalex.org/A5001445148 |
| ORCID iD | https://orcid.org/0000-0002-1155-3626 |
| Works | 313 |

## 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/)
- [TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum](https://scholariq.org/papers/ttc21b-contributes-both-causal-and-modifying-alleles-across-the-ciliopathy/)
- [A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies](https://scholariq.org/papers/a-common-allele-in-rpgrip1l-is-a-modifier-of-retinal-degeneration-in/)

## Researcher topics

- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Hedgehog Signaling Pathway Studies](https://scholariq.org/topics/hedgehog-signaling-pathway-studies/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Fetal and Pediatric Neurological Disorders](https://scholariq.org/topics/fetal-and-pediatric-neurological-disorders/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Researcher university

- [Hôpital Necker-Enfants Malades](https://scholariq.org/institutions/hopital-necker-enfants-malades/)

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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.