# Émilie Cornec-Le Gall

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/emilie-cornec-le-gall/

## Facts

| Field | Value |
| --- | --- |
| Citations | 5,820 |
| Field | Genetic and Kidney Cyst Diseases |
| h-index | 35 |
| i10-index | 55 |
| Last Known Institution | Université de Bretagne Occidentale |
| OpenAlex ID | https://openalex.org/A5091002248 |
| ORCID iD | 0000-0003-1958-4459 |
| Works | 156 |

## Researcher papers

- [Autosomal dominant polycystic kidney disease](https://scholariq.org/papers/autosomal-dominant-polycystic-kidney-disease-2/)
- [Type of PKD1 Mutation Influences Renal Outcome in ADPKD](https://scholariq.org/papers/type-of-pkd1-mutation-influences-renal-outcome-in-adpkd/)
- [Mutations in GANAB , Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease](https://scholariq.org/papers/mutations-in-ganab-encoding-the-glucosidase-ii-subunit-cause-autosomal-dominant/)
- [Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases](https://scholariq.org/papers/genetic-complexity-of-autosomal-dominant-polycystic-kidney-and-liver-diseases/)
- [The PROPKD Score](https://scholariq.org/papers/the-propkd-score/)
- [Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease](https://scholariq.org/papers/monoallelic-mutations-to-dnajb11-cause-atypical-autosomal-dominant-polycystic/)
- [ANCA-associated vasculitis — clinical utility of using ANCA specificity to classify patients](https://scholariq.org/papers/anca-associated-vasculitis-clinical-utility-of-using-anca-specificity-to/)
- [Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference](https://scholariq.org/papers/genetics-in-chronic-kidney-disease-conclusions-from-a-kidney-disease-improving/)
- [Autosomal dominant polycystic kidney disease: Comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients](https://scholariq.org/papers/autosomal-dominant-polycystic-kidney-disease-comprehensive-mutation-analysis-of/)
- [Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype](https://scholariq.org/papers/monoallelic-ift140-pathogenic-variants-are-an-important-cause-of-the-autosomal/)
- [What Is Autosomal Dominant Polycystic Kidney Disease?](https://scholariq.org/papers/what-is-autosomal-dominant-polycystic-kidney-disease/)
- [KDIGO 2025 ADPKD guideline: a commentary on diagnosis and management of hepatopancreatic manifestations by the ERA Working Group Genes & Kidney](https://scholariq.org/papers/kdigo-2025-adpkd-guideline-a-commentary-on-diagnosis-and-management-of/)

## Researcher topics

- [Genetic and Kidney Cyst Diseases](https://scholariq.org/topics/genetic-and-kidney-cyst-diseases/)
- [Renal and related cancers](https://scholariq.org/topics/renal-and-related-cancers/)
- [Renal Diseases and Glomerulopathies](https://scholariq.org/topics/renal-diseases-and-glomerulopathies/)
- [Pediatric Urology and Nephrology Studies](https://scholariq.org/topics/pediatric-urology-and-nephrology-studies/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Researcher university

- [Université de Bretagne Occidentale](https://scholariq.org/institutions/universite-de-bretagne-occidentale/)

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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.