# Vincent Plagnol

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/vincent-plagnol/

## Facts

| Field | Value |
| --- | --- |
| Citations | 36,844 |
| Field | Genetic Associations and Epidemiology |
| h-index | 93 |
| i10-index | 205 |
| Last Known Institution | Genomics (United Kingdom) |
| OpenAlex ID | https://openalex.org/A5068852782 |
| ORCID iD | https://orcid.org/0000-0002-5597-9215 |
| Works | 355 |

## Researcher papers

- [Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes](https://scholariq.org/papers/robust-associations-of-four-new-chromosome-regions-from-genome-wide-analyses-of/)
- [Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease](https://scholariq.org/papers/dense-genotyping-identifies-and-localizes-multiple-common-and-rare-variant/)
- [Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls](https://scholariq.org/papers/genome-wide-association-study-of-cnvs-in-16-000-cases-of-eight-common-diseases/)
- [Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage](https://scholariq.org/papers/phosphoinositide-3-kinase-gene-mutation-predisposes-to-respiratory-infection-and/)
- [Atlas of the clinical genetics of human dilated cardiomyopathy](https://scholariq.org/papers/atlas-of-the-clinical-genetics-of-human-dilated-cardiomyopathy/)
- [Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease](https://scholariq.org/papers/comprehensive-rare-variant-analysis-via-whole-genome-sequencing-to-determine-the/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease](https://scholariq.org/papers/unbiased-screen-for-interactors-of-leucine-rich-repeat-kinase-2-supports-a/)
- [DYX1C1 is required for axonemal dynein assembly and ciliary motility](https://scholariq.org/papers/dyx1c1-is-required-for-axonemal-dynein-assembly-and-ciliary-motility/)
- [Copy number of <i>FCGR3B,</i> which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake](https://scholariq.org/papers/copy-number-of-i-fcgr3b-i-which-is-associated-with-systemic-lupus-erythematosus/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)
- [Lung Cancer Treatments and Mutations](https://scholariq.org/topics/lung-cancer-treatments-and-mutations/)
- [Retinal Development and Disorders](https://scholariq.org/topics/retinal-development-and-disorders/)
- [RNA Research and Splicing](https://scholariq.org/topics/rna-research-and-splicing/)

## Researcher university

- [Genomics (United Kingdom)](https://scholariq.org/institutions/genomics-united-kingdom/)

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