# Jean‐Baptiste Gourraud

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/jean-baptiste-gourraud/

## Facts

| Field | Value |
| --- | --- |
| Citations | 4,480 |
| Field | Cardiac electrophysiology and arrhythmias |
| h-index | 36 |
| i10-index | 65 |
| Last Known Institution | Centre National de la Recherche Scientifique |
| OpenAlex ID | https://openalex.org/A5009366353 |
| ORCID iD | 0000-0002-6961-2131 |
| Works | 175 |

## Researcher papers

- [Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death](https://scholariq.org/papers/common-variants-at-scn5a-scn10a-and-hey2-are-associated-with-brugada-syndrome-a/)
- [Outcome After Implantation of a Cardioverter-Defibrillator in Patients With Brugada Syndrome](https://scholariq.org/papers/outcome-after-implantation-of-a-cardioverter-defibrillator-in-patients-with/)
- [Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse](https://scholariq.org/papers/replacement-myocardial-fibrosis-in-patients-with-mitral-valve-prolapse/)
- [Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-brugada-syndrome-risk-loci-and/)
- [Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome](https://scholariq.org/papers/transethnic-genome-wide-association-study-provides-insights-in-the-genetic/)
- [Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome](https://scholariq.org/papers/testing-the-burden-of-rare-variation-in-arrhythmia-susceptibility-genes-provides/)
- [Prevalence and Prognostic Role of Various Conduction Disturbances in Patients With the Brugada Syndrome](https://scholariq.org/papers/prevalence-and-prognostic-role-of-various-conduction-disturbances-in-patients/)
- [Impact of clinical and genetic findings on the management of young patients with Brugada syndrome](https://scholariq.org/papers/impact-of-clinical-and-genetic-findings-on-the-management-of-young-patients-with/)
- [Age of First Arrhythmic Event in Brugada Syndrome](https://scholariq.org/papers/age-of-first-arrhythmic-event-in-brugada-syndrome/)
- [Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls](https://scholariq.org/papers/enhancing-rare-variant-interpretation-in-inherited-arrhythmias-through/)
- [Renal replacement therapy in type 2 severe cardiorenal syndrome: a randomized controlled trial](https://scholariq.org/papers/renal-replacement-therapy-in-type-2-severe-cardiorenal-syndrome-a-randomized/)

## Researcher topics

- [Cardiac electrophysiology and arrhythmias](https://scholariq.org/topics/cardiac-electrophysiology-and-arrhythmias/)
- [Cardiac Arrhythmias and Treatments](https://scholariq.org/topics/cardiac-arrhythmias-and-treatments/)
- [Ion channel regulation and function](https://scholariq.org/topics/ion-channel-regulation-and-function/)
- [ECG Monitoring and Analysis](https://scholariq.org/topics/ecg-monitoring-and-analysis/)
- [Cardiac pacing and defibrillation studies](https://scholariq.org/topics/cardiac-pacing-and-defibrillation-studies/)

## 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.