Meet ApplyKite Twin, the application assistant that learns with you

Meet your Twin, it learns with you

Your Twin learns with you

Launch week codes:30% off annual Pro20% off monthly Pro

Ends in00h00m00s

John Rendu

Has grant

Assistant prof

Université Grenoble Alpes

France

Research Interests

Explore related searches

Professors in France Professors in Cell Biology Cell Biology professors in France

Recent Grants

Grant: Open

Myo-CLASSIFAI

Open Date: 2026-01-01

Close Date: 2028-03-01

Grant: Open

Smooth PIPO

Open Date: 2023-09-01

Close Date: 2027-08-01

Grant: Close

ClassifAI-RYR1

Open Date: 2021-09-01

Close Date: 2025-03-01

Articles (20)

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2026

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Collaborators (10)

Shannon McNulty Gray

Clinical Assistant Professor

University of North Carolina at Chapel Hill

UNITED STATES

View details

Katarina Pelin

University of Helsinki

FINLAND

View details

Sheila Riazi

Staff Anesthesiologist

University Health Network

CANADA

View details

Florence Petit

Université de Lille

FRANCE

View details

Guillaume Mortamet

FRANCE

View details

Alan Beggs

Sir Edwin & Lady Manton Professor

Harvard Medical School

UNITED STATES

View details

Edoardo Malfatti

Full Professor

FRANCE

View details

Luuk René van den Bersselaar

Radboud University Medical Center

NETHERLANDS

View details

Slim Azouzi

Etablissement Français du Sang

FRANCE

View details

Philip Hopkins

Professor of Anaesthesia

University of Leeds

UNITED KINGDOM

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

John Rendu

Research Interests

Explore related searches

Recent Grants

Articles (20)

Biallelic <scp> <i>PIGB</i> </scp> Variants Cause Motor Neuropathy with Conduction Blocks and Peripheral Nerve Hyperexcitability

2025 update of the National French consensus on gene lists for the diagnosis of muscle diseases using high-throughput sequencing

Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin‐Related Congenital Myopathy

<i>Drosophila</i> ryanodine receptor gene triggers functional and developmental muscle properties and could be used to assess the impact of human <i>RYR1</i> mutations

A De Novo Variant in <i>NALCN</i> Associated With Arthrogryposis and Neonatal Respiratory Failure: A Case Report

Identification of a novel <i>de novo RYR1</i> variant associated with malignant hyperthermia

International Forum on Visceral Myopathy 2024: Advances in the Knowledge of the Disease

Phenotype-specific muscle proteomic profiling in titinopathies

Reducing Body Myopathy in Female Patients With <i>FHL1</i> Variants Showing Rapid and Severe Evolution Mimicking Inflammatory Myopathy

Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review

Clinical validity of congenital myopathy genes determined by the ClinGen Congenital Myopathies Expert Panel

Disease Trajectories of a Large French Cohort of 142 Congenital Myopathy Patients in Adult Age

Drosophila ryanodine receptor gene triggers functional and developmental muscle properties and could be used to assess the impact of human RYR1 mutations

Expanding the spectrum of <i>TNNC2</i> variants in neonatal hypotonia - a family report of a homozygous loss of function

Limited pre-clinical relevance of the heterozygous RYR1-I4895T/+ mouse model due to its mild phenotype

Novel Dominant Splicing Variant in MPZ Associated With Unusual Charcot-Marie-Tooth Disease

Skin transient receptor potential channels expression and microvascular reactivity to cooling in primary and secondary Raynaud's phenomenon

Myopathic manifestations across the adult lifespan of patients with malignant hyperthermia susceptibility: a narrative review

From gene to cell Functional validation of RYR1 variants

Functional benefit of CRISPR-Cas9-induced allele deletion for <i>RYR1</i> dominant mutation

Collaborators (10)

Shannon McNulty Gray

Katarina Pelin

Sheila Riazi

Florence Petit

Guillaume Mortamet

Alan Beggs

Edoardo Malfatti

Luuk René van den Bersselaar

Slim Azouzi

Philip Hopkins

Make your next move.