Sylvie Bannwarth
Nice, France
Last Updated: 09/26/2026
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Found 54 publications
Sporadic amyotrophic lateral sclerosis: what is the impact of the mitochondrial genome?
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: July 01, 2025
From variant interpretation to structural discovery: A new Zinc-binding domain in PARS2.
Journal: Mitochondrion
Published: June 23, 2025
Accelerate the discovery of genetic variants in mitochondrial diseases with Variant prIOritization using Latent spAce.
Journal: Briefings in bioinformatics
Published: June 18, 2025
"Mitochondrial medicine" in the light of the fourth national plan for rare diseases (PNMR4): The example of the MITOMICS project
Journal: Medecine sciences : M/S
Published: March 03, 2025
Primary mitochondrial disorders and mimics: Insights from a large French cohort.
Journal: Annals of clinical and translational neurology
Published: February 26, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease models.
Journal: Brain : a journal of neurology
Published: February 23, 2024
Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variability.
Journal: European journal of medical genetics
Published: April 28, 2022
A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare Diseases.
Journal: International journal of molecular sciences
Published: September 14, 2021
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability.
Journal: Brain : a journal of neurology
Published: July 27, 2021
ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing data.
Journal: Bioinformatics (Oxford, England)
Published: July 12, 2021
Last Updated: 09/26/2026