Françoise Lespinasse

Author

Also Known As

F Lespinasse, F. Lespinasse, Françoise Lespinasse, Francoise Lespinasse, Franqoise Lespinasse, Françoise Lespinasse, Lespinasse, Françoise

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique Université Côte d'Azur Institut de Recherche sur le Cancer et le Vieillissement de Nice Centre Hospitalier Universitaire de Nice

About

Françoise Lespinasse is an author at Inserm specializing in medicine, oncology, and tumor biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	976
2	Health Sciences	3	3	58
3	Natural Sciences	3	3	60
4	Engineering	1	1	16
5	Public Health	1	1	56

Françoise Lespinasse

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Brain Motor Neuron DiseaseGeneticsMitochondrial MyopathyAlzheimer's DiseaseMitochondrial Origin	2014	490
<i> <scp>CHCHD</scp> 10 </i> mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis Emmanuelle C. Genin, Morgane Plutino, Sylvie Bannwarth, EMBO Molecular Medicine	2015	199
MSH4 acts in conjunction with MLH1 during mammalian meiosis Sabine Santucci‐Darmanin, Deepika Walpita, Françoise Lespinasse, The FASEB Journal	2000	138
Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse Emmanuelle C. Genin, Blandine Madji Hounoum, Sylvie Bannwarth, Acta Neuropathologica Mitochondrial MyopathyMitochondrial DefectMitochondrial FunctionChchd10s59l/+ MouseMedicine	2019	114
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy Samira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gušić, The American Journal of Human Genetics	2016	89
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases Emmanuelle C. Genin, Sylvie Bannwarth, Françoise Lespinasse, Neurobiology of Disease Genome InstabilityMitochondrial DamageMicos Complex IntegrityMitochondrial FunctionGenetics	2018	79
Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis Sophie Neyton, Françoise Lespinasse, Peter B. Møens, Molecular Human Reproduction SpermatogenesisReciprocal ExchangesGeneticsMolecular BiologyMsh4 Gene Results	2004	56
Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice Sylvie Bannwarth, Laetitia Berg-Alonso, Gaëlle Augé, Mitochondrion Mitochondrial MyopathyMitophagyMitochondrial FunctionBiochemistryNatural Sciences	2016	38
The human MSH5 (MutS Homolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage Sylvie Bannwarth, Alexia C. Figueroa, Konstantina Fragaki, Mitochondrion Reductive StressMitophagyMitochondrial BiogenesisMitochondrial FunctionGenetics	2012	29
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability Emmanuelle C. Genin, Sylvie Bannwarth, Baptiste Ropert, Brain	2022	29

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