France Leturcq

Université Paris Cité FR

233

Publications

7,533

Citations

H-Index

101

i10-Index

0.62

2yr Mean Cite

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Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar

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Publication & Citation Trends

Publications

233 total

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies PDF

Karim Wahbi, Rabah Ben Yaou, Estelle Gandjbakhch, Frédéric Anselme, Thomas Gossios et al. - Circulation, 2019

Cited by 254 OpenAlex

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase PDF

Sylvie Tuffery‐Giraud, Christophe Béroud, France Leturcq, Rabah Ben Yaou, Dalil Hamroun et al. - Human Mutation, 2009

Cited by 365 OpenAlex

Endomysial Fibrosis in Duchenne Muscular Dystrophy: A Marker of Poor Outcome Associated With Macrophage Alternative Activation PDF

Isabelle Desguerre, M Mayer, France Leturcq, J Barbet, Romain K. Gherardi et al. - Journal of Neuropathology & Experimental Neurology, 2009

Cited by 225 OpenAlex

Phenotypic Study in 40 Patients With Dysferlin Gene Mutations

Karine Nguyen, Guillaume Bassez, Martin Krahn, Rafaëlle Bernard, Pascal Laforêt et al. - Archives of Neurology, 2007

Cited by 263 OpenAlex

C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy

Virginie Carmignac, Mustafa A. Salih, Susana Quijano‐Roy, Sylvie Marchand, Molham M. Al Rayess et al. - Annals of Neurology, 2007

Cited by 247 OpenAlex

Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping

Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, France Leturcq, Jean‐Claude Kaplan et al. - Science, 2004

Cited by 475 OpenAlex

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Steven L. Roberds, France Leturcq, Valérie Allamand, Fédérica Piccolo, Marc Jeanpierre et al. - Cell, 1994

Cited by 457 OpenAlex

Research Topics

Muscle Physiology and Disorders (150) Cardiomyopathy and Myosin Studies (48) RNA Research and Splicing (38) Genetic Neurodegenerative Diseases (34) Nuclear Structure and Function (33)

Affiliations

Université Claude Bernard Lyon 1

FR 2007 - 2007

Délégation Paris 5

FR 2025 - 1994

University of Copenhagen

DK 2015 - 2015

Centre National de la Recherche Scientifique

FR 2017 - 2004

University of Padua

IT 2015 - 2015

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France Leturcq

Publication & Citation Trends

Publications

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies PDF

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase PDF

Endomysial Fibrosis in Duchenne Muscular Dystrophy: A Marker of Poor Outcome Associated With Macrophage Alternative Activation PDF

Phenotypic Study in 40 Patients With Dysferlin Gene Mutations

C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy

Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Research Topics

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