Valérie Allamand - Concepedia

Author

Valérie Allamand

Also Known As

Allamand, V., Allamand, Valérie, Claire-Sophie Davoine, Léna Guillot-Noel, P Alfieri, Teresinha Evangelista, V ALLAMAND, V Allamand, V, Allamand, V. Allamand

176

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

Inserm Sorbonne Université Institut de Myologie Centre National de la Recherche Scientifique Centre de Recherche en Myologie

About

Valérie Allamand is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	26	2.6K
2	Engineering	2	2	37
3	Health Sciences	1	1	102
4	Natural Sciences	1	1	94
5	Public Health	1	1	13

Valérie Allamand

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy Steven L. Roberds, France Leturcq, Valérie Allamand, Cell Rare DiseasesMissense MutationsDevelopmental BiologyMendelian DisorderGenetic Disorder	1994	456
β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 Leland E. Lim, Franck Duclos, Odile Broux, Nature Genetics MechanobiologySkeletal MusclePathologyLimb–girdle Muscular DystrophyMedicine	1995	447
Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Molecular Cell Skeletal MuscleMedicinePathologyDegenerative DiseaseDisease Gene Identification	2000	208
Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy Ercan Demir, Patrizia Sabatelli, Valérie Allamand, The American Journal of Human Genetics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsPathology	2002	167
Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment Laure Bidou, Isabelle Hatin, Norma Pérez, Gene Therapy MedicineDegenerative DiseaseBroad SpectrumMuscular DystrophiesAntisense Therapy	2004	150
Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin) Valérie Allamand, Pascale Guicheney European Journal of Human Genetics Rare DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderMedicine	2002	141
Early onset collagen VI myopathies: Genetic and clinical correlations Laura Briñas, Pascale Richard, Susana Quijano‐Roy, Annals of Neurology	2010	132
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin 2-Chain Valérie Allamand, Yoshihide Sunada, Mustafa A. Salih, Human Molecular Genetics Rare DiseasesDevelopmental BiologyMendelian DisorderInternally Deleted LamininSplice Site Mutation	1997	121
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A Virginie Carmignac, Martina Svensson, Zandra Körner, Human Molecular Genetics	2011	118
ColVI myopathies: where do we stand, where do we go? Valérie Allamand, Laura Briñas, Pascale Richard, Skeletal Muscle Mendelian DisorderCollagen Vi MyopathiesSkeletal MuscleGenetic DisorderGenetics	2011	109

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