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Jean-Claude Kaplan

Jean-Claude Kaplan

D-Index & Metrics

Genetics

D-Index
57
Citations
15103
World Ranking
3386
National Ranking
170

Overview

Jean-Claude Kaplan is affiliated with Université Paris Cité in France and conducts research focused primarily on muscle physiology, metabolism, and related disorders. Their work spans several interconnected fields including Biochemistry, Genetics and Molecular Biology, and Medicine. Within these broader fields, their research addresses subfields such as Molecular Biology, Cell Biology, Physiology, Genetics, and Neurology.

The scientist's research concentrates on key topics including:

  • Muscle Physiology and Disorders
  • Muscle Metabolism and Nutrition
  • Adipose Tissue and Metabolism
  • Neurogenetic and Muscular Disorders Research
  • Neurological Diseases and Metabolism
  • Hereditary Neurological Disorders

Among Jean-Claude Kaplan's recent publications are the following papers:

  • "X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation," 2020, published in Skeletal Muscle
  • "L'Homme Gelé () et le déficit en cristalline αB," 2020, published in médecine/sciences
  • "X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization," 2020, published in Research Square (Research Square)
  • "X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization," 2020, published in Research Square (Research Square)

Jean-Claude Kaplan frequently publishes in venues such as Research Square (Research Square), Skeletal Muscle, and médecine/sciences.

The scientist collaborates often with coauthors including Inès Barthélémy, Nadège Calmels, Robert B. Weiss, Laurent Tiret, and Adeline Vulin, indicating a collaborative research environment focused on muscular disorders and molecular characterizations.

Best Publications

  • THE MOLECULAR BASIS FOR DUCHENNE VERSUS BECKER MUSCULAR DYSTROPHY: CORRELATION OF SEVERITY WITH TYPE OF DELETION

    M. Koenig;A. H. Beggs;M. Moyer;S. Scherpf

  • Transcription of the dystrophin gene in human muscle and non-muscle tissues

    Jamel Chelly;Jean-Claude Kaplan;Pascal Maire;Sophie Gautron

  • Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

    F Muscatelli;T M Strom;A P Walker;E Zanaria

  • Illegitimate transcription: transcription of any gene in any cell type.

    Jamel Chelly;Jean-Paul Concordet;Jean-Claude Kaplan;Axel Kahn

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

    Steven L. Roberds;Valérie Allamand;Federica Piccolo

  • International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis.

    E. Beutler;K. G. Blume;J. C. Kaplan;G. W. Löhr

  • Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping

    Aurélie Goyenvalle;Adeline Vulin;Françoise Fougerousse

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

    Sylvie Tuffery-Giraud;Sylvie Tuffery-Giraud;Christophe Béroud;Christophe Béroud;Rabah Ben Yaou;Rabah Ben Yaou

  • Modification of enzymatically amplified DNA for the detection of point mutations.

    A. Haliassos;J.C. Chomel;L. Tesson;M. Baudis

  • Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.

    Tejvir S. Khurana;Tejvir S. Khurana;Simon C. Watkins;Philippe Chafey;Jamel Chelly

  • Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

    Kiichiro Matsumura;Fernando M. S. Tomé;Huguette Collin;Kemal Azibi

  • Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cells.

    Jamel Chelly;Didier Montarras;Christian Pinset;Yoheved Berwald-Netter

  • Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

    F. Piccolo;S.L. Roberds;M. Jeanpierre;F. Leturcq

  • Long–term correction of mouse dystrophic degeneration by adenovirus–mediated transfer of a minidystrophin gene

    Nathalie Vincent;Thierry Ragot;Hélè Gilgenkrantz;Dominique Couton

  • International Committee for Standardization in Haematology: recommended screening test for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.

    E. Beutler;K. G. Blume;J. C. Kaplan;G. W. Löhr

  • Dystrophin gene transcribed from different promoters in neuronal and glial cells

    Jamel Chelly;Ghislaine Hamard;Annette Koulakoff;Jean-Claude Kaplan

  • Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.

    A. Haliassos;J.C. Chomel;S. Grandjouan;J. Kruh

  • Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies

    Jamel Chelly;Hélène Gilgenkrantz;Martine Lambert;Ghislaine Hamard

  • Limb-girdle muscular dystrophy in Guipúzcoa (Basque Country, Spain).

    M Urtasun;A Sáenz;C Roudaut;J J Poza

  • Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophy.

    Norma B. Romero;Serge Braun;Olivier Benveniste

Frequent Co-Authors

Thierry Bienvenu
Thierry Bienvenu Université Paris Cité
Roland Berger
Roland Berger Necker-Enfants Malades Hospital
Ray White
Ray White University of Utah
Peter L. Pearson
Peter L. Pearson Universidade de São Paulo
Kenneth K. Kidd
Kenneth K. Kidd Yale University
Hans-Hilger Ropers
Hans-Hilger Ropers Max Planck Society
Stephanie L. Sherman
Stephanie L. Sherman Emory University
Mark H. Skolnick
Mark H. Skolnick Myriad Genetics (Germany)

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