World's Best Scientists 2026 revealed!
Jean-Claude Kaplan

Jean-Claude Kaplan

D-Index & Metrics

Genetics

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

Jean-Claude Kaplan publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Jean-Claude Kaplan sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 223 publications — 58th percentile

58% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Jean-Claude Kaplan D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Jean-Claude Kaplan sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 57 D-Index — 23rd percentile

23% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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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