World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
63
Citations
11813
World Ranking
2915
National Ranking
140

Joël Lunardi 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 Joël Lunardi 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: 149 publications — 29th percentile

29% of scientists in this discipline score the same or lower.

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

Joël Lunardi 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 Joël Lunardi 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: 63 D-Index — 35th percentile

35% of scientists in this discipline score the same or lower.

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

Overview

Joël Lunardi is a researcher affiliated with Grenoble Alpes University in France, specializing in fields related to biochemistry, genetics, molecular biology, and medicine. Their research spans multiple subfields including molecular biology as well as cardiology and cardiovascular medicine.

The main topics of Joël Lunardi's work include:

  • Ion channel regulation and function
  • Cardiomyopathy and myosin studies
  • Mitochondrial function and pathology

Among their recent scholarly contributions is the paper titled La grande variabilité phénotypique des mutations du gène RYR1, published in 2022 in the journal médecine/sciences. This publication addresses the phenotypic variability arising from mutations in the RYR1 gene.

Joël Lunardi has collaborated frequently with several researchers, including Mohamed Islam Kediha, Sonia Nouioua, Mériem Tazir, Damien Sternberg, and Lamia Ali Pacha, reflecting a collaborative approach in their scientific projects.

Their research output predominantly appears in the journal médecine/sciences, indicating a focus on publishing within medical and scientific forums that align with their fields of study.

Best Publications

  • Improvement of the solubilization of proteins in two-dimensional electrophoresis with immobilized pH gradients.

    Thierry Rabilloud;Céline Adessi;Anne Giraudel;Joël Lunardi

  • Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia

    Meiso Hayashi;Isabelle Denjoy;Fabrice Extramiana;Alice Maltret

  • Malignant-Hyperthermia Susceptibility Is Associated with a Mutation of the a1-Subunit of the Human Dihydropyridine-Sensitive L-Type Voltage-Dependent Calcium-Channel Receptor in Skeletal Muscle

    Nicole Monnier;Vincent Procaccio;Paul Stieglitz;Joël. Lunardi

  • New zwitterionic detergents improve the analysis of membrane proteins by two-dimensional electrophoresis.

    Mireille Chevallet;Véronique Santoni;Alexandra Poinas;David Rouquié

  • A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels.

    Thierry Rabilloud;Jean-Marc Strub;Sylvie Luche;Alain van Dorsselaer

  • Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility.

    Klaus Dieterich;Ricardo Soto Rifo;Ricardo Soto Rifo;Anne Karen Faure;Anne Karen Faure;Sylviane Hennebicq;Sylviane Hennebicq

  • Absence of Triadin, a Protein of the Calcium Release Complex, is Responsible for Cardiac Arrhythmia with Sudden Death in Human

    Nathalie Roux-Buisson;Marine Cacheux;Marine Cacheux;Anne Fourest-Lieuvin;Anne Fourest-Lieuvin;Jeremy Fauconnier

  • Two‐dimensional electrophoresis of human placental mitochondria and protein identification by mass spectrometry: Toward a human mitochondrial proteome

    Thierry Rabilloud;Sylvie Kieffer;Vincent Procaccio;Mathilde Louwagie

  • Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis.

    Fadia Medja;S. Allouche;Paule Frachon;Claude Jardel;Claude Jardel

  • A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene.

    Ana Ferreiro;Nicole Monnier;Norma B. Romero;Jean-Paul Leroy

  • A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

    Radu Harbuz;Radu Harbuz;Raoudha Zouari;Virginie Pierre;Virginie Pierre;Mariem Ben Khelifa;Mariem Ben Khelifa

  • Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia

    Norma Beatriz Romero;Nicole Monnier;Louis Viollet;Anne Cortey

  • Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

    Nicole Monnier;Norma Beatriz Romero;Joëlle Lerale;Pierre Landrieu

  • Analysis of membrane proteins by two-dimensional electrophoresis: comparison of the proteins extracted from normal or Plasmodium falciparum-infected erythrocyte ghosts.

    Thierry Rabilloud;Thierry Blisnick;Manfred Heller;Sylvie Luche

  • A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia

    Nicole Monnier;Ana Ferreiro;Isabelle Marty;Annick Labarre-Vila

  • Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion

    Nigel F. Clarke;Leigh B. Waddell;Leigh B. Waddell;Sandra T. Cooper;Sandra T. Cooper;Margaret Perry;Margaret Perry

  • An appraisal of the functional significance of the inhibitory effect of long chain acyl-CoAs on mitochondrial transports

    F. Morel;G. Lauquin;J. Lunardi;J. Duszynski

  • From Lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes.

    Haifa Hichri;John Rendu;Nicole Monnier;Charles Coutton

  • The 49‐kDa subunit of NADH‐ubiquinone oxidoreductase (Complex I) is involved in the binding of piericidin and rotenone, two quinone‐related inhibitors

    Elisabeth Darrouzet;Jean-Paul Issartel;Joël Lunardi;Alain Dupuis

  • Chemical probes of the mitochondrial ATP synthesis and translocation

    Pierre V. Vignais;Joël Lunardi

Frequent Co-Authors

Pierre V. Vignais
Pierre V. Vignais CEA Grenoble
Pierre F. Ray
Pierre F. Ray Grenoble Alpes University
Pascale Guicheney
Pascale Guicheney Sorbonne University
Thierry Rabilloud
Thierry Rabilloud Centre national de la recherche scientifique, CNRS
Christophe Arnoult
Christophe Arnoult Grenoble Alpes University
Michel Fardeau
Michel Fardeau Grenoble Alpes University
Vincent Procaccio
Vincent Procaccio University of Angers
Jérôme Garin
Jérôme Garin CEA Grenoble
Dominique Figarella-Branger
Dominique Figarella-Branger Aix-Marseille University
Alain Lacampagne
Alain Lacampagne University of Montpellier

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