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Genetics
Germany
2024
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Genetics and Molecular Biology
Germany
2024

D-Index & Metrics

Genetics

D-Index
94
Citations
34423
World Ranking
931
National Ranking
78

Medicine

D-Index
94
Citations
34768
World Ranking
10435
National Ranking
570

Jörg T. Epplen 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 Jörg T. Epplen 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: 547 publications — 95th percentile

95% of scientists in this discipline score the same or lower.

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

Jörg T. Epplen 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 Jörg T. Epplen 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: 94 D-Index — 79th percentile

79% of scientists in this discipline score the same or lower.

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

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award

Overview

Jörg T. Epplen is affiliated with Ruhr University Bochum in Germany. Their research spans across multiple fields, primarily focusing on medicine, biochemistry, genetics, molecular biology, and neuroscience.

The main subfields of their work include cellular and molecular neuroscience, molecular biology, pathology and forensic medicine, genetics, and physiology. Their research topics cover areas such as telomeres, telomerase, and senescence; RNA regulation and disease; multiple sclerosis research studies; cancer cells and metastasis; cancer research and treatments; 3D printing in biomedical research; and health and medical studies.

Their recent publications include:

  • Association between shorter leukocyte telomeres and multiple sclerosis, 2020, Journal of Neuroimmunology
  • Comparison of hybrid clones derived from human breast epithelial cells and three different cancer cell lines regarding in vitro cancer stem/initiating cell properties, 2020, BMC Cancer
  • Humangenetische Beratung in Deutschland: Entwicklung der Inanspruchnahme, 2020, Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz
  • Endocannabinergic modulation of central serotonergic activity in healthy human volunteers, 2023, Annals of General Psychiatry
  • EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder, 2025, Movement Disorders

Their publications appear regularly in venues such as Movement Disorders, Journal of Neuroimmunology, BMC Cancer, Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz, and Annals of General Psychiatry.

Frequent collaborators in their scientific work include Larissa Arning, Jörg Schmidtke, Ralf Glaubitz, Cleo Schwarz, and Florian Bartenschlager.

Best Publications

  • Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.

    Rejko Krüger;Wilfried Kuhn;Thomas Müller;Dirk Woitalla

  • Multiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity

    R. H.S.R. Roxburgh;S. R. Seaman;T. Masterman;A. E. Hensiek

  • Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

    Frank Rutsch;Nico Ruf;Sucheta Vaingankar;Mohammad R Toliat

  • Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

    Susan E. Holmes;Elizabeth E. O'Hearn;Melvin G. McInnis;Daniel A. Gorelick-Feldman

  • Worldwide Ethnic Distribution of the G Protein β3 Subunit 825T Allele and Its Association with Obesity in Caucasian, Chinese, and Black African Individuals

    Winfried Siffert;Peter Forster;Karl-Heinz Jöckel;David A. Mvere

  • Suppression of experimentally induced autoimmune encephalomyelitis by cytolytic T–T cell interactions

    Deming Sun;Yufen Qin;Johanna Chluba;Jörg T. Epplen

  • Myelin autoreactivity in multiple sclerosis: recognition of myelin basic protein in the context of HLA-DR2 products by T lymphocytes of multiple-sclerosis patients and healthy donors.

    Martin Pette;Kyoko Fujita;David Wilkinson;Daniel M. Altmann

  • DNA finger printing by oligonucleotide probes specific for simple repeats.

    S. Ali;C. R. Müller;J. T. Epplen

  • Genetic and population study of a Y-linked tetranucleotide repeat DNA polymorphism with a simple non-isotopic technique.

    Fabricio R. Santos;Sergio D. J. Pena;Jiirg T. Epplen

  • Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

    Ludger Schöls;Georgios Amoiridis;Thomas Büttner;Horst Przuntek

  • Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts.

    L Roewer;J Arnemann;N K Spurr;K H Grzeschik

  • Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype.

    Rejko Krüger;Ana Maria Menezes Vieira‐Saecker;Wilfried Kuhn;Daniela Berg

  • Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

    Ludger Schöls;Rejko Krüger;Georgios Amoiridis;Horst Przuntek

  • Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

    M Meins;J Lehmann;F Gerresheim;J Herchenbach

  • Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.

    Paul A Lyons;James E Peters;Federico Alberici;Federico Alberici;James Liley;James Liley

  • T cell receptor β chain usage in myelin basic protein-specific rat T lymphocytes

    Johanna Chluba;Christiane Steeg;Andrea Becker;Hartmut Wekerle

  • An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.

    Thorsten Schmidt;G. Bernhard Landwehrmeyer;Ina Schmitt;Yvon Trottier

  • Friedreich's ataxia. Revision of the phenotype according to molecular genetics.

    L Schöls;G Amoiridis;H Przuntek;G Frank

  • Optimized oligonucleotide probes for DNA fingerprinting

    Renate Schäfer;Hans Zischler;Uli Birsner;Andrea Becker

  • Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease

    H. P. Torok;J. Glas;L. Tonenchi;P. Lohse

Frequent Co-Authors

Olaf Riess
Olaf Riess University of Tübingen
Horst Przuntek
Horst Przuntek Ruhr University Bochum
Thomas Lubjuhn
Thomas Lubjuhn University of Cologne
Peter Nürnberg
Peter Nürnberg University of Cologne
Manfred Schartl
Manfred Schartl University of Würzburg
Carsten Saft
Carsten Saft Ruhr University Bochum
Stephan Brand
Stephan Brand Ludwig-Maximilians-Universität München
Bertram Müller-Myhsok
Bertram Müller-Myhsok Max Planck Society
Indrajit Nanda
Indrajit Nanda University of Würzburg

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