World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
46
Citations
42162
World Ranking
4132
National Ranking
215

Roland Heilig 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 Roland Heilig 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: 72 publications — 1st percentile

1% of scientists in this discipline score the same or lower.

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

Roland Heilig 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 Roland Heilig 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: 46 D-Index — 5th percentile

5% of scientists in this discipline score the same or lower.

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

Overview

Roland Heilig is affiliated with the University of Paris-Saclay in France. Their work encompasses research in molecular biology, biomaterials, and ecology, contributing to a nuanced understanding of microbial and ecological systems at a genetic and functional level.

The scientist's research topics include:

  • Diatoms and Algae Research
  • Microbial Community Ecology and Physiology
  • Genomics and Phylogenetic Studies

Heilig has coauthored scholarly articles frequently with several researchers, including:

  • Olivier Jaillon
  • Patrick Wincker
  • Shinya Sato
  • Deepak Nanjappa
  • Richard G. Dorrell

Their publication venues reveal contributions to high-impact scientific journals such as:

  • Scientific Reports
  • Nature

Among the notable recent papers authored by Roland Heilig are:

  • Genome-enabled phylogenetic and functional reconstruction of an araphid pennate diatom Plagiostriata sp. CCMP470, previously assigned as a radial centric diatom, and its bacterial commensal, 2020, Scientific Reports
  • Publisher Correction: The DNA sequence and analysis of human chromosome 14, 2023, Nature

The 2020 publication delves into the genomic and phylogenetic analysis of diatoms and their bacterial relationships, advancing knowledge in microbial community ecology and physiology. The 2023 correction note relates to human chromosome 14 sequencing, indicating involvement in large-scale genomics projects.

The wide range of topics covered highlights Heilig's interdisciplinary approach, integrating molecular biology techniques with ecological and biomaterial perspectives to explore functional genomics and phylogenetics.

Best Publications

  • Initial sequencing and analysis of the human genome.

    Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum

  • A candidate gene for familial Mediterranean fever

    Alain Bernot;Christian Clepet;Corinne Dasilva

  • A physical map of the human genome.

    John Douglas Mcpherson;Marco Marra;Marco Marra;La Deana Hillier;Robert H. Waterston

  • Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

    Jamilé Hazan;Nùria Fonknechten;Delphine Mavel;Caroline Paternotte

  • A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

    Abdelhak S;Kalatzis;Heilig R;Compain S

  • Continuum of overlapping clones spanning the entire human chromosome 21q.

    Ilya Chumakov;Philippe Rigault;Sophie Guillou;Pierre Ougen

  • Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

    Caroline Lefèvre;Florence Jobard;Frédéric Caux;Bakar Bouadjar

  • A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.

    O A Bernard;M Busson-LeConiat;P Ballerini;M Mauchauffé

  • The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis.

    Isabelle Chambaud;Roland Heilig;Stéphane Ferris;Valérie Barbe

  • Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

    Caroline Lefèvre;Stéphanie Audebert;Florence Jobard;Bakar Bouadjar

  • Bacterial Mode of Replication with Eukaryotic-Like Machinery in a Hyperthermophilic Archaeon

    Hannu Myllykallio;Philippe Lopez;Purificación López-Garcı́a;Roland Heilig

  • Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

    Sonia Abdelhak;Vasiliki Kalatzis;Roland Heilig;Sylvie Compain

  • Mutations in the gene encoding SLURP-1 in Mal de Meleda

    Judith Fischer;Bakar Bouadjar;Roland Heilig;Marcel Huber

  • An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi

    Georges N. Cohen;Valérie Barbe;Didier Flament;Michael Galperin

  • DNA Replication Origin Interference Increases the Spacing between Initiation Events in Human Cells

    Ronald Lebofsky;Roland Heilig;Max Sonnleitner;Jean Weissenbach

  • Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

    Isabelle Oberle;Giovanna Camerino;Roland Heilig;Lelia Grunebaum

  • Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)

    G Camerino;K H Grzeschik;M Jaye

  • A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis.

    S Saunier;J Calado;R Heilig;F Silbermann

  • Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

    Sophie Saunier;Joaquim Calado;Flora Silbermann

  • Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans.

    Franz P. W. Radner;Slaheddine Marrakchi;Peter Kirchmeier;Peter Kirchmeier;Gwang-Jin Kim;Gwang-Jin Kim

Frequent Co-Authors

Jean Weissenbach
Jean Weissenbach Centre national de la recherche scientifique, CNRS
Jean-Louis Mandel
Jean-Louis Mandel Institute of Genetics and Molecular and Cellular Biology
Alan T. Nurden
Alan T. Nurden Centre national de la recherche scientifique, CNRS
Lee Rowen
Lee Rowen Institute for Systems Biology in Seattle
Asao Fujiyama
Asao Fujiyama National Institute of Genetics
Yoshiyuki Sakaki
Yoshiyuki Sakaki Toyohashi University of Technology
Masahira Hattori
Masahira Hattori Waseda University
Marco A. Marra
Marco A. Marra University of British Columbia
Leroy Hood
Leroy Hood University of Washington
Richard K. Wilson
Richard K. Wilson Nationwide Children's Hospital

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