World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
84
Citations
29830
World Ranking
1355
National Ranking
20

Medicine

D-Index
85
Citations
30192
World Ranking
14496
National Ranking
181

Marc Cruts 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 Marc Cruts 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: 211 publications — 54th percentile

54% of scientists in this discipline score the same or lower.

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

Marc Cruts 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 Marc Cruts 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: 84 D-Index — 69th percentile

69% of scientists in this discipline score the same or lower.

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

Overview

Marc Cruts is a researcher affiliated with the University of Antwerp in Belgium. Their work primarily spans the fields of Medicine and Biochemistry, Genetics and Molecular Biology, with a focus on several subfields including Neurology, Physiology, Molecular Biology, and Aging.

The main research topics covered by Marc Cruts include:

  • Parkinson's Disease Mechanisms and Treatments
  • Neurological diseases and metabolism
  • Alzheimer's disease research and treatments
  • Amyotrophic Lateral Sclerosis Research
  • Epigenetics and DNA Methylation
  • Genetics, Aging, and Longevity in Model Organisms

Marc Cruts has contributed to publications in several noted academic venues, with the following journals featuring their recent papers:

  • Biological Psychiatry
  • Scientific Reports
  • Acta Neuropathologica

Their recent papers include:

  • "Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood," 2022, Biological Psychiatry
  • "Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis," 2020, Scientific Reports
  • "Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins," 2024, Acta Neuropathologica

Throughout their career, Marc Cruts has frequently collaborated with several researchers, including:

  • Christine Van Broeckhoven
  • Raffaele Ferrari
  • Dena Hernandez
  • Michael A. Nalls
  • Jonathan D. Rohrer

Best Publications

  • NanoPack: visualizing and processing long-read sequencing data.

    Wouter De Coster;Svenn D’Hert;Darrin T Schultz;Marc Cruts

  • Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

    Marc Cruts;Ilse Gijselinck;Julie van der Zee;Sebastiaan Engelborghs

  • The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS

    Kohji Mori;Shih-Ming Weng;Thomas Arzberger;Stephanie May

  • Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

    Lydia Hendriks;Cornelia M. van Duijn;Patrick Cras;Marc Cruts

  • A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

    Ilse Gijselinck;Tim Van Langenhove;Julie van der Zee;Kristel Sleegers

  • Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

    Karen Nuytemans;Jessie Theuns;Marc Cruts;Christine Van Broeckhoven

  • Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases

    Marc Cruts;Jessie Theuns;Christine Van Broeckhoven

  • Genetic association of apolipoprotein E with age-related macular degeneration

    Caroline C.W. Klaver;Mike Kliffen;Cornelia M. van Duijn;Albert Hofman

  • Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's disease

    C.M. van Duijn;P. de Knijff;M. Cruts;A. Wehnert;A. Wehnert

  • Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

    Kohji Mori;Thomas Arzberger;Thomas Arzberger;Friedrich A. Grässer;Ilse Gijselinck

  • Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

    Marc Cruts;Cornelia M. van Duijn;Hubert Backhovens;Marleen Van den Broeck

  • Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study.

    Arjen J. C. Slooter;Marc Cruts;Sandra Kalmijn;Albert Hofman

  • APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.

    Kristel Sleegers;Nathalie Brouwers;Ilse Gijselinck;Jessie Theuns

  • Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40†‡§

    Samir Kumar-Singh;Jessie Theuns;Bianca Van Broeck;Daniel Pirici

  • Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3

    C Van Broeckhoven;H Backhovens;H Backhovens;M Cruts;G De Winter;G De Winter

  • Frontotemporal dementia and its subtypes: a genome-wide association study

    Raffaele Ferrari;Raffaele Ferrari;Dena G Hernandez;Dena G Hernandez;Michael A Nalls;Jonathan D Rohrer

  • The role of tau (MAPT) in frontotemporal dementia and related tauopathies.

    R. Rademakers;M. Cruts;C. van Broeckhoven

  • hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

    Kohji Mori;Sven Lammich;Ian R. A. Mackenzie;Ignasi Forné

  • The genetics and neuropathology of frontotemporal lobar degeneration

    Anne Sieben;Tim Van Langenhove;Sebastiaan Engelborghs;Jean-Jacques Martin

  • A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

    Julie van der Zee;Ilse Gijselinck;Lubina Dillen;Tim Van Langenhove

Frequent Co-Authors

Christine Van Broeckhoven
Christine Van Broeckhoven University of Antwerp
Sebastiaan Engelborghs
Sebastiaan Engelborghs Vrije Universiteit Brussel
Peter Paul De Deyn
Peter Paul De Deyn University of Antwerp
Kristel Sleegers
Kristel Sleegers University of Antwerp
Patrick Cras
Patrick Cras University of Antwerp
Rosa Rademakers
Rosa Rademakers University of Antwerp
Samir Kumar-Singh
Samir Kumar-Singh University of Antwerp
Albert Hofman
Albert Hofman Harvard University
Jurgen Del-Favero
Jurgen Del-Favero University of Antwerp

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