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Genetics
Belgium
2026

D-Index & Metrics

Genetics

D-Index
94
Citations
28225
World Ranking
938
National Ranking
10

Medicine

D-Index
94
Citations
29308
World Ranking
10564
National Ranking
121

Guy Van Camp 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 Guy Van Camp 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: 371 publications — 85th percentile

85% of scientists in this discipline score the same or lower.

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

Guy Van Camp 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 Guy Van Camp 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

  • 2026 - Research.com Genetics in Belgium Leader Award
  • 2024 - Research.com Genetics in Belgium Leader Award

Overview

Guy Van Camp is affiliated with the University of Antwerp in Belgium and has contributed extensively to research primarily within the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their work spans several subfields, most notably Molecular Biology, Oncology, Sensory Systems, Cancer Research, and Pulmonary and Respiratory Medicine.

The scientist's research covers a range of topics, with significant publications addressing Hearing, Cochlea, Tinnitus, and Genetics; Epigenetics and DNA Methylation; Cancer Genomics and Diagnostics; RNA modifications and cancer; Colorectal Cancer Treatments and Studies; Vestibular and auditory disorders; and Hearing Loss and Rehabilitation.

Among the recent papers produced by Guy Van Camp are the following:

  • Punching Holes in Cellular Membranes: Biology and Evolution of Gasdermins, 2021, Trends in Cell Biology
  • GSDME and its role in cancer: From behind the scenes to the front of the stage, 2020, International Journal of Cancer
  • Methylation biomarkers for early cancer detection and diagnosis: Current and future perspectives, 2022, European Journal of Cancer
  • DNA Methylation as a Diagnostic Biomarker for Malignant Mesothelioma: A Systematic Review and Meta-Analysis, 2021, Journal of Thoracic Oncology
  • Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss, 2021, Genetics in Medicine

Guy Van Camp frequently collaborates with several researchers, including:

  • Ken Op de Beeck
  • Marc Peeters
  • Erik Fransén
  • Joe Ibrahim
  • Vincent Van Rompaey

Major publication venues for Guy Van Camp include:

  • Otology & Neurotology
  • Molecular Oncology
  • Clinical Epigenetics
  • ESMO Open
  • Genes

Best Publications

  • GJB2 mutations and degree of hearing loss: a multicenter study.

    Rikkert L. Snoeckx;Patrick L M Huygen;Delphine Feldmann;Sandrine Marlin

  • Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

    Nele Hilgert;Richard J.H. Smith;Guy Van Camp

  • Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma

    Behrouz Hassannia;Bartosz Wiernicki;Irina Ingold;Feng Qu

  • Congenital hearing loss.

    Anna M.H. Korver;Richard J.H. Smith;Guy Van Camp;Mark R. Schleiss

  • NONSYNDROMIC HEARING IMPAIRMENT: UNPARALLELED HETEROGENEITY

    G. Van Camp;P. J. Willems;R. J. H. Smith

  • Mutations in the human |[alpha]|-tectorin gene cause autosomal dominant non-syndromic hearing impairment

    Kristien Verhoeven;Lut Van Laer;Karin Kirschhofer;P Kevin Legan

  • A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

    F. J. Del Castillo;M. Rodriguez-Ballesteros;A. Alvarez;T. Hutchin

  • Nonsyndromic hearing impairment is associated with a mutation in DFNA5

    Lut Van Laer;Egbert H Huizing;Margriet Verstreken;Diederick van Zuijlen

  • Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

    Sedigheh Delmaghani;Francisco J del Castillo;Vincent Michel;Michel Leibovici

  • Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

    Shin Ichi Usami;Satoko Abe;Mike D. Weston;Hideichi Shinkawa

  • Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

    Ignacio Del Castillo;Miguel A. Moreno-Pelayo;Francisco J. Del Castillo;Zippora Brownstein

  • The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors

    E. Van Eyken;G. Van Camp;L. Van Laer

  • Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study.

    Erik Fransen;Vedat Topsakal;Jan Jaap Hendrickx;Lut Van Laer

  • Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

    Kumar N. Alagramam;Huijun Yuan;Markus H. Kuehn;Crystal L. Murcia

  • Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

    Irina N. Bespalova;Irina N. Bespalova;Guy Van Camp;Steven J.H. Bom;David J. Brown

  • Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

    W. T. Mcguirt;S. D. Prasad;A. J. Griffith;H. P. M. Kunst

  • Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

    D. A. Scott;M. L. Kraft;R. Carmi;A. Ramesh

  • Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

    Sigrid Wayne;Nahid G. Robertson;Frank DeClau;Nancy Chen

  • A genotype-phenotype correlation for GJB2 (connexin 26) deafness.

    K Cryns;E Orzan;A Murgia;P L M Huygen

  • The hereditary hearing loss homepage

    G. Van Camp;R.J.H. Smith

Frequent Co-Authors

Lut Van Laer
Lut Van Laer University of Antwerp
Erik Fransen
Erik Fransen University of Antwerp
Richard J.H. Smith
Richard J.H. Smith University of Iowa
Paul Van de Heyning
Paul Van de Heyning University of Antwerp
Cor W. R. J. Cremers
Cor W. R. J. Cremers Radboud University
Marc Peeters
Marc Peeters University of Antwerp
Wim Vanden Berghe
Wim Vanden Berghe University of Antwerp
Patrick Pauwels
Patrick Pauwels University of Antwerp
Hannie Kremer
Hannie Kremer Radboud University

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