World's Best Scientists 2026 revealed!
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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

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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