Guy Van Camp

25.5k citations
385 papers · 14.3k · 1 hit paper · h-index 65

Impact in

Papers in

  • Sensory Systems 179
    • Hearing, Cochlea, Tinnitus, Genetics 177
  • Molecular Biology 155
    • Connexins and lens biology 32
    • RNA regulation and disease 24
    • Epigenetics and DNA Methylation 20
    • RNA and protein synthesis mechanisms 15
Co-authors
Richard J. Smith (75 shared papers)Ken Op de Beeck (61 shared papers)Erik Fransén (70 shared papers)Lut Van Laer (29 shared papers)Paul Van de Heyning (48 shared papers)Nele Hilgert (12 shared papers)Patrick J. Willems (26 shared papers)Paul Coucke (34 shared papers)
Journals
European Journal of Human Genetics (19 papers)Human Genetics (18 papers)Otology & Neurotology (14 papers)Human Mutation (13 papers)The American Journal of Human Genetics (12 papers)
Partner nations
BelgiumUnited StatesNetherlands

In The Last Decade

Guy Van Camp

379 papers receiving 14.0k citations

Guy Van Camp's Hit Papers

Congenital hearing loss 2017 · 341 citations
3410+3+6Years since publication100200300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2017 Nature Reviews Disease Primers

Peers

Guy Van Camp
Comparison fields: 5 of 174
  • Sensory Systems 7.3k
  • Otorhinolaryngology 2.1k
  • Neurology 3.2k
  • Endocrine and Autonomic Systems 887
  • Cognitive Neuroscience 2.4k
Replace Bradley A. Schulte with:
Bradley A. Schulte United States
Cynthia C. Morton United States
Karen B. Avraham Israel
Xavier Estivill Spain
Val C. Sheffield United States
Sheikh Riazuddin Pakistan
David P. Kelsell United Kingdom
Arnold Münnich France
Peter Nürnberg Germany
Suzanne M. Leal United States
Guy Van Camp relative to Bradley A. Schulte United States Bradley A. Schulte's profile →
Citations per field
00.5×2×4×5.4×
Bradley A. Schulte · 1×
Citations per year

Countries citing papers authored by Guy Van Camp

Since Specialization
Citations

This map shows the geographic impact of Guy Van Camp's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Guy Van Camp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Guy Van Camp more than expected).

Fields of papers citing papers by Guy Van Camp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guy Van Camp. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Guy Van Camp. The network helps show where Guy Van Camp may publish in the future.

Co-authors

The 25 scholars most cited alongside Guy Van Camp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Guy Van Camp Line = papers co-authored together Guy Van Camp links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 385 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness
New England Journal of Medicine ·Robert J. Morell, Hung Jeff Kim, Linda J. Hood, Leah Goforth, Karen H. Friderici, Rachel Fisher, Guy Van Camp, Charles I. Berlín, Carole Oddoux, Harry Ostrer, Bronya J.B. Keats, Thomas B. Friedman, Theresa San Agustin, Jan E. Dumon
1998432
2
Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?
Mutation Research/Reviews in Mutation Research ·Nele Hilgert, Richard J. Smith, Guy Van Camp
2008354
3
Congenital hearing loss
Nature Reviews Disease Primers ·Anna M.H. Korver, Richard J. Smith, Guy Van Camp, Mark R. Schleiss, Maria Bitner‐Glindzicz, Lawrence R. Lustig, Shin‐ichi Usami, An Boudewyns
Hit paper breakdown →		2017341
4
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
Nature Genetics ·Lut Van Laer, E. H. Huizing, Margriet Verstreken, Diederick van Zuijlen, J. Wauters, Paul Bossuyt, Paul Van de Heyning, Wyman T. McGuirt, Richard J. Smith, Patrick J. Willems, P. Kevin Legan, Guy P. Richardson, Guy Van Camp
1998315
5
Nonsyndromic hearing impairment: unparalleled heterogeneity.
PubMed ·Guy Van Camp, P J Willems, Richard J. Smith
1997279
6
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
Nature Genetics ·Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer, P. Kevin Legan, David C. Hughes, Isabelle Schatteman, Margriet Verstreken, Peter Van Hauwe, Paul Coucke, Achih Chen, Richard J. Smith, Thomas Somers, F. Erwin Offeciers, Paul Van de Heyning, Guy P. Richardson, F. Wachtler, William J. Kimberling, Patrick J. Willems, Paul Govaerts, Guy Van Camp
1998253
7
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy
Nature Genetics ·Sedigheh Delmaghani, Francisco Castillo, Vincent Michel, Michel Leibovici, Asadollah Aghaie, Uri Ron, Lut Van Laer, Nir Ben‐Tal, Guy Van Camp, Dominique Weil, Francina Langa, Mark Lathrop, Paul Avan, Christine Petit
2006239
8
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations
Human Genetics ·Shin‐ichi Usami, Satoko Abe, Mike D. Weston, Hideichi Shinkawa, Guy Van Camp, William J. Kimberling
1999227
9
The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors
Audiology and Neurotology ·Els Van Eyken, Guy Van Camp, L. Van Laer
2007220
10
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
Human Mutation ·DA Scott, ML Kraft, Rivka Carmi, A. Ramesh, Khalil Elbedour, Yael Yairi, C. R. Srikumari Srisailapathy, S. Rosengren, AF Markham, Mueller Rf, Nicholas Lench, Guy Van Camp, Richard J. Smith, Val C. Sheffield
1998196
11
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
Nature Genetics ·Wyman T. McGuirt, Sai Prasad, Andrew J. Griffith, Henricus P. M. Kunst, Glenn E. Green, Karl B. Shpargel, Christina L. Runge, Christy Huybrechts, Robert F. Mueller, Eric D. Lynch, Mary‐Claire King, Han G. Brunner, Cor W. R. J. Cremers, Masamine Takanosu, Shiwu Li, Machiko Arita, Richard Mayne, Darwin J. Prockop, Guy Van Camp, Richard J. Smith
1999193
12
CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1
European Journal of Human Genetics ·Erik Fransén, Vance Lemmon, Guy Van Camp, Lieve Vits, Paul Coucke, Patrick J. Willems
1995169
13
The hereditary hearing loss homepage
Guy Van Camp, Richard J. Smith
1997161
14
Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies
Annals of Oncology ·Nele Boeckx, Reija Koukakis, Ken Op de Beeck, Christian Rolfo, Guy Van Camp, Salvatore Siena, Josep Tabernero, Jean‐Yves Douillard, Thierry André, Marc Peeters
2017156
15
Two Frequent Missense Mutations in Pendred Syndrome
Human Molecular Genetics ·Peter Van Hauwe, Lorraine A. Everett, Paul Coucke, Daryl A. Scott, Michelle L. Kraft, Carrie Ris‐Stalpers, Cuny Bolder, B.J. Otten, Jan J. M. de Vijlder, Nicole Dietrich, A. Ramesh, S. C. R. Srisailapathy, Agnete Parving, C. W. R. J. Cremers, Patrick J. Willems, Richard J. Smith, Eric D. Green, Guy Van Camp
1998143
16
Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease
Human Mutation ·Kim Cryns, Theru A. Sivakumaran, Jody M.W. van den Ouweland, Ronald J. E. Pennings, Cor W. R. J. Cremers, Kris Flothmann, Terry‐Lynn Young, Richard J. Smith, Marci M. Lesperance, Guy Van Camp
2003142
17
Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment
Audiological Medicine ·Manuela Mazzoli, Guy Van Camp, Valerie Newton, N. Giarbini, Frank Declau, Agnete Parving
2003135
18
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation
Human Genetics ·Akihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, Atsushi Namba, Satoko Abe, Lut Van Laer, Guy Van Camp, Shin‐ichi Usami
2003133
19
Function and Expression Pattern of Nonsyndromic Deafness Genes
Current Molecular Medicine ·Nele Hilgert, Richard J. Smith, Guy Van Camp
2009123
20
A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene
The American Journal of Human Genetics ·Guy Van Camp, Rikkert L. Snoeckx, Nele Hilgert, Jenneke van den Ende, Hisakumi Fukuoka, Michio Wagatsuma, Hiroaki Suzuki, R.M. Erica Smets, Filip Vanhoenacker, Frank Declau, Paul Van de Heyning, Shin‐ichi Usami
2006120

About Guy Van Camp

Guy Van Camp is a scholar working on Sensory Systems, Molecular Biology, Neurology, Cognitive Neuroscience and Otorhinolaryngology, having authored 385 papers that have together received 14.3k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (177 papers), Vestibular and auditory disorders (63 papers), Hearing Loss and Rehabilitation (54 papers), Ear Surgery and Otitis Media (52 papers), Connexins and lens biology (32 papers), RNA regulation and disease (24 papers), Epigenetics and DNA Methylation (20 papers) and RNA and protein synthesis mechanisms (15 papers). The work is most often cited by research in Sensory Systems (7.3k citations), Otorhinolaryngology (2.1k citations), Neurology (3.2k citations), Endocrine and Autonomic Systems (887 citations) and Cognitive Neuroscience (2.4k citations). Guy Van Camp has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Richard J. Smith, Ken Op de Beeck, Erik Fransén, Lut Van Laer, Paul Van de Heyning, Nele Hilgert, Patrick J. Willems, Paul Coucke, Cor W. R. J. Cremers and Marc Peeters. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Otology & Neurotology, Human Mutation and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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