Guy Van Camp

25.5k total citations · 1 hit paper
385 papers, 14.3k citations indexed

About

Guy Van Camp is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Guy Van Camp has authored 385 papers receiving a total of 14.3k indexed citations (citations by other indexed papers that have themselves been cited), including 179 papers in Sensory Systems, 155 papers in Molecular Biology and 63 papers in Neurology. Recurrent topics in Guy Van Camp's work include Hearing, Cochlea, Tinnitus, Genetics (177 papers), Vestibular and auditory disorders (63 papers) and Hearing Loss and Rehabilitation (54 papers). Guy Van Camp is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (177 papers), Vestibular and auditory disorders (63 papers) and Hearing Loss and Rehabilitation (54 papers). Guy Van Camp collaborates with scholars based in Belgium, United States and Netherlands. Guy Van Camp's 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 and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Guy Van Camp

379 papers receiving 14.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Congenital hearing loss

2017 341 citations Richard J. Smith, Guy Van Camp et al. profile →

Peers

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-authorship network of co-authors of Guy Van Camp

This figure shows the co-authorship network connecting the top 25 collaborators of Guy Van Camp. A scholar is included among the top collaborators of Guy Van Camp based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Guy Van Camp. Guy Van Camp is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Lineages and sublineages of high-risk human papillomavirus types associated with cervical cancer and precancer: a systematic review and meta-analysis 2025 ·JNCI Journal of the National Cancer Institute ·(unknown), Margo Bell, Ken Op de Beeck, Guy Van Camp, Severien Van Keer, Alex Vorsters	1
2	IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assay 2024 ·British Journal of Cancer ·(unknown), (unknown), (unknown), Joe Ibrahim, Arvid Suls, Dieter Peeters, (unknown), Alexander Hoischen, Erik Fransén, Marc Peeters, Guy Van Camp, Ken Op de Beeck	6
3	Simultaneous detection of eight cancer types using a multiplex droplet digital PCR assay 2024 ·Molecular Oncology ·(unknown), (unknown), (unknown), (unknown), Dieter Peeters, Marc Peeters, Guy Van Camp, Ken Op de Beeck	3
4	NPY Methylated ctDNA is a Promising Biomarker for Treatment Response Monitoring in Metastatic Colorectal Cancer 2023 ·Clinical Cancer Research ·(unknown), Greetje Vanhoutte, Willem Lybaert, Wim Demey, Jochen Decaestecker, (unknown), (unknown), Karen Zwaenepoel, Patrick Pauwels, Erik Fransén, Ken Op de Beeck, Guy Van Camp, Christian Rolfo, Marc Peeters	12
5	Same Day Discharge Strategy by Default in a Tertiary Catheterization Laboratory in Belgium: Value Based Healthcare-Change in Practice 2023 ·Health Policy ·Eric Wyffels, (unknown), (unknown), (unknown), Tom De Potter, Guy Van Camp, Carlos Collet, Jeroen Sonck, Marc Vanderheyden, Jozef Bartúnek, Emanuele Barbato, Konstantinos Bermpeis, Dario Tino Bertolone, Emanuele Gallinoro, Giuseppe Esposito, (unknown), (unknown), (unknown), Bernard De Bruyne	4
6	Singlet oxygen-based photoelectrochemical detection of single-point mutations in the KRAS oncogene 2023 ·Biosensors and Bioelectronics ·Elise Daems, (unknown), (unknown), (unknown), (unknown), Karen Zwaenepoel, Timon Vandamme, Ken Op de Beeck, Senada Koljenović, Marc Peeters, Guy Van Camp, Karolien De Wael	7
7	Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability 2021 ·Genes ·Maria Pina Concas, Anna Morgan, (unknown), A. Paul Nagtegaal, Berthe C. Oosterloo, Sudha Seshadri, Nancy L. Heard‐Costa, Guy Van Camp, Erik Fransén, Margherita Francescatto, Giancarlo Logroscino, Rodolfo Sardone, Nicola Quaranta, Paolo Gasparini, Giorgia Girotto	4
8	Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes 2021 ·European Journal of Human Genetics ·Erik Fransén, (unknown), (unknown), Manou Sommen, R. de Ridder, Geert Vandeweyer, Luigi Bisceglia, Vincent Soler, Alexander Hoischen, Geert Mortier, François Malecaze, Carina Koppen, Guy Van Camp	12
9	Establishment and characterization of cetuximab resistant head and neck squamous cell carcinoma cell lines: focus on the contribution of the AP-1 transcription factor. 2015 ·PubMed Central ·Carolien Boeckx, (unknown), Ken Op de Beeck, Ridha Limame, Guy Van Camp, Marc Peeters, Jan B. Vermorken, Pol Specenier, An Wouters, Marc Baay, Filip Lardon	24
10	Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia 2010 ·Annals of Human Genetics ·(unknown), Isabelle Schrauwen, (unknown), Erik Fransén, (unknown), Megan Ealy, (unknown), Hammadi Ayadi, (unknown), Nabil Driss, Abdelmonem Ghorbel, Richard J. Smith, Saber Masmoudi, Guy Van Camp	17
11	Safety of ultrasound contrast agents: 'Primum non nocere'? 2009 ·Acta Cardiologica ·Bernard Cosyns, A. Pasquet, Guy Van Camp, Sophie Hernot, Steven Droogmans, (unknown), Johan De Sutter, Patrizio Lancellotti	2
12	A New, Easy, and Rapid High-Throughput Detection Method for the Common GJB2 ( CX26 ), 35delG Mutation 2007 ·Genetic Testing ·Els Van Eyken, Guy Van Camp, Jan Hendrickx, (unknown), Ann Vandevelde, (unknown), Paul Van de Heyning, L. Van Laer	3
13	Low frequency of the GJB6 342 Kb deletion in the belgian deaf population. 2002 ·The American Journal of Human Genetics ·(unknown), Wim Wuyts, Ignacio del Castillo, (unknown), Nils Peeters, (unknown), (unknown), (unknown), Fabián Moreno, Guy Van Camp, Lionel Van Maldergem	2
14	A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13 2001 ·Clinical Otolaryngology ·R.J.H. Ensink, P.L.M. Huygen, (unknown), (unknown), Guy Van Camp, (unknown)	6
15	The M34T Allele Variant of Connexin 26 2000 ·Genetic Testing ·Robert A. Cucci, Sai Prasad, Philip M. Kelley, Glenn E. Green, Katrien Storm, (unknown), Edward Cohn, Guy Van Camp, Richard J. Smith	43
16	Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome 1999 ·Journal of Medical Genetics ·Paul Coucke, Peter Van Hauwe, Lorraine A. Everett, Osman Demırhan, (unknown), Nicole Dietrich, Richard J. Smith, Beth Coyle, William Reardon, Richard C. Trembath, P J Willems, (unknown), Guy Van Camp	40
17	Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea. 1998 ·PubMed ·(unknown), Guy Van Camp, (unknown), Ed Green, Margriet Verstreken, Isabelle Schatteman, Paul Van de Heyning, Wendy Balemans, Paul Coucke, (unknown), Richard J. Smith, E. H. Huizing, Patrick J. Willems	18
18	Review paper. Recent developments in genetic hearing impairment. 1998 ·Journal of Audiovisual Media in Medicine ·Guy Van Camp, PJ Willems, (unknown), Henri A. M. Marres	0
19	Branchio-Oto-Renal Syndrome: Identification of Novel Mutations, Molecular Characterization, Mutation Distribution, and Prospects for Genetic Testing 1997 ·Genetic Testing ·Shrawan Kumar, Karen Deffenbacher, Cor W. R. J. Cremers, Guy Van Camp, William J. Kimberling	40
20	Localisation of the gene for Van Buchem disease to a candidate region of less than 1 cM on chromosome 17. 1997 ·Data Archiving and Networked Services (DANS) ·Wendy Balemans, Wim Van Hul, Els Van Hul, (unknown), Robert J. Stokroos, Guy Van Camp, PJ Willems	1

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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