Peter Van Hauwe

1.3k total citations
18 papers, 787 citations indexed

About

Peter Van Hauwe is a scholar working on Sensory Systems, Molecular Biology and Otorhinolaryngology. According to data from OpenAlex, Peter Van Hauwe has authored 18 papers receiving a total of 787 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Sensory Systems, 10 papers in Molecular Biology and 3 papers in Otorhinolaryngology. Recurrent topics in Peter Van Hauwe's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Ion channel regulation and function (3 papers) and Ear Surgery and Otitis Media (3 papers). Peter Van Hauwe is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Ion channel regulation and function (3 papers) and Ear Surgery and Otitis Media (3 papers). Peter Van Hauwe collaborates with scholars based in Belgium, United States and Netherlands. Peter Van Hauwe's co-authors include Guy Van Camp, Paul Coucke, Richard J. Smith, Patrick J. Willems, Cor W. R. J. Cremers, Lorraine A. Everett, Achih Chen, P.L.M. Huygen, Isabelle Schatteman and Paul Van de Heyning and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

Peter Van Hauwe

18 papers receiving 764 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Peter Van Hauwe Belgium 12 611 356 317 197 137 18 787
Hans-Peter Zenner Germany 12 548 0.9× 246 0.7× 265 0.8× 69 0.4× 191 1.4× 14 717
R Mueller United Kingdom 9 928 1.5× 938 2.6× 256 0.8× 119 0.6× 244 1.8× 22 1.4k
C. R. Srikumari Srisailapathy India 12 598 1.0× 482 1.4× 204 0.6× 75 0.4× 133 1.0× 34 757
Katsuhisa Ikeda Japan 12 458 0.7× 322 0.9× 149 0.5× 137 0.7× 105 0.8× 14 710
Elie El‐Zir Lebanon 5 402 0.7× 274 0.8× 142 0.4× 45 0.2× 144 1.1× 6 552
Ibis Menéndez United States 11 590 1.0× 487 1.4× 173 0.5× 106 0.5× 131 1.0× 20 776
L. Van Laer Belgium 11 629 1.0× 304 0.9× 260 0.8× 83 0.4× 316 2.3× 17 811
Achih Chen United States 6 355 0.6× 221 0.6× 154 0.5× 84 0.4× 93 0.7× 7 514
Christina Sloan-Heggen United States 7 610 1.0× 366 1.0× 186 0.6× 202 1.0× 175 1.3× 10 742
Hidekane Yoshimura Japan 16 494 0.8× 451 1.3× 127 0.4× 118 0.6× 180 1.3× 46 845

Countries citing papers authored by Peter Van Hauwe

Since Specialization
Citations

This map shows the geographic impact of Peter Van Hauwe'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 Peter Van Hauwe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Van Hauwe more than expected).

Fields of papers citing papers by Peter Van Hauwe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Van Hauwe. 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 Peter Van Hauwe. The network helps show where Peter Van Hauwe may publish in the future.

Co-authorship network of co-authors of Peter Van Hauwe

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Van Hauwe. A scholar is included among the top collaborators of Peter Van Hauwe 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 Peter Van Hauwe. Peter Van Hauwe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Baere, Thierry De, Peter Van Hauwe, Hans De Beenhouwer, et al.. (2005). An interlaboratory comparison of ITS2-PCR for the identification of yeasts, using the ABI Prism 310 and CEQ8000 capillary electrophoresis systems. BMC Microbiology. 5(1). 7 indexed citations
2.
Brouwer, Arjan Pm de, Ronald J. E. Pennings, Peter Van Hauwe, et al.. (2003). Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family. Human Genetics. 112(2). 156–163. 37 indexed citations
3.
Ensink, R.J.H., P.L.M. Huygen, Peter Van Hauwe, et al.. (2000). A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region. European Archives of Oto-Rhino-Laryngology. 257(2). 62–67. 11 indexed citations
4.
Hauwe, Peter Van, Paul Coucke, R.J.H. Ensink, et al.. (2000). Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region. American Journal of Medical Genetics. 93(3). 184–187. 55 indexed citations
5.
Camp, Guy Van, Paul Coucke, Peter Van Hauwe, et al.. (2000). DFNA 2, 5, 8, 12. Advances in oto-rhino-laryngology. 56. 68–77. 2 indexed citations
6.
Coucke, Paul, Peter Van Hauwe, Lorraine A. Everett, et al.. (1999). Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome. Journal of Medical Genetics. 36(6). 475–477. 40 indexed citations
7.
Hauwe, Peter Van, Paul Coucke, & Guy Van Camp. (1999). The Dfna2 Locus for Hearing Impairment: Two Genes Regulating K+ Ion Recycling in the Inner Ear. British Journal of Audiology. 33(5). 285–289. 10 indexed citations
8.
Cremers, C. W. R. J., R.J.C. Admiraal, Lorraine A. Everett, et al.. (1998). Progressive Sensorineural Hearing Loss and a Widened Vestibular Aqueduct in Pendred Syndrome. Archives of Otolaryngology - Head and Neck Surgery. 124(5). 501–501. 59 indexed citations
9.
Kunst, Henricus P. M., Henri A. M. Marres, P.L.M. Huygen, et al.. (1998). Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2. The Laryngoscope. 108(1). 74–80. 21 indexed citations
10.
Verhoeven, Kristien, Karin Kirschhofer, P. Kevin Legan, et al.. (1998). Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nature Genetics. 19(1). 60–62. 253 indexed citations
11.
Hauwe, Peter Van, Lorraine A. Everett, Paul Coucke, et al.. (1998). Two Frequent Missense Mutations in Pendred Syndrome. Human Molecular Genetics. 7(7). 1099–1104. 143 indexed citations
12.
Kastury, Kumar, Wayne E. Taylor, Stefan Arver, et al.. (1997). Complementary Deoxyribonucleic Acid Cloning and Characterization of a Putative Human Axonemal Dynein Light Chain Gene1. The Journal of Clinical Endocrinology & Metabolism. 82(9). 3047–3053. 20 indexed citations
13.
Coucke, Paul, Guy Van Camp, Osman Demırhan, et al.. (1997). The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q. Genomics. 40(1). 48–54. 24 indexed citations
14.
Kastury, Kumar, Wayne E. Taylor, Paul Coucke, et al.. (1997). Chromosomal Mapping of Two Members of the Human Dynein Gene Family to Chromosome Regions 7p15 and 11q13 near the Deafness Loci DFNA 5 and DFNA 11. Genomics. 44(3). 362–364. 4 indexed citations
15.
Camp, Guy Van, Paul Coucke, Isabelle Schatteman, et al.. (1997). Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1p. Genomics. 41(1). 70–74. 38 indexed citations
16.
Chen, Achih, Sigrid Wayne, Adam Bell, et al.. (1997). New gene for autosomal recessive non‐syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 7 indexed citations
17.
Chen, Achih, Sigrid Wayne, Arabandi Ramesh, et al.. (1997). New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 39 indexed citations
18.
Springael, Dirk, Annemie Ryngaert, Peter Van Hauwe, et al.. (1996). RP4::Mu3A-mediated in vivo cloning and transfer of a chlorobiphenyl catabolic pathway. Microbiology. 142(11). 3283–3293. 17 indexed citations

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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