P.L.M. Huygen

8.2k total citations
235 papers, 5.0k citations indexed

About

P.L.M. Huygen is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, P.L.M. Huygen has authored 235 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Sensory Systems, 100 papers in Neurology and 57 papers in Molecular Biology. Recurrent topics in P.L.M. Huygen's work include Hearing, Cochlea, Tinnitus, Genetics (120 papers), Vestibular and auditory disorders (99 papers) and Hearing Loss and Rehabilitation (39 papers). P.L.M. Huygen is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (120 papers), Vestibular and auditory disorders (99 papers) and Hearing Loss and Rehabilitation (39 papers). P.L.M. Huygen collaborates with scholars based in Netherlands, United States and Belgium. P.L.M. Huygen's co-authors include Cor W. R. J. Cremers, W. I. M. Verhagen, R.J.C. Admiraal, Hannie Kremer, Ronald J. E. Pennings, Guy Van Camp, Henricus P. M. Kunst, W. R. J. Cremers, F.B.M. Joosten and Henri A. M. Marres and has published in prestigious journals such as New England Journal of Medicine, Scientific Reports and Annals of the New York Academy of Sciences.

In The Last Decade

P.L.M. Huygen

228 papers receiving 4.9k citations

Peers

P.L.M. Huygen

NEURO

OTORH

Shin‐ichi Usami Japan

Lawrence R. Lustig United States

Kaoru Ogawa Japan

Kimitaka Kaga Japan

Matti Anniko Sweden

Daniel Choo United States

Maria Bitner‐Glindzicz United Kingdom

Patricia A. Schachern United States

Leopoldo Zelante Italy

Françoise Denoyelle France

Shin‐ichi Usami Japan

P.L.M. Huygen

5.3k ×1.9

2.5k ×1.4

NEURO

3.3k ×2.0

1.7k ×1.6

OTORH

1.8k ×1.9

Citations per year, relative to P.L.M. Huygen P.L.M. Huygen (= 1×) peers Shin‐ichi Usami

Countries citing papers authored by P.L.M. Huygen

Since Specialization

Citations

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

Fields of papers citing papers by P.L.M. Huygen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P.L.M. Huygen. 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 P.L.M. Huygen. The network helps show where P.L.M. Huygen may publish in the future.

Co-authorship network of co-authors of P.L.M. Huygen

This figure shows the co-authorship network connecting the top 25 collaborators of P.L.M. Huygen. A scholar is included among the top collaborators of P.L.M. Huygen 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 P.L.M. Huygen. P.L.M. Huygen 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

Morin, Matías, Kevin T. Booth, P.L.M. Huygen, et al.. (2020). Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants. Scientific Reports. 10(1). 6213–6213. 66 indexed citations

Oonk, Anne M.M., Ronald J. E. Pennings, Ilse Feenstra, et al.. (2015). Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment. Ear and Hearing. 37(1). 103–111. 14 indexed citations

Oonk, Anne M.M., P.L.M. Huygen, Margit Schraders, et al.. (2014). Similar Phenotypes Caused by Mutations in OTOG and OTOGL. Ear and Hearing. 35(3). e84–e91. 18 indexed citations

Huygen, P.L.M., et al.. (2011). Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family. Hearing Research. 282(1-2). 167–177. 12 indexed citations

Pennings, Ronald J. E., et al.. (2011). Phenotypes of Two Dutch DFNA3 Families with Mutations in GJB2. Annals of Otology Rhinology & Laryngology. 120(3). 191–197. 10 indexed citations

Schraders, Margit, Kwanghyuk Lee, Jaap Oostrik, et al.. (2010). Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. The American Journal of Human Genetics. 86(2). 138–147. 50 indexed citations

Meulstee, Jan, et al.. (2010). Usefulness of additional measurements of the median nerve with ultrasonography. Neurological Sciences. 31(6). 721–725. 25 indexed citations

Hildebrand, Michael S., Luke C. Gandolfo, A. Eliot Shearer, et al.. (2010). A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss. The Laryngoscope. 120(12). 2489–2493. 17 indexed citations

Huygen, P.L.M., et al.. (2009). Audiometric and Vestibular Features in a Second Dutch DFNA20/26 Family with a Novel Mutation in ACTG1. Annals of Otology Rhinology & Laryngology. 118(5). 382–390. 19 indexed citations

10.

Pauw, Robert J., et al.. (2009). Vestibular Impairment in a Dutch DFNA15 Family with an L289F Mutation in POU4F3. Audiology and Neurotology. 14(5). 303–307. 11 indexed citations

11.

Pauw, Robert J., et al.. (2008). Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in <i>TECTA</i>. Audiology and Neurotology. 14(3). 153–162. 14 indexed citations

12.

Topsakal, Vedat, Ronald J. E. Pennings, Heleen te Brinke, et al.. (2005). Phenotype Determination Guides Swift Genotyping of a DFNA2/KCNQ4 Family With a Hot Spot Mutation (W276S). Otology & Neurotology. 26(1). 52–58. 30 indexed citations

13.

Huygen, P.L.M., et al.. (2003). Longitudinal Analysis of Hearing Loss in a Case of Hemosiderosis of the Central Nervous System. Otology & Neurotology. 24(5). 738–742. 27 indexed citations

14.

Ensink, R.J.H., et al.. (2001). A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13. Clinical Otolaryngology. 26(4). 310–316. 6 indexed citations

15.

Kunst, Henricus P. M., et al.. (2000). The phenotype of DFNA13/: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment. American Journal of Otolaryngology. 21(2). 181–187. 25 indexed citations

16.

Admiraal, R.J.C., et al.. (2000). Hearing Loss in the Nonocular Stickler Syndrome Caused by a COL11A2 Mutation. The Laryngoscope. 110(3). 457–461. 19 indexed citations

17.

Admiraal, R.J.C. & P.L.M. Huygen. (1997). Vestibular areflexia as a cause of delayed motor skill development in children with the CHARGE association. International Journal of Pediatric Otorhinolaryngology. 39(3). 205–222. 35 indexed citations

18.

Cremers, Cor W. R. J., et al.. (1995). The Treacher Collins Syndrome: A Clinical, Radiological, and Genetic Linkage Study on Two Pedigrees. Archives of Otolaryngology - Head and Neck Surgery. 121(5). 509–514. 49 indexed citations

19.

Huygen, P.L.M., et al.. (1994). Auditory Abnormalities, Including 'Precocious Presbyacusis', in Myotonic Dystrophy. International Journal of Audiology. 33(2). 73–84. 13 indexed citations

20.

Manni, Johannes J., et al.. (1990). Hyperostosis Cranialis Interna. New England Journal of Medicine. 322(7). 450–454. 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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