Els Van Eyken

1.5k total citations
9 papers, 430 citations indexed

About

Els Van Eyken is a scholar working on Sensory Systems, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Els Van Eyken has authored 9 papers receiving a total of 430 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Sensory Systems, 4 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Els Van Eyken's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), Mitochondrial Function and Pathology (3 papers) and Genetic and phenotypic traits in livestock (2 papers). Els Van Eyken is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), Mitochondrial Function and Pathology (3 papers) and Genetic and phenotypic traits in livestock (2 papers). Els Van Eyken collaborates with scholars based in Belgium, Netherlands and Finland. Els Van Eyken's co-authors include Guy Van Camp, L. Van Laer, Ann Vandevelde, Erik Fransén, Martti Sorri, Pekka Aikio, Jeroen R. Huyghe, Matthew J. Huentelman, Paul Van de Heyning and Elina Mäki‐Torkko and has published in prestigious journals such as Human Mutation, European Journal of Human Genetics and Mitochondrion.

In The Last Decade

Els Van Eyken

9 papers receiving 419 citations

Peers

Els Van Eyken

SS

CN

NEURO

MB

SH

Agneta Viberg Sweden

Frances Mapes United States

Jing‐Yi Jeng United Kingdom

L. Van Laer Belgium

Ann Vandevelde Belgium

Wouter J. F. ten Cate United States

Annelies Konings Belgium

Christina Hederstierna Sweden

Montserrat Rodríguez-Ballesteros Spain

Borka Ćeranić United Kingdom

Agneta Viberg Sweden

Els Van Eyken

278 ×0.9

SS

152 ×0.8

CN

97 ×0.8

NEURO

66 ×0.7

MB

52 ×0.7

SH

Citations per year, relative to Els Van Eyken Els Van Eyken (= 1×) peers Agneta Viberg

Countries citing papers authored by Els Van Eyken

Since Specialization

Citations

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

Fields of papers citing papers by Els Van Eyken

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Els Van Eyken

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

All Works

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9 of 9 papers shown

1.

Voets, A.M., B.J.C. van den Bosch, Alphons P. M. Stassen, et al.. (2011). Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution. Mitochondrion. 11(6). 964–972. 6 indexed citations

2.

Fransén, Erik, Els Van Eyken, L. Van Laer, et al.. (2011). Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population. Mitochondrion. 11(5). 729–734. 7 indexed citations

3.

Huyghe, Jeroen R., Erik Fransén, Samuli Hannula, et al.. (2010). A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies. European Journal of Human Genetics. 19(3). 347–352. 12 indexed citations

4.

Huyghe, Jeroen R., Samuli Hannula, Els Van Eyken, et al.. (2010). A genome-wide association study for age-related hearing impairment in the Saami. European Journal of Human Genetics. 18(6). 685–693. 73 indexed citations

5.

Huyghe, Jeroen R., Erik Fransén, Samuli Hannula, et al.. (2009). Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami. European Journal of Human Genetics. 18(5). 569–574. 4 indexed citations

6.

Konings, Annelies, Guy Van Camp, Els Van Eyken, et al.. (2008). Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients. Mitochondrion. 8(5-6). 377–382. 31 indexed citations

7.

Eyken, Els Van, Guy Van Camp, Jan Hendrickx, et al.. (2007). A New, Easy, and Rapid High-Throughput Detection Method for the Common GJB2 ( CX26 ), 35delG Mutation. Genetic Testing. 11(3). 231–234. 3 indexed citations

8.

Eyken, Els Van, Guy Van Camp, & L. Van Laer. (2007). The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors. Audiology and Neurotology. 12(6). 345–358. 220 indexed citations

9.

Eyken, Els Van, L. Van Laer, Erik Fransén, et al.. (2006). KCNQ4: a gene for age-related hearing impairment?. Human Mutation. 27(10). 1007–1016. 74 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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