L. Van Laer

1.2k total citations
17 papers, 811 citations indexed

About

L. Van Laer is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, L. Van Laer has authored 17 papers receiving a total of 811 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Sensory Systems, 6 papers in Neurology and 5 papers in Molecular Biology. Recurrent topics in L. Van Laer's work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (6 papers) and Hearing Loss and Rehabilitation (4 papers). L. Van Laer is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (6 papers) and Hearing Loss and Rehabilitation (4 papers). L. Van Laer collaborates with scholars based in Belgium, United States and Netherlands. L. Van Laer's co-authors include Guy Van Camp, Els Van Eyken, Paul Van de Heyning, Richard J. Smith, Erik Fransén, Ann Vandevelde, S. D. Smith, Vedat Topsakal, Wendy Balemans and Matthew Brown and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

L. Van Laer

17 papers receiving 792 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. Van Laer Belgium	11	629	316	304	260	112	17	811
Masatsugu Masuda Japan	11	664 1.1×	185 0.6×	220 0.7×	392 1.5×	103 0.9×	32	939
Hans-Peter Zenner Germany	12	548 0.9×	191 0.6×	246 0.8×	265 1.0×	25 0.2×	14	717
Edward Cohn United States	16	823 1.3×	265 0.8×	488 1.6×	387 1.5×	28 0.3×	24	1.1k
Suoqiang Zhai China	17	441 0.7×	115 0.4×	411 1.4×	146 0.6×	35 0.3×	42	781
Ken Kojima Japan	16	467 0.7×	161 0.5×	236 0.8×	110 0.4×	31 0.3×	38	642
Pietro Scimemi Italy	12	436 0.7×	221 0.7×	259 0.9×	154 0.6×	40 0.4×	23	575
C. R. Srikumari Srisailapathy India	12	598 1.0×	133 0.4×	482 1.6×	204 0.8×	14 0.1×	34	757
Winston Tan United States	13	376 0.6×	185 0.6×	176 0.6×	171 0.7×	52 0.5×	19	591
Atsushi Namba Japan	10	469 0.7×	107 0.3×	208 0.7×	258 1.0×	21 0.2×	18	605

Countries citing papers authored by L. Van Laer

Since Specialization

Citations

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

Fields of papers citing papers by L. Van Laer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Van Laer

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

All Works

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17 of 17 papers shown

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

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

Schrauwen, Isabelle, Koen Venken, Kathleen Vanderstraeten, et al.. (2010). Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2. Genes and Immunity. 11(3). 246–253. 10 indexed citations

Konings, Annelies, L. Van Laer, Elżbieta Rajkowska, et al.. (2009). Candidate Gene Association Study for Noise‐induced Hearing Loss in Two Independent Noise‐exposed Populations. Annals of Human Genetics. 73(2). 215–224. 64 indexed citations

Baur, Manuela, Erik Fransén, Anke Tropitzsch, et al.. (2009). Einfluss exogener Faktoren auf Altersschwerhörigkeit. HNO. 57(10). 1023–1028. 5 indexed citations

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

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

Wieringen, Astrid Van, Jan Hendrickx, Vedat Topsakal, et al.. (2007). Prevalence of tinnitus and audiometric shape.. PubMed. 3 Suppl 7. 37–49. 35 indexed citations

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

10.

Laer, L. Van, et al.. (2004). DFNA5: hearing impairment exon instead of hearing impairment gene?. Journal of Medical Genetics. 41(6). 401–406. 51 indexed citations

11.

Laer, L. Van, et al.. (2001). A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment. Journal of Medical Genetics. 38(8). 515–518. 152 indexed citations

12.

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

13.

Laer, L. Van, Wyman T. McGuirt, Tian Yang, Richard J. Smith, & Guy Van Camp. (1999). Autosomal dominant nonsyndromic hearing impairment. American Journal of Medical Genetics. 89(3). 167–167. 3 indexed citations

14.

Brown, Matthew, L. Van Laer, S. D. Smith, et al.. (1997). A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p. The American Journal of Human Genetics. 61(4). 924–927. 36 indexed citations

15.

Laer, L. Van, Guy Van Camp, Margriet Verstreken, et al.. (1997). 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. European Journal of Human Genetics. 5(6). 397–405. 19 indexed citations

16.

Verhoeven, K., Guy Van Camp, Paul Govaerts, et al.. (1997). A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.. PubMed. 60(5). 1168–73. 45 indexed citations

17.

Camp, Guy Van, Paul Coucke, Wendy Balemans, et al.. (1995). Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Human Molecular Genetics. 4(11). 2159–2163. 79 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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