Erik Fransén

836 total citations
14 papers, 529 citations indexed

About

Erik Fransén is a scholar working on Sensory Systems, Cognitive Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Erik Fransén has authored 14 papers receiving a total of 529 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Sensory Systems, 6 papers in Cognitive Neuroscience and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Erik Fransén's work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), Hearing Loss and Rehabilitation (6 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Erik Fransén is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (8 papers), Hearing Loss and Rehabilitation (6 papers) and Fetal and Pediatric Neurological Disorders (2 papers). Erik Fransén collaborates with scholars based in Belgium, Netherlands and United States. Erik Fransén's co-authors include Guy Van Camp, Lieve Vits, Paul Coucke, Patrick J. Willems, Vance Lemmon, Golder N. Wilson, Charles Schwartz, Edwin Reyniers, Annemarie Poustka and Bernhard Korn and has published in prestigious journals such as Nature Genetics, Scientific Reports and British Journal of Cancer.

In The Last Decade

Erik Fransén

14 papers receiving 520 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erik Fransén Belgium	8	182	171	170	107	101	14	529
M. De Silva Australia	13	337 1.9×	274 1.6×	121 0.7×	146 1.4×	61 0.6×	24	661
Leïla Abbas United Kingdom	11	290 1.6×	401 2.3×	116 0.7×	96 0.9×	63 0.6×	14	703
RoseAnn Berlin United States	13	124 0.7×	157 0.9×	227 1.3×	89 0.8×	155 1.5×	16	704
Jin‐Young Koh United States	12	99 0.5×	233 1.4×	187 1.1×	59 0.6×	49 0.5×	24	543
Heiko Locher Netherlands	11	210 1.2×	188 1.1×	60 0.4×	78 0.7×	59 0.6×	22	511
Jaclynn M. Lett United States	8	152 0.8×	257 1.5×	136 0.8×	63 0.6×	81 0.8×	10	432
Fabrice Giraudet France	13	257 1.4×	137 0.8×	100 0.6×	180 1.7×	106 1.0×	33	567
Kärin Halsey United States	13	317 1.7×	162 0.9×	36 0.2×	171 1.6×	123 1.2×	15	544
Jennifer W. McKee-Johnson United States	6	145 0.8×	322 1.9×	161 0.9×	54 0.5×	46 0.5×	8	511

Countries citing papers authored by Erik Fransén

Since Specialization

Citations

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

Fields of papers citing papers by Erik Fransén

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erik Fransén. 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 Erik Fransén. The network helps show where Erik Fransén may publish in the future.

Co-authorship network of co-authors of Erik Fransén

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

All Works

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14 of 14 papers shown

Gilles, Annick, Dyan Ramekers, Griet Mertens, et al.. (2025). Cochlear health in a cohort of cochlear implant users carrying the p.Pro51Ser variant in the COCH gene (DFNA9): A cross-sectional study evaluating the changes in the electrically evoked compound action potential (eCAP). Hearing Research. 460. 109240–109240. 2 indexed citations

Gilles, Annick, Griet Mertens, Marc J. W. Lammers, et al.. (2024). Interaural and sex differences in the natural evolution of hearing levels in pre-symptomatic and symptomatic carriers of the p.Pro51Ser variant in the COCH gene. Scientific Reports. 14(1). 184–184. 1 indexed citations

Ibrahim, Joe, Arvid Suls, Dieter Peeters, et al.. (2024). IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assay. British Journal of Cancer. 131(7). 1224–1236. 6 indexed citations

Cools, Nathalie, et al.. (2024). Endurance Exercise Does Not Exacerbate Cardiac Inflammation in BALB/c Mice Following mRNA COVID-19 Vaccination. Vaccines. 12(9). 966–966. 1 indexed citations

Fransén, Erik, An Verrijken, Eveline Dirinck, et al.. (2024). A Case–Control Study Supports Genetic Contribution of the PON Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver Disease. Antioxidants. 13(9). 1051–1051. 1 indexed citations

Fransén, Erik, L. Cassiers, Viktoria Chubar, et al.. (2023). Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress. Psychiatric Genetics. 33(4). 134–144. 3 indexed citations

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

Carlsson, Per‐Inge, et al.. (2007). The influence of genetic factors, smoking and cardiovascular diseases on human noise susceptibility. Audiological Medicine. 5(2). 82–91. 10 indexed citations

Pfister, Markus, Hölger Thiele, Guy Van Camp, et al.. (2004). A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by <i>TECTA</i> Mutations. Cellular Physiology and Biochemistry. 14(4-6). 369–376. 46 indexed citations

10.

Fransén, Erik. (2003). Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects. Experimental Gerontology. 38(4). 353–359. 64 indexed citations

11.

Verhagen, W. I. M., Steven J. H. Bom, P.L.M. Huygen, et al.. (2000). Familial Progressive Vestibulocochlear Dysfunction Caused by a COCH Mutation (DFNA9). Archives of Neurology. 57(7). 1045–1045. 23 indexed citations

12.

Verhagen, W. I. M., Ronald Bartels, Erik Fransén, et al.. (1998). Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression. Journal of the Neurological Sciences. 158(1). 101–105. 20 indexed citations

13.

Fransén, Erik, Vance Lemmon, Guy Van Camp, et al.. (1995). CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1. European Journal of Human Genetics. 3(5). 273–284. 169 indexed citations

14.

Vits, Lieve, Guy Van Camp, Paul Coucke, et al.. (1994). MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. Nature Genetics. 7(3). 408–413. 110 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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