Kris Flothmann

577 total citations
8 papers, 409 citations indexed

About

Kris Flothmann is a scholar working on Sensory Systems, Cognitive Neuroscience and Neurology. According to data from OpenAlex, Kris Flothmann has authored 8 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Sensory Systems, 4 papers in Cognitive Neuroscience and 3 papers in Neurology. Recurrent topics in Kris Flothmann's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Hearing Loss and Rehabilitation (4 papers) and Vestibular and auditory disorders (3 papers). Kris Flothmann is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Hearing Loss and Rehabilitation (4 papers) and Vestibular and auditory disorders (3 papers). Kris Flothmann collaborates with scholars based in Belgium, Netherlands and United States. Kris Flothmann's co-authors include Guy Van Camp, Cor W. R. J. Cremers, Kim Cryns, Ronald J. E. Pennings, Katrien Storm, Richard J. Smith, Marci M. Lesperance, Jody M.W. van den Ouweland, Terry‐Lynn Young and Theru A. Sivakumaran and has published in prestigious journals such as Genome Research, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Kris Flothmann

8 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kris Flothmann Belgium 8 237 233 113 90 77 8 409
Edi Lúcia Sartorato Brazil 15 377 1.6× 422 1.8× 44 0.4× 156 1.7× 109 1.4× 64 689
TB Friedman United States 9 238 1.0× 260 1.1× 81 0.7× 110 1.2× 46 0.6× 9 407
Marzieh Mohseni Iran 13 259 1.1× 223 1.0× 20 0.2× 125 1.4× 27 0.4× 37 470
Min Young Kim South Korea 13 182 0.8× 240 1.0× 21 0.2× 99 1.1× 72 0.9× 31 379
Qing‐qing Jiang China 9 193 0.8× 85 0.4× 68 0.6× 35 0.4× 42 0.5× 24 387
Dilip Deshmukh United States 5 218 0.9× 257 1.1× 28 0.2× 83 0.9× 45 0.6× 6 331
Liang Zong China 12 302 1.3× 337 1.4× 10 0.1× 108 1.2× 103 1.3× 23 468
Aenea Hendry United Kingdom 7 119 0.5× 128 0.5× 18 0.2× 44 0.5× 58 0.8× 7 304
Yang Wei–yan China 10 80 0.3× 254 1.1× 25 0.2× 121 1.3× 111 1.4× 24 319
Amrit Singh‐Estivalet France 9 218 0.9× 107 0.5× 37 0.3× 37 0.4× 17 0.2× 11 362

Countries citing papers authored by Kris Flothmann

Since Specialization
Citations

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

Fields of papers citing papers by Kris Flothmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kris Flothmann

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

All Works

8 of 8 papers shown
1.
Fransén, Erik, Lut Van Laer, Nele Lemkens, et al.. (2004). A Novel Z-Score–Based Method to Analyze Candidate Genes for Age-Related Hearing Impairment. Ear and Hearing. 25(2). 133–141. 20 indexed citations
2.
Cryns, Kim, Theru A. Sivakumaran, Jody M.W. van den Ouweland, et al.. (2003). Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Human Mutation. 22(4). 275–287. 142 indexed citations
3.
Pennings, Ronald J. E., Steven J. H. Bom, Kim Cryns, et al.. (2003). Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1). Archives of Otolaryngology - Head and Neck Surgery. 129(4). 421–421. 31 indexed citations
4.
Cryns, Kim, Markus Pfister, Ronald J. E. Pennings, et al.. (2002). Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110(5). 389–394. 71 indexed citations
5.
Laer, Lut Van, Anita L. DeStefano, Richard H. Myers, et al.. (2002). Is DFNA5 a susceptibility gene for age-related hearing impairment?. European Journal of Human Genetics. 10(12). 883–886. 19 indexed citations
6.
Cryns, Kim, Kris Flothmann, Paul Van de Heyning, et al.. (2002). Vestibular Dysfunction in the Epistatic circler Mouse Is Caused by Phenotypic Interaction of One Recessive Gene and Three Modifier Genes. Genome Research. 12(4). 613–617. 12 indexed citations
7.
8.
Camp, Guy Van, Henricus P. M. Kunst, Kris Flothmann, et al.. (1999). A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. Journal of Medical Genetics. 36(7). 532–536. 35 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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