Kenneth R. Johnson

7.1k total citations · 1 hit paper
102 papers, 5.5k citations indexed

About

Kenneth R. Johnson is a scholar working on Molecular Biology, Sensory Systems and Nutrition and Dietetics. According to data from OpenAlex, Kenneth R. Johnson has authored 102 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 49 papers in Sensory Systems and 18 papers in Nutrition and Dietetics. Recurrent topics in Kenneth R. Johnson's work include Hearing, Cochlea, Tinnitus, Genetics (48 papers), Biochemical Analysis and Sensing Techniques (17 papers) and Vestibular and auditory disorders (11 papers). Kenneth R. Johnson is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (48 papers), Biochemical Analysis and Sensing Techniques (17 papers) and Vestibular and auditory disorders (11 papers). Kenneth R. Johnson collaborates with scholars based in United States, Germany and United Kingdom. Kenneth R. Johnson's co-authors include Qing Yin Zheng, Lawrence C. Erway, Konrad Noben‐Trauth, Leona H. Gagnon, Chantal M. Longo-Guess, Susan A. Cook, Heping Yu, James F. Willott, Muriel T. Davisson and Belinda S. Harris and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Kenneth R. Johnson

102 papers receiving 5.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1999 695 citations Qing Yin Zheng, Kenneth R. Johnson et al. Hearing Research profile →

Peers

Kenneth R. Johnson

NEURO

GENET

Qing Yin Zheng United States

Jeffrey R. Holt United States

Andrew J. Griffith United States

A. Amraoui France

Lawrence C. Erway United States

Gary D. Housley New Zealand

Andrew Forge United Kingdom

Robert J. Morell United States

Inna A. Belyantseva United States

Shin‐ichi Usami Japan

Qing Yin Zheng United States

Kenneth R. Johnson

2.4k ×0.9

1.9k ×0.8

811 ×0.8

887 ×0.9

NEURO

522 ×0.8

GENET

Citations per year, relative to Kenneth R. Johnson Kenneth R. Johnson (= 1×) peers Qing Yin Zheng

Countries citing papers authored by Kenneth R. Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Kenneth R. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kenneth R. Johnson. 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 Kenneth R. Johnson. The network helps show where Kenneth R. Johnson may publish in the future.

Co-authorship network of co-authors of Kenneth R. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth R. Johnson. A scholar is included among the top collaborators of Kenneth R. Johnson 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 Kenneth R. Johnson. Kenneth R. Johnson 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

Tian, Cong, Kenneth R. Johnson, Jaclynn M. Lett, et al.. (2021). CACHD1-deficient mice exhibit hearing and balance deficits associated with a disruption of calcium homeostasis in the inner ear. Hearing Research. 409. 108327–108327. 4 indexed citations

Vijayakumar, Sarath, Sherri M. Jones, Timothy A. Jones, Cong Tian, & Kenneth R. Johnson. (2019). Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions. Scientific Reports. 9(1). 12430–12430. 13 indexed citations

Ohlemiller, Kevin K., Sherri M. Jones, & Kenneth R. Johnson. (2016). Application of Mouse Models to Research in Hearing and Balance. Journal of the Association for Research in Otolaryngology. 17(6). 493–523. 90 indexed citations

Buzhdygan, Tetyana P., Joshua G. Lisinicchia, Vipulkumar Patel, et al.. (2016). Neuropsychological, Neurovirological and Neuroimmune Aspects of Abnormal GABAergic Transmission in HIV Infection. Journal of Neuroimmune Pharmacology. 11(2). 279–293. 29 indexed citations

Hosur, Vishnu, Melissa L. Cox, Lisa Burzenski, et al.. (2013). Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 (Tal1) Gene Is Associated with Severe Renal Disease and Patchy Alopecia in Hairpatches (Hpt) Mice. PLoS ONE. 8(1). e53426–e53426. 5 indexed citations

Longo-Guess, Chantal M., et al.. (2011). Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice. Hearing Research. 283(1-2). 80–88. 138 indexed citations

Odeh, Hana M., Kristina L. Hunker, Inna A. Belyantseva, et al.. (2010). Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse. The American Journal of Human Genetics. 86(2). 148–160. 40 indexed citations

Munroe, Robert J., Vinay Prabhu, Kenneth R. Johnson, et al.. (2009). Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. BMC Developmental Biology. 9(1). 27–27. 44 indexed citations

Johnson, Kenneth R., et al.. (2007). Congenital Hypothyroidism, Dwarfism, and Hearing Impairment Caused by a Missense Mutation in the Mouse Dual Oxidase 2 Gene, Duox2. Molecular Endocrinology. 21(7). 1593–1602. 87 indexed citations

10.

Longo-Guess, Chantal M., Leona H. Gagnon, David E. Bergstrom, & Kenneth R. Johnson. (2007). A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9. Hearing Research. 234(1-2). 21–28. 42 indexed citations

11.

Károlyi, I, Kärin Halsey, Lisa A. Beyer, et al.. (2007). Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice. Mammalian Genome. 18(8). 596–608. 31 indexed citations

12.

Longo-Guess, Chantal M., et al.. (2005). A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry ( hscy ) mice. Proceedings of the National Academy of Sciences. 102(22). 7894–7899. 83 indexed citations

13.

Zheng, Qing Yin, Denise Yan, Xiao Mei Ouyang, et al.. (2004). Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans. Human Molecular Genetics. 14(1). 103–111. 115 indexed citations

14.

Bruneau, S., Kenneth R. Johnson, Masakazu Yamamoto, Atsushi Kuroiwa, & Denis Duboule. (2001). The Mouse Hoxd13spdh Mutation, a Polyalanine Expansion Similar to Human Type II Synpolydactyly (SPD), Disrupts the Function but Not the Expression of Other Hoxd Genes. Developmental Biology. 237(2). 345–353. 68 indexed citations

15.

Sidow, Arend, Anne W. Kerrebrock, Bruce W. Birren, et al.. (1999). A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nature Genetics. 23(1). 104–107. 79 indexed citations

16.

Hinsdale, Myron E., Susan C. Farmer, Kenneth R. Johnson, et al.. (1995). RNA Expression and Chromosomal Location of the Mouse Long-Chain Acyl-CoA Dehydrogenase Gene. Genomics. 28(2). 163–170. 11 indexed citations

17.

Johnson, Kenneth R., et al.. (1995). Assignment to chromosome 11 of mouse p68 RNA helicase gene (Hlrl) and pseudogene (Hlrl ps1). FEBS Letters. 363(1-2). 25–28. 2 indexed citations

18.

Cone, Roger D., Kathleen G. Mountjoy, Linda S. Robbins, et al.. (1993). Cloning and Functional Characterization of a Family of Receptors for the Melanotropic Peptides. Annals of the New York Academy of Sciences. 680(1). 342–363. 112 indexed citations

19.

Wang, Shupei, Joseph H. Nadeau, Alessandra M.V. Duncan, et al.. (1993). 3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes. Mammalian Genome. 4(7). 382–387. 28 indexed citations

20.

Johnson, Kenneth R., et al.. (1992). Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins. Genomics. 12(3). 503–509. 63 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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