Yoshiaki Kikkawa

2.9k total citations
89 papers, 2.3k citations indexed

About

Yoshiaki Kikkawa is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Yoshiaki Kikkawa has authored 89 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 26 papers in Sensory Systems and 24 papers in Genetics. Recurrent topics in Yoshiaki Kikkawa's work include Hearing, Cochlea, Tinnitus, Genetics (26 papers), Genetic and phenotypic traits in livestock (9 papers) and Connexins and lens biology (9 papers). Yoshiaki Kikkawa is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (26 papers), Genetic and phenotypic traits in livestock (9 papers) and Connexins and lens biology (9 papers). Yoshiaki Kikkawa collaborates with scholars based in Japan, United Kingdom and Australia. Yoshiaki Kikkawa's co-authors include Hiromichi Yonekawa, Takashi Amano, Hidetaro Yasumitsu, Kaoru Miyazaki, Toyoyuki Takada, Makoto Umeda, Ryo Kominami, Hitoshi Suzuki, Toshihiko Shiroishi and Ayako Nakamura and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Yoshiaki Kikkawa

89 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yoshiaki Kikkawa Japan	28	1.1k	683	573	342	290	89	2.3k
Suzanne L. Mansour United States	26	3.0k 2.8×	1.0k 1.5×	618 1.1×	296 0.9×	77 0.3×	45	3.9k
I.M. Leigh United Kingdom	15	1.7k 1.6×	249 0.4×	923 1.6×	464 1.4×	51 0.2×	21	2.9k
Gabriele Richard United States	41	3.2k 2.9×	1.6k 2.3×	446 0.8×	1.3k 3.7×	131 0.5×	90	5.2k
Delphine Samson France	11	2.0k 1.9×	1.4k 2.1×	157 0.3×	437 1.3×	64 0.2×	13	4.1k
Isabelle Roux France	33	2.9k 2.7×	335 0.5×	1.3k 2.3×	552 1.6×	68 0.2×	62	4.6k
Elisabeth M. Busch‐Nentwich United Kingdom	20	1.3k 1.2×	280 0.4×	317 0.6×	611 1.8×	33 0.1×	46	2.2k
Erwin van Wijk Netherlands	27	1.8k 1.7×	692 1.0×	836 1.5×	433 1.3×	70 0.2×	75	2.7k
Jacques Loiselet Lebanon	25	1.3k 1.3×	490 0.7×	547 1.0×	373 1.1×	26 0.1×	60	2.6k
Stephen J. Davies United States	29	905 0.8×	119 0.2×	155 0.3×	453 1.3×	105 0.4×	72	4.0k
Kenji Tanigaki Japan	29	2.7k 2.5×	420 0.6×	166 0.3×	408 1.2×	147 0.5×	47	4.8k

Countries citing papers authored by Yoshiaki Kikkawa

Since Specialization

Citations

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

Fields of papers citing papers by Yoshiaki Kikkawa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshiaki Kikkawa

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshiaki Kikkawa. A scholar is included among the top collaborators of Yoshiaki Kikkawa 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 Yoshiaki Kikkawa. Yoshiaki Kikkawa 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

Fukuda, Tatsuya, et al.. (2023). Serum chemokine CC‐motif ligand 17 is a predictive marker of severe COVID‐19 in haemodialysis patients: A retrospective observational study. Nephrology. 28(4). 240–248. 2 indexed citations

Fukuda, Tatsuya, et al.. (2023). Comparative outcomes of hemodialysis patients facing pre‐Omicron and Omicron COVID‐19 epidemics. Therapeutic Apheresis and Dialysis. 28(1). 51–60. 3 indexed citations

Yasuda, Shumpei P., et al.. (2023). Impacts of an age-related hearing loss allele of cadherin 23 on severity of hearing loss in ICR and NOD/Shi mice. Biochemical and Biophysical Research Communications. 674. 147–153. 1 indexed citations

Yasuda, Shumpei P., Yuki Miyasaka, Hiroshi Shitara, et al.. (2022). Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice. Biomedicines. 10(9). 2221–2221. 4 indexed citations

Balan, Shabeesh, Tetsuo Ohnishi, Akiko Watanabe, et al.. (2021). Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia. Schizophrenia Bulletin. 47(4). 1190–1200. 11 indexed citations

Matsuoka, Kunie, Kenta Wada, Yuki Miyasaka, et al.. (2019). OHC-TRECK: A Novel System Using a Mouse Model for Investigation of the Molecular Mechanisms Associated with Outer Hair Cell Death in the Inner Ear. Scientific Reports. 9(1). 5285–5285. 3 indexed citations

Miyasaka, Yuki, Shumpei P. Yasuda, Kunie Matsuoka, et al.. (2017). A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells. PLoS ONE. 12(8). e0183477–e0183477. 16 indexed citations

Sanada, Takahiro, Yuichi Hirata, Yutaka Naito, et al.. (2016). Transmission of HBV DNA Mediated by Ceramide-Triggered Extracellular Vesicles. Cellular and Molecular Gastroenterology and Hepatology. 3(2). 272–283. 49 indexed citations

Horie, Masao, Kazuyuki Mekada, Hiromi Sano, et al.. (2016). Characterization of novel dystonia musculorum mutant mice: Implications for central nervous system abnormality. Neurobiology of Disease. 96. 271–283. 16 indexed citations

10.

Ogata, Genki, Shushi Nagamori, Noriyoshi Isozumi, et al.. (2015). Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea. European Journal of Neuroscience. 42(3). 1984–2002. 19 indexed citations

11.

Nakajima, Mitsunari, et al.. (2014). Dilation of the inferior colliculus and hypersensitivity to sound in Wnt1-cre and Wnt1-GAL4 double-transgenic mice. Neuroscience Letters. 566. 236–240. 2 indexed citations

12.

Wada, Kenta, Yukiko Maeda, Kei Watanabe, et al.. (2011). A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice. Mammalian Genome. 22(11-12). 693–702. 13 indexed citations

13.

Dang, Ruihua, Daisuke Torigoe, Yoshiaki Kikkawa, et al.. (2011). Genetic Background Strongly Modifies the Severity of Symptoms of Hirschsprung Disease, but Not Hearing Loss in Rats Carrying Ednrbsl Mutations. PLoS ONE. 6(9). e24086–e24086. 25 indexed citations

14.

Okumura, Kazuhiro, Michinari Yokohama, Hisashi Yamakawa, et al.. (2009). Protein 4.1 expression in the developing hair cells of the mouse inner ear. Brain Research. 1307. 53–62. 11 indexed citations

15.

Takada, Toyoyuki, Akihiko Mita, Akiteru Maeno, et al.. (2008). Mouse inter-subspecific consomic strains for genetic dissection of quantitative complex traits. Genome Research. 18(3). 500–508. 73 indexed citations

16.

Sekine, Michiko, Hiroshi Shitara, Yoshiaki Kikkawa, et al.. (2005). The cis-Regulatory Element Gsl5 Is Indispensable for Proximal Straight Tubule Cell-specific Transcription of Core 2 β-1,6-N-Acetylglucosaminyltransferase in the Mouse Kidney. Journal of Biological Chemistry. 281(2). 1008–1015. 10 indexed citations

17.

Kikkawa, Yoshiaki. (2003). Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice. Human Molecular Genetics. 12(5). 453–461. 5 indexed citations

18.

Sekine, Michiko, Choji Taya, Yoshiaki Kikkawa, et al.. (2001). Regulation of mouse kidney tubular epithelial cell‐specific expression of core 2 GlcNAc transferase. European Journal of Biochemistry. 268(4). 1129–1135. 8 indexed citations

19.

Wakabayashi, Yuichi, Yoshiaki Takahashi, Yoshiaki Kikkawa, et al.. (1998). A Novel Type of Myosin Encoded by the Mouse Deafness Geneshaker-2. Biochemical and Biophysical Research Communications. 248(3). 655–659. 14 indexed citations

20.

Wakabayashi, Yuichi, Yoshiaki Kikkawa, Yasuo Matsumoto, et al.. (1997). Genetic and Physical Delineation of the Region of the Mouse Deafness Mutationshaker-2. Biochemical and Biophysical Research Communications. 234(1). 107–110. 8 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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