Yukiko Arimoto

479 total citations
23 papers, 351 citations indexed

About

Yukiko Arimoto is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Yukiko Arimoto has authored 23 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Sensory Systems, 9 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in Yukiko Arimoto's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Vestibular and auditory disorders (9 papers) and Ear Surgery and Otitis Media (4 papers). Yukiko Arimoto is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Vestibular and auditory disorders (9 papers) and Ear Surgery and Otitis Media (4 papers). Yukiko Arimoto collaborates with scholars based in Japan, United Kingdom and United States. Yukiko Arimoto's co-authors include Atsuko Nakano, Tatsuo Matsunaga, Hideki Mutai, Kimitaka Kaga, Noriko Morimoto, Sawako Masuda, Hirokazu Sakamoto, Hiroshi Nagata, Kazunori Namba and Takuya Tomemori and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Gene and The Laryngoscope.

In The Last Decade

Yukiko Arimoto

21 papers receiving 341 citations

Peers

Yukiko Arimoto
Ah Reum Kim South Korea
Arnaud P. J. Giese United States
Kyu Yup Lee South Korea
Xue Gao China
Elyssa L. Monzack United States
Seungmin Lee South Korea
Yukiko Arimoto
Citations per year, relative to Yukiko Arimoto Yukiko Arimoto (= 1×) peers Ryotaro Omichi

Countries citing papers authored by Yukiko Arimoto

Since Specialization
Citations

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

Fields of papers citing papers by Yukiko Arimoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yukiko Arimoto

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

All Works

20 of 20 papers shown
1.
Nakano, Atsuko, et al.. (2021). Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts. International Journal of Pediatric Otorhinolaryngology. 152. 110975–110975. 2 indexed citations
2.
Yonekura, Syuji, Tomohisa Iinuma, Yukiko Arimoto, et al.. (2020). The influence of tonsillectomy on allergic diseases in pediatric patients. International Journal of Pediatric Otorhinolaryngology. 140. 110503–110503. 1 indexed citations
3.
Fujioka, Masato, Makoto Hosoya, Kiyomitsu Nara, et al.. (2020). Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations. Auris Nasus Larynx. 47(6). 938–942. 4 indexed citations
4.
Nakano, Atsuko, Yukiko Arimoto, Hideki Mutai, & Tatsuo Matsunaga. (2020). Clinical Features of <i>GJB2―</i>associated Hearing Loss Children. Nippon Jibiinkoka Gakkai Kaiho. 123(10). 1225–1230. 2 indexed citations
5.
Nakano, Atsuko, Yukiko Arimoto, Hideki Mutai, et al.. (2018). High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy. International Journal of Pediatric Otorhinolaryngology. 108. 125–131. 3 indexed citations
6.
Mutai, Hideki, Kazunori Namba, Noriko Morimoto, et al.. (2018). Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds. Ear and Hearing. 40(1). 184–191. 17 indexed citations
7.
Kaneko, Yuka, Atsuko Nakano, Yukiko Arimoto, et al.. (2017). The first sporadic case of DFNA11 identified by next-generation sequencing. International Journal of Pediatric Otorhinolaryngology. 100. 183–186. 6 indexed citations
8.
Hoshino, Tadashi, Noriko Takeuchi, Hiroko Sato, et al.. (2016). Analysis of Streptococcus pneumoniae and Haemophilus influenzae isolated from middle ear fluid before and after the introduction of government subsidies for pneumococcal and H. influenzae type b vaccines in Japan. Journal of Infection and Chemotherapy. 23(2). 85–89. 10 indexed citations
9.
Masuda, Masatsugu, Hideki Mutai, Yukiko Arimoto, Atsuko Nakano, & Tatsuo Matsunaga. (2015). A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9. Biochemical and Biophysical Research Communications. 469(2). 270–274. 7 indexed citations
10.
Arimoto, Yukiko, Kazunori Namba, Atsuko Nakano, & Tatsuo Matsunaga. (2014). Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome. Gene. 540(2). 258–262. 5 indexed citations
11.
Nakano, Atsuko, Yukiko Arimoto, & Tatsuo Matsunaga. (2013). Cochlear Nerve Deficiency and Associated Clinical Features in Patients With Bilateral and Unilateral Hearing Loss. Otology & Neurotology. 34(3). 554–558. 51 indexed citations
12.
Minami, Shujiro, Hideki Mutai, Atsuko Nakano, et al.. (2013). GJB2-associated hearing loss undetected by hearing screening of newborns. Gene. 532(1). 41–45. 37 indexed citations
13.
Matsunaga, Tatsuo, Hideki Mutai, Shinji Kunishima, et al.. (2012). A prevalent founder mutation and genotype–phenotype correlations of OTOF in Japanese patients with auditory neuropathy. Clinical Genetics. 82(5). 425–432. 62 indexed citations
14.
Arimoto, Yukiko, et al.. (2008). Bacteriology of Nasal Discharge in Children. Nihon Bika Gakkai Kaishi (Japanese Journal of Rhinology). 47(2). 115–119. 1 indexed citations
15.
Nakano, Atsuko, et al.. (2007). Audiometric Re-examination and Follow-up after Newborn Hearing Screening at Chiba Children's Hospital. AUDIOLOGY JAPAN. 50(6). 665–670. 1 indexed citations
16.
Nagata, Hiroshi, Ken Watanabe, Norio Shimizu, et al.. (2005). Suppression of inflammation by dexamethasone prolongs adenoviral vector-mediated transgene expression in murine nasal mucosa. Acta Oto-Laryngologica. 125(12). 1301–1306. 6 indexed citations
17.
Nagata, Hiroshi, Yuji Shino, Yukiko Arimoto, et al.. (2004). Effects of adenoviral vector-mediated BDNF expression on the bulbectomy-induced apoptosis of olfactory receptor neurons. Molecular Brain Research. 129(1-2). 88–95. 11 indexed citations
18.
Arimoto, Yukiko, et al.. (2002). In vivo Expression of Adenovirus-mediated lacZ Gene in Murine Nasal Mucosa. Acta Oto-Laryngologica. 122(6). 627–633. 14 indexed citations
20.
Nagata, Hiroshi, Hironori Mutoh, Yukiko Arimoto, et al.. (2001). Association between nasal allergy and a coding variant of the Fc ε RI β gene Glu237Gly in a Japanese population. Human Genetics. 109(3). 262–266. 34 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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