Satoko Abe

2.7k total citations
56 papers, 2.0k citations indexed

About

Satoko Abe is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Satoko Abe has authored 56 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Sensory Systems, 21 papers in Neurology and 16 papers in Molecular Biology. Recurrent topics in Satoko Abe's work include Hearing, Cochlea, Tinnitus, Genetics (36 papers), Vestibular and auditory disorders (21 papers) and Ear Surgery and Otitis Media (15 papers). Satoko Abe is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (36 papers), Vestibular and auditory disorders (21 papers) and Ear Surgery and Otitis Media (15 papers). Satoko Abe collaborates with scholars based in Japan, United States and Germany. Satoko Abe's co-authors include Shin‐ichi Usami, Hideichi Shinkawa, Guy Van Camp, Atsushi Namba, William J. Kimberling, Yusuke Nakamura, Hiroaki Suzuki, Koji Tsukamoto, Shin‐ya Nishio and Daisuke Harada and has published in prestigious journals such as PLoS ONE, Physical Review B and Scientific Reports.

In The Last Decade

Satoko Abe

55 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Satoko Abe Japan 26 1.3k 799 716 462 269 56 2.0k
Toshihiko Kikuchi Japan 22 1.4k 1.0× 1.0k 1.3× 357 0.5× 171 0.4× 310 1.2× 53 2.0k
Tatsuo Matsunaga Japan 22 1.1k 0.8× 760 1.0× 446 0.6× 268 0.6× 319 1.2× 144 1.9k
Takayuki Okano Japan 18 547 0.4× 300 0.4× 250 0.3× 98 0.2× 160 0.6× 53 1.4k
Jieyu Qi China 20 938 0.7× 703 0.9× 259 0.4× 67 0.1× 210 0.8× 52 1.5k
Kazuaki Homma United States 23 427 0.3× 831 1.0× 145 0.2× 30 0.1× 294 1.1× 67 1.9k
Donald Coling United States 25 904 0.7× 652 0.8× 300 0.4× 82 0.2× 374 1.4× 45 1.6k
Thomas Weber Germany 21 346 0.3× 385 0.5× 101 0.1× 18 0.0× 138 0.5× 40 1.3k
Yoshihiro Noguchi Japan 18 392 0.3× 253 0.3× 321 0.4× 123 0.3× 112 0.4× 92 924
Fabienne Lévi-Acobas France 15 762 0.6× 1.3k 1.6× 225 0.3× 84 0.2× 118 0.4× 30 1.7k
Hirofumi Sakaguchi Japan 18 713 0.5× 645 0.8× 277 0.4× 103 0.2× 177 0.7× 43 1.4k

Countries citing papers authored by Satoko Abe

Since Specialization
Citations

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

Fields of papers citing papers by Satoko Abe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoko Abe

This figure shows the co-authorship network connecting the top 25 collaborators of Satoko Abe. A scholar is included among the top collaborators of Satoko Abe 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 Satoko Abe. Satoko Abe 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.
Abe, Satoko, et al.. (2024). Quantification of HPV16 E7 Oncoproteins in Urine Specimens from Women with Cervical Intraepithelial Neoplasia. Microorganisms. 12(6). 1205–1205. 6 indexed citations
2.
Moteki, Hideaki, Shin‐ya Nishio, Kenji Ohyama, et al.. (2020). Prevalence and clinical features of hearing loss caused by EYA4 variants. Scientific Reports. 10(1). 3662–3662. 21 indexed citations
3.
Moteki, Hideaki, Shin‐ya Nishio, Tomomi Yamaguchi, et al.. (2019). Frequency and clinical features of hearing loss caused by STRC deletions. Scientific Reports. 9(1). 4408–4408. 51 indexed citations
4.
5.
Iwasa, Yoh-ichiro, Shin‐ya Nishio, Hidekane Yoshimura, et al.. (2013). OTOF mutation screening in Japanese severe to profound recessive hearing loss patients. BMC Medical Genetics. 14(1). 95–95. 35 indexed citations
6.
Ozaki, Shinji, Eisuke Fukuma, Mitsuhiro Tozaki, et al.. (2008). THE USE OF NON-SURGICAL CRYOABLATION FOR MINIMAL BREAST CANCER. Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 69(12). 3038–3047. 2 indexed citations
7.
Usami, Shin‐ichi, Hisakuni Fukuoka, Hiroaki Suzuki, et al.. (2008). The responsible genes in Japanese deafness patients and clinical application using Invader assay. Acta Oto-Laryngologica. 128(4). 446–454. 36 indexed citations
8.
Usami, Shin‐ichi, Yutaka Takumi, Aki Oshima, et al.. (2008). The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea. Neuroscience. 154(1). 22–28. 25 indexed citations
9.
Abe, Satoko, Toshikazu Yamaguchi, & Shin‐ichi Usami. (2007). Application of Deafness Diagnostic Screening Panel Based on Deafness Mutation/Gene Database Using Invader Assay. Genetic Testing. 11(3). 333–340. 30 indexed citations
10.
Suzuki, Hiroaki, Aki Oshima, Koji Tsukamoto, et al.. (2007). Clinical characteristics and genotype–phenotype correlation of hearing loss patients withSLC26A4mutations. Acta Oto-Laryngologica. 127(12). 1292–1297. 46 indexed citations
11.
Abe, Satoko, Yasutada Imamura, Attila Aszódi, et al.. (2005). Type IX collagen is crucial for normal hearing. Neuroscience. 132(2). 493–500. 42 indexed citations
12.
Suzuki, Nobuyoshi, Yutaka Takumi, Satoko Abe, et al.. (2005). Type IX collagen knock-out mouse shows progressive hearing loss. Neuroscience Research. 51(3). 293–298. 35 indexed citations
13.
Usami, Shin‐ichi, Kentaro Takahashi, Atsushi Namba, et al.. (2003). Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. European Journal of Human Genetics. 11(10). 744–748. 74 indexed citations
14.
15.
Abe, Satoko, Shin‐ichi Usami, & Yusuke Nakamura. (2003). Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss. Journal of Human Genetics. 48(11). 564–570. 110 indexed citations
16.
Tsukamoto, Koji, Hiroaki Suzuki, Daisuke Harada, et al.. (2003). Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese. European Journal of Human Genetics. 11(12). 916–922. 199 indexed citations
17.
Tono, Tetsuya, Keiji Matsuda, Shizuo Komune, et al.. (2001). Different Clinical Characteristics of Aminoglycoside-Induced Profound Deafness with and without the 1555 A→G Mitochondrial Mutation. ORL. 63(1). 25–30. 27 indexed citations
18.
Abe, Satoko, et al.. (2001). Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese. Journal of Human Genetics. 46(7). 355–361. 35 indexed citations
19.
Abe, Satoko, et al.. (2001). Compositional Dependence of Superconducting Transition Temperature and Long Range Order Parameter in A15 Type V<SUB>3</SUB>Ga. Journal of the Japan Institute of Metals and Materials. 65(9). 795–798. 1 indexed citations
20.
Umezawa, Kazuo, Karo Tanaka, Takashi Hori, et al.. (1991). Induction of morphological change by tyrosine kinase inhibitors in Rous sarcoma virus‐transformed rat kidney cells. FEBS Letters. 279(1). 132–136. 11 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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