Yoshihiko Kitoh

499 total citations
8 papers, 423 citations indexed

About

Yoshihiko Kitoh is a scholar working on Molecular Biology, Genetics and Biomaterials. According to data from OpenAlex, Yoshihiko Kitoh has authored 8 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Biomaterials. Recurrent topics in Yoshihiko Kitoh's work include Muscle Physiology and Disorders (7 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA Research and Splicing (3 papers). Yoshihiko Kitoh is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA Research and Splicing (3 papers). Yoshihiko Kitoh collaborates with scholars based in Japan and United States. Yoshihiko Kitoh's co-authors include Hajime Nakamura, Masafumi Matsuo, Hisahide Nishio, Yuto Ishikawa, Toru Takumi, Junichi Koga, Takehiro Masumura, Naoko Narita, Rumi Minami and Takeshi Nakajima and has published in prestigious journals such as Journal of Clinical Investigation, Biochemical and Biophysical Research Communications and Journal of Neurology.

In The Last Decade

Yoshihiko Kitoh

8 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yoshihiko Kitoh Japan	6	393	105	68	60	57	8	423
Petr Dmitriev France	12	459 1.2×	32 0.3×	35 0.5×	68 1.1×	41 0.7×	20	517
Tanja Lalic Serbia	6	251 0.6×	32 0.3×	99 1.5×	77 1.3×	78 1.4×	10	320
Marija Guć‐Šćekić Serbia	9	230 0.6×	42 0.4×	76 1.1×	54 0.9×	47 0.8×	23	299
Junqiu Chen China	8	266 0.7×	116 1.1×	58 0.9×	30 0.5×	16 0.3×	15	407
Damelys Calderon France	8	337 0.9×	30 0.3×	77 1.1×	23 0.4×	35 0.6×	11	394
Zoltán Simándi Hungary	12	320 0.8×	28 0.3×	42 0.6×	24 0.4×	12 0.2×	19	457
Chao-Jen Wong United States	9	520 1.3×	39 0.4×	46 0.7×	57 0.9×	86 1.5×	11	541
Т. Тодоров Bulgaria	8	146 0.4×	21 0.2×	49 0.7×	20 0.3×	19 0.3×	26	258
Isabella M. Salamone United States	8	316 0.8×	37 0.4×	197 2.9×	17 0.3×	20 0.4×	10	407
Ivone Bruno United States	7	392 1.0×	17 0.2×	28 0.4×	24 0.4×	20 0.4×	11	453

Countries citing papers authored by Yoshihiko Kitoh

Since Specialization

Citations

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

Fields of papers citing papers by Yoshihiko Kitoh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshihiko Kitoh

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

Hagiwara, Yoshihiro, Hisahide Nishio, Yoshihiko Kitoh, et al.. (1994). A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.. PubMed. 54(1). 53–61. 39 indexed citations

Narita, Naoko, Hisahide Nishio, Yoshihiko Kitoh, et al.. (1993). Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.. Journal of Clinical Investigation. 91(5). 1862–1867. 167 indexed citations

Nishio, Hisahide, Masafumi Matsuo, Yoshihiko Kitoh, et al.. (1993). Brain- and muscle-type promoters of the dystrophin gene are selected in peripheral lymphocytes and Epstein Barr virus-transformed lymphoplastoid cells. Journal of Neurology. 241(2). 81–86. 2 indexed citations

Kitoh, Yoshihiko, Masafumi Matsuo, Hisahide Nishio, et al.. (1992). Amplification of ten deletion‐rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy. American Journal of Medical Genetics. 42(4). 453–457. 16 indexed citations

Matsuo, Masafumi, et al.. (1992). Partial deletion of a dystrophin gene leads to exon skipping and to loss of an intra-exon hairpin structure from the predicted mRNA precursor. Biochemical and Biophysical Research Communications. 182(2). 495–500. 18 indexed citations

Matsuo, Masafumi, Takehiro Masumura, Hisahide Nishio, et al.. (1991). Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.. Journal of Clinical Investigation. 87(6). 2127–2131. 130 indexed citations

Nakajima, Takeshi, Masafumi Matsuo, Yoshihiko Kitoh, et al.. (1991). Screening of gene deletions by polymerase chain reaction in Japanese patients with Duchenne muscular dystrophy. Journal of Neurology. 238(1). 6–8. 5 indexed citations

Matsuo, Masafumi, Takehiro Masumura, Toshihiro Nakajima, et al.. (1990). A very small frame-shifting deletion within exon 19 of the Duchenne muscular dystrophy gene. Biochemical and Biophysical Research Communications. 170(2). 963–967. 46 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.

Explore authors with similar magnitude of impact