Yoshihito Kishita

2.3k total citations
38 papers, 693 citations indexed

About

Yoshihito Kishita is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Yoshihito Kishita has authored 38 papers receiving a total of 693 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 18 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Yoshihito Kishita's work include Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (18 papers) and ATP Synthase and ATPases Research (16 papers). Yoshihito Kishita is often cited by papers focused on Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (18 papers) and ATP Synthase and ATPases Research (16 papers). Yoshihito Kishita collaborates with scholars based in Japan, Canada and Switzerland. Yoshihito Kishita's co-authors include Kei Murayama, Yasushi Okazaki, Akira Ohtake, Masakazu Kohda, Toshiro Aigaki, Manabu Tsuda, Masaru Shimura, Takuya Fushimi, Keiko Ichimoto and Yukiko Yatsuka and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Yoshihito Kishita

36 papers receiving 687 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshihito Kishita Japan 14 589 240 66 30 30 38 693
Rolf J. R. J. Janssen Netherlands 9 662 1.1× 279 1.2× 51 0.8× 37 1.2× 42 1.4× 9 765
Johannes Koch Austria 17 688 1.2× 438 1.8× 72 1.1× 41 1.4× 39 1.3× 27 933
Marris G. Dibley Australia 4 502 0.9× 132 0.6× 38 0.6× 31 1.0× 37 1.2× 4 585
Chaya Miller Israel 15 1.1k 1.8× 455 1.9× 88 1.3× 61 2.0× 57 1.9× 20 1.2k
Lena Böttinger Germany 14 840 1.4× 238 1.0× 31 0.5× 38 1.3× 45 1.5× 17 965
Aaron R. D’Souza United Kingdom 8 589 1.0× 102 0.4× 35 0.5× 15 0.5× 67 2.2× 11 646
Irina Kuznetsova Australia 12 580 1.0× 93 0.4× 34 0.5× 21 0.7× 54 1.8× 20 662
Julia Philippou‐Massier Germany 10 576 1.0× 42 0.2× 59 0.9× 27 0.9× 57 1.9× 14 751
Sarah F. Pearce United Kingdom 16 849 1.4× 120 0.5× 48 0.7× 23 0.8× 126 4.2× 20 937
Inge Kühl France 13 1.1k 1.9× 320 1.3× 54 0.8× 48 1.6× 62 2.1× 21 1.2k

Countries citing papers authored by Yoshihito Kishita

Since Specialization
Citations

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

Fields of papers citing papers by Yoshihito Kishita

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshihito Kishita

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshihito Kishita. A scholar is included among the top collaborators of Yoshihito Kishita 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 Yoshihito Kishita. Yoshihito Kishita 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.
Yatsuka, Yukiko, Akira Hasegawa, Takeya Kasukawa, et al.. (2025). Successful Diagnosis of Sengers Syndrome Using a Comprehensive Genomic Analysis. Molecular Genetics & Genomic Medicine. 13(1). e70048–e70048.
2.
Miyauchi, Akihiko, Chika Watanabe, Naoya Yamada, et al.. (2024). Apomorphine is a potent inhibitor of ferroptosis independent of dopaminergic receptors. Scientific Reports. 14(1). 4820–4820. 11 indexed citations
3.
Kishita, Yoshihito, Ayumu Sugiura, Tetsuro Matsuhashi, et al.. (2023). Strategic validation of variants of uncertain significance in ECHS1 genetic testing. Journal of Medical Genetics. 60(10). 1006–1015. 2 indexed citations
4.
Kishita, Yoshihito, Mina Nakama, Hideo Sasai, et al.. (2023). Novel ITPA variants identified by whole genome sequencing and RNA sequencing. Journal of Human Genetics. 68(9). 649–652. 2 indexed citations
5.
Imasawa, Toshiyuki, Masakiyo Wakasugi, Hiroshi Kitamura, et al.. (2023). Focal segmental glomerulosclerosis with a mutation in the mitochondrially encoded NADH dehydrogenase 5 gene: A case report. Molecular Genetics and Metabolism Reports. 35. 100963–100963. 4 indexed citations
6.
Tsuruoka, Tomoko, Masaru Shimura, Makiko Tajika, et al.. (2022). Severe spinal cord hypoplasia due to a novel ATAD3A compound heterozygous deletion. Molecular Genetics and Metabolism Reports. 33. 100912–100912. 4 indexed citations
7.
Kishita, Yoshihito, Kaori Ishikawa, Kazuto Nakada, et al.. (2021). A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome. Scientific Reports. 11(1). 11123–11123. 12 indexed citations
8.
Shimura, Masaru, Taro Yamazaki, Hiroko Harashima, et al.. (2021). Prenatal diagnosis of severe mitochondrial diseases caused by nuclear gene defects: a study in Japan. Scientific Reports. 11(1). 3531–3531. 1 indexed citations
9.
Shimura, Masaru, Tetsuro Matsuhashi, Takuya Fushimi, et al.. (2021). Development of Leigh syndrome with a high probability of cardiac manifestations in infantile-onset patients with m.14453G > A. Mitochondrion. 63. 1–8. 7 indexed citations
10.
Borna, Nurun Nahar, Yoshihito Kishita, Norio Sakai, et al.. (2020). Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL. Genes. 11(11). 1325–1325. 8 indexed citations
11.
Doi, Toshiki, Yukinari Masuda, Yoshihito Kishita, et al.. (2020). A case report of adult-onset COQ8B nephropathy presenting focal segmental glomerulosclerosis with granular swollen podocytes. BMC Nephrology. 21(1). 376–376. 8 indexed citations
12.
Hirono, Keiichi, Fukiko Ichida, Minako Ogawa‐Tominaga, et al.. (2019). Mitochondrial complex deficiency by novel compound heterozygous TMEM 70 variants and correlation with developmental delay, undescended testicle, and left ventricular noncompaction in a Japanese patient: A case report. SHILAP Revista de lepidopterología. 7(3). 553–557. 13 indexed citations
13.
Tozawa, Takenori, H. Kondo, Zenro Kizaki, et al.. (2019). Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185 T > C variant in the MT-ATP6 gene: Expanding the clinical spectrum. Brain and Development. 42(1). 69–72. 9 indexed citations
14.
Kishita, Yoshihito, Masakazu Kohda, Yosuke Mizuno, et al.. (2019). Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International Journal of Cardiology. 279. 115–121. 33 indexed citations
15.
Yao, Yue, Motoi Nishimura, Kei Murayama, et al.. (2019). A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing. Scientific Reports. 9(1). 17411–17411. 22 indexed citations
16.
Borna, Nurun Nahar, Yoshihito Kishita, Masakazu Kohda, et al.. (2019). Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. Neurogenetics. 20(1). 9–25. 44 indexed citations
17.
Asano, Kana, Takeo Suzuki, Ayaka Saito, et al.. (2018). Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease. Nucleic Acids Research. 46(4). 1565–1583. 117 indexed citations
18.
Borna, Nurun Nahar, Yoshihito Kishita, Kaori Ishikawa, et al.. (2017). A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy. Journal of Human Genetics. 62(5). 539–547. 5 indexed citations
19.
Ohtake, Akira, Kei Murayama, Masayuki Mori, et al.. (2014). Diagnosis and molecular basis of mitochondrial respiratory chain disorders: Exome sequencing for disease gene identification. Biochimica et Biophysica Acta (BBA) - General Subjects. 1840(4). 1355–1359. 43 indexed citations
20.
Tsuda, Manabu, et al.. (2010). Loss of Trx‐2 enhances oxidative stress‐dependent phenotypes in Drosophila. FEBS Letters. 584(15). 3398–3401. 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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