Yutaka Nishigaki

4.4k total citations · 1 hit paper
67 papers, 3.4k citations indexed

About

Yutaka Nishigaki is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, Yutaka Nishigaki has authored 67 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 26 papers in Clinical Biochemistry and 11 papers in Epidemiology. Recurrent topics in Yutaka Nishigaki's work include Mitochondrial Function and Pathology (29 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (8 papers). Yutaka Nishigaki is often cited by papers focused on Mitochondrial Function and Pathology (29 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (8 papers). Yutaka Nishigaki collaborates with scholars based in Japan, United States and India. Yutaka Nishigaki's co-authors include Peramaiyan Rajendran, Thamaraiselvan Rengarajan, Dhanapal Sakthisekaran, Ikuo Nishigaki, Jayakumar Thangavel, Michio Hirano, Gautam Sethi, Ramón Martí, Noriyuki Fuku and Masashi Tanaka and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Cancer.

In The Last Decade

Yutaka Nishigaki

62 papers receiving 3.3k citations

Hit Papers

The Vascular Endothelium and Human Diseases 2013 2026 2017 2021 2013 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yutaka Nishigaki Japan 28 1.9k 889 418 313 253 67 3.4k
Feng Zheng China 38 1.1k 0.6× 942 1.1× 579 1.4× 184 0.6× 367 1.5× 74 3.6k
Satoru Sugiyama Japan 35 1.9k 1.0× 635 0.7× 515 1.2× 470 1.5× 357 1.4× 166 3.7k
Isabel Tavares de Almeida Portugal 32 1.9k 1.0× 1.3k 1.4× 549 1.3× 92 0.3× 308 1.2× 112 3.8k
Manuela Bartoli United States 31 1.6k 0.8× 319 0.4× 649 1.6× 204 0.7× 213 0.8× 88 4.0k
Xue Du China 8 1.2k 0.6× 1.4k 1.5× 1.1k 2.6× 409 1.3× 357 1.4× 17 3.6k
Li Xiao China 34 2.1k 1.1× 460 0.5× 467 1.1× 245 0.8× 444 1.8× 169 4.4k
Hiroki Fujita Japan 30 1.2k 0.6× 280 0.3× 624 1.5× 262 0.8× 543 2.1× 103 3.7k
Stefano Menini Italy 41 1.3k 0.7× 491 0.6× 889 2.1× 392 1.3× 472 1.9× 72 4.0k
Michelle S. Johnson United States 32 2.0k 1.0× 274 0.3× 616 1.5× 235 0.8× 211 0.8× 59 3.7k
Glenn L. Wilson United States 43 3.3k 1.7× 701 0.8× 895 2.1× 163 0.5× 567 2.2× 97 5.2k

Countries citing papers authored by Yutaka Nishigaki

Since Specialization
Citations

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

Fields of papers citing papers by Yutaka Nishigaki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yutaka Nishigaki

This figure shows the co-authorship network connecting the top 25 collaborators of Yutaka Nishigaki. A scholar is included among the top collaborators of Yutaka Nishigaki 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 Yutaka Nishigaki. Yutaka Nishigaki 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.
Rajendran, Peramaiyan, et al.. (2015). In vitrostudies on mangiferin protection against cadmium-induced human renal endothelial damage and cell death via the MAP kinase and NF-κB pathways. Journal of Receptors and Signal Transduction. 36(1). 57–66. 18 indexed citations
2.
Rajendran, Peramaiyan, Thamaraiselvan Rengarajan, Natarajan Nandakumar, et al.. (2014). Kaempferol, a potential cytostatic and cure for inflammatory disorders. European Journal of Medicinal Chemistry. 86. 103–112. 199 indexed citations
3.
Nishigaki, Yutaka, Yoshihiro Noguchi, Noriyuki Fuku, et al.. (2012). Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. Journal of Human Genetics. 57(12). 772–775. 1 indexed citations
4.
Sawabe, Motoji, Masashi Tanaka, Kouji Chida, et al.. (2011). Mitochondrial Haplogroups A and M7a Confer a Genetic Risk for Coronary Atherosclerosis in the Japanese Elderly: An Autopsy Study of 1,536 Patients. Journal of Atherosclerosis and Thrombosis. 18(2). 166–175. 26 indexed citations
6.
Nishigaki, Yutaka, Hitomi Ueno, Jorida Çoku, et al.. (2010). Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion. 10(3). 300–308. 24 indexed citations
7.
Nishigaki, Ikuo, Rajkapoor Balasubramanian, Peramaiyan Rajendran, et al.. (2010). Effect of fresh apple extract on glycated protein/iron chelate-induced toxicity in human umbilical vein endothelial cellsin vitro. Natural Product Research. 24(7). 599–609. 4 indexed citations
8.
Ueno, Hitomi, Yutaka Nishigaki, Qing‐Peng Kong, et al.. (2009). Analysis of mitochondrial DNA variants in Japanese patients with schizophrenia. Mitochondrion. 9(6). 385–393. 59 indexed citations
9.
Yoshida, Tetsuro, Kimihiko Kato, Kiyoshi Yokoi, et al.. (2009). Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension. Hypertension Research. 32(5). 411–418. 19 indexed citations
10.
Yamämoto, Yasushi, et al.. (2008). Resistin Is Closely Related to Systemic Inflammation in Obstructive Sleep Apnea. Respiration. 76(4). 377–385. 44 indexed citations
12.
Hirano, Michio, Clotilde Lagier‐Tourenne, Maria Lucia Valentino, Ramón Martí, & Yutaka Nishigaki. (2005). Thymidine phosphorylase mutations cause instability of mitochondrial DNA. Gene. 354. 152–156. 44 indexed citations
13.
Martí, Ramón, Antonella Spinazzola, Saba Tadesse, et al.. (2004). Definitive Diagnosis of Mitochondrial Neurogastrointestinal Encephalomyopathy by Biochemical Assays. Clinical Chemistry. 50(1). 120–124. 87 indexed citations
14.
Nishigaki, Yutaka, Ramón Martí, William C. Copeland, & Michio Hirano. (2003). Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency. Journal of Clinical Investigation. 111(12). 1913–1921. 153 indexed citations
15.
Fujita, Yuka, Satoru Fujiuchi, Yutaka Nishigaki, et al.. (2003). The diagnostic and prognostic relevance of human telomerase reverse transcriptase mRNA expression detected in situ in patients with nonsmall cell lung carcinoma. Cancer. 98(5). 1008–1013. 46 indexed citations
16.
Filosto, Massimiliano, Michelangelo Mancuso, Yutaka Nishigaki, et al.. (2003). Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase γ. Archives of Neurology. 60(9). 1279–84. 96 indexed citations
17.
Nishigaki, Yutaka, Saba Tadesse, Eduardo Bonilla, et al.. (2003). A novel mitochondrial tRNALeu(UUR) mutation in a patient with features of MERRF and Kearns–Sayre syndrome. Neuromuscular Disorders. 13(4). 334–340. 50 indexed citations
18.
Yamämoto, Yasushi, Hiroshi Ide, Yutaka Nishigaki, et al.. (2002). [Pulmonary sarcoidosis in a case of dermatomyositis under long-term steroid therapy].. PubMed. 40(4). 311–5. 2 indexed citations
19.
Ohsaki, Yoshinobu, Sachie Tanno, Eri Toyoshima, et al.. (2001). Detection of Photofrin Fluorescence From Malignant and Premalignant Lesions in the Bronchus using a Full‐color Endoscopic Fluorescence Imaging System. Diagnostic and therapeutic endoscopy. 7(3-4). 187–195. 7 indexed citations
20.
Hirano, Michio, Ramón Martí, Saba Tadesse, et al.. (2001). Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA. Seminars in Cell and Developmental Biology. 12(6). 417–427. 89 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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