Satoshi Horai

9.8k total citations · 1 hit paper
93 papers, 7.4k citations indexed

About

Satoshi Horai is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Satoshi Horai has authored 93 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 32 papers in Clinical Biochemistry and 28 papers in Genetics. Recurrent topics in Satoshi Horai's work include Mitochondrial Function and Pathology (36 papers), Metabolism and Genetic Disorders (32 papers) and Forensic and Genetic Research (22 papers). Satoshi Horai is often cited by papers focused on Mitochondrial Function and Pathology (36 papers), Metabolism and Genetic Disorders (32 papers) and Forensic and Genetic Research (22 papers). Satoshi Horai collaborates with scholars based in Japan, United States and Taiwan. Satoshi Horai's co-authors include Yu‐ichi Goto, Ikuya Nonaka, Kenji Hayasaka, Michael F. Hammer, R Kondo, Ei Matsunaga, Kazuo Tsugane, Naoyuki Takahata, Masami Hasegawa and Yasutoshi Koga and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Satoshi Horai

92 papers receiving 7.1k citations

Hit Papers

A mutation in the tRNALeu(UUR) gene associated with the M... 1990 2026 2002 2014 1990 500 1000 1.5k

Peers

Satoshi Horai
M.H.L. de Bruijn United Kingdom
Ian C. Eperon United Kingdom
Theodore G. Schurr United States
Thomas J. Parsons United States
Anna Di Rienzo United States
Henrik Kaessmann Switzerland
M.H.L. de Bruijn United Kingdom
Satoshi Horai
Citations per year, relative to Satoshi Horai Satoshi Horai (= 1×) peers M.H.L. de Bruijn

Countries citing papers authored by Satoshi Horai

Since Specialization
Citations

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

Fields of papers citing papers by Satoshi Horai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoshi Horai

This figure shows the co-authorship network connecting the top 25 collaborators of Satoshi Horai. A scholar is included among the top collaborators of Satoshi Horai 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 Satoshi Horai. Satoshi Horai 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.
Shi, Li, Jun Ohashi, Hao Sun, et al.. (2005). HLA‐A, HLA‐B, and HLA‐DRB1 alleles and haplotypes in Naxi and Han populations in southwestern China (Yunnan province). Tissue Antigens. 67(1). 38–44. 38 indexed citations
2.
Tajima, Atsushi, Masanori Hayami, Katsushi Tokunaga, et al.. (2004). Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages. Journal of Human Genetics. 49(4). 187–193. 98 indexed citations
3.
Tajima, Atsushi, et al.. (2003). Mitochondrial DNA polymorphisms in nine aboriginal groups of Taiwan: implications for the population history of aboriginal Taiwanese. Human Genetics. 113(1). 24–33. 41 indexed citations
4.
Fucharoen, Goonnapa, Supan Fucharoen, & Satoshi Horai. (2001). Mitochondrial DNA polymorphisms in Thailand. Journal of Human Genetics. 46(3). 115–125. 71 indexed citations
5.
Tajima, Atsushi, I-Hung Pan, Goonnapa Fucharoen, et al.. (2001). Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia. Human Genetics. 110(1). 80–88. 57 indexed citations
6.
Abe, Satoko, et al.. (1998). Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation. European Journal of Human Genetics. 6(6). 563–569. 27 indexed citations
7.
Horai, Satoshi, et al.. (1998). Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome. Neuromuscular Disorders. 8(3-4). 149–151. 34 indexed citations
8.
Goto, Yu-ichi, Ichizo Nishino, Satoshi Horai, & Ikuya Nonaka. (1996). Detection of DNA Fragments Encompassing the Deletion Junction of Mitochondrial Genome. Biochemical and Biophysical Research Communications. 222(2). 215–219. 12 indexed citations
9.
Hammer, Michael F. & Satoshi Horai. (1995). Y chromosomal DNA variation and the peopling of Japan.. PubMed Central. 303 indexed citations
10.
Goto, Yu‐ichi, Ikuya Nonaka, & Satoshi Horai. (1994). Insertion near the mitochondrial tyrosine tRNA gene in patients with mitochondrial diseases. The American Journal of Human Genetics. 55. 1 indexed citations
11.
Kondo, Rumi, Satoshi Horai, Yoko Satta, & Naoyuki Takahata. (1993). Evolution of hominoid mitochondrial DNA with special reference to the silent substitution rate over the genome. Journal of Molecular Evolution. 36(6). 517–531. 44 indexed citations
12.
Goto, Yu‐ichi, et al.. (1992). A novel point mutation in the mitochondrial tRNALeu(UUR) gene in a family with mitochondrial myopathy. Annals of Neurology. 31(6). 672–675. 89 indexed citations
13.
Horai, Satoshi, Rumi Kondo, Kumiko Murayama, et al.. (1991). Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNA. Philosophical Transactions of the Royal Society B Biological Sciences. 333(1268). 409–417. 87 indexed citations
14.
Hayasaka, Kenji, Takashi Ishida, & Satoshi Horai. (1991). Heteroplasmy and polymorphism in the major noncoding region of mitochondrial DNA in Japanese monkeys: association with tandemly repeated sequences.. Molecular Biology and Evolution. 8(4). 399–415. 79 indexed citations
15.
Goto, Yu‐ichi, Yasutoshi Koga, Satoshi Horai, & Ikuya Nonaka. (1990). Chronic progressive external ophthalmoplegia: A correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies. Journal of the Neurological Sciences. 100(1-2). 63–69. 88 indexed citations
16.
Goto, Yu‐ichi, Ikuya Nonaka, & Satoshi Horai. (1990). A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature. 348(6302). 651–653. 1587 indexed citations breakdown →
17.
Yamamoto, Akiko, Satoshi Horai, & Yasuhito Yuasa. (1989). Increased level of mitochondrial gene expression in polyps of familial polyposis coli patients. Biochemical and Biophysical Research Communications. 159(3). 1100–1106. 42 indexed citations
18.
Yoneda, Makoto, Masashi Tanaka, Morimitsu Nishikimi, et al.. (1989). Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS). Journal of the Neurological Sciences. 92(2-3). 143–158. 36 indexed citations
19.
Horai, Satoshi, J.J. van der Poel, & Els Goulmy. (1982). Differential recognition of the serologically defined HLA-A2 antigen by allogeneic cytotoxic T Cells. Immunogenetics. 16(2). 135–142. 34 indexed citations
20.

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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