Ichiro Satokata

4.6k total citations · 2 hit papers
27 papers, 3.8k citations indexed

About

Ichiro Satokata is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ichiro Satokata has authored 27 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Surgery. Recurrent topics in Ichiro Satokata's work include DNA Repair Mechanisms (9 papers), dental development and anomalies (7 papers) and Renal and related cancers (4 papers). Ichiro Satokata is often cited by papers focused on DNA Repair Mechanisms (9 papers), dental development and anomalies (7 papers) and Renal and related cancers (4 papers). Ichiro Satokata collaborates with scholars based in Japan, United States and France. Ichiro Satokata's co-authors include Richard L. Maas, Gail V. Benson, Ian Woo, Marianna Bei, Hyunjung Jade Lim, Sudhansu K. Dey, Bibhash C. Paria, Yiping Chen, Naoyuki Miura and Yoshiaki Satoh and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Ichiro Satokata

27 papers receiving 3.7k citations

Hit Papers

Msx1 deficient mice exhibit cleft palate and abnormalitie... 1994 2026 2004 2015 1994 2000 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    1994 1.0k citations Ichiro Satokata, Richard L. Maas Nature Genetics profile →
  2. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
    2000 597 citations Ichiro Satokata, Liang Ma et al. Nature Genetics profile →

Peers

Ichiro Satokata
B L Hogan United States
Annette Neubüser Germany
Rulang Jiang United States
Eric Schoenmakers Belgium
Kentaro Suzuki Japan
Y Ninomiya Japan
Rong Mo Canada
Andrea Vortkamp Germany
Kirsi Sainio Finland
Yu Lan United States
B L Hogan United States
Ichiro Satokata
Citations per year, relative to Ichiro Satokata Ichiro Satokata (= 1×) peers B L Hogan

Countries citing papers authored by Ichiro Satokata

Since Specialization
Citations

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

Fields of papers citing papers by Ichiro Satokata

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ichiro Satokata

This figure shows the co-authorship network connecting the top 25 collaborators of Ichiro Satokata. A scholar is included among the top collaborators of Ichiro Satokata 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 Ichiro Satokata. Ichiro Satokata 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.
Yoshida, Akiko, Hiroko Morisaki, Masataka Kitano, et al.. (2015). Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease. Journal of Human Genetics. 61(2). 157–162. 31 indexed citations
2.
Ida‐Yonemochi, Hiroko, Ichiro Satokata, Hayato Ohshima, et al.. (2011). Morphogenetic roles of perlecan in the tooth enamel organ: An analysis of overexpression using transgenic mice. Matrix Biology. 30(7-8). 379–388. 23 indexed citations
3.
Itoh, Takehiko, et al.. (2009). Odontogenic Potential of Post-natal Oral Mucosal Epithelium. Journal of Dental Research. 88(3). 219–223. 25 indexed citations
4.
Yokota, Masayuki, Takaomi C. Saido, Ichiro Satokata, et al.. (2005). Spatial resolution of calpain-catalyzed proteolysis in focal cerebral ischemia. Brain Research. 1040(1-2). 36–43. 14 indexed citations
5.
Yokota, Masayuki, Takaomi C. Saido, Hideki Kamitani, et al.. (2003). Calpain induces proteolysis of neuronal cytoskeleton in ischemic gerbil forebrain. Brain Research. 984(1-2). 122–132. 26 indexed citations
6.
Satokata, Ichiro, Liang Ma, Hayato Ohshima, et al.. (2000). Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nature Genetics. 24(4). 391–395. 597 indexed citations breakdown →
7.
Kuratani, Shigeru, Ichiro Satokata, Yoshihiro Komatsu, et al.. (1999). Middle ear defects associated with the double knock out mutation of murine goosecoid and Msx1 genes.. PubMed. 45(5). 589–99. 9 indexed citations
8.
Maas, Richard L., Yi Ping Chen, Marianna Bei, Ian Woo, & Ichiro Satokata. (1996). The Role of Msx Genes in Mammalian Developmenta. Annals of the New York Academy of Sciences. 785(1). 171–181. 32 indexed citations
9.
Shirai, Manabu, Akinori Miyashita, Yasuhiro Itoh, et al.. (1996). A Gene Trap Strategy for Identifying the Gene Expressed in the Embryonic Nervous System. ZOOLOGICAL SCIENCE. 13(2). 277–283. 17 indexed citations
10.
Benson, Gail V., Hyunjung Jade Lim, Bibhash C. Paria, et al.. (1996). Mechanisms of reduced fertility in Hoxa-10 mutant mice: uterine homeosis and loss of maternal Hoxa-10 expression. Development. 122(9). 2687–2696. 407 indexed citations
11.
Satokata, Ichiro, Gail V. Benson, & Richard L. Maas. (1995). Sexually dimorphic sterility phenotypes in HoxalO-deficient mice. Nature. 374(6521). 460–463. 439 indexed citations
12.
Satokata, Ichiro, Makoto Uchiyama, & Kiyoji Tanaka. (1995). Two novel splicing mutations in the XPA gene in patients with group A xeroderma pigmentosum. Human Molecular Genetics. 4(10). 1993–1994. 9 indexed citations
13.
Satokata, Ichiro & M Uchiyama. (1995). [Mice carrying null mutations of the homeotic genes Hoxa10 and Msx1].. PubMed. 40(14). 2134–43. 2 indexed citations
14.
Satokata, Ichiro & Richard L. Maas. (1994). Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nature Genetics. 6(4). 348–356. 1043 indexed citations breakdown →
15.
Satokata, Ichiro, Kunimitsu Iwai, Toshiro Matsuda, Yoshio Okada, & Kiyoji Tanaka. (1993). Genomic characterization of the human DNA excision repair-controlling geneXPAC. Gene. 136(1-2). 345–348. 25 indexed citations
16.
Satokata, Ichiro, Keiji Tanaka, Shunsuke Yuba, & Yasunori Okada. (1992). Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosum. Mutation Research/DNA Repair. 273(2). 203–212. 60 indexed citations
17.
Satokata, Ichiro, Keiji Tanaka, Naoyuki Miura, et al.. (1992). Three nonsense mutations responsible for group A xeroderma pigmentosum. Mutation Research/DNA Repair. 273(2). 193–202. 72 indexed citations
18.
Tanaka, Kiyoji, Naoyuki Miura, Ichiro Satokata, et al.. (1990). Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain. Nature. 348(6296). 73–76. 320 indexed citations
19.
Uchiyama, Makoto, et al.. (1987). Effect of various drugs on plasma atrial natriuretic peptide levels in childhood. 35(2). 77–81. 1 indexed citations
20.
Uchiyama, Makoto, et al.. (1987). Plasma Atrial Natriuretic Peptide in Congenital Heart Disease. Acta Paediatrica. 76(4). 669–670. 9 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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