Satoshi Ishikiriyama

1.5k total citations
21 papers, 472 citations indexed

About

Satoshi Ishikiriyama is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Satoshi Ishikiriyama has authored 21 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Satoshi Ishikiriyama's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and Connective tissue disorders research (4 papers). Satoshi Ishikiriyama is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and Connective tissue disorders research (4 papers). Satoshi Ishikiriyama collaborates with scholars based in Japan and United States. Satoshi Ishikiriyama's co-authors include Norio Niikawa, Hirofumi Ohashi, Yoshimitsu Fukushima, Kyohko Abe, Naoki Harada, Hidefumi Tonoki, Shinki Chin, Tsutomu Kamei, H. Tonoki and Naoki Hase and has published in prestigious journals such as Human Genetics, American Journal of Medical Genetics and Dermatology.

In The Last Decade

Satoshi Ishikiriyama

20 papers receiving 455 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Satoshi Ishikiriyama Japan 10 289 283 128 69 52 21 472
Yoshinori Izumikawa Japan 12 216 0.7× 252 0.9× 82 0.6× 29 0.4× 27 0.5× 19 368
Piergiorgio Franceschini Italy 8 410 1.4× 263 0.9× 56 0.4× 23 0.3× 24 0.5× 13 598
Cheryl DeScipio United States 15 337 1.2× 334 1.2× 404 3.2× 35 0.5× 67 1.3× 18 834
Grange S. Coffin United States 8 274 0.9× 294 1.0× 82 0.6× 23 0.3× 66 1.3× 12 467
Judith Dagan Israel 12 231 0.8× 223 0.8× 96 0.8× 19 0.3× 88 1.7× 27 457
Michael J. Macera United States 13 165 0.6× 193 0.7× 76 0.6× 34 0.5× 130 2.5× 43 400
Isabelle Gicquel France 13 312 1.1× 236 0.8× 93 0.7× 27 0.4× 24 0.5× 21 453
Raymond Lewandowski United States 14 140 0.5× 272 1.0× 119 0.9× 9 0.1× 88 1.7× 16 380
Janice Zunich United States 11 197 0.7× 236 0.8× 47 0.4× 33 0.5× 27 0.5× 14 420
L. Wiśniewski Poland 11 134 0.5× 305 1.1× 115 0.9× 12 0.2× 129 2.5× 28 390

Countries citing papers authored by Satoshi Ishikiriyama

Since Specialization
Citations

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

Fields of papers citing papers by Satoshi Ishikiriyama

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoshi Ishikiriyama

This figure shows the co-authorship network connecting the top 25 collaborators of Satoshi Ishikiriyama. A scholar is included among the top collaborators of Satoshi Ishikiriyama 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 Ishikiriyama. Satoshi Ishikiriyama 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.
Naruse, Ichiro, et al.. (2009). Birth defects caused by mutations in human GLI3 and mouse Gli3 genes. Congenital Anomalies. 50(1). 1–7. 21 indexed citations
2.
Ariga, Tadashi, Satoshi Ishikiriyama, Makoto Otsu, et al.. (2008). Detection of a novel silent deletion, a missense mutation and a nonsense mutation in TCOF1. Pediatrics International. 50(6). 806–809. 6 indexed citations
3.
Nishimura, Akira, Haruya Sakai, Shiro Ikegawa, et al.. (2007). FBN2, FBN1, TGFBR1, and TGFBR2 analyses in congenital contractural arachnodactyly. American Journal of Medical Genetics Part A. 143A(7). 694–698. 21 indexed citations
4.
Niihori, Tetsuya, Yoko Aoki, Hirofumi Ohashi, et al.. (2005). Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. Journal of Human Genetics. 50(4). 192–202. 87 indexed citations
5.
Nakashima, Eiji, Akihiko Mabuchi, Mitsuru Kubota, et al.. (2004). Novel and recurrent exon 13 mutations of COMP in pseudoachondroplasia. American Journal of Medical Genetics Part A. 132A(1). 108–109. 3 indexed citations
6.
Hatamochi, Atsushi, Keisuke Kuroda, Hiroshi Shinkai, et al.. (2000). Costello Syndrome with Decreased Gene Expression of Elastin in Cultured Dermal Fibroblasts. Dermatology. 201(4). 366–369. 12 indexed citations
7.
Ishikiriyama, Satoshi. (2000). [Congenital insensitivity to pain with anhidrosis, Nishida syndrome].. PubMed. 288–90. 2 indexed citations
8.
Okamoto, Nobuhiko, Yoshinao Wada, Hidehiko Kawabata, Satoshi Ishikiriyama, & Satoru Takahashi. (1996). A novel mutation in LICAM gene in a Japanese patient with x-linked hydrocephalus. The Japanese Journal of Human Genetics. 41(4). 431–437. 5 indexed citations
9.
Wakui, Keiko, et al.. (1996). Interstitial duplication 8q22-q24: Report of a case proven by FISH with mapped cosmid probes. American Journal of Medical Genetics. 65(1). 36–39. 3 indexed citations
10.
Sato, Hirokazu, Shigeki Miyamoto, Satoshi Ishikiriyama, Nozomu Sasaki, & Hiroo Niimi. (1995). Klinefelter's Syndrome with Growth Hormone Deficiency. Clinical Pediatric Endocrinology. 4(Supple6). 127–129.
11.
Ishikiriyama, Satoshi, et al.. (1994). Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) and microcephaly. American Journal of Medical Genetics. 52(2). 245–245. 8 indexed citations
12.
Ohashi, Hirofumi, Satoshi Ishikiriyama, & Yoshimitsu Fukushima. (1993). New diagnostic method for Pallister‐Killian syndrome: Detection of i(12p) in interphase nuclei of buccal mucosa by fluorscence in situ hybridization. American Journal of Medical Genetics. 45(1). 123–128. 35 indexed citations
13.
Ishikiriyama, Satoshi, Mizue Iai, & Yuzo Tanabe. (1993). Lack of X inactivation: Loss of one X inactivation center in a case with mos45,X, –21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2). American Journal of Medical Genetics. 47(1). 41–44. 6 indexed citations
14.
Ishikiriyama, Satoshi, et al.. (1993). Blepharophimosis sequence (BPES) and microcephaly in a girl with del(3) (q22.2q23): A putative gene responsible for microcephaly close to the BPES gene?. American Journal of Medical Genetics. 47(4). 487–489. 16 indexed citations
15.
Ishikiriyama, Satoshi, et al.. (1991). Crossed polydactyly type I in a mother and son: An autosomal dominant trait?. American Journal of Medical Genetics. 40(1). 41–43. 9 indexed citations
16.
Ishikiriyama, Satoshi, Hidefumi Tonoki, Shinki Chin, et al.. (1989). Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3). American Journal of Medical Genetics. 33(4). 505–507. 72 indexed citations
17.
18.
Niikawa, Norio, Satoshi Ishikiriyama, Satoshi Takahashi, et al.. (1986). The Wiedemann‐Beckwith syndrome: Pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. American Journal of Medical Genetics. 24(1). 41–55. 80 indexed citations
19.
Ishikiriyama, Satoshi & Norio Niikawa. (1984). Origin of extra chromosome in Patau syndrome. Human Genetics. 68(3). 266–268. 22 indexed citations
20.
Tonoki, H., et al.. (1983). The Coffin‐Lowry Syndrome: Four New Cases In Three Families. Pediatrics International. 25(3). 298–303. 2 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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