Hidefumi Tonoki

3.1k total citations
48 papers, 1.5k citations indexed

About

Hidefumi Tonoki is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hidefumi Tonoki has authored 48 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 26 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hidefumi Tonoki's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (13 papers) and Genetic Syndromes and Imprinting (7 papers). Hidefumi Tonoki is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (13 papers) and Genetic Syndromes and Imprinting (7 papers). Hidefumi Tonoki collaborates with scholars based in Japan, India and United States. Hidefumi Tonoki's co-authors include Mohammad A. Karim, Yutaka Awaya, Tomoyasu Kawano, Yasuhiro Indo, Kohji Ohta, Hiroshi Mitsubuchi, Ichiro Matsuda, Tetsuya Moriuchi, Norio Niikawa and Naoki Harada and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Gastroenterology.

In The Last Decade

Hidefumi Tonoki

46 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hidefumi Tonoki Japan 18 751 518 310 186 185 48 1.5k
David Goudie United Kingdom 25 1.2k 1.5× 663 1.3× 441 1.4× 112 0.6× 206 1.1× 69 2.6k
J D Gearhart United States 25 1.1k 1.5× 586 1.1× 177 0.6× 113 0.6× 354 1.9× 35 2.0k
Mitsunobu Shimadzu Japan 22 812 1.1× 195 0.4× 452 1.5× 83 0.4× 176 1.0× 43 1.7k
Ellen J. Collarini United States 18 951 1.3× 385 0.7× 338 1.1× 82 0.4× 77 0.4× 38 1.7k
Sharon Zeligson Israel 19 731 1.0× 281 0.5× 167 0.5× 166 0.9× 91 0.5× 41 1.3k
J.‐C. Kaplan France 22 988 1.3× 279 0.5× 175 0.6× 157 0.8× 217 1.2× 54 1.5k
Takumi Takizawa Japan 20 1.5k 2.0× 345 0.7× 328 1.1× 66 0.4× 146 0.8× 68 2.2k
Tamae Ohye Japan 27 1.4k 1.8× 569 1.1× 697 2.2× 261 1.4× 172 0.9× 71 2.6k
Andrea Gashler United States 9 1.6k 2.1× 270 0.5× 288 0.9× 115 0.6× 77 0.4× 9 2.1k
Yufang Zheng China 24 989 1.3× 255 0.5× 239 0.8× 127 0.7× 72 0.4× 64 1.7k

Countries citing papers authored by Hidefumi Tonoki

Since Specialization
Citations

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

Fields of papers citing papers by Hidefumi Tonoki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hidefumi Tonoki

This figure shows the co-authorship network connecting the top 25 collaborators of Hidefumi Tonoki. A scholar is included among the top collaborators of Hidefumi Tonoki 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 Hidefumi Tonoki. Hidefumi Tonoki 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.
2.
Saitsu, Hirotomo, Gen Nishimura, Rika Kosaki, et al.. (2019). Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2). European Journal of Human Genetics. 27(12). 1845–1857. 7 indexed citations
3.
Kurahashi, Hiroki, Makiko Tsutsumi, Naoko Fujita, et al.. (2018). A constitutional jumping translocation involving the Y and acrocentric chromosomes. Asian Journal of Andrology. 21(1). 101–101. 1 indexed citations
4.
Watari, Michiko, Tomoharu Tokutomi, K Okuhara, et al.. (2016). Genetic and prenatal findings in two Japanese patients with Schinzel–Giedion syndrome. Clinical Case Reports. 5(1). 5–8. 2 indexed citations
5.
Kishimoto, Kenji, Ryōji Kobayashi, Hiroshi Yamamoto, et al.. (2014). Refractory Sacrococcygeal Germ Cell Tumor in Schinzel-Giedion Syndrome. Journal of Pediatric Hematology/Oncology. 37(4). e238–e241. 7 indexed citations
6.
Yoshiura, Koh-ichiro, Tatsuro Kondoh, Hirofumi Ohashi, et al.. (2009). Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome. Journal of Human Genetics. 54(5). 304–309. 27 indexed citations
7.
Sato, Daisuke, Osamu Shimokawa, Naoki Harada, et al.. (2007). A girl with Down syndrome and partial trisomy for 21pter‐q22.13: A clue to narrow the Down syndrome critical region. American Journal of Medical Genetics Part A. 146A(1). 124–127. 4 indexed citations
8.
Nakashima, Taiji, Yoshihiko Watarai, Ken Morita, et al.. (2006). Renal failure due to tubulointerstitial nephropathy in an infant with cranioectodermal dysplasia. Pediatric Nephrology. 21(4). 574–576. 4 indexed citations
9.
Nagai, Toshiro, Hidefumi Tonoki, Yoshimitsu Fukushima, et al.. (2000). Standard growth curves for Japanese patients with Prader-Willi syndrome. American Journal of Medical Genetics. 95(2). 130–134. 32 indexed citations
10.
Takahashi, Masato, Hidefumi Tonoki, Mitsuhiro Tada, et al.. (2000). Distinct prognostic values ofp53 mutations and loss of estrogen receptor and their cumulative effect in primary breast cancers. International Journal of Cancer. 89(1). 92–99. 27 indexed citations
11.
Kobayashi, Ichiro, Mitsuru Kubota, Susumu Ishikawa, et al.. (1999). Identification of an autoimmune enteropathy–related 75-kilodalton antigen. Gastroenterology. 117(4). 823–830. 68 indexed citations
12.
Yamamoto, Kazuhisa, Mitsuhiro Tada, Hidefumi Tonoki, et al.. (1999). A functional and quantitative mutational analysis ofp53 mutations in yeast indicates strand biases and different roles of mutations in DMBA- and BBN-induced tumors in rats. International Journal of Cancer. 83(5). 700–705. 7 indexed citations
13.
Tonoki, Hidefumi, Shinji Saitoh, & Kunihiko Kobayashi. (1998). Patient with del(12)(q12q13.12) manifesting abnormalities compatible with Noonan syndrome. American Journal of Medical Genetics. 75(4). 416–418. 25 indexed citations
14.
Hoshi, Nobuhiko, Hidefumi Tonoki, Takafumi Fujino, et al.. (1998). Prenatal identification ofmos 45, X/46, X, +mar in a normal male baby by cytogenetic and molecular analysis. Prenatal Diagnosis. 18(12). 1316–1322. 6 indexed citations
15.
Kashiwazaki, Haruhiko, Hidefumi Tonoki, Mitsuhiro Tada, et al.. (1997). High frequency of p53 mutations in human oral epithelial dysplasia and primary squamous cell carcinoma detected by yeast functional assay. Oncogene. 15(22). 2667–2674. 74 indexed citations
16.
Tonoki, Hidefumi, Jun Nakae, Toshihiro Tajima, et al.. (1995). Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasia. The Japanese Journal of Human Genetics. 40(4). 347–349. 3 indexed citations
17.
Fukushima, Yoshimitsu, Naoki Harada, Kyohko Abe, et al.. (1991). Molecular study of the Prader‐Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients. American Journal of Medical Genetics. 41(1). 54–63. 58 indexed citations
18.
Tonoki, Hidefumi, et al.. (1991). Identification of a marker chromosome as inv dup(15) by molecular analysis. Clinical Genetics. 40(3). 233–236. 17 indexed citations
19.
Tonoki, Hidefumi, et al.. (1990). A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs. American Journal of Medical Genetics. 36(1). 89–93. 5 indexed citations
20.
Kondoh, Tatsuro, Hidefumi Tonoki, Tadashi Matsumoto, Masato Tsukahara, & Norio Niikawa. (1988). Origin of the extra chromosome in trisomy 18. Human Genetics. 79(4). 377–8. 20 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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