Toshiro Nagai

9.0k total citations
138 papers, 3.5k citations indexed

About

Toshiro Nagai is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Toshiro Nagai has authored 138 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Genetics, 71 papers in Molecular Biology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Toshiro Nagai's work include Genetic Syndromes and Imprinting (47 papers), Prenatal Screening and Diagnostics (27 papers) and Genomic variations and chromosomal abnormalities (17 papers). Toshiro Nagai is often cited by papers focused on Genetic Syndromes and Imprinting (47 papers), Prenatal Screening and Diagnostics (27 papers) and Genomic variations and chromosomal abnormalities (17 papers). Toshiro Nagai collaborates with scholars based in Japan, United States and Australia. Toshiro Nagai's co-authors include Tsutomu Ogata, Nobuyuki Murakami, Tomonobu Hasegawa, Maki Fukami, Hirofumi Ohashi, Lam‐Son Phan Tran, Yoshifumi Itoh, Gen Nishimura, Nobutake Matsuo and Yukihiro Hasegawa and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

In The Last Decade

Toshiro Nagai

135 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toshiro Nagai Japan 33 2.0k 1.8k 616 327 250 138 3.5k
Mitsuhiro Kato Japan 38 2.4k 1.2× 2.0k 1.1× 603 1.0× 268 0.8× 159 0.6× 214 5.0k
Taneli Raivio Finland 38 2.5k 1.3× 1.8k 1.0× 312 0.5× 384 1.2× 172 0.7× 135 5.0k
D. Holmes Morton United States 39 2.5k 1.2× 925 0.5× 487 0.8× 303 0.9× 201 0.8× 76 4.7k
Robert M. Greene United States 33 1.9k 1.0× 1.1k 0.7× 209 0.3× 487 1.5× 138 0.6× 155 3.4k
V. Reid Sutton United States 41 2.5k 1.3× 2.2k 1.2× 770 1.3× 415 1.3× 98 0.4× 146 4.7k
Dani Bercovich Israel 28 1.2k 0.6× 696 0.4× 139 0.2× 284 0.9× 230 0.9× 74 2.9k
Thomas Günther Germany 26 3.1k 1.6× 701 0.4× 136 0.2× 182 0.6× 212 0.8× 65 4.2k
Kazuhiko Nakabayashi Japan 40 3.5k 1.8× 1.9k 1.1× 884 1.4× 220 0.7× 267 1.1× 222 5.0k
Yang Yu China 35 2.2k 1.1× 384 0.2× 448 0.7× 272 0.8× 364 1.5× 160 4.0k
Julián Nevado Spain 26 892 0.5× 621 0.4× 245 0.4× 126 0.4× 132 0.5× 118 2.0k

Countries citing papers authored by Toshiro Nagai

Since Specialization
Citations

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

Fields of papers citing papers by Toshiro Nagai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshiro Nagai

This figure shows the co-authorship network connecting the top 25 collaborators of Toshiro Nagai. A scholar is included among the top collaborators of Toshiro Nagai 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 Toshiro Nagai. Toshiro Nagai 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.
Oto, Yuji, Nobuyuki Murakami, Takeshi Inoue, et al.. (2023). Perinatal and neonatal characteristics of Prader–Willi syndrome in Japan. Pediatrics International. 65(1). e15540–e15540. 1 indexed citations
2.
Naoi, Sotaro, Hisamitsu Hayashi, Takeshi Inoue, et al.. (2014). Improved Liver Function and Relieved Pruritus after 4-Phenylbutyrate Therapy in a Patient with Progressive Familial Intrahepatic Cholestasis Type 2. The Journal of Pediatrics. 164(5). 1219–1227.e3. 54 indexed citations
3.
Sawada, Masayuki, et al.. (2014). Comparative analysis of autistic traits and behavioral disorders in Prader–Willi syndrome and Asperger disorder. American Journal of Medical Genetics Part A. 167(1). 64–68. 13 indexed citations
4.
Suzuki, Junichi, Noriyuki Azuma, Sumito Dateki, et al.. (2014). Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities. Journal of Human Genetics. 59(6). 353–356. 12 indexed citations
5.
Kido, Yasuhiro, Christopher T. Gordon, Satoru Sakazume, et al.. (2013). Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations. American Journal of Medical Genetics Part A. 161(9). 2339–2346. 20 indexed citations
6.
Kido, Yasuhiro, Satoru Sakazume, Yoshiko Abe, et al.. (2013). Testosterone replacement therapy to improve secondary sexual characteristics and body composition without adverse behavioral problems in adult male patients with Prader–Willi syndrome: An observational study. American Journal of Medical Genetics Part A. 161(9). 2167–2173. 29 indexed citations
7.
Inoue, Takeshi, et al.. (2011). [Three cases of Fanconi syndrome associated with valproate sodium treatment].. PubMed. 43(3). 233–7. 9 indexed citations
8.
Tanaka, Yuriko, et al.. (2011). Five cases of West syndrome complicated by nephrocalcinosis during combination therapy with ACTH and zonisamide. Japanese journal of pediatric nephrology. 24(1). 86–91.
9.
Tsunoda, Tomoyuki, Ayano Inui, Tsuyoshi Sogo, et al.. (2011). Long-term effect of the Japanese hepatitis B immunization program in newborn infants born to HBV carrier mothers in Japan. Kanzo. 52(7). 491–493. 1 indexed citations
10.
Nagai, Toshiro, et al.. (2010). Incidents of Violence and Verbal Abuse from Patients and Their Relatives against Nurses in Dokkyo Medical University Koshigaya Hospital. 37(1). 1–8. 2 indexed citations
11.
Fukami, Maki, Toshiro Nagai, Hiroshi Mochizuki, et al.. (2010). Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency. Molecular Genetics and Metabolism. 100(3). 269–273. 21 indexed citations
12.
Rock, Matthew J., Jean Prenen, Vincent Funari, et al.. (2008). Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia. Nature Genetics. 40(8). 999–1003. 176 indexed citations
13.
Sakuta, Ryoichi, et al.. (2005). Diagnostic Significance of Membrane Attack Complex and Vitronectin in Childhood Dermatomyositis. Journal of Child Neurology. 20(7). 597–602. 13 indexed citations
14.
Murakami, Nobuyuki, et al.. (2005). An adolescent with pharyngeal-cervical-brachial variant of Guillain–Barré syndrome after cytomegalovirus infection. Brain and Development. 28(4). 269–271. 11 indexed citations
15.
Miyake, Noriko, Naoki Harada, Osamu Shimokawa, et al.. (2004). On the reported 8p22‐p23.1 duplication in Kabuki make‐up syndrome (KMS) and its absence in patients with typical KMS. American Journal of Medical Genetics Part A. 128A(2). 170–172. 24 indexed citations
16.
Ozawa, Hiroshi, et al.. (2004). Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II. Brain and Development. 27(3). 237–240. 13 indexed citations
17.
Muramatsu, Kanako, et al.. (1997). Stimulative Effect of Phytone on the Production of Sticky Materials in Bacillus subtilis(natto).. Nippon Shokuhin Kagaku Kogaku Kaishi. 44(11). 812–815. 5 indexed citations
18.
Nagai, Toshiro, et al.. (1993). Symmetrical thalamic lesions on CT in influenza A virus infection presenting with or without Reye syndrome. Brain and Development. 15(1). 67–73. 32 indexed citations
19.
Nagai, Toshiro, et al.. (1992). Infantile polymyositis: A case report. Brain and Development. 14(3). 167–169. 5 indexed citations
20.
Kang, Ellen S., et al.. (1989). Serum lipolytic activity in Reye's syndrome. Clinica Chimica Acta. 184(1). 107–114. 3 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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