Hideyuki Ohtani

1.2k total citations
17 papers, 375 citations indexed

About

Hideyuki Ohtani is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Hideyuki Ohtani has authored 17 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Psychiatry and Mental health, 8 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Hideyuki Ohtani's work include Epilepsy research and treatment (10 papers), Pharmacological Effects and Toxicity Studies (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Hideyuki Ohtani is often cited by papers focused on Epilepsy research and treatment (10 papers), Pharmacological Effects and Toxicity Studies (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Hideyuki Ohtani collaborates with scholars based in Japan, China and United States. Hideyuki Ohtani's co-authors include Yushi Inoue, Kazuhiro Yamakawa, Ikuo Ogiwara, Yukitoshi Takahashi, Emi Mazaki, Tojo Nakayama, Shigeru Tsuchiya, Tetsushi Yamagata, Katsuyuki Fukushima and Jun Tohyama and has published in prestigious journals such as Epilepsia, Journal of the Neurological Sciences and Human Mutation.

In The Last Decade

Hideyuki Ohtani

17 papers receiving 370 citations

Peers

Hideyuki Ohtani

PMH

CMN

GENET

PPCH

Suha Mercho Canada

Manyee Gee United States

Jan‐Peter Ernst Germany

Amedeo Bianchi Italy

Daniela Buti Italy

Sibylle Wallace United States

Yasuhiro Suzuki Japan

Kristien Verhaert Belgium

Ritu Kumari India

Giulia Iapadre Italy

Suha Mercho Canada

Hideyuki Ohtani

280 ×1.2

PMH

182 ×1.3

164 ×1.2

CMN

173 ×1.6

GENET

96 ×0.9

PPCH

Citations per year, relative to Hideyuki Ohtani Hideyuki Ohtani (= 1×) peers Suha Mercho

Countries citing papers authored by Hideyuki Ohtani

Since Specialization

Citations

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

Fields of papers citing papers by Hideyuki Ohtani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hideyuki Ohtani

This figure shows the co-authorship network connecting the top 25 collaborators of Hideyuki Ohtani. A scholar is included among the top collaborators of Hideyuki Ohtani 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 Hideyuki Ohtani. Hideyuki Ohtani is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Nishida, Takuji, Hitoshi Ikeda, Hiroko Ikeda, et al.. (2025). Long‐term seizure and psychosocial outcomes of patients with ring chromosome 20 syndrome: A cohort study of 47 cases. Epilepsia. 66(7). 2444–2453. 1 indexed citations

Takahashi, Satoru, Ryosuke Tanaka, Takayoshi Koike, et al.. (2022). CDKL5 deficiency causes epileptic seizures independent of cellular mosaicism. Journal of the Neurological Sciences. 443. 120498–120498. 3 indexed citations

Mine, Jun, et al.. (2020). Efficacy of a Psychoeducational Program for Children with Epilepsy and Their Parents (Famoses) in Japan. Journal of the Japan Epilepsy Society. 38(1). 43–53. 1 indexed citations

Ogiwara, Ikuo, Hiroyuki Miyamoto, Tetsuya Tatsukawa, et al.. (2018). Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice. Communications Biology. 1(1). 96–96. 65 indexed citations

Ohtani, Hideyuki, Masaki Tanaka, Mutsuo Sasagawa, et al.. (2016). Japanese Results of the European Registry of Antiepileptic Drugs and Pregnancy (EURAP): (Second Report). Journal of the Japan Epilepsy Society. 33(3). 663–671. 1 indexed citations

Takahashi, Yukitoshi, Tokito Yamaguchi, Yuki Ueda, et al.. (2015). Three patients manifesting early infantile epileptic spasms associated with 2q24.3 microduplications. Brain and Development. 37(9). 874–879. 8 indexed citations

Yamamoto, Yoshiaki, Yukitoshi Takahashi, Katsumi Imai, et al.. (2014). Individualized Phenytoin Therapy for Japanese Pediatric Patients With Epilepsy Based on CYP2C9 and CYP2C19 Genotypes. Therapeutic Drug Monitoring. 37(2). 229–235. 10 indexed citations

Cao, Dezhi, Hideyuki Ohtani, Ikuo Ogiwara, et al.. (2012). Efficacy of stiripentol in hyperthermia‐induced seizures in a mouse model of Dravet syndrome. Epilepsia. 53(7). 1140–1145. 42 indexed citations

Ogiwara, Ikuo, Tojo Nakayama, Tetsushi Yamagata, et al.. (2012). A homozygous mutation of voltage‐gated sodium channel β _I gene SCN1B in a patient with Dravet syndrome. Epilepsia. 53(12). e200–3. 70 indexed citations

10.

Mogami, Yukiko, Yukitoshi Takahashi, Rumiko Takayama, et al.. (2012). [Sleepiness:a frequent adverse reaction of antiepileptic drugs in patients with epilepsy after encephalitis/encephalopathy].. PubMed. 44(6). 472–6. 1 indexed citations

11.

Mogami, Yukiko, Yukitoshi Takahashi, Rumiko Takayama, et al.. (2011). Cutaneous adverse drug reaction in patients with epilepsy after acute encephalitis. Brain and Development. 34(6). 496–503. 6 indexed citations

12.

Takahashi, Hiroka, Yukitoshi Takahashi, Jun Mine, et al.. (2010). [Effectiveness of topiramate in eleven patients with Dravet syndrome].. PubMed. 42(4). 273–6. 4 indexed citations

13.

Nakayama, Tojo, Ikuo Ogiwara, Koichi Ito, et al.. (2010). Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome. Human Mutation. 31(7). 820–829. 41 indexed citations

14.

Inoue, Yushi, Yoko Ohtsuka, Hirokazu Oguni, et al.. (2009). Stiripentol open study in Japanese patients with Dravet syndrome. Epilepsia. 50(11). 2362–2368. 83 indexed citations

15.

Ohtani, Hideyuki, Takuya Kida, Takeaki Uno, & Hiroki Arimura. (2009). Efficient serial episode mining with minimal occurrences. 457–464. 6 indexed citations

16.

Ohtani, Hideyuki, et al.. (2006). Development of Industrial Control Programming Environment Enhanced by Extensible Graphic Symbols. 2006 SICE-ICASE International Joint Conference. 5169–5172. 2 indexed citations

17.

Ohta, Toshiyuki, Takashi Sakano, Hideyuki Ohtani, et al.. (2004). Reversible posterior leukoencephalopathy in a patient with Wegener granulomatosis. Pediatric Nephrology. 19(4). 442–444. 31 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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