Iori Ohmori

2.1k total citations
57 papers, 1.5k citations indexed

About

Iori Ohmori is a scholar working on Psychiatry and Mental health, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Iori Ohmori has authored 57 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Psychiatry and Mental health, 25 papers in Molecular Biology and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Iori Ohmori's work include Epilepsy research and treatment (32 papers), Neuroscience and Neuropharmacology Research (17 papers) and Ion channel regulation and function (10 papers). Iori Ohmori is often cited by papers focused on Epilepsy research and treatment (32 papers), Neuroscience and Neuropharmacology Research (17 papers) and Ion channel regulation and function (10 papers). Iori Ohmori collaborates with scholars based in Japan, United States and France. Iori Ohmori's co-authors include Yoko Ohtsuka, Mamoru Ouchida, Eiji Oka, Hideki Matsui, Tei‐ichi Nishiki, Kazuhito Tomizawa, Kenji Shimizu, Hiroyuki Michiue, Katsuhiro Kobayashi and Thomas H. Rhodes and has published in prestigious journals such as Journal of Neuroscience, The EMBO Journal and PLoS ONE.

In The Last Decade

Iori Ohmori

57 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iori Ohmori Japan 24 744 604 407 369 241 57 1.5k
Hadassa Goldberg‐Stern Israel 23 790 1.1× 378 0.6× 429 1.1× 350 0.9× 388 1.6× 51 1.6k
Heather E. Olson United States 21 753 1.0× 513 0.8× 345 0.8× 861 2.3× 307 1.3× 58 1.8k
Bernd A. Neubauer Germany 28 1.1k 1.5× 680 1.1× 661 1.6× 604 1.6× 538 2.2× 128 2.3k
Giuseppe Gobbi Italy 28 1.2k 1.6× 435 0.7× 433 1.1× 551 1.5× 649 2.7× 85 2.1k
Paolo Balestri Italy 30 811 1.1× 944 1.6× 383 0.9× 835 2.3× 725 3.0× 109 2.8k
Tae‐Sung Ko South Korea 24 999 1.3× 216 0.4× 362 0.9× 232 0.6× 597 2.5× 116 1.7k
Ki Joong Kim South Korea 28 1.1k 1.5× 892 1.5× 396 1.0× 407 1.1× 633 2.6× 199 3.0k
Edda Haberlandt Austria 25 641 0.9× 371 0.6× 217 0.5× 288 0.8× 477 2.0× 89 1.7k
Andy Peiffer United States 15 575 0.8× 1.5k 2.5× 806 2.0× 499 1.4× 118 0.5× 19 2.6k
Francesca Darra Italy 24 819 1.1× 365 0.6× 285 0.7× 522 1.4× 440 1.8× 86 1.6k

Countries citing papers authored by Iori Ohmori

Since Specialization
Citations

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

Fields of papers citing papers by Iori Ohmori

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iori Ohmori

This figure shows the co-authorship network connecting the top 25 collaborators of Iori Ohmori. A scholar is included among the top collaborators of Iori Ohmori 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 Iori Ohmori. Iori Ohmori 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.
Ohmori, Iori, et al.. (2020). Scn1a and Cacna1a mutations mutually alter their original phenotypes in rats. Neurochemistry International. 141. 104859–104859. 3 indexed citations
2.
Saitoh, Makiko, Iori Ohmori, Keiko Tanaka, et al.. (2016). Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS. Journal of the Neurological Sciences. 368. 272–276. 46 indexed citations
3.
Kobayashi, Katsuhiro, Tomoyuki Akiyama, Iori Ohmori, Harumi Yoshinaga, & Jean Gotman. (2014). Action potentials contribute to epileptic high-frequency oscillations recorded with electrodes remote from neurons. Clinical Neurophysiology. 126(5). 873–881. 8 indexed citations
4.
Kobayashi, Katsuhiro, Hiroki Ohzono, Makiko Saitoh, et al.. (2012). Acute encephalopathy with a novel point mutation in the SCN2A gene. Epilepsy Research. 102(1-2). 109–112. 24 indexed citations
5.
Michiue, Hiroyuki, Atsushi Fujimura, Atsuhito Uneda, et al.. (2012). Combining poly-arginine with the hydrophobic counter-anion 4-(1-pyrenyl)-butyric acid for protein transduction in transdermal delivery. Biomaterials. 33(27). 6468–6475. 32 indexed citations
6.
Michiue, Hiroyuki, Mizuki Kitamatsu, Atsushi Fujimura, et al.. (2012). A protein transduction method using oligo-arginine (3R) for the delivery of transcription factors into cell nuclei. Biomaterials. 33(18). 4665–4672. 32 indexed citations
7.
Suzuki, Koichiro, Iori Ohmori, Hiroyuki Michiue, et al.. (2011). Ca2+-independent syntaxin binding to the C2B effector region of synaptotagmin. Molecular and Cellular Neuroscience. 49(1). 1–8. 8 indexed citations
8.
Ouchida, Mamoru, Tomoji Mashimo, Tei‐ichi Nishiki, et al.. (2011). Therapy for hyperthermia-induced seizures in Scn1a mutant rats. Epilepsia. 52(5). 1010–1017. 20 indexed citations
9.
Fujimura, Atsushi, Hiroyuki Michiue, Tei‐ichi Nishiki, et al.. (2011). Expression of a Constitutively Active Calcineurin Encoded by an Intron-Retaining mRNA in Follicular Keratinocytes. PLoS ONE. 6(3). e17685–e17685. 11 indexed citations
10.
Kobayashi, Katsuhiro, Mamoru Ouchida, Akihisa Okumura, et al.. (2010). Genetic seizure susceptibility underlying acute encephalopathies in childhood. Epilepsy Research. 91(2-3). 143–152. 23 indexed citations
11.
Ohmori, Iori, Mamoru Ouchida, Takafumi Miki, et al.. (2008). A CACNB4 mutation shows that altered Cav2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy. Neurobiology of Disease. 32(3). 349–354. 45 indexed citations
12.
Ohtsuka, Yoko, Iori Ohmori, Tatsuya Ogino, et al.. (2003). Paroxysmal movement disorders in severe myoclonic epilepsy in infancy. Brain and Development. 25(6). 401–405. 12 indexed citations
13.
Kobayashi, Katsuhiro, et al.. (2003). Clinical and electroencephalographic characteristics of children with febrile seizures plus. Brain and Development. 26(4). 262–268. 2 indexed citations
14.
Yoshinaga, Harumi, et al.. (2003). EEG in childhood absence epilepsy. Seizure. 13(5). 296–302. 30 indexed citations
15.
Ohmori, Iori, Yoko Ohtsuka, Tatsuya Ogino, et al.. (2002). The Relationship between Paroxysmal Kinesigenic Choreoathetosis and Epilepsy. Neuropediatrics. 33(1). 15–20. 17 indexed citations
16.
Ohmori, Iori, Mamoru Ouchida, Yoko Ohtsuka, Eiji Oka, & Kenji Shimizu. (2002). Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy. Biochemical and Biophysical Research Communications. 295(1). 17–23. 180 indexed citations
17.
Oka, Eiji, Nagako Murakami, Iori Ohmori, & Tatsuya Ogino. (2001). A population-based neuroepidemiological survey of West syndrome in Okayama Prefecture, Japan. Brain and Development. 23(7). 580–583. 3 indexed citations
18.
Ohtsuka, Yoko, Iori Ohmori, & Eiji Oka. (1998). Long‐Term Follow‐Up of Childhood Epilepsy Associated with Tuberous Sclerosis. Epilepsia. 39(11). 1158–1163. 31 indexed citations
19.
Ohmori, Iori, et al.. (1997). Electroclinical study of localization-related epilepsies in early infancy. Pediatric Neurology. 16(2). 131–136. 6 indexed citations
20.
Ohmori, Iori, et al.. (1981). Dental care for severely handicapped children.. PubMed. 31(3). 177–84. 15 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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