Hiroyuki Torisu

1.6k total citations
57 papers, 804 citations indexed

About

Hiroyuki Torisu is a scholar working on Molecular Biology, Infectious Diseases and Genetics. According to data from OpenAlex, Hiroyuki Torisu has authored 57 papers receiving a total of 804 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Infectious Diseases and 13 papers in Genetics. Recurrent topics in Hiroyuki Torisu's work include Infectious Encephalopathies and Encephalitis (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Virology and Viral Diseases (6 papers). Hiroyuki Torisu is often cited by papers focused on Infectious Encephalopathies and Encephalitis (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Virology and Viral Diseases (6 papers). Hiroyuki Torisu collaborates with scholars based in Japan, United States and South Korea. Hiroyuki Torisu's co-authors include Toshiro Hara, Yasunari Sakai, Masafumi Sanefuji, Ryutaro Kira, Yoshito Ishizaki, Megumi Takemoto, Koichi Kusuhara, Kenji Ihara, Satoshi Akamine and Yuki Matsushita and has published in prestigious journals such as NeuroImage, Neurology and Clinical Infectious Diseases.

In The Last Decade

Hiroyuki Torisu

56 papers receiving 782 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hiroyuki Torisu Japan 17 193 174 150 143 123 57 804
Yoshito Ishizaki Japan 15 278 1.4× 150 0.9× 88 0.6× 129 0.9× 104 0.8× 38 788
İlknur Erol Türkiye 18 141 0.7× 238 1.4× 89 0.6× 199 1.4× 91 0.7× 78 896
Mauri Reunanen Finland 18 143 0.7× 177 1.0× 113 0.8× 150 1.0× 83 0.7× 59 970
Louise Wienholt Australia 12 173 0.9× 94 0.5× 109 0.7× 370 2.6× 152 1.2× 36 901
Sabiha Aysun Türkiye 18 144 0.7× 208 1.2× 94 0.6× 176 1.2× 140 1.1× 59 903
Tatsuro Izumi Japan 16 225 1.2× 226 1.3× 84 0.6× 71 0.5× 50 0.4× 70 895
Timothy Lotze United States 19 417 2.2× 106 0.6× 147 1.0× 468 3.3× 166 1.3× 63 1.4k
Sushil Bandodkar Australia 13 141 0.7× 103 0.6× 105 0.7× 200 1.4× 55 0.4× 25 548
Steffen Leiz Germany 11 111 0.6× 226 1.3× 70 0.5× 148 1.0× 46 0.4× 24 586
Şenay Haspolat Türkiye 14 103 0.5× 168 1.0× 119 0.8× 141 1.0× 66 0.5× 54 663

Countries citing papers authored by Hiroyuki Torisu

Since Specialization
Citations

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

Fields of papers citing papers by Hiroyuki Torisu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroyuki Torisu

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroyuki Torisu. A scholar is included among the top collaborators of Hiroyuki Torisu 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 Hiroyuki Torisu. Hiroyuki Torisu 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.
Fujii, Fumihiko, Yuki Matsushita, Daiki Setoyama, et al.. (2023). Shank3a/b isoforms regulate the susceptibility to seizures and thalamocortical development in the early postnatal period of mice. Neuroscience Research. 193. 13–19. 3 indexed citations
2.
Chong, Pin Fee, Hiroyuki Torisu, Sawa Yasumoto, et al.. (2021). Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study. Clinical Neurophysiology. 132(10). 2456–2463. 4 indexed citations
3.
Torio, Michiko, Hirosuke Inoue, Masayuki Ochiai, et al.. (2020). Neurodevelopmental Outcomes of High-Risk Preterm Infants. Neurology Clinical Practice. 11(5). 398–405. 6 indexed citations
4.
Torisu, Hiroyuki & Kenji Okada. (2019). Vaccination-associated acute disseminated encephalomyelitis. Vaccine. 37(8). 1126–1129. 5 indexed citations
5.
Fukai, Ryoko, Noriko Miyake, Soo-Young Lee, et al.. (2018). An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome. Brain and Development. 41(4). 378–381. 3 indexed citations
6.
Sakai, Yasunari, Fumiya Yamashita, Satoshi Akamine, et al.. (2017). Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion. Brain and Development. 39(7). 621–624. 7 indexed citations
7.
Matsushita, Yuki, Yasunari Sakai, Hiroshi Shigeto, et al.. (2016). Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice. Scientific Reports. 6(1). 22991–22991. 22 indexed citations
8.
Hoshina, Takayuki, Yuhki Koga, Masayuki Ochiai, et al.. (2016). Analysis of Death Due to Infectious Diseases in Patients Hospitalized in the Pediatric Ward of a Single Japanese Tertiary Medical Facility. Japanese Journal of Infectious Diseases. 69(6). 464–470. 3 indexed citations
9.
Fukai, Ryoko, Yasunari Sakai, Michiko Torio, et al.. (2016). De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. BMC Neurology. 16(1). 174–174. 20 indexed citations
10.
Torisu, Hiroyuki & Toshiro Hara. (2014). [Clinical features of pediatric multiple sclerosis: epidemiology and treatment].. PubMed. 72(11). 2061–6. 1 indexed citations
11.
Sakai, Yasunari, Ryota Souzaki, Hidetaka Yamamoto, et al.. (2014). Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome. BMC Medical Genomics. 7(1). 19–19. 2 indexed citations
12.
Sakai, Yasunari, Yuki Matsushita, Satoshi Akamine, et al.. (2013). Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus. European Journal of Medical Genetics. 56(9). 475–483. 6 indexed citations
13.
Torisu, Hiroyuki, Akiko Iwaki, Kenzo Takeshita, et al.. (2012). Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion. Brain and Development. 34(10). 852–856. 16 indexed citations
14.
Sanefuji, Masafumi, Kenji Watanabe, Ayumi Uematsu, et al.. (2011). Clinical and MRI characteristics of acute encephalopathy in congenital adrenal hyperplasia. Journal of the Neurological Sciences. 306(1-2). 91–93. 15 indexed citations
15.
Sanefuji, Masafumi, Ryutaro Kira, Kenichi Matsumoto, et al.. (2010). Autopsy Case of Later-Onset Pontocerebellar Hypoplasia Type 1: Pontine Atrophy and Pyramidal Tract Involvement. Journal of Child Neurology. 25(11). 1429–1434. 1 indexed citations
16.
Kira, Ryutaro, Yoshito Ishizaki, Hiroyuki Torisu, et al.. (2009). Genetic susceptibility to febrile seizures: Case-control association studies. Brain and Development. 32(1). 57–63. 23 indexed citations
17.
18.
Takemoto, Megumi, Ryutaro Kira, Koichi Kusuhara, et al.. (2005). Gene expression profiles in peripheral blood mononuclear cells from patients with subacute sclerosing panencephalitis using oligonucleotide microarrays. Journal of NeuroVirology. 11(3). 299–305. 5 indexed citations
19.
Tamura, Hiroshi, Takayuki Takahashi, Nobuhiro Ban, et al.. (2005). Niemann–Pick type C disease: Novel NPC1 mutations and characterization of the concomitant acid sphingomyelinase deficiency. Molecular Genetics and Metabolism. 87(2). 113–121. 26 indexed citations
20.
Torisu, Hiroyuki, Toshiyuki Yamamoto, Mitsutaka Kadota, et al.. (2004). Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1). American Journal of Medical Genetics Part A. 131A(1). 94–98. 21 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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