Hidetoshi Date

3.3k total citations
20 papers, 1.2k citations indexed

About

Hidetoshi Date is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Hidetoshi Date has authored 20 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 8 papers in Neurology. Recurrent topics in Hidetoshi Date's work include Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (7 papers) and DNA Repair Mechanisms (4 papers). Hidetoshi Date is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (7 papers) and DNA Repair Mechanisms (4 papers). Hidetoshi Date collaborates with scholars based in Japan, Spain and United States. Hidetoshi Date's co-authors include Shoji Tsuji, Atsushi Iwata, Lumine Matsumoto, Akira Tamaoka, Hiroshi Takuma, Hiroshi Kurisaki, Shuichi Igarashi, Hiroki Takano, Mutsuo Oyake and Hitoshi Takahashi and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Hidetoshi Date

19 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hidetoshi Date Japan 14 764 546 424 184 150 20 1.2k
D. Sau Italy 12 630 0.8× 315 0.6× 441 1.0× 132 0.7× 223 1.5× 15 1.2k
Norma B. Romero France 22 1.2k 1.5× 291 0.5× 304 0.7× 174 0.9× 182 1.2× 44 1.7k
Jianwen Deng China 19 810 1.1× 395 0.7× 651 1.5× 182 1.0× 108 0.7× 85 1.4k
Beate Schlotter‐Weigel Germany 15 779 1.0× 338 0.6× 125 0.3× 348 1.9× 240 1.6× 24 1.3k
Giulietta Riboldi Italy 19 846 1.1× 353 0.6× 432 1.0× 226 1.2× 104 0.7× 43 1.4k
Jiasheng Zhang United States 13 590 0.8× 178 0.3× 484 1.1× 241 1.3× 118 0.8× 18 1.2k
Vı́ctor Volpini Spain 23 605 0.8× 532 1.0× 395 0.9× 41 0.2× 75 0.5× 45 1.2k
Simon Hammans United Kingdom 25 1.4k 1.8× 425 0.8× 211 0.5× 96 0.5× 91 0.6× 45 1.7k
Silvia Rathke‐Hartlieb Germany 9 554 0.7× 325 0.6× 317 0.7× 103 0.6× 119 0.8× 9 979
Jelena Mojsilovic‐Petrovic United States 13 575 0.8× 225 0.4× 255 0.6× 83 0.5× 76 0.5× 17 1.1k

Countries citing papers authored by Hidetoshi Date

Since Specialization
Citations

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

Fields of papers citing papers by Hidetoshi Date

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hidetoshi Date

This figure shows the co-authorship network connecting the top 25 collaborators of Hidetoshi Date. A scholar is included among the top collaborators of Hidetoshi Date 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 Hidetoshi Date. Hidetoshi Date 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.
Ishihara, Tomohiko, Sachiko Hirokawa, Hidetoshi Date, et al.. (2025). Redefining the Pathogenic CAG Repeat Units Threshold in CACNA1A for Spinocerebellar Ataxia Type 6. Neurology Genetics. 11(2). e200245–e200245.
2.
Hama, Yuka, Hidetoshi Date, Hiroyuki Ishiura, et al.. (2022). A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity. The Cerebellum. 22(6). 1308–1311. 1 indexed citations
3.
Ikenaga, Chiseko, Hidetoshi Date, Motoi Kanagawa, et al.. (2022). Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis. Annals of Neurology. 91(3). 317–328. 12 indexed citations
4.
Ishiura, Hiroyuki, Jun Mitsui, Hidetoshi Date, et al.. (2017). Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation. Neurobiology of Aging. 61. 255.e9–255.e16. 39 indexed citations
5.
Ishiura, Hiroyuki, Hidetoshi Date, Minoru Tanaka, et al.. (2017). Search for target genes of transcriptional regulation by Dentatorubral-pallidoluysian atrophy protein that acts as a transcriptional co-regulator. Journal of the Neurological Sciences. 381. 57–57. 1 indexed citations
6.
7.
Ishiura, Hiroyuki, Yuji Takahashi, Jun Mitsui, et al.. (2012). C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan. Archives of Neurology. 69(9). 1154–8. 69 indexed citations
8.
Chen, F., et al.. (2012). Pulmonary arterioplasty for the remaining arterial stump of the donor and the arterial cuff of the donor graft in living-donor lobar lung transplantation. European Journal of Cardio-Thoracic Surgery. 42(5). e138–e139. 11 indexed citations
9.
Yokoseki, Akio, Tomohiko Ishihara, Akihide Koyama, et al.. (2011). Genotype–phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia. Brain. 134(5). 1387–1399. 21 indexed citations
10.
Matsumoto, Lumine, Hiroshi Takuma, Akira Tamaoka, et al.. (2010). CpG Demethylation Enhances Alpha-Synuclein Expression and Affects the Pathogenesis of Parkinson's Disease. PLoS ONE. 5(11). e15522–e15522. 240 indexed citations
11.
Iwata, Atsushi, Yu Nagashima, Lumine Matsumoto, et al.. (2009). Intranuclear Degradation of Polyglutamine Aggregates by the Ubiquitin-Proteasome System. Journal of Biological Chemistry. 284(15). 9796–9803. 75 indexed citations
12.
Mitsui, Jun, Ikuko Mizuta, Atsushi Toyoda, et al.. (2009). Mutations for Gaucher Disease Confer High Susceptibility to Parkinson Disease. Archives of Neurology. 66(5). 571–6. 150 indexed citations
13.
Fukuda, Y., Yasuo Nakahara, Hidetoshi Date, et al.. (2009). SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data. BMC Bioinformatics. 10(1). 121–121. 21 indexed citations
14.
Takahashi, Tetsuya, Masayoshi Tada, Shuichi Igarashi, et al.. (2007). Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends. Nucleic Acids Research. 35(11). 3797–3809. 46 indexed citations
15.
Date, Hidetoshi, Shuichi Igarashi, Yasuteru Sano, et al.. (2004). The FHA domain of aprataxin interacts with the C-terminal region of XRCC1. Biochemical and Biophysical Research Communications. 325(4). 1279–1285. 49 indexed citations
16.
Sano, Yasuteru, Hidetoshi Date, Shuichi Igarashi, et al.. (2004). Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein. Annals of Neurology. 55(2). 241–249. 61 indexed citations
17.
Sekijima, Yoshiki, Takao Hashimoto, Osamu Onodera, et al.. (2003). Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation. Movement Disorders. 18(10). 1198–1200. 20 indexed citations
18.
Tanaka, Keiko, Takeshi Ikeuchi, Shuichi Igarashi, et al.. (2002). A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees. Annals of Neurology. 52(4). 516–519. 42 indexed citations
19.
Shimazaki, Haruo, Yoshihisa Takiyama, Kumi Sakoe, et al.. (2002). Early-onset ataxia with ocular motor apraxia and hypoalbuminemia. Neurology. 59(4). 590–595. 60 indexed citations
20.
Igarashi, Shuichi, Reiji Koide, Takayoshi Shimohata, et al.. (1998). Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch. Nature Genetics. 18(2). 111–117. 299 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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