Koichiro Doi

3.6k total citations
28 papers, 382 citations indexed

About

Koichiro Doi is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Koichiro Doi has authored 28 papers receiving a total of 382 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Neurology. Recurrent topics in Koichiro Doi's work include Neurogenetic and Muscular Disorders Research (6 papers), Human auditory perception and evaluation (5 papers) and Amyotrophic Lateral Sclerosis Research (4 papers). Koichiro Doi is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Human auditory perception and evaluation (5 papers) and Amyotrophic Lateral Sclerosis Research (4 papers). Koichiro Doi collaborates with scholars based in Japan. Koichiro Doi's co-authors include Shinichi Morishita, Jun Yoshimura, Shoji Tsuji, Hiroyuki Ishiura, Jun Mitsui, Hiroshi Imai, Yuji Takahashi, Jun Goto, Takashi Matsukawa and Ryohei Nakamura and has published in prestigious journals such as Nature Communications, Bioinformatics and Scientific Reports.

In The Last Decade

Koichiro Doi

25 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Koichiro Doi Japan 11 251 84 79 66 51 28 382
Abigail L. Pfaff Australia 11 178 0.7× 84 1.0× 57 0.7× 30 0.5× 42 0.8× 33 276
Vitaliy V. Bondar United States 9 292 1.2× 111 1.3× 67 0.8× 75 1.1× 41 0.8× 10 590
И. В. Честков Russia 8 292 1.2× 33 0.4× 64 0.8× 97 1.5× 28 0.5× 11 367
E. Koenig United States 6 232 0.9× 131 1.6× 45 0.6× 88 1.3× 38 0.7× 13 405
Xiao-Hong Lin China 11 165 0.7× 39 0.5× 39 0.5× 125 1.9× 65 1.3× 18 545
Devon Lamb Thrush United States 10 218 0.9× 19 0.2× 141 1.8× 54 0.8× 25 0.5× 19 334
Fabienne Wavrant De Vrieze United States 5 232 0.9× 181 2.2× 250 3.2× 90 1.4× 19 0.4× 6 543
Claire Guissart France 12 174 0.7× 65 0.8× 73 0.9× 76 1.2× 40 0.8× 22 301
Jenny Blechingberg Denmark 10 294 1.2× 41 0.5× 67 0.8× 34 0.5× 32 0.6× 18 388
Parul Jayakar United States 15 383 1.5× 27 0.3× 217 2.7× 99 1.5× 27 0.5× 32 615

Countries citing papers authored by Koichiro Doi

Since Specialization
Citations

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

Fields of papers citing papers by Koichiro Doi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Koichiro Doi

This figure shows the co-authorship network connecting the top 25 collaborators of Koichiro Doi. A scholar is included among the top collaborators of Koichiro Doi 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 Koichiro Doi. Koichiro Doi 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.
Ikeda, Yoshiki, et al.. (2025). Global DNA methylation level sensing using methyl-CpG binding domain-fused luciferase and fluorescent protein. Sensors and Actuators B Chemical. 438. 137797–137797. 1 indexed citations
2.
Doi, Koichiro, et al.. (2020). Self-demodulation characteristics of amplitude-modulated bone-conducted ultrasound in the human body presented to the neck, trunk and arm. Japanese Journal of Applied Physics. 59(SK). SKKE26–SKKE26. 3 indexed citations
3.
Ishiura, Hiroyuki, Jun Mitsui, Yuji Takahashi, et al.. (2020). Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population. Journal of Human Genetics. 66(3). 237–241. 11 indexed citations
4.
Hongo, Hiroki, Satoru Miyawaki, Hideaki Imai, et al.. (2020). Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis. Scientific Reports. 10(1). 11942–11942. 10 indexed citations
5.
6.
Ishiura, Hiroyuki, Jun Mitsui, Yuji Takahashi, et al.. (2020). Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis. Neurogenetics. 22(1). 11–17. 8 indexed citations
7.
Nakagawa, Seiji, et al.. (2019). Propagation characteristics of amplitude-modulated bone-conducted ultrasound presented to the neck, trunk and arms. Japanese Journal of Applied Physics. 58(SG). SGGE18–SGGE18. 4 indexed citations
8.
Doi, Koichiro, et al.. (2019). Propagation and perception characteristics of distantly-presented bone-conducted sounds-Comparison between ultrasonic and low-frequency ranges-. 5–5.
9.
Ishiura, Hiroyuki, Jun Mitsui, Yuji Takahashi, et al.. (2018). Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS. Journal of Neurology Neurosurgery & Psychiatry. 90(5). 537–542. 27 indexed citations
10.
Ichinose, Yuta, Hiroyuki Ishiura, Masaki Tanaka, et al.. (2018). Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. Parkinsonism & Related Disorders. 61. 57–63. 6 indexed citations
11.
Ichikawa, Kazuki, Yuta Suzuki, Ryohei Nakamura, et al.. (2017). Centromere evolution and CpG methylation during vertebrate speciation. Nature Communications. 8(1). 1833–1833. 68 indexed citations
12.
Yamashita, Toru, Jun Mitsui, Nobuyuki Shimozawa, et al.. (2017). Ataxic form of autosomal recessive PEX10-related peroxisome biogenesis disorders with a novel compound heterozygous gene mutation and characteristic clinical phenotype. Journal of the Neurological Sciences. 375. 424–429. 8 indexed citations
13.
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
14.
Kurihara, Masanori, Hiroyuki Ishiura, Takuya Sasaki, et al.. (2017). Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia. The Cerebellum. 17(2). 237–242. 16 indexed citations
15.
Ikeda, Toshio, Rie Nagano, Hiroshi Moritake, et al.. (2016). TBCD may be a causal gene in progressive neurodegenerative encephalopathy with atypical infantile spinal muscular atrophy. Journal of Human Genetics. 62(4). 473–480. 13 indexed citations
16.
Fujimori, Koki, Hiroyuki Ishiura, Jun Mitsui, et al.. (2016). Modeling neurological diseases with induced pluripotent cells reprogrammed from immortalized lymphoblastoid cell lines. Molecular Brain. 9(1). 88–88. 19 indexed citations
17.
Matsukawa, Takashi, Jun Mitsui, Hiroyuki Ishiura, et al.. (2016). Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing. Journal of the Neurological Sciences. 372. 6–10. 10 indexed citations
18.
Ichikawa, Yaeko, Hiroyuki Ishiura, Jun Mitsui, et al.. (2013). Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1. Journal of the Neurological Sciences. 331(1-2). 158–160. 4 indexed citations
19.
Doi, Koichiro & Hiroshi Imai. (2000). Sequencing by hybridization in the presence of hybridization errors.. PubMed. 11. 53–62. 2 indexed citations
20.
Doi, Koichiro & Hiroshi Imai. (1999). A Greedy Algorithm for Minimizing the Number of Primers in Multiple PCR Experiments.. PubMed. 10. 73–82. 18 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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