Ryosuke Ohsawa

1.4k total citations
20 papers, 1.1k citations indexed

About

Ryosuke Ohsawa is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Ryosuke Ohsawa has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Ryosuke Ohsawa's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Ryosuke Ohsawa is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Ryosuke Ohsawa collaborates with scholars based in Japan, United States and Portugal. Ryosuke Ohsawa's co-authors include Ryoichiro Kageyama, Toshiyuki Ohtsuka, Jun Hatakeyama, Xiaoyan Zhu, Jessica Tollkühn, François Guillemot, Michael G. Rosenfeld, Jie Zhang, Emery H. Bresnick and Hiroyuki Morino and has published in prestigious journals such as Journal of Neuroscience, Genes & Development and PLoS ONE.

In The Last Decade

Ryosuke Ohsawa

20 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryosuke Ohsawa Japan 10 825 229 213 161 108 20 1.1k
Joanne M. Britto Australia 15 518 0.6× 234 1.0× 226 1.1× 146 0.9× 128 1.2× 28 992
Mireille Rossel France 17 810 1.0× 285 1.2× 237 1.1× 194 1.2× 86 0.8× 45 1.3k
Clare Faux United Kingdom 14 660 0.8× 343 1.5× 379 1.8× 135 0.8× 59 0.5× 15 1.1k
Zhoufeng Chen United States 10 962 1.2× 393 1.7× 140 0.7× 292 1.8× 47 0.4× 13 1.4k
Eumorphia Remboutsika Greece 16 677 0.8× 109 0.5× 112 0.5× 127 0.8× 60 0.6× 27 971
Ann-Sofie Nilsson Sweden 7 442 0.5× 473 2.1× 314 1.5× 125 0.8× 69 0.6× 8 943
Alex Paul United States 5 459 0.6× 107 0.5× 358 1.7× 145 0.9× 95 0.9× 5 731
Vivian Capilla‐González Spain 22 508 0.6× 165 0.7× 344 1.6× 87 0.5× 78 0.7× 35 1.3k
Dirk Junghans Germany 17 633 0.8× 314 1.4× 228 1.1× 124 0.8× 22 0.2× 20 1.0k
Ming‐Ji Fann Taiwan 12 576 0.7× 309 1.3× 103 0.5× 77 0.5× 31 0.3× 18 936

Countries citing papers authored by Ryosuke Ohsawa

Since Specialization
Citations

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

Fields of papers citing papers by Ryosuke Ohsawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryosuke Ohsawa

This figure shows the co-authorship network connecting the top 25 collaborators of Ryosuke Ohsawa. A scholar is included among the top collaborators of Ryosuke Ohsawa 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 Ryosuke Ohsawa. Ryosuke Ohsawa 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.
Fukushi, Masaya, Ryosuke Ohsawa, Yasushi Okinaka, et al.. (2023). Optineurin deficiency impairs autophagy to cause interferon beta overproduction and increased survival of mice following viral infection. PLoS ONE. 18(6). e0287545–e0287545. 1 indexed citations
2.
Kume, Kodai, Hiroyuki Morino, Ryosuke Ohsawa, et al.. (2021). Analysis of genetic risk factors in Japanese patients with Parkinson’s disease. Journal of Human Genetics. 66(10). 957–964. 4 indexed citations
3.
Kurashige, Takashi, Masahito Kuramochi, Ryosuke Ohsawa, et al.. (2020). Optineurin defects cause TDP43-pathology with autophagic vacuolar formation. Neurobiology of Disease. 148. 105215–105215. 19 indexed citations
4.
Kume, Kodai, Yukiko Matsuda, Takashi Kurashige, et al.. (2020). Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia. Journal of Human Genetics. 65(4). 363–369. 9 indexed citations
5.
Kume, Kodai, Hiroyuki Morino, Yukiko Matsuda, et al.. (2020). The first Japanese case of primary familial brain calcification caused by an MYORG variant. Journal of Human Genetics. 65(10). 917–920. 7 indexed citations
6.
Kume, Kodai, Hiroyuki Morino, Ryosuke Miyamoto, et al.. (2020). Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report. BMC Medical Genetics. 21(1). 68–68. 8 indexed citations
7.
Mizuno, Noriyoshi, Kodai Kume, Shinji Matsuda, et al.. (2020). Aggressive periodontitis and NOD2 variants. Journal of Human Genetics. 65(10). 841–846. 8 indexed citations
8.
Matsuda, Yukiko, Hiroyuki Morino, Ryosuke Miyamoto, et al.. (2020). Biallelic mutation of HSD17B4 induces middle age–onset spinocerebellar ataxia. Neurology Genetics. 6(1). e396–e396. 6 indexed citations
9.
Ramos, Amanda, Mafalda Raposo, Uzma Shamim, et al.. (2018). MitochondrialDNAhaplogroups and age at onset of Machado–Joseph disease/spinocerebellar ataxia type 3: a study in patients from multiple populations. European Journal of Neurology. 26(3). 506–512. 6 indexed citations
10.
Pal, Sangita, Hillary K. Graves, Ryosuke Ohsawa, et al.. (2016). The Commercial Antibodies Widely Used to Measure H3 K56 Acetylation Are Non-Specific in Human and Drosophila Cells. PLoS ONE. 11(5). e0155409–e0155409. 11 indexed citations
11.
Morino, Hiroyuki, Yukiko Matsuda, Keiko Muguruma, et al.. (2015). A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia. Molecular Brain. 8(1). 89–89. 77 indexed citations
12.
Morino, Hiroyuki, Sarah B. Pierce, Yukiko Matsuda, et al.. (2014). Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologic features. Neurology. 83(22). 2054–2061. 75 indexed citations
13.
Ohsawa, Ryosuke, et al.. (2013). At the intersection of non-coding transcription, DNA repair, chromatin structure, and cellular senescence. Frontiers in Genetics. 4. 136–136. 21 indexed citations
14.
Ohsawa, Ryosuke, Melissa W. Adkins, & Jessica K. Tyler. (2009). Epigenetic inheritance of an inducibly nucleosome-depleted promoter and its associated transcriptional state in the apparent absence of transcriptional activators. Epigenetics & Chromatin. 2(1). 11–11. 9 indexed citations
15.
Ohsawa, Ryosuke & Ryoichiro Kageyama. (2007). Regulation of retinal cell fate specification by multiple transcription factors. Brain Research. 1192. 90–98. 141 indexed citations
16.
Kita, Aya, Itaru Imayoshi, Masato Hojo, et al.. (2007). Hes1 and Hes5 Control the Progenitor Pool, Intermediate Lobe Specification, and Posterior Lobe Formation in the Pituitary Development. Molecular Endocrinology. 21(6). 1458–1466. 73 indexed citations
17.
Zhu, Xiaoyan, Jie Zhang, Jessica Tollkühn, et al.. (2006). Sustained Notch signaling in progenitors is required for sequential emergence of distinct cell lineages during organogenesis. Genes & Development. 20(19). 2739–2753. 151 indexed citations
18.
Ohsawa, Ryosuke, Toshiyuki Ohtsuka, & Ryoichiro Kageyama. (2005). Mash1andMath3Are Required for Development of Branchiomotor Neurons and Maintenance of Neural Progenitors. Journal of Neuroscience. 25(25). 5857–5865. 39 indexed citations
19.
Kageyama, Ryoichiro, Toshiyuki Ohtsuka, Jun Hatakeyama, & Ryosuke Ohsawa. (2005). Roles of bHLH genes in neural stem cell differentiation. Experimental Cell Research. 306(2). 343–348. 388 indexed citations
20.
Suehiro, Makiko, et al.. (1981). [13C-trioctanoin breath test for diagnosis of fat malabsorption (author's transl)].. PubMed. 18(2). 211–4. 1 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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