Tomohiro Chiyonobu

1.7k total citations
56 papers, 966 citations indexed

About

Tomohiro Chiyonobu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tomohiro Chiyonobu has authored 56 papers receiving a total of 966 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tomohiro Chiyonobu's work include Genetics and Neurodevelopmental Disorders (11 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Advanced Neuroimaging Techniques and Applications (6 papers). Tomohiro Chiyonobu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Advanced Neuroimaging Techniques and Applications (6 papers). Tomohiro Chiyonobu collaborates with scholars based in Japan, United Kingdom and United States. Tomohiro Chiyonobu's co-authors include Masafumi Morimoto, Hajime Hosoi, Tatsushi Toda, Takenori Tozawa, Norimitsu Inoue, Yoshiko Murakami, Taroh Kinoshita, Tatsuji Hasegawa, Satoshi Takeda and Kei Yamada and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain Research.

In The Last Decade

Tomohiro Chiyonobu

55 papers receiving 964 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomohiro Chiyonobu Japan 20 455 217 176 140 135 56 966
Yong Seung Hwang South Korea 22 553 1.2× 213 1.0× 284 1.6× 367 2.6× 135 1.0× 89 1.4k
Katsuo Sugita Japan 22 790 1.7× 268 1.2× 197 1.1× 114 0.8× 151 1.1× 101 1.6k
Christine Barnérias France 20 704 1.5× 283 1.3× 140 0.8× 133 0.9× 137 1.0× 73 1.4k
Andreas Hahn Germany 21 680 1.5× 183 0.8× 90 0.5× 198 1.4× 174 1.3× 93 1.3k
Soo Yeon Kim South Korea 17 327 0.7× 197 0.9× 100 0.6× 180 1.3× 132 1.0× 109 899
Kenji Yokochi Japan 20 587 1.3× 197 0.9× 460 2.6× 285 2.0× 131 1.0× 72 1.4k
Satoko Kumada Japan 20 630 1.4× 423 1.9× 129 0.7× 202 1.4× 289 2.1× 86 1.4k
Jeehun Lee South Korea 17 204 0.4× 99 0.5× 219 1.2× 250 1.8× 101 0.7× 80 855
Toru Kurokawa Japan 20 589 1.3× 97 0.4× 164 0.9× 304 2.2× 267 2.0× 62 1.4k
Francesca Madia Italy 18 351 0.8× 292 1.3× 70 0.4× 180 1.3× 290 2.1× 62 1.0k

Countries citing papers authored by Tomohiro Chiyonobu

Since Specialization
Citations

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

Fields of papers citing papers by Tomohiro Chiyonobu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomohiro Chiyonobu

This figure shows the co-authorship network connecting the top 25 collaborators of Tomohiro Chiyonobu. A scholar is included among the top collaborators of Tomohiro Chiyonobu 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 Tomohiro Chiyonobu. Tomohiro Chiyonobu 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.
Okanishi, Tohru, Yosuke Miyamoto, Ryuki Matsuura, et al.. (2024). Predictive modeling based on functional connectivity of interictal scalp EEG for infantile epileptic spasms syndrome. Clinical Neurophysiology. 167. 37–48. 2 indexed citations
2.
Tozawa, Takenori, et al.. (2024). Bilateral choroid plexus resection in a 9p hexasomy/tetrasomy mosaic patient. Human Genome Variation. 11(1). 9–9.
3.
Chiyonobu, Tomohiro, et al.. (2023). Knockdown of Chronophage in the nervous system mimics features of neurodevelopmental disorders caused by BCL11A/B variants. Experimental Cell Research. 433(2). 113827–113827. 2 indexed citations
4.
Tozawa, Takenori, et al.. (2023). Myosin Va, a Novel Interaction Partner of STXBP1, Is Required to Transport Syntaxin1A to the Plasma Membrane. Neuroscience. 524. 256–268. 1 indexed citations
5.
Tozawa, Takenori, Kenichi Isoda, Tomohiro Chiyonobu, et al.. (2023). Leigh-like syndrome with progressive cerebellar atrophy caused by novel HIBCH variants. Human Genome Variation. 10(1). 23–23. 2 indexed citations
6.
Chiyonobu, Tomohiro, Shinsaku Tokuda, Mitsuru Miyachi, et al.. (2022). Pleomorphic rhabdomyosarcoma in a young adult harboring a novel germline MSH2 variant. Human Genome Variation. 9(1). 8–8. 4 indexed citations
7.
Mori, Jun, Tatsuji Hasegawa, Yosuke Miyamoto, et al.. (2022). Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation. Human Genome Variation. 9(1). 18–18. 2 indexed citations
8.
Tozawa, Takenori, Akira Nishimura, Takeshi Yoshida, et al.. (2021). Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants. Human Genome Variation. 8(1). 4–4. 4 indexed citations
9.
Hasegawa, Tatsuji, Koji Sakai, Takenori Tozawa, et al.. (2021). Low‐grade IVH in preterm infants causes cerebellar damage, motor, and cognitive impairment. Pediatrics International. 63(11). 1327–1333. 8 indexed citations
10.
Yamaguchi, Masamitsu, et al.. (2020). Investigating Developmental and Epileptic Encephalopathy Using Drosophila melanogaster. International Journal of Molecular Sciences. 21(17). 6442–6442. 16 indexed citations
11.
Chiyonobu, Tomohiro, Ryo Tanaka, Takenori Tozawa, et al.. (2020). A novel Drosophila model for neurodevelopmental disorders associated with Shwachman–Diamond syndrome. Neuroscience Letters. 739. 135449–135449. 7 indexed citations
12.
Chiyonobu, Tomohiro, et al.. (2019). Novel genetic link between the ATP-binding cassette subfamily A gene and hippo gene in Drosophila. Experimental Cell Research. 386(2). 111733–111733. 5 indexed citations
13.
Tozawa, Takenori, H. Kondo, Zenro Kizaki, et al.. (2019). Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185 T > C variant in the MT-ATP6 gene: Expanding the clinical spectrum. Brain and Development. 42(1). 69–72. 9 indexed citations
14.
15.
Kodo, Kazuki, Kenichi Sakamoto, Mitsuru Miyachi, et al.. (2018). Cytomegalovirus-associated biliary atresia. Journal of Pediatric Surgery Case Reports. 35. 17–20. 4 indexed citations
16.
Yoshida, Michiko, Mitsuko Nakashima, Tohru Okanishi, et al.. (2017). Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum. Clinical Genetics. 93(2). 368–373. 26 indexed citations
17.
Nishimura, Agnes L., Masafumi Morimoto, Takashi Morita, et al.. (2013). Altered somatosensory barrel cortex refinement in the developing brain of Mecp2-null mice. Brain Research. 1537. 319–326. 6 indexed citations
18.
Kanagawa, Motoi, Tomohiro Chiyonobu, Satoshi Takeda, et al.. (2008). Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy. Human Molecular Genetics. 18(4). 621–631. 61 indexed citations
19.
Chiyonobu, Tomohiro, Shin Hayashi, Kazuhiro Kobayashi, et al.. (2007). Partial tandem duplication of GRIA3 in a male with mental retardation. American Journal of Medical Genetics Part A. 143A(13). 1448–1455. 19 indexed citations
20.
Morimoto, Akira, Tomohiro Chiyonobu, Tohru Sugimoto, et al.. (2004). Early Blastic Transformation Following Complete Cytogenetic Response in a Pediatric Chronic Myeloid Leukemia Patient Treated With Imatinib Mesylate. Journal of Pediatric Hematology/Oncology. 26(5). 320–322. 6 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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