Fuyuki Miya

3.0k total citations
84 papers, 1.0k citations indexed

About

Fuyuki Miya is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Fuyuki Miya has authored 84 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 31 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Fuyuki Miya's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and RNA modifications and cancer (10 papers). Fuyuki Miya is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and RNA modifications and cancer (10 papers). Fuyuki Miya collaborates with scholars based in Japan, United States and United Kingdom. Fuyuki Miya's co-authors include Tatsuhiko Tsunoda, Kenjiro Kosaki, Nobuhiko Okamoto, Shinji Saitoh, Yonehiro Kanemura, Mitsuhiro Kato, Mami Yamasaki, Tatsuo Matsunaga, Hideki Mutai and Chise Tateno and has published in prestigious journals such as Nature Communications, Immunity and PLoS ONE.

In The Last Decade

Fuyuki Miya

75 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
Fuyuki Miya Japan 19 509 299 126 126 100 84 1.0k
Bin Cai China 18 316 0.6× 261 0.9× 101 0.8× 119 0.9× 75 0.8× 54 944
Mark E. Samuels Canada 21 615 1.2× 412 1.4× 135 1.1× 113 0.9× 43 0.4× 41 1.2k
Ortal Barel Israel 15 450 0.9× 247 0.8× 104 0.8× 189 1.5× 73 0.7× 63 868
Ramu Elango Saudi Arabia 19 447 0.9× 263 0.9× 145 1.2× 112 0.9× 60 0.6× 76 1.0k
Sharon Zeligson Israel 19 731 1.4× 281 0.9× 51 0.4× 96 0.8× 97 1.0× 41 1.3k
Bartolomeo Augello Italy 18 439 0.9× 199 0.7× 63 0.5× 184 1.5× 80 0.8× 33 882
Dominique Marchant France 22 752 1.5× 260 0.9× 66 0.5× 105 0.8× 50 0.5× 54 1.3k
Itay Chowers Israel 20 862 1.7× 134 0.4× 71 0.6× 123 1.0× 93 0.9× 87 1.5k
Asaf Ta‐Shma Israel 16 450 0.9× 224 0.7× 102 0.8× 126 1.0× 43 0.4× 19 988
Karen Duran Netherlands 21 755 1.5× 575 1.9× 80 0.6× 121 1.0× 135 1.4× 28 1.4k

Countries citing papers authored by Fuyuki Miya

Since Specialization
Citations

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

Fields of papers citing papers by Fuyuki Miya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fuyuki Miya

This figure shows the co-authorship network connecting the top 25 collaborators of Fuyuki Miya. A scholar is included among the top collaborators of Fuyuki Miya 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 Fuyuki Miya. Fuyuki Miya 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.
Kobayashi, Yu, Satoru Sakuma, Emiko Morimoto, et al.. (2025). Refractory myoclonic epilepsy and progressive movement disorder arising from recurrent DHDDS variants in Japanese patients: a case series. Brain and Development. 47(6). 104478–104478.
2.
Sato, Taku, Mihoko Kajita, Fuyuki Miya, et al.. (2025). An organoid library of human esophageal squamous cell carcinomas (ESCCs) uncovers the chemotherapy-resistant ESCC features. Communications Biology. 8(1). 507–507. 2 indexed citations
3.
Imaizumi, Kent, Fuyuki Miya, Mamiko Yamada, et al.. (2025). Rescue of imprinted genes by epigenome editing in human cellular models of Prader-Willi syndrome. Nature Communications. 16(1). 9442–9442.
4.
Sato, Taku, Hajime Sato, Fuyuki Miya, et al.. (2024). Comparative analysis of tongue cancer organoids among patients identifies the heritable nature of minimal residual disease. Developmental Cell. 60(3). 396–413.e6. 5 indexed citations
5.
Nishiuchi, Ritsuo, et al.. (2024). Sibling cases of DEPDC5-related developmental and epileptic encephalopathy successfully treated with lacosamide. 2(4). 100044–100044. 1 indexed citations
6.
Tanaka, Yumiko, Mai Yamagishi, Yasutaka Motomura, et al.. (2023). Time-dependent cell-state selection identifies transiently expressed genes regulating ILC2 activation. Communications Biology. 6(1). 915–915. 2 indexed citations
7.
Yamada, Mamiko, Hisato Suzuki, Atsuko Noguchi, et al.. (2022). Diagnosis of SLC25A46-related pontocerebellar hypoplasia in two siblings with fulminant neonatal course: role of postmortem CT and whole genomic analysis: a case report. BMC Neurology. 22(1). 20–20. 2 indexed citations
8.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2021). Four pedigrees with aminoacyl-tRNA synthetase abnormalities. Neurological Sciences. 43(4). 2765–2774. 10 indexed citations
9.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2021). Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability. Neurological Sciences. 42(7). 2975–2978. 5 indexed citations
10.
Matsumoto, Ayumi, Karin Kojima, Fuyuki Miya, et al.. (2021). Two cases of DYNC1H1 mutations with intractable epilepsy. Brain and Development. 43(8). 857–862. 7 indexed citations
11.
Nishiguchi, Koji M., Kosuke Fujita, Fuyuki Miya, et al.. (2020). Serum anti‐recoverin antibodies is found in elderly patients with retinitis pigmentosa and cancer. Acta Ophthalmologica. 98(6). e722–e729. 2 indexed citations
12.
Mutai, Hideki, Koichiro Wasano, Yukihide Momozawa, et al.. (2020). Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans. PLoS Genetics. 16(4). e1008643–e1008643. 40 indexed citations
13.
Hori, Ikumi, Fuyuki Miya, Yutaka Negishi, et al.. (2018). A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome. Journal of Human Genetics. 63(9). 957–963. 10 indexed citations
14.
Tamai, Kei, Katsuhiko Tada, Akihito Takeuchi, et al.. (2018). Fetal ultrasonographic findings including cerebral hyperechogenicity in a patient with non‐lethal form of Raine syndrome. American Journal of Medical Genetics Part A. 176(3). 682–686. 13 indexed citations
15.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2017). Novel MCA/ID syndrome with ASH1L mutation. American Journal of Medical Genetics Part A. 173(6). 1644–1648. 29 indexed citations
16.
Okamoto, Nobuhiko, Fuyuki Miya, Tatsuhiko Tsunoda, et al.. (2017). A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology. American Journal of Medical Genetics Part A. 173(10). 2690–2696. 7 indexed citations
17.
Kato, Koji, Fuyuki Miya, Ikumi Hori, et al.. (2017). A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate. Journal of Human Genetics. 62(9). 861–863. 18 indexed citations
18.
Kawamura, Shunsuke, Nobuyuki Onai, Fuyuki Miya, et al.. (2017). Identification of a Human Clonogenic Progenitor with Strict Monocyte Differentiation Potential: A Counterpart of Mouse cMoPs. Immunity. 46(5). 835–848.e4. 64 indexed citations
19.
Hamada, Nanako, Yutaka Negishi, Makoto Mizuno, et al.. (2016). Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability. Journal of Neurochemistry. 140(1). 82–95. 13 indexed citations
20.
Negishi, Yutaka, Fuyuki Miya, Ayako Hattori, et al.. (2015). Truncating mutation in NFIA causes brain malformation and urinary tract defects. Human Genome Variation. 2(1). 15007–15007. 19 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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