Takeshi Mizuguchi

8.2k total citations
126 papers, 2.7k citations indexed

About

Takeshi Mizuguchi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Takeshi Mizuguchi has authored 126 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Molecular Biology, 57 papers in Genetics and 18 papers in Cellular and Molecular Neuroscience. Recurrent topics in Takeshi Mizuguchi's work include Genetics and Neurodevelopmental Disorders (27 papers), Genomics and Rare Diseases (22 papers) and Genomic variations and chromosomal abnormalities (17 papers). Takeshi Mizuguchi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Genomics and Rare Diseases (22 papers) and Genomic variations and chromosomal abnormalities (17 papers). Takeshi Mizuguchi collaborates with scholars based in Japan, United States and Malaysia. Takeshi Mizuguchi's co-authors include Naomichi Matsumoto, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Shiv I. S. Grewal, Mitsuhiro Kato, Akira Nishimura, Kazuhiro Ogata, Satomi Mitsuhashi and Hitoshi Osaka and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Takeshi Mizuguchi

119 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takeshi Mizuguchi Japan 28 1.6k 1.2k 381 274 266 126 2.7k
Andreas Tzschach Germany 30 2.1k 1.3× 1.8k 1.6× 238 0.6× 206 0.8× 266 1.0× 104 3.3k
Diana Baralle United Kingdom 24 1.8k 1.1× 761 0.7× 142 0.4× 97 0.4× 426 1.6× 84 2.7k
Keiko Shimojima Japan 25 1.0k 0.6× 1.2k 1.0× 190 0.5× 130 0.5× 190 0.7× 125 1.9k
Francisco Martı́nez Spain 24 1.1k 0.6× 837 0.7× 301 0.8× 121 0.4× 130 0.5× 118 1.8k
Victoria Mok Siu Canada 25 1.3k 0.8× 868 0.7× 150 0.4× 152 0.6× 149 0.6× 73 1.9k
Roderick T. Bronson United States 7 1.6k 1.0× 815 0.7× 218 0.6× 41 0.1× 237 0.9× 7 3.0k
Līvija Medne United States 25 1.1k 0.7× 928 0.8× 145 0.4× 141 0.5× 130 0.5× 53 1.8k
Alfredo Brusco Italy 32 2.2k 1.3× 799 0.7× 859 2.3× 53 0.2× 188 0.7× 141 3.3k
Pascale Saugier-Véber France 28 1.1k 0.7× 672 0.6× 437 1.1× 39 0.1× 156 0.6× 82 2.3k
X. Shawn Liu United States 24 2.3k 1.4× 631 0.5× 146 0.4× 115 0.4× 434 1.6× 41 3.1k

Countries citing papers authored by Takeshi Mizuguchi

Since Specialization
Citations

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

Fields of papers citing papers by Takeshi Mizuguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takeshi Mizuguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Takeshi Mizuguchi. A scholar is included among the top collaborators of Takeshi Mizuguchi 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 Takeshi Mizuguchi. Takeshi Mizuguchi 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.
Mizuguchi, Takeshi, Keisuke Hamada, Kotaro Yuge, et al.. (2025). Hemizygous SMARCA1 variants cause X-linked intellectual disability. Journal of Human Genetics. 70(7). 359–363.
2.
Koshimizu, Eriko, Mitsuhiro Kato, Kazuharu Misawa, et al.. (2024). Detection of hidden intronic DDC variant in aromatic L-amino acid decarboxylase deficiency by adaptive sampling. Journal of Human Genetics. 69(3-4). 153–157. 1 indexed citations
3.
Fu, Lina, Yuka Yamamoto, Takashi Yao, et al.. (2024). Biallelic missense CEP55 variants cause prenatal MARCH syndrome. Journal of Human Genetics. 70(1). 63–66.
4.
Tsuchida, Naomi, Chong Ae Kim, Rachel Sayuri Honjo, et al.. (2024). Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. Journal of Human Genetics. 69(3-4). 163–167. 2 indexed citations
5.
Kurosawa, Kenji, Kazuhiro Iwama, Nobuhiko Okamoto, et al.. (2023). A heterozygous germline deletion within USP8 causes severe neurodevelopmental delay with multiorgan abnormalities. Journal of Human Genetics. 69(2). 85–90. 1 indexed citations
6.
Fukuda, Hiromi, Takeshi Mizuguchi, Hiroshi Doi, et al.. (2023). Long-read sequencing revealing intragenic deletions in exome-negative spastic paraplegias. Journal of Human Genetics. 68(10). 689–697. 3 indexed citations
7.
Uchiyama, Yuri, Kohei Hamanaka, Atsushi Fujita, et al.. (2023). Distal arthrogryposis in a girl arising from a novel TNNI2 variant inherited from paternal somatic mosaicism. Journal of Human Genetics. 68(5). 363–367. 3 indexed citations
8.
Kuki, Ichiro, Takeshi Inoue, Nobuhiko Okamoto, et al.. (2023). Abnormal axonal development and severe epileptic phenotype in Dynamin‐1 (DNM1) encephalopathy. Epileptic Disorders. 26(1). 139–143. 1 indexed citations
9.
Mizuguchi, Takeshi, Hiroshi Doi, Shigeru Koyano, et al.. (2022). Patients with biallelic GGC repeat expansions in NOTCH2NLC exhibiting a typical neuronal intranuclear inclusion disease phenotype. Genomics. 114(5). 110469–110469. 4 indexed citations
10.
Okamoto, Nobuhiko, Eriko Koshimizu, Naomi Tsuchida, et al.. (2022). A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8. Journal of Human Genetics. 68(4). 247–253. 2 indexed citations
11.
Saida, Ken, Masayuki Sasaki, Eriko Koshimizu, et al.. (2021). Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clinical Genetics. 100(6). 722–730. 18 indexed citations
12.
Itai, Toshiyuki, Satoko Miyatake, Naomi Tsuchida, et al.. (2021). Novel CLTC variants cause new brain and kidney phenotypes. Journal of Human Genetics. 67(1). 1–7. 6 indexed citations
13.
Troncoso, M., Nobuhiko Okamoto, Kohei Hamanaka, et al.. (2020). A novel ITPA variant causes epileptic encephalopathy with multiple-organ dysfunction. Journal of Human Genetics. 65(9). 751–757. 11 indexed citations
14.
Iwama, Kazuhiro, Futoshi Sekiguchi, Satoko Kumada, et al.. (2020). Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. Journal of Human Genetics. 66(4). 401–407. 13 indexed citations
15.
Tsuchida, Naomi, Yohei Kirino, Masafumi Onodera, et al.. (2019). Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease. Arthritis Research & Therapy. 21(1). 137–137. 43 indexed citations
16.
Saida, Ken, Atsushi Fujita, Kohei Hamanaka, et al.. (2018). SOFT syndrome in a patient from Chile. American Journal of Medical Genetics Part A. 179(3). 338–340. 10 indexed citations
17.
Imagawa, Eri, Yutaka Yamamoto, Satomi Mitsuhashi, et al.. (2018). PRUNE1‐related disorder: Expanding the clinical spectrum. Clinical Genetics. 94(3-4). 362–367. 8 indexed citations
18.
Uchiyama, Yuri, Shinji Kunishima, Masaaki Shiina, et al.. (2018). A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia. Clinical Genetics. 94(6). 548–553. 20 indexed citations
19.
Sekiguchi, Futoshi, Maryam Sedghi, Mansoor Salehi, et al.. (2018). A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features. Journal of Human Genetics. 63(4). 487–491. 10 indexed citations
20.
Saitsu, Hirotomo, Kenji Kurosawa, Takeshi Mizuguchi, et al.. (2009). Characterization of the complex 7q21.3 rearrangement in a patient with bilateral split‐foot malformation and hearing loss. American Journal of Medical Genetics Part A. 149A(6). 1224–1230. 14 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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