Seiji Mizuno

5.9k total citations
132 papers, 2.4k citations indexed

About

Seiji Mizuno is a scholar working on Genetics, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Seiji Mizuno has authored 132 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 39 papers in Molecular Biology and 27 papers in Materials Chemistry. Recurrent topics in Seiji Mizuno's work include Genomic variations and chromosomal abnormalities (30 papers), Acoustic Wave Resonator Technologies (16 papers) and Genetic Syndromes and Imprinting (15 papers). Seiji Mizuno is often cited by papers focused on Genomic variations and chromosomal abnormalities (30 papers), Acoustic Wave Resonator Technologies (16 papers) and Genetic Syndromes and Imprinting (15 papers). Seiji Mizuno collaborates with scholars based in Japan, United States and United Kingdom. Seiji Mizuno's co-authors include Shin-ichiro Tamura, Yuji Ishikawa, Nobuhiko Okamoto, Hirofumi Ohashi, Tsutomu Ogata, Kenjiro Kosaki, Kenji Nakao, Naomichi Matsumoto, Kenji Kurosawa and Masayo Kagami and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Physical review. B, Condensed matter.

In The Last Decade

Seiji Mizuno

127 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seiji Mizuno Japan 28 947 918 360 317 314 132 2.4k
Patrizia De Marco Italy 32 1.2k 1.2× 566 0.6× 378 1.1× 470 1.5× 320 1.0× 101 2.7k
David A. Stevenson United States 30 822 0.9× 400 0.4× 443 1.2× 128 0.4× 531 1.7× 149 2.9k
Weirong Xing United States 32 1.1k 1.2× 470 0.5× 577 1.6× 55 0.2× 272 0.9× 79 2.8k
Takashi Yamashiro Japan 38 2.3k 2.4× 678 0.7× 543 1.5× 27 0.1× 392 1.2× 240 5.0k
Jingtao Li China 27 691 0.7× 457 0.5× 123 0.3× 18 0.1× 463 1.5× 154 2.5k
Virginia L. Ferguson United States 37 999 1.1× 437 0.5× 114 0.3× 155 0.5× 205 0.7× 152 4.1k
Yi Qi United States 32 663 0.7× 133 0.1× 351 1.0× 163 0.5× 591 1.9× 117 4.0k
Yasuhiro Ono Japan 34 880 0.9× 241 0.3× 273 0.8× 29 0.1× 1.1k 3.5× 171 3.8k
Christopher P. Smith United States 36 404 0.4× 116 0.1× 405 1.1× 42 0.1× 117 0.4× 160 4.3k
David Barba Canada 26 404 0.4× 191 0.2× 602 1.7× 23 0.1× 671 2.1× 95 2.3k

Countries citing papers authored by Seiji Mizuno

Since Specialization
Citations

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

Fields of papers citing papers by Seiji Mizuno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seiji Mizuno

This figure shows the co-authorship network connecting the top 25 collaborators of Seiji Mizuno. A scholar is included among the top collaborators of Seiji Mizuno 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 Seiji Mizuno. Seiji Mizuno 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.
Nishikawa, Masashi, Shin Hayashi, Hidenori Ito, et al.. (2024). Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephaly. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(1). 167520–167520. 1 indexed citations
2.
Suzuki, Y., Noriko Nomura, Kenichiro Yamada, et al.. (2023). Pathogenicity evaluation of variants of uncertain significance at exon-intron junction by splicing assay in patients with Mowat–Wilson syndrome. European Journal of Medical Genetics. 66(12). 104882–104882.
3.
Tsujita, Maki, Marlène Rio, Céline Huber, et al.. (2022). Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome. Journal of Medical Genetics. 60(4). 359–367. 9 indexed citations
4.
Mariya, Tasuku, Takema Kato, Hidehito Inagaki, et al.. (2022). Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes. Journal of Human Genetics. 67(6). 363–368. 9 indexed citations
5.
Fujimoto, Masanori, Y. Nakamura, Daisuke Ieda, et al.. (2022). Angelman syndrome with mosaic paternal uniparental disomy suggestive of mitotic nondisjunction. Journal of Human Genetics. 68(2). 87–90. 1 indexed citations
6.
Mizuno, Seiji. (2021). Analytical expressions for real and complex Fano parameters in a simple classical harmonic oscillator system. Japanese Journal of Applied Physics. 61(SG). SG1010–SG1010. 3 indexed citations
7.
Kato, Takema, et al.. (2020). Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases. Cytogenetic and Genome Research. 160(3). 118–123. 2 indexed citations
8.
Mishima, Kenichi, Atsushi Fujita, Seiji Mizuno, et al.. (2020). Legg‐Calvé‐Perthes disease in a patient with Bardet‐Biedl syndrome: A case report of a novel MKKS/BBS6 mutation. SHILAP Revista de lepidopterología. 8(12). 3109–3114. 2 indexed citations
9.
Shimbo, Hiroko, Noriko Aida, Seiji Mizuno, et al.. (2017). Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome. Molecular Genetics & Genomic Medicine. 5(4). 429–437. 20 indexed citations
10.
Takenouchi, Toshiki, Kiyokuni Miura, Tomoko Uehara, Seiji Mizuno, & Kenjiro Kosaki. (2016). Establishing SON in 21q22.11 as a cause a new syndromic form of intellectual disability: Possible contribution to Braddock–Carey syndrome phenotype. American Journal of Medical Genetics Part A. 170(10). 2587–2590. 36 indexed citations
11.
Shimojima, Keiko, Yumiko Ondo, Eriko Nishi, et al.. (2016). Loss-of-function mutations and global rearrangements in GPC3 in patients with Simpson–Golabi–Behmel syndrome. Human Genome Variation. 3(1). 16033–16033. 10 indexed citations
12.
Nishi, Eriko, Satoshi Takamizawa, Yasumasa Yamada, et al.. (2013). Surgical intervention for esophageal atresia in patients with trisomy 18. American Journal of Medical Genetics Part A. 164(2). 324–330. 36 indexed citations
13.
Tsurusaki, Yoshinori, Nobuhiko Okamoto, Hirofumi Ohashi, et al.. (2013). Coffin–Siris syndrome is a SWI/SNF complex disorder. Clinical Genetics. 85(6). 548–554. 103 indexed citations
14.
Miyajima, Yuji, et al.. (2011). [Acute lymphoblastic leukemia in a pediatric patient with Marfan's syndrome].. PubMed. 52(1). 28–31. 1 indexed citations
15.
Komatsuzaki, Shoko, Yoko Aoki, Tetsuya Niihori, et al.. (2010). Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies. Journal of Human Genetics. 55(12). 801–809. 35 indexed citations
16.
Mizuno, Seiji & Norihiko Nishiguchi. (2009). Acoustic phonon modes and dispersion relations of nanowire superlattices. Journal of Physics Condensed Matter. 21(19). 195303–195303. 16 indexed citations
17.
Hayashi, Shin, Seiji Mizuno, Ohsuke Migita, et al.. (2008). The CASK gene harbored in a deletion detected by array‐CGH as a potential candidate for a gene causative of X‐linked dominant mental retardation. American Journal of Medical Genetics Part A. 146A(16). 2145–2151. 34 indexed citations
18.
Mizuno, Seiji, Kenjiro Kosaki, Junichiro Machida, et al.. (2006). Monopolar preparation of human lymphocytes for evaluation of the metaphase chromosome alignment. Chromosome science. 9(3). 75–83. 1 indexed citations
19.
Suzuki, Yoshiko, Toshiyuki Kumagai, Chiemi Hayakawa, et al.. (2005). [Tracheostomy for home-care patients with severe motor and intellectual disabilities].. PubMed. 37(4). 293–8. 2 indexed citations
20.
Mizuno, Seiji & Shin-ichiro Tamura. (2002). Anomalous delay of phonons reflected from the surface of a superlattice. Applied Surface Science. 190(1-4). 200–204. 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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