Yo Okizuka

489 total citations
18 papers, 363 citations indexed

About

Yo Okizuka is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Epidemiology. According to data from OpenAlex, Yo Okizuka has authored 18 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Epidemiology. Recurrent topics in Yo Okizuka's work include Muscle Physiology and Disorders (9 papers), RNA Research and Splicing (8 papers) and RNA regulation and disease (4 papers). Yo Okizuka is often cited by papers focused on Muscle Physiology and Disorders (9 papers), RNA Research and Splicing (8 papers) and RNA regulation and disease (4 papers). Yo Okizuka collaborates with scholars based in Japan. Yo Okizuka's co-authors include Masafumi Matsuo, Yasuhiro Takeshima, Mariko Yagi, Hiroyuki Awano, Zhujun Zhang, Yumiko Yamauchi, Hisahide Nishio, Atsushi Nishiyama, Masayuki Yagi and Kayoko Saiki and has published in prestigious journals such as Scientific Reports, Gene and Nutrients.

In The Last Decade

Yo Okizuka

17 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yo Okizuka Japan 10 307 75 69 66 37 18 363
Sara Scapolan Italy 10 271 0.9× 34 0.5× 57 0.8× 49 0.7× 43 1.2× 11 348
C R Müller Germany 12 262 0.9× 55 0.7× 44 0.6× 70 1.1× 44 1.2× 17 387
Royston Ong Australia 6 229 0.7× 103 1.4× 127 1.8× 82 1.2× 55 1.5× 10 330
Tianyou Yuan China 9 243 0.8× 8 0.1× 55 0.8× 41 0.6× 26 0.7× 14 350
Emanuela Abiusi Italy 7 214 0.7× 61 0.8× 254 3.7× 35 0.5× 23 0.6× 8 376
Irene Colombo Italy 7 155 0.5× 53 0.7× 63 0.9× 14 0.2× 30 0.8× 14 198
Mohammad Yahya Vahidi Mehrjardi Iran 13 184 0.6× 16 0.2× 14 0.2× 68 1.0× 15 0.4× 38 323
R. Mercelis Belgium 11 252 0.8× 14 0.2× 26 0.4× 16 0.2× 54 1.5× 15 301
Julia Morere France 6 253 0.8× 62 0.8× 42 0.6× 38 0.6× 24 0.6× 6 327

Countries citing papers authored by Yo Okizuka

Since Specialization
Citations

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

Fields of papers citing papers by Yo Okizuka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yo Okizuka

This figure shows the co-authorship network connecting the top 25 collaborators of Yo Okizuka. A scholar is included among the top collaborators of Yo Okizuka 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 Yo Okizuka. Yo Okizuka is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
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Lee, Tomoko, Yasuhiro Takeshima, Yo Okizuka, et al.. (2012). A Japanese child with geleophysic dysplasia caused by a novel mutation of FBN1. Gene. 512(2). 456–459. 14 indexed citations
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Nakagawa, Taku, Yo Okizuka, Yuichi Takami, et al.. (2012). Treatment of preterm infants with West syndrome: Differences due to etiology. Pediatrics International. 54(6). 892–898. 2 indexed citations
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Takeshima, Yasuhiro, Mariko Yagi, Yo Okizuka, et al.. (2010). Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center. Journal of Human Genetics. 55(6). 379–388. 188 indexed citations
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Okizuka, Yo, Yasuhiro Takeshima, Kyoko Itoh, et al.. (2010). Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD. BMC Medical Genetics. 11(1). 49–49. 10 indexed citations
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Awano, Hiroyuki, Rusdy Ghazali Malueka, Mariko Yagi, et al.. (2010). Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA. Journal of Human Genetics. 55(12). 785–790. 14 indexed citations
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Yagi, Mariko, Tsutomu Nakamura, Yo Okizuka, et al.. (2010). Effect of CPS14217C>A genotype on valproic‐acid‐induced hyperammonemia. Pediatrics International. 52(5). 744–748. 24 indexed citations
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Takeshima, Yasuhiro, Masahiro Enomoto, Yo Okizuka, et al.. (2010). Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity.. PubMed. 16. 2590–7. 5 indexed citations
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Okizuka, Yo, Yasuhiro Takeshima, Hiroyuki Awano, et al.. (2009). Small Mutations Detected by Multiplex Ligation-Dependent Probe Amplification of the Dystrophin Gene. Genetic Testing and Molecular Biomarkers. 13(3). 427–431. 16 indexed citations
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Zhang, Zhujun, Mariko Yagi, Yo Okizuka, et al.. (2009). Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene. Journal of Human Genetics. 54(8). 466–473. 5 indexed citations
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Nishiyama, Atsushi, Mariko Yagi, Hiroyuki Awano, et al.. (2009). Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations. Pediatrics International. 51(6). 775–779. 12 indexed citations
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Zhang, Zhujun, Yasuhiro Takeshima, Hiroyuki Awano, et al.. (2007). Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy. Journal of Human Genetics. 53(3). 215–219. 12 indexed citations
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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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