Mariko Yagi

1.9k total citations
66 papers, 1.5k citations indexed

About

Mariko Yagi is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Mariko Yagi has authored 66 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 10 papers in Physiology and 9 papers in Genetics. Recurrent topics in Mariko Yagi's work include Muscle Physiology and Disorders (38 papers), RNA Research and Splicing (26 papers) and RNA Interference and Gene Delivery (9 papers). Mariko Yagi is often cited by papers focused on Muscle Physiology and Disorders (38 papers), RNA Research and Splicing (26 papers) and RNA Interference and Gene Delivery (9 papers). Mariko Yagi collaborates with scholars based in Japan, United States and Vietnam. Mariko Yagi's co-authors include Masafumi Matsuo, Yasuhiro Takeshima, Hiroyuki Awano, Hiroko Wada, Zhujun Zhang, Yo Okizuka, Atsushi Nishiyama, Yumiko Yamauchi, Tomoko Lee and Hisahide Nishio and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Mariko Yagi

64 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mariko Yagi Japan 21 1.1k 226 225 190 127 66 1.5k
Hiroyuki Awano Japan 21 1.2k 1.0× 191 0.8× 306 1.4× 320 1.7× 54 0.4× 125 1.5k
Hui Xiong China 17 652 0.6× 97 0.4× 123 0.5× 239 1.3× 57 0.4× 116 1.0k
Rosário Santos Portugal 19 491 0.4× 224 1.0× 87 0.4× 115 0.6× 153 1.2× 79 821
Pilar Camaño Spain 11 1.1k 0.9× 119 0.5× 254 1.1× 227 1.2× 34 0.3× 22 1.3k
Denise Cassandrini Italy 23 735 0.7× 176 0.8× 169 0.8× 132 0.7× 57 0.4× 62 1.3k
Reeval Segel Israel 18 649 0.6× 249 1.1× 34 0.2× 102 0.5× 211 1.7× 40 1.1k
Anthony Donsante United States 17 744 0.7× 468 2.1× 59 0.3× 80 0.4× 36 0.3× 27 1.3k
Barbara Illi Italy 23 1.2k 1.1× 150 0.7× 82 0.4× 100 0.5× 43 0.3× 42 1.6k
W.B. Bowler United Kingdom 16 442 0.4× 82 0.4× 92 0.4× 81 0.4× 50 0.4× 24 1.1k
Ivo Kremensky Bulgaria 18 753 0.7× 295 1.3× 45 0.2× 118 0.6× 84 0.7× 75 1.4k

Countries citing papers authored by Mariko Yagi

Since Specialization
Citations

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

Fields of papers citing papers by Mariko Yagi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariko Yagi

This figure shows the co-authorship network connecting the top 25 collaborators of Mariko Yagi. A scholar is included among the top collaborators of Mariko Yagi 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 Mariko Yagi. Mariko Yagi 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.
Yagi, Mariko, Masahiro Miyake, Yuki Mori, et al.. (2022). Natural Course of Pachychoroid Pigment Epitheliopathy. SHILAP Revista de lepidopterología. 2(4). 100201–100201. 16 indexed citations
2.
Miyazaki, Teruo, Hironori Nagasaka, Haruki Komatsu, et al.. (2018). Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period. JIMD Reports. 43. 53–61. 9 indexed citations
3.
Nagasaka, Hironori, Haruki Komatsu, Ayano Inui, et al.. (2016). Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment. Molecular Genetics and Metabolism. 120(3). 207–212. 14 indexed citations
4.
Hayashi, Shin, Mariko Yagi, Ichijiro Morisaki, & Johji Inazawa. (2015). Identical deletion at 14q13.3 including PAX9 and NKX2-1 in siblings from mosaicism of unaffected parent. Journal of Human Genetics. 60(4). 203–206. 10 indexed citations
5.
Fujioka, Kazumichi, Akio Shibata, Tomoyuki Yokota, et al.. (2014). Association of a vascular endothelial growth factor polymorphism with the development of bronchopulmonary dysplasia in Japanese premature newborns. Scientific Reports. 4(1). 4459–4459. 22 indexed citations
6.
Lee, Tomoko, Mariko Yagi, Tsubasa Koda, et al.. (2014). Standard values for the urine HVA/VMA ratio in neonates as a screen for Menkes disease. Brain and Development. 37(1). 114–119. 14 indexed citations
7.
Takeshima, Yasuhiro, Mariko Yagi, & Masafumi Matsuo. (2012). Optimizing RNA/ENA Chimeric Antisense Oligonucleotides Using In Vitro Splicing. Methods in molecular biology. 867. 131–141. 6 indexed citations
8.
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
9.
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
10.
Zhang, Zhujun, Yasuaki Habara, Atsushi Nishiyama, et al.. (2007). Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exons. Journal of Human Genetics. 52(7). 607–617. 18 indexed citations
11.
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
12.
Takeshima, Yasuhiro, Mariko Yagi, Hiroko Wada, et al.. (2006). Intravenous Infusion of an Antisense Oligonucleotide Results in Exon Skipping in Muscle Dystrophin mRNA of Duchenne Muscular Dystrophy. Pediatric Research. 59(5). 690–694. 80 indexed citations
13.
Sakaeda, Toshiyuki, Noboru Okamura, Akinobu Gotoh, et al.. (2005). EGFR mRNA is Upregulated, but Somatic Mutations of the Gene are Hardly Found in Renal Cell Carcinoma in Japanese Patients. Pharmaceutical Research. 22(10). 1757–1761. 15 indexed citations
14.
Takeshima, Yasuhiro, et al.. (2005). A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro. Molecular Genetics and Metabolism. 85(3). 213–219. 53 indexed citations
15.
16.
Takeshima, Yasuhiro, et al.. (2004). C-Terminal Truncated Dystrophin Identified in Skeletal Muscle of an Asymptomatic Boy with a Novel Nonsense Mutation of the Dystrophin Gene. Pediatric Research. 56(5). 739–743. 11 indexed citations
17.
Morisawa, Takeshi, Mariko Yagi, Agus Surono, et al.. (2004). Novel double-deletion mutations of the OFD1 gene creating multiple novel transcripts. Human Genetics. 115(2). 97–103. 13 indexed citations
18.
Adachi, Kayo, Yasuhiro Takeshima, Hiroko Wada, et al.. (2003). Heterogous Dystrophin mRNA Produced by a Novel Splice Acceptor Site Mutation in Intermediate Dystrophinopathy. Pediatric Research. 53(1). 125–131. 18 indexed citations
19.
Yagi, Mariko, Yasuhiro Takeshima, Hiroko Wada, Hajime Nakamura, & Masafumi Matsuo. (2003). Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy. Human Genetics. 112(2). 164–170. 19 indexed citations
20.
Takeshima, Yasuhiro, Hiroko Wada, Mariko Yagi, et al.. (2001). Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient. Brain and Development. 23(8). 788–790. 65 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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