Eri Imagawa

1.3k total citations
30 papers, 418 citations indexed

About

Eri Imagawa is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Eri Imagawa has authored 30 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Clinical Biochemistry. Recurrent topics in Eri Imagawa's work include Metabolism and Genetic Disorders (5 papers), RNA modifications and cancer (5 papers) and Epigenetics and DNA Methylation (4 papers). Eri Imagawa is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), RNA modifications and cancer (5 papers) and Epigenetics and DNA Methylation (4 papers). Eri Imagawa collaborates with scholars based in Japan, United States and Israel. Eri Imagawa's co-authors include Naomichi Matsumoto, Noriko Miyake, Satoko Miyatake, Mitsuko Nakashima, Hirotomo Saitsu, Takeshi Mizuguchi, Yoshinori Tsurusaki, Atsushi Fujita, Atsushi Takata and Satomi Mitsuhashi and has published in prestigious journals such as Journal of Hepatology, Journal of Neurology Neurosurgery & Psychiatry and American Journal of Roentgenology.

In The Last Decade

Eri Imagawa

29 papers receiving 417 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eri Imagawa Japan 13 250 170 41 33 31 30 418
Eyby Leon United States 9 263 1.1× 104 0.6× 22 0.5× 29 0.9× 60 1.9× 29 379
Adi Mory Israel 15 245 1.0× 147 0.9× 38 0.9× 78 2.4× 33 1.1× 40 592
Marjan M. Nezarati Canada 10 232 0.9× 198 1.2× 57 1.4× 13 0.4× 15 0.5× 17 447
Angela L. Duker United States 10 284 1.1× 267 1.6× 28 0.7× 28 0.8× 13 0.4× 25 471
Thomas Cullup United Kingdom 15 434 1.7× 130 0.8× 42 1.0× 17 0.5× 27 0.9× 24 615
Martina Klempt Germany 12 235 0.9× 86 0.5× 29 0.7× 20 0.6× 13 0.4× 18 397
Chalurmpon Srichomthong Thailand 16 342 1.4× 356 2.1× 74 1.8× 49 1.5× 30 1.0× 49 676
Wee Teik Keng Malaysia 11 183 0.7× 183 1.1× 100 2.4× 15 0.5× 58 1.9× 20 420
Naoya Morisada Japan 15 367 1.5× 205 1.2× 45 1.1× 17 0.5× 10 0.3× 46 585
Suna Önengüt United States 11 396 1.6× 120 0.7× 30 0.7× 7 0.2× 29 0.9× 11 551

Countries citing papers authored by Eri Imagawa

Since Specialization
Citations

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

Fields of papers citing papers by Eri Imagawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eri Imagawa

This figure shows the co-authorship network connecting the top 25 collaborators of Eri Imagawa. A scholar is included among the top collaborators of Eri Imagawa 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 Eri Imagawa. Eri Imagawa 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.
Ow, Jin Rong, Eri Imagawa, Feng Chen, et al.. (2025). Developing splice-switching oligonucleotides for urea cycle disorder using an integrated diagnostic and therapeutic platform. Journal of Hepatology. 83(2). 411–425. 2 indexed citations
2.
Oishi, Kimihiko, et al.. (2024). Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population. Human Genome Variation. 11(1). 24–24. 1 indexed citations
3.
Imagawa, Eri, et al.. (2023). Functional insight into a neurodevelopmental disorder caused by missense variants in an RNA-binding protein, RBM10. Journal of Human Genetics. 68(9). 643–648. 1 indexed citations
4.
Imagawa, Eri, Yuri Uchiyama, Rachel Sayuri Honjo, et al.. (2023). Imagawa–Matsumoto syndrome: SUZ12 ‐related overgrowth disorder. Clinical Genetics. 103(4). 383–391. 12 indexed citations
5.
Shiohama, Tadashi, Tomohiko Ichikawa, Eri Imagawa, et al.. (2021). Remitting and exacerbating white matter lesions in leukoencephalopathy with thalamus and brainstem involvement and high lactate. Brain and Development. 43(7). 798–803.
6.
Graber, Denis, Eri Imagawa, Noriko Miyake, et al.. (2021). Polymicrogyria in a child with KCNMA1-related channelopathy. Brain and Development. 44(2). 173–177. 9 indexed citations
7.
Imagawa, Eri, et al.. (2020). A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features. Clinical Genetics. 98(6). 606–612. 8 indexed citations
8.
Oishi, Kimihiko, et al.. (2020). Novel missense variants in PCK1 gene cause cytosolic PEPCK deficiency with growth failure from inadequate caloric intake. Journal of Human Genetics. 66(3). 321–325. 10 indexed citations
9.
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
10.
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
11.
Imagawa, Eri, Bertrand Isidor, Satomi Mitsuhashi, et al.. (2018). Novel SUZ12 mutations in Weaver‐like syndrome. Clinical Genetics. 94(5). 461–466. 28 indexed citations
12.
Hamanaka, Kohei, Satoko Miyatake, Ayelet Zerem, et al.. (2018). Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic. Journal of Human Genetics. 63(12). 1223–1229. 14 indexed citations
13.
Takeda, Kazuki, Ikuyo Kou, Noriaki Kawakami, et al.. (2017). Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype inTBX6Causes Congenital Scoliosis. Human Mutation. 38(3). 317–323. 30 indexed citations
14.
Imagawa, Eri, Aviva Fattal‐Valevski, Satoko Miyatake, et al.. (2015). Homozygous p.V116* mutation inC12orf65results in Leigh syndrome. Journal of Neurology Neurosurgery & Psychiatry. 87(2). jnnp–2014. 15 indexed citations
15.
Behnam, Mahdiyeh, et al.. (2015). A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract. Journal of Human Genetics. 61(2). 177–179. 17 indexed citations
16.
Imagawa, Eri, Ryoko Fukai, Mahdiyeh Behnam, et al.. (2015). Two novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome. Human Genome Variation. 2(1). 15034–15034. 8 indexed citations
17.
Miyatake, Satoko, Eriko Koshimizu, Atsushi Fujita, et al.. (2015). Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an ‘exome-first’ approach. Journal of Human Genetics. 60(4). 175–182. 41 indexed citations
18.
Imagawa, Eri, Hitoshi Osaka, Akio Yamashita, et al.. (2013). A hemizygous GYG2 mutation and Leigh syndrome: a possible link?. Human Genetics. 133(2). 225–234. 16 indexed citations
19.
Matsuda, Kazuyuki, Eiko Hidaka, Fumihiro Ishida, et al.. (2006). A case of acute myelogenous leukemia with MLL–AF10 fusion caused by insertion of 5′ MLL into 10p12, with concurrent 3′ MLL deletion. Cancer Genetics and Cytogenetics. 171(1). 24–30. 11 indexed citations
20.
Suekane, H., Eri Imagawa, Mitsuo Iida, et al.. (1997). Duodenal obstruction due to Henoch-Schönlein purpura.. American Journal of Roentgenology. 168(4). 969–970. 7 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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