Eri Imagawa

1.3k citations

30 papers · 442 · h-index 14

Impact in

Genetics
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Clinical Biochemistry
- Metabolism and Genetic Disorders

Papers in

Molecular Biology 20
- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 4
- RNA Research and Splicing 3
- Mitochondrial Function and Pathology 3
Genetics 10
- Genomics and Rare Diseases 3

Co-authors: Naomichi Matsumoto (20 shared papers)Noriko Miyake (19 shared papers)Satoko Miyatake (9 shared papers)Mitsuko Nakashima (8 shared papers)Hirotomo Saitsu (7 shared papers)Takeshi Mizuguchi (7 shared papers)Yoshinori Tsurusaki (5 shared papers)Satomi Mitsuhashi (5 shared papers)
Journals: Clinical Genetics (5 papers)Brain and Development (3 papers)Human Mutation (2 papers)Clinical Transplantation (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: Japan United States Israel

In The Last Decade

Eri Imagawa

30 papers receiving 439 citations

Peers

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-authors

The 25 scholars most cited alongside Eri Imagawa, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eri Imagawa Line = papers co-authored together Eri Imagawa links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome Human Mutation ·Eri Imagawa, Ken Higashimoto, Yasunari Sakai, Chikahiko Numakura, Nobuhiko Okamoto, Satoko Matsunaga, Akihide Ryo, Yoshinori Sato, Masafumi Sanefuji, Kenji Ihara, Yui Takada, Gen Nishimura, Hirotomo Saitsu, Takeshi Mizuguchi, Satoko Miyatake, Mitsuko Nakashima, Noriko Miyake, Hidenobu Soejima, Naomichi Matsumoto	2017	75
2	Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an ‘exome-first’ approach Journal of Human Genetics ·Satoko Miyatake, Eriko Koshimizu, Atsushi Fujita, Ryoko Fukai, Eri Imagawa, Chihiro Ohba, Ichiro Kuki, Megumi Nukui, Atsushi Araki, Yoshio Makita, Tsutomu Ogata, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto	2015	41
3	Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype inTBX6Causes Congenital Scoliosis Human Mutation ·Kazuki Takeda, Ikuyo Kou, Noriaki Kawakami, Aritoshi Iida, Masahiro Nakajima, Yoji Ogura, Eri Imagawa, Noriko Miyake, Naomichi Matsumoto, Yukuto Yasuhiko, Hideki Sudo, Toshiaki Kotani, Masaya Nakamura, Morio Matsumoto, Kota Watanabe, Shiro Ikegawa	2017	32
4	Novel SUZ12 mutations in Weaver‐like syndrome Clinical Genetics ·Eri Imagawa, Edoarda Vasco de Albuquerque Albuquerque, Bertrand Isidor, Satomi Mitsuhashi, Takeshi Mizuguchi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Margaret Cristina da Silva Boguszewski, César Luiz Boguszewski, Antônio Marcondes Lerário, Mariana A. Funari, Alexander A.L. Jorge, Naomichi Matsumoto	2018	30
5	De novo autoimmune hepatitis following living‐donor liver transplantation for primary biliary cirrhosis Clinical Transplantation ·Kaname Yoshizawa, Haruaki Shirakawa, Tetsuya Ichijo, Takeji Umemura, Eiji Tanaka, Kendo Kiyosawa, Eri Imagawa, Kazuyuki Matsuda, Eiko Hidaka, Kenji Sano, Yūichi Nakazawa, Toshihiko Ikegami, Yasuhiko Hashikura, Shinichi Miyagawa, Masao Ôta, Masayuki Nakano	2008	25
6	Biotin-responsive basal ganglia disease: a case diagnosed by whole exome sequencing Journal of Human Genetics ·Kensaku Kohrogi, Eri Imagawa, Yuichiro Muto, Katsuki Hirai, Masahiro Migita, Hiroshi Mitsubuchi, Noriko Miyake, Naomichi Matsumoto, Kimitoshi Nakamura, Fumio Endo	2015	24
7	A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia Clinical Genetics ·Yuri Uchiyama, Kunio Yanagisawa, Shinji Kunishima, Masaaki Shiina, Yoshiyuki Ogawa, Mitsuko Nakashima, Junko Hirato, Eri Imagawa, Atsushi Fujita, Kohei Hamanaka, Satoko Miyatake, Satomi Mitsuhashi, Atsushi Takata, Noriko Miyake, Kazuhiro Ogata, Hiroshi Handa, Naomichi Matsumoto, Takeshi Mizuguchi	2018	21
8	A novel missense SNAP25b mutation in two affected siblings from an Israeli family showing seizures and cerebellar ataxia Journal of Human Genetics ·Hiroyuki Fukuda, Eri Imagawa, Kohei Hamanaka, Atsushi Fujita, Satomi Mitsuhashi, Satoko Miyatake, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Uri Kramer, Naomichi Matsumoto, Aviva Fattal‐Valevski	2018	18
9	A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract Journal of Human Genetics ·Mahdiyeh Behnam, Eri Imagawa, Ahmad Reza Salehi Chaleshtori, Firooze Ronasian, Mansoor Salehi, Noriko Miyake, Naomichi Matsumoto	2015	17
10	A hemizygous GYG2 mutation and Leigh syndrome: a possible link? Human Genetics ·Eri Imagawa, Hitoshi Osaka, Akio Yamashita, Masaaki Shiina, Eihiko Takahashi, Hideo Sugie, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Kazuhiro Ogata, Naomichi Matsumoto, Noriko Miyake	2013	16
11	Homozygous p.V116* mutation inC12orf65results in Leigh syndrome Journal of Neurology Neurosurgery & Psychiatry ·Eri Imagawa, Aviva Fattal‐Valevski, Ori Eyal, Satoko Miyatake, Ann Saada, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto	2015	15
12	Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic Journal of Human Genetics ·Kohei Hamanaka, Satoko Miyatake, Ayelet Zerem, Dorit Lev, Luba Blumkin, Kenji Yokochi, Atsushi Fujita, Eri Imagawa, Kazuhiro Iwama, Mitsuko Nakashima, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Hirotomo Saitsu, Marjo S. van der Knaap, Tally Lerman‐Sagie, Naomichi Matsumoto	2018	14
13	Imagawa–Matsumoto syndrome: SUZ12 ‐related overgrowth disorder Clinical Genetics ·Eri Imagawa, Rie Seyama, Hiromi Aoi, Yuri Uchiyama, Bruno Guimaraes Marcarini, Isabel Furquim, Rachel Sayuri Honjo, Débora Romeo Bertola, Chong Ae Kim, Naomichi Matsumoto	2023	13
14	Severe manifestations of hand‐foot‐genital syndrome associated with a novel HOXA13 mutation American Journal of Medical Genetics Part A ·Eri Imagawa, Hülya Kayserili, Gen Nishimura, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Shiro Ikegawa, Naomichi Matsumoto, Noriko Miyake	2014	13
15	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 ·Kazuyuki Matsuda, Eiko Hidaka, Fumihiro Ishida, Kazuyoshi Yamauchi, Hideki Makishima, Toshiro Ito, Takefumi Suzuki, Eri Imagawa, Kenji Sano, Tsutomu Katsuyama, Hiroyoshi Ota	2006	11
16	Novel missense variants in PCK1 gene cause cytosolic PEPCK deficiency with growth failure from inadequate caloric intake Journal of Human Genetics ·Kimihiko Oishi, Casey M Siegel, Emalyn Cork, Hongjie Chen, Eri Imagawa	2020	10
17	The presence of diminished white matter and corpus callosal thinning in a case with a SOX9 mutation Brain and Development ·Ayumi Matsumoto, Eri Imagawa, Noriko Miyake, Takahiro Ikeda, Mizuki Kobayashi, Masahide Goto, Naomichi Matsumoto, Takanori Yamagata, Hitoshi Osaka	2017	10
18	PRUNE1‐related disorder: Expanding the clinical spectrum Clinical Genetics ·Eri Imagawa, Yutaka Yamamoto, Satomi Mitsuhashi, Bertrand Isidor, Tetsuhiro Fukuyama, Mitsuhiro Kato, Masayuki Sasaki, Saori Tanabe, Satoko Miyatake, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	2018	9
19	Polymicrogyria in a child with KCNMA1-related channelopathy Brain and Development ·Denis Graber, Eri Imagawa, Noriko Miyake, Naomichi Matsumoto, Satoko Miyatake, Marianne Graber, Bertrand Isidor	2021	9
20	A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features Clinical Genetics ·Eri Imagawa, Tsuyoshi Konuma, Emalyn Cork, George A. Diaz, Kimihiko Oishi	2020	8

About Eri Imagawa

Eri Imagawa is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Hematology and Physiology, having authored 30 papers that have together received 442 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Metabolism and Genetic Disorders (4 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (3 papers), Genomics and Rare Diseases (3 papers), Mitochondrial Function and Pathology (3 papers), Cellular transport and secretion (2 papers) and Erythrocyte Function and Pathophysiology (2 papers). The work is most often cited by research in Genetics (165 citations), Clinical Biochemistry (27 citations), Molecular Biology (247 citations), Hepatology (24 citations) and Developmental Biology (7 citations). Eri Imagawa has collaborated with scholars based in Japan, United States and Israel. Frequent co-authors include Naomichi Matsumoto, Noriko Miyake, Satoko Miyatake, Mitsuko Nakashima, Hirotomo Saitsu, Takeshi Mizuguchi, Yoshinori Tsurusaki, Satomi Mitsuhashi, Atsushi Fujita and Atsushi Takata. Their work appears in journals such as Clinical Genetics, Brain and Development, Human Mutation, Clinical Transplantation and Journal of Medical Genetics.

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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Eri Imagawa

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Eri Imagawa

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About Eri Imagawa

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