Emi Mazaki

2.4k total citations · 1 hit paper
21 papers, 1.7k citations indexed

About

Emi Mazaki is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Emi Mazaki has authored 21 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Psychiatry and Mental health, 13 papers in Cellular and Molecular Neuroscience and 12 papers in Molecular Biology. Recurrent topics in Emi Mazaki's work include Epilepsy research and treatment (15 papers), Neuroscience and Neuropharmacology Research (13 papers) and Ion channel regulation and function (10 papers). Emi Mazaki is often cited by papers focused on Epilepsy research and treatment (15 papers), Neuroscience and Neuropharmacology Research (13 papers) and Ion channel regulation and function (10 papers). Emi Mazaki collaborates with scholars based in Japan, United States and Australia. Emi Mazaki's co-authors include Kazuhiro Yamakawa, Ikuo Ogiwara, Shigeyoshi Itohara, Hiroyuki Miyamoto, Yuchio Yanagawa, Takao K. Hensch, Ikuyo Inoue, Nafiseh Atapour, Yushi Inoue and Tamaki Takeuchi and has published in prestigious journals such as Nature Communications, Journal of Neuroscience and Neurology.

In The Last Decade

Emi Mazaki

20 papers receiving 1.7k citations

Hit Papers

Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibit... 2007 2026 2013 2019 2007 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emi Mazaki Japan 16 968 924 838 532 274 21 1.7k
Ikuo Ogiwara Japan 21 1.2k 1.2× 1.1k 1.2× 1.0k 1.2× 608 1.1× 316 1.2× 30 2.1k
Franck Kalume United States 16 1.3k 1.3× 1.5k 1.6× 1.4k 1.7× 588 1.1× 365 1.3× 29 2.7k
Wangzhen Shen United States 26 916 0.9× 820 0.9× 467 0.6× 451 0.8× 100 0.4× 51 1.5k
Ikuyo Inoue Japan 10 576 0.6× 527 0.6× 512 0.6× 324 0.6× 128 0.5× 19 1.1k
Heather A. O’Malley United States 15 888 0.9× 735 0.8× 427 0.5× 236 0.4× 65 0.2× 18 1.3k
Jack Kronengold United States 17 1.2k 1.2× 430 0.5× 259 0.3× 625 1.2× 246 0.9× 17 1.6k
Edward Glasscock United States 18 628 0.6× 542 0.6× 395 0.5× 130 0.2× 155 0.6× 38 1.1k
Paolo Scalmani Italy 15 510 0.5× 511 0.6× 353 0.4× 200 0.4× 211 0.8× 24 897
Tara Klassen Canada 15 589 0.6× 449 0.5× 303 0.4× 159 0.3× 107 0.4× 22 1.0k
Nanda A. Singh United States 11 1.8k 1.8× 1.4k 1.5× 747 0.9× 553 1.0× 52 0.2× 12 2.4k

Countries citing papers authored by Emi Mazaki

Since Specialization
Citations

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

Fields of papers citing papers by Emi Mazaki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emi Mazaki

This figure shows the co-authorship network connecting the top 25 collaborators of Emi Mazaki. A scholar is included among the top collaborators of Emi Mazaki 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 Emi Mazaki. Emi Mazaki 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.
Miyamoto, Hiroyuki, et al.. (2025). Rapid and cumulative adult plasticity in the mouse visual cortex. Frontiers in Neural Circuits. 19. 1537305–1537305.
2.
Yamagata, Tetsushi, Ikuo Ogiwara, Tetsuya Tatsukawa, et al.. (2023). Scn1a-GFP transgenic mouse revealed Nav1.1 expression in neocortical pyramidal tract projection neurons. eLife. 12. 5 indexed citations
3.
Tatsukawa, Tetsuya, Matthieu Raveau, Ikuo Ogiwara, et al.. (2019). Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity. Molecular Autism. 10(1). 15–15. 58 indexed citations
4.
Miyamoto, Hiroyuki, Tetsuya Tatsukawa, Atsushi Shimohata, et al.. (2019). Impaired cortico-striatal excitatory transmission triggers epilepsy. Nature Communications. 10(1). 1917–1917. 75 indexed citations
5.
Ogiwara, Ikuo, Hiroyuki Miyamoto, Tetsuya Tatsukawa, et al.. (2018). Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice. Communications Biology. 1(1). 96–96. 65 indexed citations
6.
Tatsukawa, Tetsuya, Ikuo Ogiwara, Emi Mazaki, Atsushi Shimohata, & Kazuhiro Yamakawa. (2018). Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells. Neurobiology of Disease. 112. 24–34. 38 indexed citations
7.
Haginoya, Kazuhiro, Noriko Togashi, Tomohiro Kaneta, et al.. (2018). [18F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome. Epilepsy Research. 147. 9–14. 10 indexed citations
8.
Yamagata, Tetsushi, Ikuo Ogiwara, Emi Mazaki, Yuchio Yanagawa, & Kazuhiro Yamakawa. (2017). Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2. Biochemical and Biophysical Research Communications. 491(4). 1070–1076. 39 indexed citations
9.
Miyamoto, Hiroyuki, Atsushi Shimohata, Manabu Abe, et al.. (2017). Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency. Human Molecular Genetics. 26(24). 4961–4974. 27 indexed citations
10.
Ogiwara, Ikuo, Takuji Iwasato, Hiroyuki Miyamoto, et al.. (2013). Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome. Human Molecular Genetics. 22(23). 4784–4804. 126 indexed citations
11.
Ogiwara, Ikuo, Tojo Nakayama, Tetsushi Yamagata, et al.. (2012). A homozygous mutation of voltage‐gated sodium channel β I gene SCN1B in a patient with Dravet syndrome. Epilepsia. 53(12). e200–3. 70 indexed citations
12.
Tsuji, Megumi, Emi Mazaki, Ikuo Ogiwara, et al.. (2011). Acute Encephalopathy in a Patient with Dravet Syndrome. Neuropediatrics. 42(2). 78–81. 8 indexed citations
13.
Nakayama, Tojo, Ikuo Ogiwara, Koichi Ito, et al.. (2010). Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome. Human Mutation. 31(7). 820–829. 41 indexed citations
14.
Takayanagi, Masaru, Kazuhiro Haginoya, Taro Kitamura, et al.. (2010). Acute encephalopathy with a truncation mutation in the SCN1A gene: A case report. Epilepsia. 51(9). 1886–1888. 32 indexed citations
15.
Ogiwara, Ikuo, Hiroyuki Miyamoto, Noriyuki Morita, et al.. (2007). Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons: A Circuit Basis for Epileptic Seizures in Mice Carrying anScn1aGene Mutation. Journal of Neuroscience. 27(22). 5903–5914. 655 indexed citations breakdown →
16.
Osaka, Hitoshi, Ikuo Ogiwara, Emi Mazaki, et al.. (2007). Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation. Epilepsy Research. 75(1). 46–51. 32 indexed citations
17.
Ogiwara, Ikuo, Hiroshi Miyamoto, Nafiseh Atapour, et al.. (2007). Nav1.1 predominantly localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in Nav1.1-deficient mice. Neuroscience Research. 58. S40–S40. 1 indexed citations
18.
Singh, B. P., Ikuo Ogiwara, Makoto Kaneda, et al.. (2006). A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy. Neurobiology of Disease. 24(2). 245–253. 97 indexed citations
19.
Morimoto, Masafumi, Emi Mazaki, Akira Nishimura, et al.. (2006). SCN1AMutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy. Epilepsia. 47(10). 1732–1736. 53 indexed citations
20.
Kamiya, Kazusaku, Makoto Kaneda, Takashi Sugawara, et al.. (2004). A Nonsense Mutation of the Sodium Channel GeneSCN2Ain a Patient with Intractable Epilepsy and Mental Decline. Journal of Neuroscience. 24(11). 2690–2698. 147 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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