Saeko Ishida

1.2k total citations
20 papers, 719 citations indexed

About

Saeko Ishida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Saeko Ishida has authored 20 papers receiving a total of 719 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 7 papers in Cell Biology. Recurrent topics in Saeko Ishida's work include Neuroscience and Neuropharmacology Research (6 papers), CRISPR and Genetic Engineering (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Saeko Ishida is often cited by papers focused on Neuroscience and Neuropharmacology Research (6 papers), CRISPR and Genetic Engineering (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Saeko Ishida collaborates with scholars based in Japan, France and United States. Saeko Ishida's co-authors include Stéphanie Baulac, Éric Leguern, Fabienne Picard, Elise Marsan, Tomoji Mashimo, Richard Miles, Michel Baulac, Virginie Lambrecq, Maïlys Daniau and Eric Noé and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Saeko Ishida

19 papers receiving 713 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saeko Ishida Japan 12 402 337 195 191 101 20 719
Alexandra Afenjar France 16 521 1.3× 621 1.8× 127 0.7× 106 0.6× 96 1.0× 42 1.0k
Pierre Cacciagli France 15 410 1.0× 391 1.2× 104 0.5× 100 0.5× 120 1.2× 25 739
Christopher M. LaCoursiere United States 6 315 0.8× 324 1.0× 142 0.7× 93 0.5× 61 0.6× 7 584
Marta A. Bayly Australia 9 181 0.5× 399 1.2× 140 0.7× 74 0.4× 52 0.5× 11 588
Shunling Guo United States 6 199 0.5× 188 0.6× 176 0.9× 176 0.9× 44 0.4× 6 533
Delphine Héron France 11 201 0.5× 157 0.5× 60 0.3× 138 0.7× 40 0.4× 27 421
Marcello Scala Italy 15 207 0.5× 178 0.5× 91 0.5× 53 0.3× 35 0.3× 61 513
A.-E. Lehesjoki Finland 12 241 0.6× 310 0.9× 133 0.7× 128 0.7× 37 0.4× 16 610
Ana María Cobo Spain 14 703 1.7× 252 0.7× 93 0.5× 393 2.1× 80 0.8× 28 979
Markus Zweier Switzerland 12 582 1.4× 547 1.6× 46 0.2× 80 0.4× 50 0.5× 23 937

Countries citing papers authored by Saeko Ishida

Since Specialization
Citations

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

Fields of papers citing papers by Saeko Ishida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saeko Ishida

This figure shows the co-authorship network connecting the top 25 collaborators of Saeko Ishida. A scholar is included among the top collaborators of Saeko Ishida 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 Saeko Ishida. Saeko Ishida 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.
Ishida, Saeko, et al.. (2025). Diverse Cre recombinase expression pattern in Albumin-Cre driver rats. EXPERIMENTAL ANIMALS. 74(3). 328–334.
2.
Yoshimi, Kazuto, Akihiro Kuno, Yuko Yamauchi, et al.. (2024). Genome editing using type I-E CRISPR-Cas3 in mice and rat zygotes. Cell Reports Methods. 4(8). 100833–100833. 1 indexed citations
3.
Asano, Kana, Kazuto Yoshimi, Kohei Takeshita, et al.. (2024). CRISPR Diagnostics for Quantification and Rapid Diagnosis of Myotonic Dystrophy Type 1 Repeat Expansion Disorders. ACS Synthetic Biology. 13(12). 3926–3935. 2 indexed citations
4.
Ishida, Saeko, et al.. (2024). A novel Kit mutant rat enables hematopoietic stem cell engraftment without irradiation. Experimental Hematology. 132. 104174–104174. 1 indexed citations
5.
Ohmori, Iori, Mamoru Ouchida, Hirohiko Imai, et al.. (2022). Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain. Neurobiology of Disease. 175. 105921–105921. 6 indexed citations
6.
Miyasaka, Yoshiki, Jinxi Wang, Yuko Yamauchi, et al.. (2022). A high-quality severe combined immunodeficiency (SCID) rat bioresource. PLoS ONE. 17(8). e0272950–e0272950. 12 indexed citations
7.
Ohmori, Iori, et al.. (2022). Novel animal model of combined generalized and focal epilepsy. Epilepsia. 63(7). e80–e85. 4 indexed citations
8.
Ishida, Saeko, et al.. (2021). Dorsal telencephalon-specific Nprl2- and Nprl3-knockout mice: novel mouse models for GATORopathy. Human Molecular Genetics. 31(9). 1519–1530. 14 indexed citations
9.
Calbiac, Hortense de, Elise Marsan, Hervé Tostivint, et al.. (2018). Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish. Annals of Clinical and Translational Neurology. 5(5). 510–523. 38 indexed citations
10.
Ishida, Saeko. (2018). DEPDC5, a new key to understand various epilepsies. Folia Pharmacologica Japonica. 152(6). 281–285. 1 indexed citations
11.
Marsan, Elise, Saeko Ishida, Adrien E. Schramm, et al.. (2016). Depdc5 knockout rat: A novel model of mTORopathy. Neurobiology of Disease. 89. 180–189. 73 indexed citations
12.
Morin‐Brureau, Mélanie, Fabienne Picard, Sarah Weckhuysen, et al.. (2015). Novel GABRG2 mutations cause familial febrile seizures. Neurology Genetics. 1(4). e35–e35. 25 indexed citations
13.
Baulac, Stéphanie, Saeko Ishida, Elise Marsan, et al.. (2015). Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations. Annals of Neurology. 77(4). 675–683. 195 indexed citations
14.
Huneau, Clément, Elise Marsan, Katia Lehongre, et al.. (2014). Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures. Brain. 137(11). 2984–2996. 40 indexed citations
15.
Mashimo, Tomoji, Saeko Ishida, Akio Ikeda, et al.. (2014). Evaluation of seizure foci and genes in the Lgi1 mutant rat. Neuroscience Research. 80. 69–75. 10 indexed citations
16.
Ishida, Saeko, Fabienne Picard, Gabrielle Rudolf, et al.. (2013). Mutations of DEPDC5 cause autosomal dominant focal epilepsies. Nature Genetics. 45(5). 552–555. 167 indexed citations
17.
Baulac, Stéphanie, Saeko Ishida, Tomoji Mashimo, et al.. (2012). A rat model for LGI1-related epilepsies. Human Molecular Genetics. 21(16). 3546–3557. 31 indexed citations
18.
Mashimo, Tomoji, Akiko Takizawa, Junya Kobayashi, et al.. (2012). Generation and Characterization of Severe Combined Immunodeficiency Rats. Cell Reports. 2(3). 685–694. 58 indexed citations
19.
Ishida, Saeko, Takeshi Nishio, Stéphanie Baulac, et al.. (2011). Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures. Brain Research. 1435. 154–166. 27 indexed citations
20.
Kodama, Hiroshi, et al.. (2008). Protective Effect of Humus Extract Against Trypanosoma brucei Infection in Mice. Journal of Veterinary Medical Science. 70(11). 1185–1190. 14 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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