Yoichi Sekita

1.3k total citations
22 papers, 775 citations indexed

About

Yoichi Sekita is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yoichi Sekita has authored 22 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yoichi Sekita's work include Epigenetics and DNA Methylation (10 papers), Genetic Syndromes and Imprinting (5 papers) and Pluripotent Stem Cells Research (5 papers). Yoichi Sekita is often cited by papers focused on Epigenetics and DNA Methylation (10 papers), Genetic Syndromes and Imprinting (5 papers) and Pluripotent Stem Cells Research (5 papers). Yoichi Sekita collaborates with scholars based in Japan, United States and United Kingdom. Yoichi Sekita's co-authors include Tohru Kimura, Miguel Constância, Abigail L. Fowden, Fumitoshi Ishino, Atsuo Ogura, Tomoko Kaneko‐Ishino, Graham J. Burton, Owen R. Vaughan, P. M. Coan and Takashi Kohda and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Nature Immunology.

In The Last Decade

Yoichi Sekita

22 papers receiving 763 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoichi Sekita Japan 15 526 325 310 151 69 22 775
Hirosuke Shiura Japan 15 655 1.2× 394 1.2× 187 0.6× 31 0.2× 167 2.4× 22 776
Zhiyuan Chen United States 16 932 1.8× 432 1.3× 329 1.1× 29 0.2× 223 3.2× 21 1.2k
Giuliano Cottone Italy 12 194 0.4× 174 0.5× 350 1.1× 35 0.2× 146 2.1× 16 615
Bruno Passet France 14 494 0.9× 133 0.4× 77 0.2× 86 0.6× 31 0.4× 45 666
Steve Bischoff United States 11 413 0.8× 213 0.7× 108 0.3× 91 0.6× 63 0.9× 21 569
Alida C. Knegt Netherlands 14 271 0.5× 257 0.8× 232 0.7× 35 0.2× 120 1.7× 35 652
Kaiyu Kubota Japan 16 330 0.6× 184 0.6× 187 0.6× 240 1.6× 140 2.0× 35 784
Leila Christie United Kingdom 8 634 1.2× 89 0.3× 87 0.3× 58 0.4× 139 2.0× 12 714
Pratik Home United States 15 717 1.4× 68 0.2× 140 0.5× 164 1.1× 134 1.9× 21 885
Winifred Mak United States 16 1.3k 2.6× 803 2.5× 361 1.2× 118 0.8× 233 3.4× 32 1.8k

Countries citing papers authored by Yoichi Sekita

Since Specialization
Citations

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

Fields of papers citing papers by Yoichi Sekita

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoichi Sekita

This figure shows the co-authorship network connecting the top 25 collaborators of Yoichi Sekita. A scholar is included among the top collaborators of Yoichi Sekita 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 Yoichi Sekita. Yoichi Sekita 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.
Sato, Kazuki, Toshiaki Ito, Naoki Gotō, et al.. (2022). Epigenome editing reveals core DNA methylation for imprinting control in the Dlk1-Dio3 imprinted domain. Nucleic Acids Research. 50(9). 5080–5094. 17 indexed citations
2.
Ito, Toshiaki, Akira Nishiyama, Kei‐ichiro Ishiguro, et al.. (2022). Switching defective/sucrose non‐fermenting chromatin remodeling complex coordinates meiotic gene activation via promoter remodeling and Meiosin activation in female germline. Genes to Cells. 28(1). 15–28. 2 indexed citations
3.
Sekita, Yoichi, Yuki Sugiura, Yuki Kawasaki, et al.. (2021). AKT signaling is associated with epigenetic reprogramming via the upregulation of TET and its cofactor, alpha-ketoglutarate during iPSC generation. Stem Cell Research & Therapy. 12(1). 510–510. 14 indexed citations
4.
Murakami, Koichi, Haruka Sasaki, Akira Nishiyama, et al.. (2021). A RUNX–CBFβ-driven enhancer directs the Irf8 dose-dependent lineage choice between DCs and monocytes. Nature Immunology. 22(3). 301–311. 35 indexed citations
5.
Ito, Toshiaki, Akira Nishiyama, Yuichi Niikura, et al.. (2021). SWI/SNF chromatin remodeling complex is required for initiation of sex-dependent differentiation in mouse germline. Scientific Reports. 11(1). 24074–24074. 14 indexed citations
6.
Sandovici, Ionel, Gemma V. Brierley, Nicola M. Smith, et al.. (2020). Mesenchyme-derived IGF2 is a major paracrine regulator of pancreatic growth and function. PLoS Genetics. 16(10). e1009069–e1009069. 13 indexed citations
7.
Yoshimura, Yuki, et al.. (2020). Five multicopy gene family genes expressed during the maternal-to-zygotic transition are not essential for mouse development. Biochemical and Biophysical Research Communications. 534. 752–757. 3 indexed citations
8.
Itakura, Yoko, Kohei Sakai, Toshiaki Ito, et al.. (2020). Mutations of histone demethylase genes encoded by X and Y chromosomes, Kdm5c and Kdm5d, lead to noncompaction cardiomyopathy in mice. Biochemical and Biophysical Research Communications. 525(1). 100–106. 14 indexed citations
9.
Ito, Toshiaki, Koji Saito, Shigekí Kato, et al.. (2020). Involvement of Nlrp9a/b/c in mouse preimplantation development. Reproduction. 160(2). 181–191. 17 indexed citations
10.
Sakai, Kohei, Chizuru Ito, Toshiaki Ito, et al.. (2019). Usp26 mutation in mice leads to defective spermatogenesis depending on genetic background. Scientific Reports. 9(1). 13757–13757. 21 indexed citations
11.
Sekita, Yoichi, Toshinobu Nakamura, & Tohru Kimura. (2016). Reprogramming of germ cells into pluripotency. World Journal of Stem Cells. 8(8). 251–251. 10 indexed citations
12.
Nakatani, Tsunetoshi, Masaaki Oda, Yasuyoshi Kimura, et al.. (2015). Stella controls chromocenter formation through regulation of Daxx expression in 2-cell embryos. Biochemical and Biophysical Research Communications. 466(1). 60–65. 15 indexed citations
13.
Kimura, Yasuyoshi, Masaaki Oda, Tsunetoshi Nakatani, et al.. (2015). CRISPR/Cas9-mediated reporter knock-in in mouse haploid embryonic stem cells. Scientific Reports. 5(1). 10710–10710. 25 indexed citations
14.
Nakatani, Tsunetoshi, Kazuo Yamagata, Tohru Kimura, et al.. (2015). Stella preserves maternal chromosome integrity by inhibiting 5hmC‐induced γH2 AX accumulation. EMBO Reports. 16(5). 582–589. 28 indexed citations
15.
Kimura, Tohru, Yoichi Sekita, Keita Fujikawa, et al.. (2014). Pluripotent Stem Cells Derived From Mouse Primordial Germ Cells by Small Molecule Compounds. Stem Cells. 33(1). 45–55. 27 indexed citations
16.
Kagami, Masayo, Kentaro Matsuoka, Toshiro Nagai, et al.. (2012). Paternal uniparental disomy 14 and related disorders. Epigenetics. 7(10). 1142–1150. 30 indexed citations
17.
Coan, P. M., Owen R. Vaughan, Yoichi Sekita, et al.. (2009). Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice. The Journal of Physiology. 588(3). 527–538. 159 indexed citations
18.
Sekita, Yoichi, Hirotaka Wagatsuma, Kenji Nakamura, et al.. (2008). Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta. Nature Genetics. 40(2). 243–248. 255 indexed citations
19.
Wakisaka, Noriko, Kimiko Inoue, Narumi Ogonuki, et al.. (2008). Ultrastructure of Placental Hyperplasia in Mice: Comparison of Placental Phenotypes with Three Different Etiologies. Placenta. 29(8). 753–759. 13 indexed citations
20.
Sekita, Yoichi, Hirotaka Wagatsuma, Shin Kobayashi, et al.. (2006). Aberrant regulation of imprinted gene expression in <i>Gtl2</i><sup>lacZ</sup> mice. Cytogenetic and Genome Research. 113(1-4). 223–229. 36 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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