Kohzoh Mitsuya

3.9k total citations · 1 hit paper
32 papers, 2.7k citations indexed

About

Kohzoh Mitsuya is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Kohzoh Mitsuya has authored 32 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Genetics and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Kohzoh Mitsuya's work include Genetic Syndromes and Imprinting (21 papers), Epigenetics and DNA Methylation (20 papers) and Prenatal Screening and Diagnostics (12 papers). Kohzoh Mitsuya is often cited by papers focused on Genetic Syndromes and Imprinting (21 papers), Epigenetics and DNA Methylation (20 papers) and Prenatal Screening and Diagnostics (12 papers). Kohzoh Mitsuya collaborates with scholars based in Japan, United States and United Kingdom. Kohzoh Mitsuya's co-authors include Mitsuo Oshimura, Jafar Sharif, Tetsuro Toyoda, Haruhiko Koseki, Yoko Mizutani-Koseki, Shin‐ichiro Takebayashi, Isao Suetake, Kunihiro Okamura, Akihiro Iwamatsu and Shoji Tajima and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Kohzoh Mitsuya

32 papers receiving 2.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA

2007 945 citations Kohzoh Mitsuya et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kohzoh Mitsuya Japan	19	2.3k	1.4k	758	222	152	32	2.7k
Martina Paulsen Germany	22	2.5k 1.1×	1.6k 1.2×	726 1.0×	442 2.0×	195 1.3×	35	2.9k
Joomyeong Kim United States	31	2.1k 0.9×	1.1k 0.8×	431 0.6×	224 1.0×	276 1.8×	91	2.5k
Matthias Begemann Germany	24	1.2k 0.5×	1.1k 0.8×	709 0.9×	96 0.4×	61 0.4×	81	1.8k
Julia Arand Germany	16	3.1k 1.3×	860 0.6×	446 0.6×	160 0.7×	335 2.2×	23	3.4k
Jun Ohgane Japan	27	2.1k 0.9×	694 0.5×	354 0.5×	187 0.8×	77 0.5×	48	2.6k
Evica Rajcan‐Separovic Canada	24	775 0.3×	770 0.6×	386 0.5×	106 0.5×	178 1.2×	58	1.6k
Naka Hattori Japan	27	2.2k 1.0×	707 0.5×	346 0.5×	180 0.8×	87 0.6×	55	2.8k
Daniel M. Messerschmidt Singapore	18	1.5k 0.6×	437 0.3×	341 0.4×	134 0.6×	139 0.9×	30	1.9k
Asaf Hellman Israel	12	1.7k 0.7×	683 0.5×	170 0.2×	269 1.2×	83 0.5×	18	1.9k
Ronald Zwart Netherlands	14	1.5k 0.7×	715 0.5×	315 0.4×	489 2.2×	74 0.5×	20	2.2k

Countries citing papers authored by Kohzoh Mitsuya

Since Specialization

Citations

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

Fields of papers citing papers by Kohzoh Mitsuya

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kohzoh Mitsuya

This figure shows the co-authorship network connecting the top 25 collaborators of Kohzoh Mitsuya. A scholar is included among the top collaborators of Kohzoh Mitsuya 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 Kohzoh Mitsuya. Kohzoh Mitsuya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

1.

Lin, Li‐Ling, Meizhen Chen, Anthony Lopez, et al.. (2022). 2-Hydroxyglutarate destabilizes chromatin regulatory landscape and lineage fidelity to promote cellular heterogeneity. Cell Reports. 38(2). 110220–110220. 16 indexed citations

2.

Chou, Chih‐Wei, Xi Tan, Kohzoh Mitsuya, et al.. (2020). Menin and Menin-Associated Proteins Coregulate Cancer Energy Metabolism. Cancers. 12(9). 2715–2715. 10 indexed citations

3.

Tan, Xi, Chih‐Wei Chou, Nameer B. Kirma, et al.. (2020). ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer. BMC Medical Genomics. 13(1). 69–69. 9 indexed citations

4.

Mitsuya, Kohzoh, et al.. (2017). Alterations in the placental methylome with maternal obesity and evidence for metabolic regulation. PLoS ONE. 12(10). e0186115–e0186115. 51 indexed citations

5.

Nijland, Mark J., Kohzoh Mitsuya, Cun Li, et al.. (2010). Epigenetic modification of fetal baboon hepatic phosphoenolpyruvate carboxykinase following exposure to moderately reduced nutrient availability. The Journal of Physiology. 588(8). 1349–1359. 93 indexed citations

6.

Haruta, Masayuki, Makiko Meguro, Yuki Sakamoto, et al.. (2005). Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells. Journal of Human Genetics. 50(3). 124–132. 1 indexed citations

7.

Lewis, Annabelle, Kohzoh Mitsuya, Miguel Constância, & Wolf Reik. (2004). Tandem Repeat Hypothesis in Imprinting: Deletion of a Conserved Direct Repeat Element Upstream of H19 Has No Effect on Imprinting in the Igf2-H19 Region. Molecular and Cellular Biology. 24(13). 5650–5656. 30 indexed citations

8.

Reik, Wolf, Adele Murrell, Annabelle Lewis, et al.. (2004). Chromosome Loops, Insulators, and Histone Methylation: New Insights into Regulation of Imprinting in Clusters. Cold Spring Harbor Symposia on Quantitative Biology. 69(0). 29–38. 17 indexed citations

9.

Reik, Wolf, Adele Murrell, Annabelle Lewis, et al.. (2004). Chromosome Loops, Insulators, and Histone Methylation: New Insights into Regulation of Imprinting in Clusters. Cold Spring Harbor Symposia on Quantitative Biology. 69(1). 1–10. 2 indexed citations

10.

Cerrato, Flavia, Wendy Dean, Kazuhiro Kagotani, et al.. (2003). Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA. Human Molecular Genetics. 12(23). 3123–3132. 15 indexed citations

11.

Yamada, Takahiro, Kohzoh Mitsuya, Tomohiko Kayashima, et al.. (2003). Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32. Genomics. 83(3). 402–412. 16 indexed citations

12.

Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations

13.

Sakatani, Takashi, Michelle Wei, Motonobu Katoh, et al.. (2001). Epigenetic Heterogeneity at Imprinted Loci in Normal Populations. Biochemical and Biophysical Research Communications. 283(5). 1124–1130. 76 indexed citations

14.

Inoue, Jun‐ichiro, Kohzoh Mitsuya, Shinji Maegawa, et al.. (2001). Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6. Journal of Human Genetics. 46(3). 137–145. 30 indexed citations

15.

Meguro, Makiko, Akiko Kashiwagi, Kohzoh Mitsuya, et al.. (2001). A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome. Nature Genetics. 28(1). 19–20. 114 indexed citations

16.

Mitsuya, Kohzoh. (1997). Paternal expression of WT1 in human fibroblasts and lymphocytes. Human Molecular Genetics. 6(13). 2243–2246. 37 indexed citations

17.

Meguro, Masaki, Kohzoh Mitsuya, Hajime Sui, et al.. (1997). Evidence for Uniparental, Paternal Expression of the Human GABAA Receptor Subunit Genes, Using Microcell-Mediated Chromosome Transfer. Human Molecular Genetics. 6(12). 2127–2133. 69 indexed citations

18.

Kugoh, Hiroyuki, Yuzuki Nakagawa, Kohzoh Mitsuya, et al.. (1995). Isolation and Mapping of 186 New DNA Markers on Human Chromosome 1. Genomics. 27(1). 207–210. 16 indexed citations

19.

Kitagawa, Kazunori, Xudong Wang, Izuho Hatada, et al.. (1995). Isolation and Mapping of Human Homologues of an Imprinted Mouse GeneU2af1-rs1. Genomics. 30(2). 257–263. 27 indexed citations

20.

Uejima, Hiroshi, Kohzoh Mitsuya, Hiroyuki Kugoh, Izumi Horikawa, & Mitsuo Oshimura. (1995). Normal human chromosome 2 induces cellular senescence in the human cervical carcinoma cell line SiHa. Genes Chromosomes and Cancer. 14(2). 120–127. 41 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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