Hiroyuki Kugoh

2.5k total citations
68 papers, 1.9k citations indexed

About

Hiroyuki Kugoh is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Hiroyuki Kugoh has authored 68 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 24 papers in Genetics and 21 papers in Physiology. Recurrent topics in Hiroyuki Kugoh's work include Telomeres, Telomerase, and Senescence (19 papers), Genetic Syndromes and Imprinting (10 papers) and Epigenetics and DNA Methylation (10 papers). Hiroyuki Kugoh is often cited by papers focused on Telomeres, Telomerase, and Senescence (19 papers), Genetic Syndromes and Imprinting (10 papers) and Epigenetics and DNA Methylation (10 papers). Hiroyuki Kugoh collaborates with scholars based in Japan, United States and Mexico. Hiroyuki Kugoh's co-authors include Mitsuo Oshimura, Kazuhiro Murakami, Hiroshi Uejima, Motoyuki Shimizu, Mitsuo Oshimura, Mitsuhiko Osaki, J. Carl Barrett, Yuji Nakayama, Izumi Horikawa and Kohzoh Mitsuya and has published in prestigious journals such as Nature Genetics, Molecular Cell and PLoS ONE.

In The Last Decade

Hiroyuki Kugoh

67 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hiroyuki Kugoh Japan 25 1.5k 712 360 309 160 68 1.9k
Effie Apostolou United States 24 4.0k 2.7× 518 0.7× 350 1.0× 281 0.9× 176 1.1× 45 4.3k
Bruce E. Hayward United Kingdom 27 1.7k 1.2× 1.3k 1.9× 418 1.2× 149 0.5× 174 1.1× 54 2.9k
Monique Losekoot Netherlands 34 1.4k 0.9× 1.3k 1.8× 259 0.7× 288 0.9× 226 1.4× 125 3.1k
Martin F. Arlt United States 22 2.1k 1.4× 1.2k 1.7× 291 0.8× 168 0.5× 596 3.7× 37 2.7k
Sigrid Swagemakers Netherlands 26 1.9k 1.2× 299 0.4× 443 1.2× 156 0.5× 481 3.0× 61 2.6k
Hidenori Kiyosawa Japan 20 1.3k 0.8× 452 0.6× 264 0.7× 87 0.3× 82 0.5× 52 1.8k
H F Willard United States 22 1.2k 0.8× 804 1.1× 168 0.5× 130 0.4× 112 0.7× 28 1.8k
Gerard Merkx Netherlands 25 1.6k 1.0× 570 0.8× 184 0.5× 71 0.2× 187 1.2× 52 2.2k
Christine Fauth Austria 22 1.5k 1.0× 790 1.1× 182 0.5× 88 0.3× 181 1.1× 66 2.3k
Sabine Loewer United States 10 1.8k 1.2× 290 0.4× 193 0.5× 261 0.8× 151 0.9× 11 2.3k

Countries citing papers authored by Hiroyuki Kugoh

Since Specialization
Citations

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

Fields of papers citing papers by Hiroyuki Kugoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroyuki Kugoh

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroyuki Kugoh. A scholar is included among the top collaborators of Hiroyuki Kugoh 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 Hiroyuki Kugoh. Hiroyuki Kugoh 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.
Tomimatsu, Kosuke, Dóra Bihary, Ioana Olan, et al.. (2021). Locus-specific induction of gene expression from heterochromatin loci during cellular senescence. Nature Aging. 2(1). 31–45. 18 indexed citations
2.
Morimoto, Masaki, Takehiko Hanaki, Kyoichi Kihara, et al.. (2021). Human chromosome 3p21.3 carries TERT transcriptional regulators in pancreatic cancer. Scientific Reports. 11(1). 15355–15355. 5 indexed citations
3.
Nakayama, Yuji, et al.. (2020). Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individual. Experimental Cell Research. 398(2). 112419–112419. 2 indexed citations
4.
Uno, Narumi, et al.. (2019). An efficient protein production system via gene amplification on a human artificial chromosome and the chromosome transfer to CHO cells. Scientific Reports. 9(1). 16954–16954. 6 indexed citations
5.
Kojima, Hirotada, Yuko Kuroda, Mitsuhiko Osaki, et al.. (2019). PITX1 protein interacts with ZCCHC10 to regulate <i>hTERT</i> mRNA transcription. Figshare. 20 indexed citations
6.
Osaki, Mitsuhiko, Kunishige Onuma, Hideki Iwamoto, et al.. (2017). Identification of MicroRNAs Involved in Resistance to Sunitinib in Renal Cell Carcinoma Cells. Anticancer Research. 37(6). 2985–2992. 43 indexed citations
7.
Oshimura, Mitsuo, et al.. (2015). Repression of hTERT transcription by the introduction of chromosome 3 into human oral squamous cell carcinoma. Biochemical and Biophysical Research Communications. 466(4). 755–759. 5 indexed citations
8.
Osaki, Mitsuhiko, Yuichi Yoshida, Osamu Yamamoto, et al.. (2013). Decreased PITX1 gene expression in human cutaneous malignant melanoma and its clinicopathological significance. European Journal of Dermatology. 23(3). 344–349. 19 indexed citations
9.
Abe, Satoshi, Hiromi Tanaka, Shin‐ichi Horike, et al.. (2010). Localization of an hTERT repressor region on human chromosome 3p21.3 using chromosome engineering. PubMed. 1(1). 6–6. 15 indexed citations
10.
Nguyen, Phuongmai, Hengmi Cui, Kheem S. Bisht, et al.. (2008). CTCFL/BORIS Is a Methylation-Independent DNA-Binding Protein That Preferentially Binds to the Paternal H19 Differentially Methylated Region. Cancer Research. 68(14). 5546–5551. 39 indexed citations
11.
Murakami, Kazuhiro, Mitsuo Oshimura, & Hiroyuki Kugoh. (2007). Suggestive evidence for chromosomal localization of non-coding RNA from imprinted LIT1. Journal of Human Genetics. 52(11). 926–933. 39 indexed citations
12.
13.
Kugoh, Hiroyuki, et al.. (2002). Human chromosome 5 carries a putative telomerase repressor gene. Genes Chromosomes and Cancer. 36(1). 37–47. 20 indexed citations
14.
Inoue, Toshiaki, Shoko Takehara, Jun Inoue, et al.. (2000). Specific Impairment of Cardiogenesis in Mouse ES Cells Containing a Human Chromosome 21. Biochemical and Biophysical Research Communications. 273(1). 219–224. 19 indexed citations
15.
Kugoh, Hiroyuki, Mutsunori Fujiwara, Kazunori Kihara, et al.. (2000). Cellular Senescence of a Human Bladder Carcinoma Cell Line (JTC-32) Induced by a Normal Chromosome 11. Cancer Genetics and Cytogenetics. 116(2). 158–163. 6 indexed citations
16.
Tomizuka, Kazuma, Hitoshi Yoshida, Hiroshi Uejima, et al.. (1997). Functional expression and germline atransmission of a human chromosome fragment in chimaeric mice. Nature Genetics. 16(2). 133–143. 207 indexed citations
17.
Horikawa, Izumi, Hideto Yamada, Hiroyuki Kugoh, et al.. (1995). Subchromosomal Mapping of a Putative Transformation Suppressor Gene on Human Chromosome 1. Japanese Journal of Cancer Research. 86(5). 444–450. 1 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.
Katoh, Motonobu, Yuzuki Nakagawa, Toshio Yawata, et al.. (1995). Cosmids and transcribed sequences from chromosome 11q23. The Japanese Journal of Human Genetics. 40(4). 307–317. 1 indexed citations
20.
Oshimura, Mitsuo, Hiroyuki Kugoh, Minoru Koi, et al.. (1990). Transfer of a normal human chromosome 11 suppresses tumorigenicity of some but not all tumor cell lines. Journal of Cellular Biochemistry. 42(3). 135–142. 66 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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