K. Okui

512 total citations
18 papers, 447 citations indexed

About

K. Okui is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, K. Okui has authored 18 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in K. Okui's work include Renal and related cancers (4 papers), Ubiquitin and proteasome pathways (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). K. Okui is often cited by papers focused on Renal and related cancers (4 papers), Ubiquitin and proteasome pathways (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). K. Okui collaborates with scholars based in Japan, Spain and India. K. Okui's co-authors include Shiro Ikegawa, Yusuke Nakamura, Kumiko Koyama, Tatsushi Toda, Ken-ichi Takita, Hiroko Saito, Takashi Sakamoto, Takaaki Sato, Mitsuo Oshimura and Yasukazu Nakamura and has published in prestigious journals such as Genomics, Human Genetics and Genes Chromosomes and Cancer.

In The Last Decade

K. Okui

18 papers receiving 439 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K. Okui Japan 13 318 119 87 65 51 18 447
E. Natt Germany 10 314 1.0× 84 0.7× 124 1.4× 28 0.4× 54 1.1× 13 510
Masahiko Shiraishi Japan 13 466 1.5× 120 1.0× 99 1.1× 40 0.6× 94 1.8× 39 607
Michael Swift United States 5 357 1.1× 177 1.5× 148 1.7× 82 1.3× 144 2.8× 7 514
K. Tago Japan 9 422 1.3× 63 0.5× 36 0.4× 38 0.6× 58 1.1× 16 559
Martha Kalff-Suske Germany 10 312 1.0× 159 1.3× 33 0.4× 26 0.4× 51 1.0× 15 475
Anne‐Marie Hutchins Australia 10 234 0.7× 176 1.5× 113 1.3× 55 0.8× 132 2.6× 12 458
Anita M. Quintana United States 12 384 1.2× 212 1.8× 50 0.6× 33 0.5× 56 1.1× 24 665
Marjo Aitola Finland 7 442 1.4× 130 1.1× 80 0.9× 20 0.3× 31 0.6× 9 542
Stef van Lieshout Netherlands 7 243 0.8× 208 1.7× 160 1.8× 72 1.1× 91 1.8× 11 519
Genevieve J. Rabiasz United Kingdom 7 298 0.9× 52 0.4× 74 0.9× 35 0.5× 85 1.7× 8 412

Countries citing papers authored by K. Okui

Since Specialization
Citations

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

Fields of papers citing papers by K. Okui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Okui

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

All Works

18 of 18 papers shown
1.
Iida, Aritoshi, M. Emi, Rumiko Matsuoka, et al.. (2000). Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation. Human Genetics. 106(3). 277–287. 9 indexed citations
2.
Iida, Aritoshi, M. Emi, Rumiko Matsuoka, et al.. (2000). Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation. Human Genetics. 106(3). 277–287. 31 indexed citations
3.
Masuno, Mitsuo, Akihiko Okawa, Minoru Isomura, et al.. (1999). Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene. Clinical Genetics. 55(6). 466–472. 10 indexed citations
4.
Isomura, Minoru, K. Okui, Tsutomu Fujiwara, Sadahito Shin, & Yusuke Nakamura. (1996). Cloning and Mapping of a Novel Human cDNA Homologous to DROER, the Enhancer of theDrosophila melanogasterRudimentary Gene. Genomics. 32(1). 125–127. 19 indexed citations
5.
Saito, Hirohisa, T. Fujiwara, Sungwon Shin, K. Okui, & Yoshimasa Nakamura. (1996). Cloning and mapping of a human novel cDNA (NHP2L1) that encodes a protein highly homologous to yeast nuclear protein NHP2. Cytogenetic and Genome Research. 72(2-3). 191–193. 17 indexed citations
6.
Isomura, Minoru, K. Okui, T. Fujiwara, Sook Shin, & Yoshimasa Nakamura. (1996). Isolation and mapping of RAB2L, a human cDNA that encodes a protein homologous to RalGDS. Cytogenetic and Genome Research. 74(4). 263–265. 10 indexed citations
7.
Ikegawa, Shiro, et al.. (1996). Isolation, characterization and chromosomal assignment of the human WNT7A gene. Cytogenetic and Genome Research. 74(1-2). 149–152. 30 indexed citations
8.
Ikegawa, Shiro, Tatsushi Toda, K. Okui, & Yusuke Nakamura. (1996). Structure and Chromosomal Assignment of the Human S1-5 Gene (FBNL) That Is Highly Homologous to Fibrillin. Genomics. 35(3). 590–592. 26 indexed citations
9.
Fujiwara, Tsutomu, et al.. (1996). Isolation and Mapping of a Novel Human Gene Encoding a Protein Containing Zinc-Finger Structures. Genomics. 31(3). 376–379. 8 indexed citations
10.
Ikegawa, Shiro, et al.. (1995). Isolation, characterization and chromosomal assignment of human colligin-2 gene (CBP2). Cytogenetic and Genome Research. 71(2). 182–186. 17 indexed citations
11.
12.
Nakamura, Yusuke, K. Okui, Eiichi Takahashi, & Kumiko Koyama. (1994). Isolation and mapping of 328 new cosmid markers on human chromosome 8: construction of a high-resolution cytogenetic map of chromosome 8 with 416 markers. Cytogenetic and Genome Research. 65(1-2). 115–118. 13 indexed citations
13.
Toda, Tatsushi, Shiro Ikegawa, K. Okui, et al.. (1994). Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.. PubMed. 55(5). 946–50. 54 indexed citations
14.
Tanaka, Toshihiro, K. Okui, & Yoshimasa Nakamura. (1994). Assignment of the human caltractin gene (CALT) to Xq28 by fluorescence in situ hybridization.. PubMed. 24(3). 609–10. 5 indexed citations
15.
Sato, Takaaki, Takashi Sakamoto, Ken-ichi Takita, et al.. (1993). The Human Prohibitin (PHB) Gene Family and Its Somatic Mutations in Human Tumors. Genomics. 17(3). 762–764. 62 indexed citations
16.
Yamakawa, Kazuhiro, Eiichi Takahashi, Motoi Murata, et al.. (1992). Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B. Genomics. 14(2). 412–416. 12 indexed citations
17.
Takahashi, Ei-ichi, et al.. (1992). Isolation and mapping of 88 new RFLP markers on human chromosome 8. Genomics. 13(4). 1261–1266. 23 indexed citations
18.
Saito, Susumu, K. Okui, Takashi Tokino, Mitsuo Oshimura, & Yusuke Nakamura. (1992). Isolation and mapping of 68 RFLP markers on human chromosome 6.. PubMed. 50(1). 65–70. 26 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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