Jibak Lee

1.5k total citations
35 papers, 1.1k citations indexed

About

Jibak Lee is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Cell Biology. According to data from OpenAlex, Jibak Lee has authored 35 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 23 papers in Public Health, Environmental and Occupational Health and 17 papers in Cell Biology. Recurrent topics in Jibak Lee's work include Reproductive Biology and Fertility (23 papers), Microtubule and mitosis dynamics (17 papers) and Genomics and Chromatin Dynamics (12 papers). Jibak Lee is often cited by papers focused on Reproductive Biology and Fertility (23 papers), Microtubule and mitosis dynamics (17 papers) and Genomics and Chromatin Dynamics (12 papers). Jibak Lee collaborates with scholars based in Japan, United Kingdom and United States. Jibak Lee's co-authors include Takashi Miyano, Tatsuya Hirano, R. M. Moor, Masakane Yamashita, Takehiro Yokota, Masashi Miyake, Toshiharu Iwai, Takashi Morita, Tomoya S. Kitajima and Yuji Tanno and has published in prestigious journals such as The Journal of Cell Biology, Nature Cell Biology and Journal of Cell Science.

In The Last Decade

Jibak Lee

33 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jibak Lee Japan 17 850 489 399 220 214 35 1.1k
Suzanne Madgwick United Kingdom 13 429 0.5× 471 1.0× 315 0.8× 206 0.9× 112 0.5× 18 802
Pascale Rassinier France 7 592 0.7× 700 1.4× 715 1.8× 97 0.4× 140 0.7× 8 1.0k
Vladimı́r Baran Slovakia 15 540 0.6× 442 0.9× 267 0.7× 97 0.4× 71 0.3× 37 761
Masashi Miyake Japan 20 717 0.8× 739 1.5× 177 0.4× 377 1.7× 77 0.4× 39 1.2k
Henri de Pennart France 6 444 0.5× 530 1.1× 306 0.8× 179 0.8× 69 0.3× 7 712
Mark Levasseur United Kingdom 11 607 0.7× 505 1.0× 533 1.3× 135 0.6× 125 0.6× 12 862
Maria S. Szöllösi France 13 730 0.9× 724 1.5× 84 0.2× 235 1.1× 71 0.3× 15 977
Pascale Debey France 11 913 1.1× 458 0.9× 50 0.1× 114 0.5× 107 0.5× 11 1.1k
Hiroki Shibuya Japan 17 1.2k 1.4× 130 0.3× 240 0.6× 63 0.3× 196 0.9× 31 1.3k
Edgar-John Vogt Germany 8 258 0.3× 347 0.7× 111 0.3× 152 0.7× 42 0.2× 8 514

Countries citing papers authored by Jibak Lee

Since Specialization
Citations

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

Fields of papers citing papers by Jibak Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jibak Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Jibak Lee. A scholar is included among the top collaborators of Jibak Lee 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 Jibak Lee. Jibak Lee 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.
Kyogoku, Hirohisa, et al.. (2024). Change in the ability of bovine granulosa cells to elongate transzonal projections and their transcriptome changes during follicle development. Journal of Reproduction and Development. 70(6). 362–371.
2.
Lee, Jibak, et al.. (2018). GDF9 and BMP15 induce development of antrum-like structures by bovine granulosa cells without oocytes. Journal of Reproduction and Development. 64(5). 423–431. 30 indexed citations
3.
Lee, Jibak. (2017). The Regulation and Function of Cohesin and Condensin in Mammalian Oocytes and Spermatocytes. Results and problems in cell differentiation. 63. 355–372. 7 indexed citations
4.
Houlard, Martin, Jonathan Godwin, Jean Metson, et al.. (2015). Condensin confers the longitudinal rigidity of chromosomes. Nature Cell Biology. 17(6). 771–781. 79 indexed citations
5.
Lee, Jibak & Tatsuya Hirano. (2011). RAD21L, a novel cohesin subunit implicated in linking homologous chromosomes in mammalian meiosis. The Journal of Cell Biology. 192(2). 263–276. 125 indexed citations
7.
Lee, Jibak, Sugako Ogushi, Mitinori Saitou, & Tatsuya Hirano. (2011). Condensins I and II are essential for construction of bivalent chromosomes in mouse oocytes. Molecular Biology of the Cell. 22(18). 3465–3477. 50 indexed citations
8.
Moniruzzaman, Mohammad, et al.. (2009). Knockdown of FOXO3 induces primordial oocyte activation in pigs. Reproduction. 139(2). 337–348. 20 indexed citations
9.
Lee, Jibak, Tomoya S. Kitajima, Yuji Tanno, et al.. (2007). Unified mode of centromeric protection by shugoshin in mammalian oocytes and somatic cells. Nature Cell Biology. 10(1). 42–52. 202 indexed citations
10.
Miyano, Takashi, Sugako Ogushi, Hong‐Thuy Bui, & Jibak Lee. (2007). Meiotic Resumption and Spindle Formation of Pig Oocytes. Journal of Mammalian Ova Research. 24(3). 92–98.
12.
Iwai, Toshiharu, et al.. (2004). THE UNIQUE MITOTIC APPARATUS AND DISTRIBUTION OF γ-TUBULIN IN SPERMATOCYTES OF THE SILKWORM, BOMBYX MORI(LEPIDOPTERA)(Developmental Biology,Abstracts of papers presented at the 75^ Annual Meeting of the Zoological Society of Japan) :. ZOOLOGICAL SCIENCE. 21(12). 1288. 1 indexed citations
13.
Iwai, Toshiharu, et al.. (2004). Changes in the expression and localization of cohesin subunits during meiosis in a non-mammalian vertebrate, the medaka fish. Gene Expression Patterns. 4(5). 495–504. 14 indexed citations
14.
Miyano, Takashi, Jibak Lee, & Josef Fulka. (2003). G2/M transition of pig oocytes: How do oocytes initiate maturation?. Reproductive Medicine and Biology. 2(3). 91–99. 6 indexed citations
15.
16.
Lee, Jibak, Takehiro Yokota, & Masakane Yamashita. (2002). Analyses of mRNA Expression Patterns of Cohesin Subunits Rad21 and Rec8 in Mice: Germ Cell-Specific Expression ofrec8mRNA in Both Male and Female Mice. ZOOLOGICAL SCIENCE. 19(5). 539–544. 25 indexed citations
17.
Lee, Jibak, Takashi Miyano, & R. M. Moor. (2000). Spindle Formation and Dynamics of γ-Tubulin and Nuclear Mitotic Apparatus Protein Distribution During Meiosis in Pig and Mouse Oocytes1. Biology of Reproduction. 62(5). 1184–1192. 86 indexed citations
18.
Miyano, Takashi, Yanfeng Dai, Jibak Lee, Koichiro Kano, & R. M. Moor. (2000). Degradation of pig cyclin B1 molecules precedes MAP kinase dephosphorylation during fertilisation of the oocytes. Zygote. 8(2). 153–158. 11 indexed citations
19.
Lee, Jibak, Takashi Miyano, Yanfeng Dai, et al.. (2000). Specific regulation of CENP-E and kinetochores during meiosis I/meiosis II transition in pig oocytes. Molecular Reproduction and Development. 56(1). 51–62. 30 indexed citations
20.
Lee, Jibak, Takashi Miyano, Yanfeng Dai, et al.. (2000). Specific regulation of CENP-E and kinetochores during meiosis I/meiosis II transition in pig oocytes. Molecular Reproduction and Development. 56(1). 51–51. 4 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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