Sun‐Cheol Choi

869 total citations
29 papers, 699 citations indexed

About

Sun‐Cheol Choi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sun‐Cheol Choi has authored 29 papers receiving a total of 699 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sun‐Cheol Choi's work include Developmental Biology and Gene Regulation (12 papers), Wnt/β-catenin signaling in development and cancer (11 papers) and TGF-β signaling in diseases (6 papers). Sun‐Cheol Choi is often cited by papers focused on Developmental Biology and Gene Regulation (12 papers), Wnt/β-catenin signaling in development and cancer (11 papers) and TGF-β signaling in diseases (6 papers). Sun‐Cheol Choi collaborates with scholars based in South Korea, United States and Switzerland. Sun‐Cheol Choi's co-authors include Jin‐Kwan Han, Sergei Y. Sokol, Gun‐Hwa Kim, Weijun Pan, Lin Li, Laura E. Swan, Louise Lucast, He Wang, Charles S. Abrams and Xiaowu Zhang and has published in prestigious journals such as Science, The EMBO Journal and Development.

In The Last Decade

Sun‐Cheol Choi

29 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sun‐Cheol Choi South Korea 14 609 200 100 69 39 29 699
Dayana Krawchuk Canada 9 623 1.0× 166 0.8× 119 1.2× 142 2.1× 48 1.2× 10 814
Daniel Maurus Germany 8 444 0.7× 94 0.5× 83 0.8× 64 0.9× 31 0.8× 9 502
Morioh Kusakabe Japan 13 887 1.5× 265 1.3× 98 1.0× 101 1.5× 82 2.1× 22 1.0k
Yusuke Mii Japan 13 458 0.8× 153 0.8× 62 0.6× 63 0.9× 28 0.7× 19 553
Aliana Egeo Italy 12 691 1.1× 319 1.6× 101 1.0× 84 1.2× 35 0.9× 15 842
Kiyomasa Nishii Japan 13 618 1.0× 83 0.4× 90 0.9× 56 0.8× 40 1.0× 18 791
Paul Wakenight United States 6 304 0.5× 117 0.6× 93 0.9× 90 1.3× 29 0.7× 8 467
Trudi A. Westfall United States 10 525 0.9× 114 0.6× 137 1.4× 65 0.9× 16 0.4× 14 608
Annabel Christ Germany 14 321 0.5× 97 0.5× 101 1.0× 71 1.0× 39 1.0× 18 556

Countries citing papers authored by Sun‐Cheol Choi

Since Specialization
Citations

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

Fields of papers citing papers by Sun‐Cheol Choi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sun‐Cheol Choi. 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 Sun‐Cheol Choi. The network helps show where Sun‐Cheol Choi may publish in the future.

Co-authorship network of co-authors of Sun‐Cheol Choi

This figure shows the co-authorship network connecting the top 25 collaborators of Sun‐Cheol Choi. A scholar is included among the top collaborators of Sun‐Cheol Choi 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 Sun‐Cheol Choi. Sun‐Cheol Choi 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.
Choi, Sun‐Cheol, et al.. (2023). Transmembrane protein 150b attenuates BMP signaling in the Xenopus organizer. Journal of Cellular Physiology. 238(8). 1850–1866. 1 indexed citations
2.
Choi, Sun‐Cheol, et al.. (2022). RNF152 negatively regulates Wnt/β-catenin signaling in Xenopus embryos. BMB Reports. 55(5). 232–237. 3 indexed citations
3.
Kim, Eun‐Young, et al.. (2020). Wip1 regulates Smad4 phosphorylation and inhibits TGF ‐β signaling. EMBO Reports. 21(5). e48693–e48693. 22 indexed citations
4.
Lee, Hyun-Kyung, Tayaba Ismail, Jeen‐Woo Park, et al.. (2016). IFT46 plays crucial roles in craniofacial and cilia development. Biochemical and Biophysical Research Communications. 477(3). 419–425. 7 indexed citations
5.
Choi, Sun‐Cheol, et al.. (2016). Tbx2 regulates anterior neural specification by repressing FGF signaling pathway. Developmental Biology. 421(2). 183–193. 13 indexed citations
6.
Kim, Gun‐Hwa, et al.. (2013). β-Arrestin 1 mediates non-canonical Wnt pathway to regulate convergent extension movements. Biochemical and Biophysical Research Communications. 435(2). 182–187. 4 indexed citations
7.
Choi, Sun‐Cheol, et al.. (2013). BMP signal attenuates FGF pathway in anteroposterior neural patterning. Biochemical and Biophysical Research Communications. 434(3). 509–515. 13 indexed citations
8.
Hong, Mina, et al.. (2013). Essential role of AWP1 in neural crest specification in Xenopus. The International Journal of Developmental Biology. 57(11-12). 829–836. 8 indexed citations
9.
Choi, Sun‐Cheol & Jin‐Kwan Han. (2011). Negative Regulation of Activin Signal Transduction. Vitamins and hormones. 85. 79–104. 9 indexed citations
10.
Choi, Sun‐Cheol, et al.. (2011). Role of Tbx2 in defining the territory of the pronephric nephron. Development. 138(3). 465–474. 20 indexed citations
11.
Park, Edmond Changkyun, et al.. (2010). The involvement of Eph–Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements. Developmental Biology. 350(2). 441–450. 33 indexed citations
12.
Choi, Sun‐Cheol & Sergei Y. Sokol. (2009). The involvement of lethal giant larvae and Wnt signaling in bottle cell formation in Xenopus embryos. Developmental Biology. 336(1). 68–75. 33 indexed citations
13.
Lee, Seung Joon, Sanghee Kim, Sun‐Cheol Choi, & Jin‐Kwan Han. (2009). XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis. Mechanisms of Development. 127(1-2). 49–61. 8 indexed citations
14.
Kim, Gun‐Hwa, et al.. (2006). Role of PKA as a negative regulator of PCP signaling pathway during Xenopus gastrulation movements. Developmental Biology. 292(2). 344–357. 32 indexed citations
15.
Choi, Sun‐Cheol, et al.. (2006). XenopusDab2 is required for embryonic angiogenesis. BMC Developmental Biology. 6(1). 63–63. 19 indexed citations
16.
Choi, Sun‐Cheol & Jin‐Kwan Han. (2005). Rap2 is required for Wnt/β‐catenin signaling pathway in Xenopus early development. The EMBO Journal. 24(5). 985–996. 34 indexed citations
17.
Song, Beom‐Seok, Sun‐Cheol Choi, & Jin‐Kwan Han. (2003). Local activation of protein kinase A inhibits morphogenetic movements during Xenopus gastrulation. Developmental Dynamics. 227(1). 91–103. 10 indexed citations
18.
Shim, Sangwoo, et al.. (2003). A putative Xenopus Rho-GTPase activating protein (XrGAP) gene is expressed in the notochord and brain during the early embryogenesis. Gene Expression Patterns. 3(2). 219–223. 4 indexed citations
19.
Choi, Sun‐Cheol & Jin‐Kwan Han. (2002). Xenopus Cdc42 Regulates Convergent Extension Movements during Gastrulation through Wnt/Ca2+ Signaling Pathway. Developmental Biology. 244(2). 342–357. 130 indexed citations
20.
Choi, Sun‐Cheol, et al.. (2001). A Novel Xenopus Acetyltransferase with a Dynamic Expression in Early Development. Biochemical and Biophysical Research Communications. 285(5). 1338–1343. 6 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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