Sang‐Wook Cha

805 total citations
28 papers, 622 citations indexed

About

Sang‐Wook Cha is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Sang‐Wook Cha has authored 28 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Sang‐Wook Cha's work include Developmental Biology and Gene Regulation (14 papers), Pluripotent Stem Cells Research (8 papers) and Wnt/β-catenin signaling in development and cancer (8 papers). Sang‐Wook Cha is often cited by papers focused on Developmental Biology and Gene Regulation (14 papers), Pluripotent Stem Cells Research (8 papers) and Wnt/β-catenin signaling in development and cancer (8 papers). Sang‐Wook Cha collaborates with scholars based in United States, South Korea and Canada. Sang‐Wook Cha's co-authors include Emmanuel Tadjuidje, Janet Heasman, Christopher Wylie, Shelby A. Blythe, Peter S. Klein, Qinghua Tao, Aaron M. Zorn, Yetki Aslan, James M. Wells and Christopher N. Mayhew and has published in prestigious journals such as PLoS ONE, Development and Current Biology.

In The Last Decade

Sang‐Wook Cha

28 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sang‐Wook Cha United States 13 558 106 69 51 35 28 622
Emmanuel Tadjuidje United States 11 572 1.0× 92 0.9× 73 1.1× 40 0.8× 27 0.8× 17 633
Fredericus Van Eeden United Kingdom 4 442 0.8× 72 0.7× 164 2.4× 47 0.9× 39 1.1× 5 552
Vincent Liu United States 8 590 1.1× 53 0.5× 65 0.9× 35 0.7× 17 0.5× 9 678
Catherine T. Nguyen United States 7 334 0.6× 106 1.0× 151 2.2× 22 0.4× 38 1.1× 11 526
Chris Showell United States 8 304 0.5× 72 0.7× 37 0.5× 33 0.6× 50 1.4× 10 385
Lan-Hsin Wang Taiwan 9 323 0.6× 78 0.7× 59 0.9× 24 0.5× 17 0.5× 12 416
Veronika Akopian United States 7 903 1.6× 135 1.3× 16 0.2× 44 0.9× 20 0.6× 9 968
Takayoshi Yamamoto Japan 9 201 0.4× 75 0.7× 93 1.3× 66 1.3× 10 0.3× 28 327
Elisabeth Mahen United States 9 601 1.1× 96 0.9× 40 0.6× 42 0.8× 14 0.4× 14 712
Naoki Mine Japan 10 416 0.7× 99 0.9× 84 1.2× 35 0.7× 28 0.8× 13 556

Countries citing papers authored by Sang‐Wook Cha

Since Specialization
Citations

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

Fields of papers citing papers by Sang‐Wook Cha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sang‐Wook Cha. 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 Sang‐Wook Cha. The network helps show where Sang‐Wook Cha may publish in the future.

Co-authorship network of co-authors of Sang‐Wook Cha

This figure shows the co-authorship network connecting the top 25 collaborators of Sang‐Wook Cha. A scholar is included among the top collaborators of Sang‐Wook Cha 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 Sang‐Wook Cha. Sang‐Wook Cha 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.
Nakayama, Takuya, Robert M. Grainger, & Sang‐Wook Cha. (2022). Homology-Directed Repair by CRISPR–Cas9 Mutagenesis inXenopusUsing Long Single-Stranded Donor DNA Templates via Simple Microinjection of Embryos. Cold Spring Harbor Protocols. 2022(12). pdb.prot107599–pdb.prot107599. 3 indexed citations
2.
Cha, Sang‐Wook. (2021). Generating Nonmosaic Mutants in Xenopus Using CRISPR–Cas in Oocytes. Cold Spring Harbor Protocols. 2022(6). pdb.prot106989–pdb.prot106989. 2 indexed citations
3.
Nasr, Talia, Pamela Mancini, Scott A. Rankin, et al.. (2019). Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation. Developmental Cell. 51(6). 665–674.e6. 36 indexed citations
4.
Tadjuidje, Emmanuel & Sang‐Wook Cha. (2018). How to Generate Non-Mosaic CRISPR/Cas9 Mediated Knock-In and Mutations in F0 Xenopus Through the Host-Transfer Technique. Methods in molecular biology. 1865. 105–117. 2 indexed citations
5.
Wang, Sha, Sang‐Wook Cha, Aaron M. Zorn, & Christopher Wylie. (2013). Par6b Regulates the Dynamics of Apicobasal Polarity during Development of the Stratified Xenopus Epidermis. PLoS ONE. 8(10). e76854–e76854. 9 indexed citations
6.
Nandadasa, Sumeda, et al.. (2012). Regulation of Classical Cadherin Membrane Expression and F-Actin Assembly by Alpha-Catenins, during Xenopus Embryogenesis. PLoS ONE. 7(6). e38756–e38756. 6 indexed citations
7.
Cha, Sang‐Wook, et al.. (2012). Foxi2 Is an Animally Localized Maternal mRNA in Xenopus, and an Activator of the Zygotic Ectoderm Activator Foxi1e. PLoS ONE. 7(7). e41782–e41782. 15 indexed citations
8.
Lee, Sungyoung, Jaeho Yoon, Sang‐Wook Cha, et al.. (2011). The Function of Heterodimeric AP-1 Comprised of c-Jun and c-Fos in Activin Mediated Spemann Organizer Gene Expression. PLoS ONE. 6(7). e21796–e21796. 9 indexed citations
9.
Lee, Sung‐Young, Sang‐Wook Cha, Jaeho Yoon, et al.. (2011). Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos. Differentiation. 82(2). 99–107. 11 indexed citations
10.
Lee, Hyun‐Shik, Sungyoung Lee, Hyosang Lee, et al.. (2011). Direct Response Elements of BMP within the PV.1A Promoter Are Essential for Its Transcriptional Regulation during Early Xenopus Development. PLoS ONE. 6(8). e22621–e22621. 16 indexed citations
11.
Tadjuidje, Emmanuel, et al.. (2011). The functions of maternal Dishevelled 2 and 3 in the Early Xenopus embryo. Developmental Dynamics. 240(7). 1727–1736. 14 indexed citations
12.
Blythe, Shelby A., Sang‐Wook Cha, Emmanuel Tadjuidje, Janet Heasman, & Peter S. Klein. (2010). Beta-catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2. Developmental Biology. 344(1). 418–418. 2 indexed citations
13.
Hwang, Yoo‐Seok, Sang‐Wook Cha, Jang-Hee Hahn, et al.. (2010). Xclaudin 1 is required for the proper gastrulation in Xenopus laevis. Biochemical and Biophysical Research Communications. 397(1). 75–81. 4 indexed citations
14.
Cha, Sang‐Wook & Janet Heasman. (2010). Using oocytes for Wnt signaling assays: Paracrine assays and Wnt-conditioned medium. Methods. 51(1). 52–55. 6 indexed citations
15.
Blythe, Shelby A., Sang‐Wook Cha, Emmanuel Tadjuidje, Janet Heasman, & Peter S. Klein. (2010). β-Catenin Primes Organizer Gene Expression by Recruiting a Histone H3 Arginine 8 Methyltransferase, Prmt2. Developmental Cell. 19(2). 220–231. 131 indexed citations
16.
Kennedy, Mark, et al.. (2009). A co‐dependent requirement of xBcl9 and Pygopus for embryonic body axis development in Xenopus. Developmental Dynamics. 239(1). 271–283. 9 indexed citations
17.
Cha, Sang‐Wook, Emmanuel Tadjuidje, James M. Wells, et al.. (2009). Wnt11/5a Complex Formation Caused by Tyrosine Sulfation Increases Canonical Signaling Activity. Current Biology. 19(18). 1573–1580. 55 indexed citations
18.
Cha, Sang‐Wook, Emmanuel Tadjuidje, Qinghua Tao, Christopher Wylie, & Janet Heasman. (2008). Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling inXenopusaxis formation. Development. 135(22). 3719–3729. 118 indexed citations
19.
Lee, Hyun‐Shik, et al.. (2003). Active repression of organizer genes by C-terminal domain of PV.1. Biochemical and Biophysical Research Communications. 308(1). 79–86. 12 indexed citations
20.
Cha, Sang‐Wook, Hyun‐Shik Lee, Sungyoung Lee, et al.. (2002). Antimorphic PV.1 Causes Secondary Axis by Inducing Ectopic Organizer. Biochemical and Biophysical Research Communications. 292(4). 1081–1086. 15 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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