Jun‐Dae Kim

1.4k total citations
31 papers, 925 citations indexed

About

Jun‐Dae Kim is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Jun‐Dae Kim has authored 31 papers receiving a total of 925 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 12 papers in Cell Biology and 6 papers in Oncology. Recurrent topics in Jun‐Dae Kim's work include Congenital heart defects research (12 papers), Zebrafish Biomedical Research Applications (9 papers) and Angiogenesis and VEGF in Cancer (8 papers). Jun‐Dae Kim is often cited by papers focused on Congenital heart defects research (12 papers), Zebrafish Biomedical Research Applications (9 papers) and Angiogenesis and VEGF in Cancer (8 papers). Jun‐Dae Kim collaborates with scholars based in United States, South Korea and Serbia. Jun‐Dae Kim's co-authors include Suk-Won Jin, Victoria L. Bautch, Charles C. Hong, David M. Wiley, Jijun Hao, Jongmin Kim, Hyung J. Chun, Yujung Kang, Jingxia Wu and Yibing Qyang and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Journal of Neuroscience.

In The Last Decade

Jun‐Dae Kim

29 papers receiving 918 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jun‐Dae Kim United States 15 606 222 157 143 136 31 925
Christian SM Helker Germany 15 673 1.1× 407 1.8× 184 1.2× 75 0.5× 129 0.9× 27 1.1k
Susan Hutchison United States 11 538 0.9× 273 1.2× 148 0.9× 63 0.4× 207 1.5× 14 1.4k
Sharina Palencia Desai United States 5 652 1.1× 177 0.8× 71 0.5× 150 1.0× 201 1.5× 7 959
Gaël Genet United States 12 445 0.7× 144 0.6× 149 0.9× 149 1.0× 77 0.6× 19 889
Isao Inoki Japan 13 862 1.4× 187 0.8× 98 0.6× 192 1.3× 303 2.2× 19 1.4k
Fréderic Larrieu-Lahargue United States 15 848 1.4× 213 1.0× 97 0.6× 229 1.6× 117 0.9× 15 1.2k
Fumitaka Muramatsu Japan 15 458 0.8× 95 0.4× 150 1.0× 151 1.1× 185 1.4× 23 809
Manuel Ehling Germany 13 840 1.4× 259 1.2× 86 0.5× 210 1.5× 249 1.8× 14 1.3k
Bikram Sharma United States 12 517 0.9× 79 0.4× 198 1.3× 76 0.5× 91 0.7× 22 790
Roxana Ola United States 14 468 0.8× 130 0.6× 174 1.1× 155 1.1× 62 0.5× 24 934

Countries citing papers authored by Jun‐Dae Kim

Since Specialization
Citations

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

Fields of papers citing papers by Jun‐Dae Kim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun‐Dae Kim. 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 Jun‐Dae Kim. The network helps show where Jun‐Dae Kim may publish in the future.

Co-authorship network of co-authors of Jun‐Dae Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Jun‐Dae Kim. A scholar is included among the top collaborators of Jun‐Dae Kim 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 Jun‐Dae Kim. Jun‐Dae Kim 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.
Kim, Jun‐Dae, Jonathan W. Astin, Philip S. Crosier, et al.. (2025). APOA1 binding protein promotes lymphatic cell fate and lymphangiogenesis by relieving caveolae-mediated inhibition of VEGFR3 signaling. Nature Communications. 16(1). 9286–9286.
2.
Lv, Jie, Shu Meng, Qilin Gu, et al.. (2023). Epigenetic landscape reveals MECOM as an endothelial lineage regulator. Nature Communications. 14(1). 2390–2390. 19 indexed citations
3.
Kim, Jun‐Dae, Lingping Zhu, Quan Sun, & Longhou Fang. (2021). Systemic metabolite profiling reveals sexual dimorphism of AIBP control of metabolism in mice. PLoS ONE. 16(4). e0248964–e0248964. 11 indexed citations
4.
Choi, Woosoung, Jun‐Dae Kim, Da‐Woon Jung, et al.. (2020). Analyses of Avascular Mutants Reveal Unique Transcriptomic Signature of Non-conventional Endothelial Cells. Frontiers in Cell and Developmental Biology. 8. 589717–589717. 5 indexed citations
5.
Kim, Jun‐Dae, et al.. (2020). Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold. Frontiers in Cell and Developmental Biology. 8. 603306–603306.
6.
Kim, Jun‐Dae, et al.. (2020). Pax9 is essential for granulopoiesis but dispensable for erythropoiesis in zebrafish. Biochemical and Biophysical Research Communications. 534. 359–366. 6 indexed citations
7.
Kim, Jun‐Dae, Benoît Zuber, Andrew N. Makanya, et al.. (2018). Synergistic interaction of sprouting and intussusceptive angiogenesis during zebrafish caudal vein plexus development. Scientific Reports. 8(1). 9840–9840. 49 indexed citations
8.
Kim, Jun‐Dae, et al.. (2016). Spatiotemporal expression pattern of the zebrafish aquaporin 8 family during early developmental stages. Gene Expression Patterns. 21(1). 1–6. 6 indexed citations
9.
Kim, Jun‐Dae, Aram Lee, Jihea Choi, et al.. (2015). Epigenetic modulation as a therapeutic approach for pulmonary arterial hypertension. Experimental & Molecular Medicine. 47(7). e175–e175. 50 indexed citations
10.
Kim, Jun‐Dae, et al.. (2015). Proper Activity of Histone H3 Lysine 4 (H3K4) Methyltransferase Is Required for Morphogenesis during Zebrafish Cardiogenesis. Molecules and Cells. 38(6). 580–586. 25 indexed citations
11.
Kim, Jun‐Dae, Hyun-Taek Kim, Jung Hwa Choi, et al.. (2014). FIH-1, a Novel Interactor of Mindbomb, Functions as an Essential Anti-Angiogenic Factor during Zebrafish Vascular Development. PLoS ONE. 9(10). e109517–e109517. 26 indexed citations
12.
Kim, Jun‐Dae & Suk-Won Jin. (2014). A Tale of Two Models: Mouse and Zebrafish as Complementary Models for Lymphatic Studies. Molecules and Cells. 37(7). 503–510. 9 indexed citations
13.
14.
Kim, Jun‐Dae, Bruno Larrivée, Min Young Lee, et al.. (2012). Context-Dependent Proangiogenic Function of Bone Morphogenetic Protein Signaling Is Mediated by Disabled Homolog 2. Developmental Cell. 23(2). 441–448. 53 indexed citations
15.
Kim, Jun‐Dae, et al.. (2012). Histone deacetylase is required for the activation of Wnt/β-catenin signaling crucial for heart valve formation in zebrafish embryos. Biochemical and Biophysical Research Communications. 423(1). 140–146. 26 indexed citations
16.
Kim, Suhyun, et al.. (2012). Antagonistic Regulation of PAF1C and p-TEFb Is Required for Oligodendrocyte Differentiation. Journal of Neuroscience. 32(24). 8201–8207. 9 indexed citations
17.
Kim, Se Hee, et al.. (2012). Vascular endothelial growth factor signaling regulates the segregation of artery and vein via ERK activity during vascular development. Biochemical and Biophysical Research Communications. 430(4). 1212–1216. 14 indexed citations
18.
Wiley, David M., et al.. (2011). Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein. Nature Cell Biology. 13(6). 686–692. 156 indexed citations
19.
Park, Jae Sun, Hyung‐Seok Kim, Jun‐Dae Kim, et al.. (2009). Isolation of a ventricle‐specific promoter for the zebrafish ventricular myosin heavy chain (vmhc) gene and its regulation by GATA factors during embryonic heart development. Developmental Dynamics. 238(6). 1574–1581. 15 indexed citations
20.
Kim, Hyung-Seok, Jimann Shin, Jun‐Dae Kim, et al.. (2006). Eye field requires the function of Sfrp1 as a Wnt antagonist. Neuroscience Letters. 414(1). 26–29. 13 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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