Diana C. Chong

1.4k total citations
18 papers, 1.0k citations indexed

About

Diana C. Chong is a scholar working on Molecular Biology, Cell Biology and Surgery. According to data from OpenAlex, Diana C. Chong has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 6 papers in Cell Biology and 3 papers in Surgery. Recurrent topics in Diana C. Chong's work include Angiogenesis and VEGF in Cancer (9 papers), Congenital heart defects research (8 papers) and TGF-β signaling in diseases (4 papers). Diana C. Chong is often cited by papers focused on Angiogenesis and VEGF in Cancer (9 papers), Congenital heart defects research (8 papers) and TGF-β signaling in diseases (4 papers). Diana C. Chong collaborates with scholars based in United States, South Korea and Italy. Diana C. Chong's co-authors include Ondine Cleaver, Alethia Villasenor, Ke Xu, Mark Henkemeyer, Victoria L. Bautch, Yeon Koo, George E. Davis, Anastasia Sacharidou, Kathryn M. Citrin and Brian Skaug and has published in prestigious journals such as Nature Communications, Nature Cell Biology and Development.

In The Last Decade

Diana C. Chong

17 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diana C. Chong United States 16 648 296 255 170 100 18 1.0k
Ara Parlakian France 17 947 1.5× 240 0.8× 203 0.8× 157 0.9× 47 0.5× 30 1.3k
Y Hiraki Japan 18 667 1.0× 242 0.8× 156 0.6× 131 0.8× 77 0.8× 30 1.3k
Arianna Caprioli United States 13 830 1.3× 285 1.0× 327 1.3× 87 0.5× 31 0.3× 13 1.1k
Paola Cattaneo Italy 14 866 1.3× 262 0.9× 100 0.4× 103 0.6× 24 0.2× 17 1.3k
William M. Mahoney United States 16 554 0.9× 162 0.5× 255 1.0× 57 0.3× 26 0.3× 25 1.0k
Jason A. Mellad United Kingdom 8 973 1.5× 300 1.0× 240 0.9× 86 0.5× 16 0.2× 8 1.6k
Andrew Beenken United States 9 1.6k 2.5× 233 0.8× 419 1.6× 238 1.4× 27 0.3× 11 2.0k
Rene C. Adam United States 11 681 1.1× 127 0.4× 204 0.8× 76 0.4× 67 0.7× 12 1.2k
Silvia Moimas Italy 18 475 0.7× 222 0.8× 51 0.2× 73 0.4× 41 0.4× 24 947
Yongshun Lin United States 21 836 1.3× 146 0.5× 138 0.5× 150 0.9× 15 0.1× 32 1.2k

Countries citing papers authored by Diana C. Chong

Since Specialization
Citations

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

Fields of papers citing papers by Diana C. Chong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diana C. Chong. 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 Diana C. Chong. The network helps show where Diana C. Chong may publish in the future.

Co-authorship network of co-authors of Diana C. Chong

This figure shows the co-authorship network connecting the top 25 collaborators of Diana C. Chong. A scholar is included among the top collaborators of Diana C. Chong 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 Diana C. Chong. Diana C. Chong 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.
Payne, Laura Beth, et al.. (2021). Pericyte migration and proliferation are tightly synchronized to endothelial cell sprouting dynamics. Integrative Biology. 13(2). 31–43. 21 indexed citations
2.
Chong, Diana C., et al.. (2020). Clonal Analysis of the Neonatal Mouse Heart using Nearest Neighbor Modeling. Journal of Visualized Experiments. 1 indexed citations
3.
Lee, Heon‐Woo, Victoria L. Bautch, Suk‐Won Jin, et al.. (2020). Alk2/ACVR1 and Alk3/BMPR1A Provide Essential Function for Bone Morphogenetic Protein–Induced Retinal AngiogenesisHighlights. UNC Libraries.
4.
Mouillesseaux, Kevin P., et al.. (2018). Developmental SMAD6 loss leads to blood vessel hemorrhage and disrupted endothelial cell junctions. Developmental Biology. 442(2). 199–209. 24 indexed citations
5.
Rojas, Juan D., Virginie Papadopoulou, Tomasz J. Czernuszewicz, et al.. (2018). Ultrasound Measurement of Vascular Density to Evaluate Response to Anti-Angiogenic Therapy in Renal Cell Carcinoma. IEEE Transactions on Biomedical Engineering. 66(3). 873–880. 23 indexed citations
6.
Rojas, Juan D., Fanglue Lin, Yun-Chen Chiang, et al.. (2017). Ultrasound Molecular Imaging of VEGFR-2 in Clear-Cell Renal Cell Carcinoma Tracks Disease Response to Antiangiogenic and Notch-Inhibition Therapy. Theranostics. 8(1). 141–155. 34 indexed citations
7.
Boucher, Joshua M., et al.. (2017). Dynamic alterations in decoy VEGF receptor-1 stability regulate angiogenesis. Nature Communications. 8(1). 15699–15699. 62 indexed citations
8.
Lee, Heon‐Woo, Diana C. Chong, Roxana Ola, et al.. (2017). Alk2/ACVR1 and Alk3/BMPR1A Provide Essential Function for Bone Morphogenetic Protein–Induced Retinal Angiogenesis. Arteriosclerosis Thrombosis and Vascular Biology. 37(4). 657–663. 35 indexed citations
9.
Chong, Diana C., Zhixian Yu, Hailey E. Brighton, James E. Bear, & Victoria L. Bautch. (2017). Tortuous Microvessels Contribute to Wound Healing via Sprouting Angiogenesis. Arteriosclerosis Thrombosis and Vascular Biology. 37(10). 1903–1912. 34 indexed citations
10.
Chong, Diana C., Alethia Villasenor, Judith Magenheim, et al.. (2016). Vascular development in the vertebrate pancreas. Developmental Biology. 420(1). 67–78. 17 indexed citations
11.
Mouillesseaux, Kevin P., Lauren M. Saunders, Erich J. Kushner, et al.. (2016). Notch regulates BMP responsiveness and lateral branching in vessel networks via SMAD6. Nature Communications. 7(1). 13247–13247. 80 indexed citations
12.
Chong, Diana C., et al.. (2011). Stepwise arteriovenous fate acquisition during mammalian vasculogenesis. Developmental Dynamics. 240(9). 2153–2165. 89 indexed citations
13.
Xu, Ke, Anastasia Sacharidou, Diana C. Chong, et al.. (2011). Blood Vessel Tubulogenesis Requires Rasip1 Regulation of GTPase Signaling. Developmental Cell. 20(4). 526–539. 124 indexed citations
14.
Iacovino, Michelina, Diana C. Chong, István Szatmári, et al.. (2010). HoxA3 is an apical regulator of haemogenic endothelium. Nature Cell Biology. 13(1). 72–78. 66 indexed citations
15.
Villasenor, Alethia, Diana C. Chong, Mark Henkemeyer, & Ondine Cleaver. (2010). Epithelial dynamics of pancreatic branching morphogenesis. Development. 137(24). 4295–4305. 171 indexed citations
16.
Xu, Ke, Diana C. Chong, Scott A. Rankin, Aaron M. Zorn, & Ondine Cleaver. (2009). Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation. Developmental Biology. 329(2). 269–279. 51 indexed citations
17.
Villasenor, Alethia, et al.. (2009). BMP and BMP receptor expression during murine organogenesis. Gene Expression Patterns. 9(5). 255–265. 88 indexed citations
18.
Villasenor, Alethia, Diana C. Chong, & Ondine Cleaver. (2008). Biphasic Ngn3 expression in the developing pancreas. Developmental Dynamics. 237(11). 3270–3279. 108 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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