Van N. Pham

3.2k total citations · 1 hit paper
24 papers, 2.2k citations indexed

About

Van N. Pham is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Van N. Pham has authored 24 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Cell Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Van N. Pham's work include Zebrafish Biomedical Research Applications (13 papers), Angiogenesis and VEGF in Cancer (10 papers) and Congenital heart defects research (6 papers). Van N. Pham is often cited by papers focused on Zebrafish Biomedical Research Applications (13 papers), Angiogenesis and VEGF in Cancer (10 papers) and Congenital heart defects research (6 papers). Van N. Pham collaborates with scholars based in United States, Hungary and Pakistan. Van N. Pham's co-authors include Brant M. Weinstein, Nathan D. Lawson, José A. Campos‐Ortega, Ajay Chitnis, Cheol‐Hee Kim, Nico Scheer, Beth L. Roman, Daniel Castranova, Mark C. Fishman and Sarah J. Childs and has published in prestigious journals such as Nature Communications, Blood and Molecular and Cellular Biology.

In The Last Decade

Van N. Pham

23 papers receiving 2.2k citations

Hit Papers

Notch signaling is required for arterial-venous different... 2001 2026 2009 2017 2001 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Van N. Pham United States 19 1.6k 1.0k 371 208 176 24 2.2k
Suk‐Won Jin United States 20 1.8k 1.1× 1.0k 1.0× 256 0.7× 283 1.4× 231 1.3× 34 2.7k
Arndt F. Siekmann Germany 24 2.1k 1.3× 1.2k 1.2× 285 0.8× 318 1.5× 278 1.6× 43 3.0k
Hanna M. Eilken Germany 11 1.2k 0.7× 553 0.5× 177 0.5× 218 1.0× 216 1.2× 13 1.9k
Melih Acar United States 17 1.2k 0.7× 529 0.5× 279 0.8× 178 0.9× 506 2.9× 26 2.3k
Inga Sörensen Germany 10 1.4k 0.8× 419 0.4× 231 0.6× 421 2.0× 166 0.9× 10 2.1k
Lisa D. Urness United States 17 1.6k 1.0× 308 0.3× 584 1.6× 247 1.2× 139 0.8× 22 2.4k
Hiroshi Hanafusa Japan 19 1.9k 1.1× 488 0.5× 153 0.4× 166 0.8× 214 1.2× 38 2.3k
Soline Estrach France 20 1.3k 0.8× 652 0.6× 507 1.4× 272 1.3× 150 0.9× 27 2.0k
Alison Miyamoto United States 14 1.7k 1.0× 292 0.3× 162 0.4× 194 0.9× 156 0.9× 17 2.1k
Jon D. Larson United States 16 1.5k 0.9× 790 0.8× 133 0.4× 220 1.1× 192 1.1× 29 2.0k

Countries citing papers authored by Van N. Pham

Since Specialization
Citations

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

Fields of papers citing papers by Van N. Pham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Van N. Pham. 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 Van N. Pham. The network helps show where Van N. Pham may publish in the future.

Co-authorship network of co-authors of Van N. Pham

This figure shows the co-authorship network connecting the top 25 collaborators of Van N. Pham. A scholar is included among the top collaborators of Van N. Pham 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 Van N. Pham. Van N. Pham 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.
Burns, Margaret C., Andrew Davis, Van N. Pham, et al.. (2024). Angiogenesis is limited by LIC1-mediated lysosomal trafficking. Angiogenesis. 27(4). 943–962.
2.
Stratman, Amber N., Margaret C. Burns, Olivia Farrelly, et al.. (2020). Chemokine mediated signalling within arteries promotes vascular smooth muscle cell recruitment. Communications Biology. 3(1). 734–734. 28 indexed citations
3.
Stratman, Amber N., Olivia Farrelly, Constantinos M. Mikelis, et al.. (2020). Anti-angiogenic effects of VEGF stimulation on endothelium deficient in phosphoinositide recycling. Nature Communications. 11(1). 1204–1204. 19 indexed citations
5.
Jung, Hyun Min, Daniel Castranova, Matthew Swift, et al.. (2017). Development of the larval lymphatic system in the zebrafish. Development. 144(11). 2070–2081. 59 indexed citations
6.
Gore, Aniket V., James Iben, Kristin Johnson, et al.. (2016). Epigenetic regulation of hematopoiesis by DNA methylation. eLife. 5. e11813–e11813. 32 indexed citations
7.
Moore, John C., Timothy S. Mulligan, Daniel Castranova, et al.. (2016). T Cell Immune Deficiency in zap70 Mutant Zebrafish. Molecular and Cellular Biology. 36(23). 2868–2876. 33 indexed citations
8.
Castranova, Daniel, Andrew Davis, Brigid D. Lo, et al.. (2016). Aminoacyl-Transfer RNA Synthetase Deficiency Promotes Angiogenesis via the Unfolded Protein Response Pathway. Arteriosclerosis Thrombosis and Vascular Biology. 36(4). 655–662. 19 indexed citations
9.
Yu, Jianxin, Daniel Castranova, Van N. Pham, & Brant M. Weinstein. (2015). Single cell analysis of endothelial morphogenesis in vivo. Development. 142(17). 2951–61. 41 indexed citations
10.
Ulrich, Florian, Jorge Carretero-Ortega, Carlos F. Narváez, et al.. (2015). Reck enables cerebrovascular development by promoting canonical Wnt signaling. Development. 143(1). 1055–1055. 52 indexed citations
11.
Swift, Matthew, et al.. (2014). SoxF factors and Notch regulate nr2f2 gene expression during venous differentiation in zebrafish. Developmental Biology. 390(2). 116–125. 42 indexed citations
12.
Pan, Weijun, Van N. Pham, Amber N. Stratman, et al.. (2012). CDP-diacylglycerol synthetase-controlled phosphoinositide availability limits VEGFA signaling and vascular morphogenesis. Blood. 120(2). 489–498. 31 indexed citations
13.
Miskinyte, S., Matthew G. Butler, Dominique Hervé, et al.. (2011). Loss of BRCC3 Deubiquitinating Enzyme Leads to Abnormal Angiogenesis and Is Associated with Syndromic Moyamoya. The American Journal of Human Genetics. 88(6). 718–728. 86 indexed citations
14.
Anderson, Matthew J., Van N. Pham, Andreas M. Vogel, Brant M. Weinstein, & Beth L. Roman. (2008). Loss of unc45a precipitates arteriovenous shunting in the aortic arches. Developmental Biology. 318(2). 258–267. 51 indexed citations
15.
Pham, Van N., Nathan D. Lawson, Joshua W. Mugford, et al.. (2006). Combinatorial function of ETS transcription factors in the developing vasculature. Developmental Biology. 303(2). 772–783. 163 indexed citations
16.
Shaw, Kenna M., Van N. Pham, Makoto Kamei, et al.. (2006). fused‐somites–like mutants exhibit defects in trunk vessel patterning. Developmental Dynamics. 235(7). 1753–1760. 18 indexed citations
17.
Pollard, Steven M., Maddy Parsons, Makoto Kamei, et al.. (2005). Essential and overlapping roles for laminin α chains in notochord and blood vessel formation. Developmental Biology. 289(1). 64–76. 82 indexed citations
18.
Torres‐Vázquez, Jesús, Aaron D. Gitler, Sherri D. Fraser, et al.. (2004). Semaphorin-Plexin Signaling Guides Patterning of the Developing Vasculature. Developmental Cell. 7(1). 117–123. 301 indexed citations
19.
Lawson, Nathan D., Nico Scheer, Van N. Pham, et al.. (2001). Notch signaling is required for arterial-venous differentiation during embryonic vascular development. Development. 128(19). 3675–3683. 698 indexed citations breakdown →
20.
Pham, Van N., Beth L. Roman, & Brant M. Weinstein. (2001). Isolation and expression analysis of three zebrafish angiopoietin genes. Developmental Dynamics. 221(4). 470–474. 46 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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