Fred Wong

1.3k total citations
20 papers, 1.2k citations indexed

About

Fred Wong is a scholar working on Molecular Biology, Immunology and Cancer Research. According to data from OpenAlex, Fred Wong has authored 20 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Immunology and 7 papers in Cancer Research. Recurrent topics in Fred Wong's work include Cell death mechanisms and regulation (7 papers), Immune Response and Inflammation (7 papers) and Developmental Biology and Gene Regulation (7 papers). Fred Wong is often cited by papers focused on Cell death mechanisms and regulation (7 papers), Immune Response and Inflammation (7 papers) and Developmental Biology and Gene Regulation (7 papers). Fred Wong collaborates with scholars based in Canada, United States and France. Fred Wong's co-authors include Aly Karsan, Patrick J. Duriez, Michela Noseda, John M. Harlan, Christopher Hull, Graeme W. McLean, Leroy Hood, Kevin G. Leong, Linda Chang and Esther Yee and has published in prestigious journals such as Journal of Biological Chemistry, Blood and The Journal of Immunology.

In The Last Decade

Fred Wong

20 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fred Wong Canada 16 720 425 280 101 81 20 1.2k
Ana Rebane Estonia 27 909 1.3× 1.0k 2.4× 481 1.7× 122 1.2× 93 1.1× 54 2.3k
Carla Mazzeo Spain 15 607 0.8× 281 0.7× 235 0.8× 63 0.6× 94 1.2× 19 983
Margaret Solon United States 15 670 0.9× 550 1.3× 220 0.8× 109 1.1× 227 2.8× 20 1.3k
Maureen A. Harrington United States 21 754 1.0× 319 0.8× 276 1.0× 194 1.9× 91 1.1× 45 1.2k
Stephen Bellum United States 15 529 0.7× 182 0.4× 121 0.4× 90 0.9× 129 1.6× 20 909
Daniela Giunciuglio Italy 15 500 0.7× 226 0.5× 216 0.8× 261 2.6× 61 0.8× 18 1.0k
Mark Baer United States 15 582 0.8× 485 1.1× 277 1.0× 222 2.2× 54 0.7× 23 1.3k
Fanyong Meng United States 17 572 0.8× 809 1.9× 147 0.5× 216 2.1× 107 1.3× 21 1.5k
Donatella Starace Italy 18 425 0.6× 594 1.4× 190 0.7× 161 1.6× 89 1.1× 23 1.2k
Vito Ruggiero Italy 14 415 0.6× 821 1.9× 197 0.7× 201 2.0× 56 0.7× 29 1.3k

Countries citing papers authored by Fred Wong

Since Specialization
Citations

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

Fields of papers citing papers by Fred Wong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fred Wong. 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 Fred Wong. The network helps show where Fred Wong may publish in the future.

Co-authorship network of co-authors of Fred Wong

This figure shows the co-authorship network connecting the top 25 collaborators of Fred Wong. A scholar is included among the top collaborators of Fred Wong 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 Fred Wong. Fred Wong 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.
Dijke, E., et al.. (2017). Regulation of Human CD27+IgM+ B Cell Activation by Cis-Binding of the Inhibitory Molecule CD22 to CD22 Ligand (CD22L). Transplantation. 101(5S-3). S5–S5. 1 indexed citations
2.
Patenaude, Alexandre, Fred Wong, Alastair H. Kyle, et al.. (2015). A novel population of local pericyte precursor cells in tumor stroma that require Notch signaling for differentiation. Microvascular Research. 101. 38–47. 12 indexed citations
3.
Patenaude, Alexandre, Megan Fuller, Linda Chang, et al.. (2014). Endothelial-Specific Notch Blockade Inhibits Vascular Function and Tumor Growth through an eNOS-Dependent Mechanism. Cancer Research. 74(9). 2402–2411. 29 indexed citations
4.
Chang, Linda, Fred Wong, Kyle Niessen, & Aly Karsan. (2013). Notch activation promotes endothelial survival through a PI3K-Slug axis. Microvascular Research. 89. 80–85. 5 indexed citations
5.
Reeves, R. Keith, T. Idil Apak Evans, Jacqueline Gillis, et al.. (2012). SIV Infection Induces Accumulation of Plasmacytoid Dendritic Cells in the Gut Mucosa. The Journal of Infectious Diseases. 206(9). 1462–1468. 61 indexed citations
6.
Wong, Nelson K.Y., Megan Fuller, Sandy Sung, Fred Wong, & Aly Karsan. (2012). Heterogeneity of breast cancer stem cells as evidenced with Notch‐dependent and Notch‐independent populations. Cancer Medicine. 1(2). 105–113. 22 indexed citations
7.
Dauphinee, Shauna, et al.. (2011). Heterotrimeric Gi/Goproteins modulate endothelial TLR signaling independent of the MyD88-dependent pathway. American Journal of Physiology-Heart and Circulatory Physiology. 301(6). H2246–H2253. 24 indexed citations
8.
Reeves, R. Keith, Jacqueline Gillis, Fred Wong, & R. Paul Johnson. (2009). Vaccination with SIVmac239Δnef activates CD4+ T cells in the absence of CD4+ T‐cell loss. Journal of Medical Primatology. 38(s1). 8–16. 8 indexed citations
9.
Noseda, Michela, Yang‐Xin Fu, Kyle Niessen, et al.. (2006). Smooth Muscle α-Actin Is a Direct Target of Notch/CSL. Circulation Research. 98(12). 1468–1470. 152 indexed citations
10.
Larrivée, Bruno, Ingrid L. Pollet, David E. Williams, et al.. (2006). Identification of Sokotrasterol Sulfate As a Novel Proangiogenic Steroid. Circulation Research. 99(3). 257–265. 15 indexed citations
11.
Duriez, Patrick J., et al.. (2004). Notch4 Inhibits Endothelial Apoptosis via RBP-Jκ-dependent and -independent Pathways. Journal of Biological Chemistry. 279(12). 11657–11663. 99 indexed citations
12.
Wong, Fred, Christopher Hull, Rachel Zhande, Jennifer Law, & Aly Karsan. (2004). Lipopolysaccharide initiates a TRAF6-mediated endothelial survival signal. Blood. 103(12). 4520–4526. 29 indexed citations
13.
Duriez, Patrick J., Bruno Larrivée, Linda Chang, et al.. (2004). Notch4-induced inhibition of endothelial sprouting requires the ankyrin repeats and involves signaling through RBP-Jκ. Blood. 104(6). 1760–1768. 36 indexed citations
14.
15.
Hull, Christopher, Graeme W. McLean, Fred Wong, Patrick J. Duriez, & Aly Karsan. (2002). Lipopolysaccharide Signals an Endothelial Apoptosis Pathway Through TNF Receptor-Associated Factor 6-Mediated Activation of c-Jun NH2-Terminal Kinase. The Journal of Immunology. 169(5). 2611–2618. 98 indexed citations
16.
Leong, Kevin G., Linheng Li, Michela Noseda, et al.. (2002). Activated Notch4 Inhibits Angiogenesis: Role of β1-Integrin Activation. Molecular and Cellular Biology. 22(8). 2830–2841. 143 indexed citations
17.
Duriez, Patrick J., Fred Wong, Katerina Dorovini‐Zis, Réza Shahidi, & Aly Karsan. (2000). A1 Functions at the Mitochondria to Delay Endothelial Apoptosis in Response to Tumor Necrosis Factor. Journal of Biological Chemistry. 275(24). 18099–18107. 86 indexed citations
18.
Choi, Kyung Bok, Fred Wong, John M. Harlan, et al.. (1998). Lipopolysaccharide Mediates Endothelial Apoptosis by a FADD-dependent Pathway. Journal of Biological Chemistry. 273(32). 20185–20188. 136 indexed citations
19.
Yee, Esther, et al.. (1998). Lipopolysaccharide Induces the Antiapoptotic Molecules, A1 and A20, in Microvascular Endothelial Cells. Blood. 92(8). 2759–2765. 126 indexed citations
20.
Yee, Esther, et al.. (1998). Lipopolysaccharide Induces the Antiapoptotic Molecules, A1 and A20, in Microvascular Endothelial Cells. Blood. 92(8). 2759–2765. 16 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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