Philip A. Barker

5.4k total citations · 1 hit paper
42 papers, 4.4k citations indexed

About

Philip A. Barker is a scholar working on Molecular Biology, Cancer Research and Cellular and Molecular Neuroscience. According to data from OpenAlex, Philip A. Barker has authored 42 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 14 papers in Cancer Research and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Philip A. Barker's work include NF-κB Signaling Pathways (13 papers), Cell death mechanisms and regulation (10 papers) and Immune Response and Inflammation (7 papers). Philip A. Barker is often cited by papers focused on NF-κB Signaling Pathways (13 papers), Cell death mechanisms and regulation (10 papers) and Immune Response and Inflammation (7 papers). Philip A. Barker collaborates with scholars based in Canada, United States and Argentina. Philip A. Barker's co-authors include Kathleen M. Dickson, Amir H. Salehi, Mathieu J.M. Bertrand, Stephen J. Morris, Asha Bhakar, Snezana Milutinovic, John W. Gillard, Jon P. Durkin, James B. Jaquith and Alain Boudreault and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and The Journal of Experimental Medicine.

In The Last Decade

Philip A. Barker

40 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

cIAP1 and cIAP2 Facilitate Cancer Cell Survival by Functioning as E3 Ligases that Promote RIP1 Ubiquitination

2008 874 citations Mathieu J.M. Bertrand, Snezana Milutinovic et al. Molecular Cell profile →

Peers

Philip A. Barker

IMMUN

CMN

ONCOL

Isabella A. Graef United States

Susan M. Kaech United States

Douglas S. Annis United States

Sourav Ghosh United States

Robert A. Hipskind France

Vincenzo Coppola United States

Katherine Conant United States

Stephen J. Crocker United States

Theo Mantamadiotis Australia

Chong Chen China

Isabella A. Graef United States

Philip A. Barker

4.1k ×1.5

965 ×0.8

IMMUN

928 ×1.0

CMN

487 ×0.6

637 ×1.3

ONCOL

Citations per year, relative to Philip A. Barker Philip A. Barker (= 1×) peers Isabella A. Graef

Countries citing papers authored by Philip A. Barker

Since Specialization

Citations

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

Fields of papers citing papers by Philip A. Barker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip A. Barker. 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 Philip A. Barker. The network helps show where Philip A. Barker may publish in the future.

Co-authorship network of co-authors of Philip A. Barker

This figure shows the co-authorship network connecting the top 25 collaborators of Philip A. Barker. A scholar is included among the top collaborators of Philip A. Barker 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 Philip A. Barker. Philip A. Barker is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Unsain, Nicolás, et al.. (2016). Calpain-dependent truncated form of TrkB-FL increases in neurodegenerative processes. Molecular and Cellular Neuroscience. 75. 81–92. 21 indexed citations

Vargas, Jorge L. Cueva, Nicolás Unsain, Mark Aurousseau, et al.. (2015). Soluble Tumor Necrosis Factor Alpha Promotes Retinal Ganglion Cell Death in Glaucoma via Calcium-Permeable AMPA Receptor Activation. Journal of Neuroscience. 35(35). 12088–12102. 105 indexed citations

Choe, Katrina Y., Perrine Gaub, Brent Shell, et al.. (2015). High Salt Intake Increases Blood Pressure via BDNF-Mediated Downregulation of KCC2 and Impaired Baroreflex Inhibition of Vasopressin Neurons. Neuron. 85(3). 549–560. 100 indexed citations

Chaineau, Mathilde, et al.. (2014). LRRK 2 localizes to endosomes and interacts with clathrin‐light chains to limit Rac1 activation. EMBO Reports. 16(1). 79–86. 44 indexed citations

Maussion, Gilles, Jennie Yang, Volodymyr Yerko, et al.. (2012). Regulation of a Truncated Form of Tropomyosin-Related Kinase B (TrkB) by Hsa-miR-185* in Frontal Cortex of Suicide Completers. PLoS ONE. 7(6). e39301–e39301. 65 indexed citations

Zhang, Zizhen, Antonio Reboreda, Ángel Alonso, Philip A. Barker, & Philippe Séguéla. (2010). TRPC channels underlie cholinergic plateau potentials and persistent activity in entorhinal cortex. Hippocampus. 21(4). 386–397. 85 indexed citations

Kommaddi, Reddy Peera, Kathleen M. Dickson, & Philip A. Barker. (2010). Stress-induced expression of the p75 neurotrophin receptor is regulated by O-GlcNAcylation of the Sp1 transcription factor. Journal of Neurochemistry. 116(3). 396–405. 22 indexed citations

Lebrun-Julien, Frédéric, Laure Duplan, Vincent Pernet, et al.. (2009). Excitotoxic Death of Retinal NeuronsIn VivoOccurs via a Non-Cell-Autonomous Mechanism. Journal of Neuroscience. 29(17). 5536–5545. 154 indexed citations

Bertrand, Mathieu J.M., Karine Doiron, Katherine Labbè, et al.. (2009). Cellular Inhibitors of Apoptosis cIAP1 and cIAP2 Are Required for Innate Immunity Signaling by the Pattern Recognition Receptors NOD1 and NOD2. Immunity. 30(6). 789–801. 278 indexed citations

10.

Bertrand, Mathieu J.M., Snezana Milutinovic, Kathleen M. Dickson, et al.. (2008). cIAP1 and cIAP2 Facilitate Cancer Cell Survival by Functioning as E3 Ligases that Promote RIP1 Ubiquitination. Molecular Cell. 30(6). 689–700. 874 indexed citations breakdown →

11.

Piton, Amélie, Jacques L. Michaud, Boon‐Peng Hoh, et al.. (2008). Mutations in the calcium-related gene IL1RAPL1 are associated with autism. Human Molecular Genetics. 17(24). 3965–3974. 149 indexed citations

12.

Bertrand, Mathieu J.M., Rajappa S. Kenchappa, M. Leclercq-Smekens, et al.. (2008). NRAGE, a p75NTR adaptor protein, is required for developmental apoptosis in vivo. Cell Death and Differentiation. 15(12). 1921–1929. 58 indexed citations

13.

Furuya, Kazushige, Toshinori Ozaki, Takayuki Hanamoto, et al.. (2007). Stabilization of p73 by Nuclear IκB Kinase-α Mediates Cisplatin-induced Apoptosis. Journal of Biological Chemistry. 282(25). 18365–18378. 25 indexed citations

14.

Sirerol-Piquer, Ma Salomé, et al.. (2006). The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface. Human Molecular Genetics. 15(23). 3436–3445. 76 indexed citations

15.

Salehi, Amir H., Stephen J. Morris, Kathleen M. Dickson, et al.. (2006). AEG3482 Is an Antiapoptotic Compound that Inhibits Jun Kinase Activity and Cell Death through Induced Expression of Heat Shock Protein 70. Chemistry & Biology. 13(2). 213–223. 43 indexed citations

16.

Dickson, Kathleen M., Asha Bhakar, & Philip A. Barker. (2004). TRAF6‐dependent NF‐kB transcriptional activity during mouse development. Developmental Dynamics. 231(1). 122–127. 44 indexed citations

17.

Roux, Philippe P., Geneviève Dorval, Mathieu Boudreau, et al.. (2002). K252a and CEP1347 Are Neuroprotective Compounds That Inhibit Mixed-lineage Kinase-3 and Induce Activation of Akt and ERK. Journal of Biological Chemistry. 277(51). 49473–49480. 88 indexed citations

18.

Roux, Philippe P., Asha Bhakar, Timothy E. Kennedy, & Philip A. Barker. (2001). The p75 Neurotrophin Receptor Activates Akt (Protein Kinase B) through a Phosphatidylinositol 3-Kinase-dependent Pathway. Journal of Biological Chemistry. 276(25). 23097–23104. 125 indexed citations

19.

Wooten, Marie W., M. Lamar Seibenhener, Vidya Mamidipudi, et al.. (2001). The Atypical Protein Kinase C-interacting Protein p62 Is a Scaffold for NF-κB Activation by Nerve Growth Factor. Journal of Biological Chemistry. 276(11). 7709–7712. 149 indexed citations

20.

Bhakar, Asha, et al.. (1999). The p75 Neurotrophin Receptor (p75NTR) Alters Tumor Necrosis Factor-mediated NF-κB Activity under Physiological Conditions, but Direct p75NTR-mediated NF-κB Activation Requires Cell Stress. Journal of Biological Chemistry. 274(30). 21443–21449. 44 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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