Gail V.W. Johnson

31.2k total citations · 2 hit papers
228 papers, 15.5k citations indexed

About

Gail V.W. Johnson is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gail V.W. Johnson has authored 228 papers receiving a total of 15.5k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Molecular Biology, 92 papers in Physiology and 69 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gail V.W. Johnson's work include Alzheimer's disease research and treatments (78 papers), Blood properties and coagulation (54 papers) and Mitochondrial Function and Pathology (39 papers). Gail V.W. Johnson is often cited by papers focused on Alzheimer's disease research and treatments (78 papers), Blood properties and coagulation (54 papers) and Mitochondrial Function and Pathology (39 papers). Gail V.W. Johnson collaborates with scholars based in United States, Canada and Chile. Gail V.W. Johnson's co-authors include Richard S. Jope, William H. Stoothoff, Philip J. Dolan, Mathieu Lesort, Janusz Tucholski, Rodrigo A. Quintanilla, Jae‐Hyeon Cho, Rodney P. Guttmann, Youngnam N. Jin and Tamara Tramišak Milaković and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Gail V.W. Johnson

225 papers receiving 15.2k citations

Hit Papers

The glamour and gloom of ... 2004 2026 2011 2018 2004 2014 400 800 1.2k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Gail V.W. Johnson 7.6k 5.9k 4.0k 2.8k 2.4k 228 15.5k
Pamela Maher 9.5k 1.2× 2.8k 0.5× 2.7k 0.7× 1.8k 0.7× 1.6k 0.7× 229 16.8k
Rajiv R. Ratan 8.7k 1.1× 2.4k 0.4× 3.2k 0.8× 971 0.3× 1.9k 0.8× 164 15.4k
Keqiang Ye 9.0k 1.2× 3.4k 0.6× 3.8k 1.0× 3.8k 1.4× 417 0.2× 244 17.1k
Jean‐Pierre Brion 4.5k 0.6× 6.1k 1.0× 2.8k 0.7× 1.4k 0.5× 431 0.2× 260 10.6k
Charleen T. Chu 6.2k 0.8× 2.6k 0.4× 2.1k 0.5× 1.3k 0.5× 726 0.3× 146 12.7k
Michael P. Vitek 6.1k 0.8× 7.0k 1.2× 2.7k 0.7× 968 0.3× 344 0.1× 181 14.5k
António Zorzano 14.6k 1.9× 5.8k 1.0× 1.8k 0.5× 3.1k 1.1× 797 0.3× 345 23.0k
Jochen Walter 5.3k 0.7× 6.0k 1.0× 2.3k 0.6× 1.6k 0.6× 340 0.1× 148 11.6k
Hiroshi Mori 4.6k 0.6× 6.6k 1.1× 2.0k 0.5× 904 0.3× 436 0.2× 273 12.3k
Carsten Culmsee 7.0k 0.9× 1.7k 0.3× 2.3k 0.6× 710 0.3× 1.5k 0.6× 162 12.7k

Countries citing papers authored by Gail V.W. Johnson

Since Specialization
Citations

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

Fields of papers citing papers by Gail V.W. Johnson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gail V.W. Johnson. 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 Gail V.W. Johnson. The network helps show where Gail V.W. Johnson may publish in the future.

Co-authorship network of co-authors of Gail V.W. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Gail V.W. Johnson. A scholar is included among the top collaborators of Gail V.W. Johnson 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 Gail V.W. Johnson. Gail V.W. Johnson 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.
Ganguly, Upasana, et al.. (2024). Mitochondrial Quality Control in Alzheimer’s Disease: Insights from Caenorhabditis elegans Models. Antioxidants. 13(11). 1343–1343.
2.
Johnson, Gail V.W., et al.. (2023). Deletion of Transglutaminase 2 from Mouse Astrocytes Significantly Improves Their Ability to Promote Neurite Outgrowth on an Inhibitory Matrix. International Journal of Molecular Sciences. 24(7). 6058–6058. 3 indexed citations
3.
Quintanilla, Rodrigo A., et al.. (2023). Caspase-3 cleaved tau impairs mitochondrial function through the opening of the mitochondrial permeability transition pore. Free Radical Biology and Medicine. 208. S164–S164. 1 indexed citations
4.
Nehrke, Keith, et al.. (2023). Site‐specific phosphorylation of tau impacts mitochondrial function and response to stressors. Journal of Neurochemistry. 168(6). 1019–1029. 6 indexed citations
5.
J., Maria Jose Perez, et al.. (2023). Caspase-3 cleaved tau impairs mitochondrial function through the opening of the mitochondrial permeability transition pore. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(1). 166898–166898. 15 indexed citations
6.
Koren, Shon A., et al.. (2023). All-optical spatiotemporal mapping of ROS dynamics across mitochondrial microdomains in situ. Nature Communications. 14(1). 6036–6036. 27 indexed citations
8.
Guha, Sanjib, Gail V.W. Johnson, & Keith Nehrke. (2020). The Crosstalk Between Pathological Tau Phosphorylation and Mitochondrial Dysfunction as a Key to Understanding and Treating Alzheimer’s Disease. Molecular Neurobiology. 57(12). 5103–5120. 40 indexed citations
9.
Guha, Sanjib, Sarah Fischer, Gail V.W. Johnson, & Keith Nehrke. (2020). Tauopathy-associated tau modifications selectively impact neurodegeneration and mitophagy in a novel C. elegans single-copy transgenic model. Molecular Neurodegeneration. 15(1). 65–65. 46 indexed citations
10.
Fu, Hongjun, Andrea Possenti, Rosie Freer, et al.. (2018). A tau homeostasis signature is linked with the cellular and regional vulnerability of excitatory neurons to tau pathology. Nature Neuroscience. 22(1). 47–56. 167 indexed citations
11.
Lin, Chi Hua Sarah, Jun Chen, Zhongtao Zhang, et al.. (2016). Endostatin and transglutaminase 2 are involved in fibrosis of the aging kidney. Kidney International. 89(6). 1281–1292. 43 indexed citations
12.
DiMaio, John, et al.. (2015). Mechanisms of tau and Aβ-induced excitotoxicity. Brain Research. 1634. 119–131. 39 indexed citations
13.
Chesser, Adrianne S., et al.. (2015). Epigallocatechin-3-gallate enhances clearance of phosphorylated tau in primary neurons. Nutritional Neuroscience. 19(1). 21–31. 65 indexed citations
14.
Jo, Chulman, et al.. (2014). Nrf2 reduces levels of phosphorylated tau protein by inducing autophagy adaptor protein NDP52. Nature Communications. 5(1). 3496–3496. 267 indexed citations
15.
Gundemir, Soner, et al.. (2012). Transglutaminase 2 facilitates or ameliorates HIF signaling and ischemic cell death depending on its conformation and localization. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(1). 1–10. 31 indexed citations
16.
Gundemir, Soner, Gozde Colak, Janusz Tucholski, & Gail V.W. Johnson. (2011). Transglutaminase 2: A molecular Swiss army knife. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1823(2). 406–419. 200 indexed citations
17.
Dolan, Philip J., et al.. (2011). The toxicity of tau in Alzheimer disease: turnover, targets and potential therapeutics. Journal of Cellular and Molecular Medicine. 15(8). 1621–1635. 64 indexed citations
18.
Quintanilla, Rodrigo A., et al.. (2009). Caspase-cleaved Tau Expression Induces Mitochondrial Dysfunction in Immortalized Cortical Neurons. Journal of Biological Chemistry. 284(28). 18754–18766. 145 indexed citations
19.
Teal, R. K., John B. Solie, M. L. Stone, et al.. (2004). By-plant precision sensing for variable nitrogen rate application in corn.. 918–932. 2 indexed citations
20.
Stoothoff, William H. & Gail V.W. Johnson. (2004). Tau phosphorylation: physiological and pathological consequences. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1739(2-3). 280–297. 355 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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