Matthew Redmann

1.1k total citations
16 papers, 911 citations indexed

About

Matthew Redmann is a scholar working on Molecular Biology, Epidemiology and Geriatrics and Gerontology. According to data from OpenAlex, Matthew Redmann has authored 16 papers receiving a total of 911 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Epidemiology and 4 papers in Geriatrics and Gerontology. Recurrent topics in Matthew Redmann's work include Autophagy in Disease and Therapy (9 papers), Mitochondrial Function and Pathology (5 papers) and Sirtuins and Resveratrol in Medicine (4 papers). Matthew Redmann is often cited by papers focused on Autophagy in Disease and Therapy (9 papers), Mitochondrial Function and Pathology (5 papers) and Sirtuins and Resveratrol in Medicine (4 papers). Matthew Redmann collaborates with scholars based in United States and France. Matthew Redmann's co-authors include Victor Darley‐Usmar, Jianhua Zhang, Matthew Dodson, Willayat Yousuf Wani, Xiaosen Ouyang, Gloria A. Benavides, Michelle S. Johnson, Namakkal S. Rajasekaran, Saranya Ravi and Michaël Boyer‐Guittaut and has published in prestigious journals such as PLoS ONE, Biochemical Journal and Free Radical Biology and Medicine.

In The Last Decade

Matthew Redmann

16 papers receiving 906 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew Redmann United States 11 519 380 162 113 112 16 911
Wiem Chaabane Sweden 7 607 1.2× 422 1.1× 226 1.4× 157 1.4× 141 1.3× 10 1.2k
Hayato Takeuchi Japan 14 780 1.5× 621 1.6× 106 0.7× 131 1.2× 149 1.3× 33 1.5k
Shiori Sekine United States 16 957 1.8× 569 1.5× 184 1.1× 194 1.7× 171 1.5× 25 1.3k
Mónica Álvarez-Córdoba Spain 20 705 1.4× 156 0.4× 161 1.0× 46 0.4× 97 0.9× 44 1.1k
Ayaka Yamamoto Japan 15 487 0.9× 440 1.2× 197 1.2× 49 0.4× 218 1.9× 37 1.4k
Nikolaos Georgakopoulos United Kingdom 12 462 0.9× 267 0.7× 106 0.7× 82 0.7× 42 0.4× 19 844
Pan Chang China 18 563 1.1× 160 0.4× 157 1.0× 121 1.1× 61 0.5× 45 1.1k
Doo Sin Jo South Korea 17 508 1.0× 221 0.6× 94 0.6× 30 0.3× 149 1.3× 41 793
Tomas Schmauck‐Medina Norway 3 331 0.6× 355 0.9× 190 1.2× 46 0.4× 98 0.9× 4 845
Salvatore Rizza Italy 16 544 1.0× 139 0.4× 270 1.7× 44 0.4× 81 0.7× 33 908

Countries citing papers authored by Matthew Redmann

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Redmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Redmann

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

All Works

16 of 16 papers shown
1.
Ouyang, Xiaosen, Willayat Yousuf Wani, Gloria A. Benavides, et al.. (2023). Cathepsin D overexpression in the nervous system rescues lethality and Aβ42 accumulation of cathepsin D systemic knockout in vivo. Acta Pharmaceutica Sinica B. 13(10). 4172–4184. 2 indexed citations
2.
Gordon, Emily R., Sara J. Cooper, Matthew Redmann, et al.. (2021). Novel dopamine receptor 3 antagonists inhibit the growth of primary and temozolomide resistant glioblastoma cells. PLoS ONE. 16(5). e0250649–e0250649. 8 indexed citations
3.
Ouyang, Xiaosen, Israr Ahmad, Michelle S. Johnson, et al.. (2020). Nuclear receptor binding factor 2 (NRBF2) is required for learning and memory. Laboratory Investigation. 100(9). 1238–1251. 9 indexed citations
4.
Redmann, Matthew, Gloria A. Benavides, Willayat Yousuf Wani, et al.. (2018). Methods for assessing mitochondrial quality control mechanisms and cellular consequences in cell culture. Redox Biology. 17. 59–69. 39 indexed citations
5.
Zhang, Sixue, Gloria A. Benavides, Sarah Scott, et al.. (2018). Identification of Compounds That Decrease Glioblastoma Growth and Glucose Uptake in Vitro. ACS Chemical Biology. 13(8). 2048–2057. 28 indexed citations
6.
Wani, Willayat Yousuf, Xiaosen Ouyang, Gloria A. Benavides, et al.. (2017). O-GlcNAc regulation of autophagy and α-synuclein homeostasis; implications for Parkinson’s disease. Molecular Brain. 10(1). 32–32. 78 indexed citations
7.
Redmann, Matthew, Willayat Yousuf Wani, Laura A. Volpicelli‐Daley, Victor Darley‐Usmar, & Jianhua Zhang. (2017). Trehalose does not improve neuronal survival on exposure to alpha-synuclein pre-formed fibrils. Redox Biology. 11. 429–437. 32 indexed citations
8.
Dodson, Matthew, Willayat Yousuf Wani, Matthew Redmann, et al.. (2017). Regulation of autophagy, mitochondrial dynamics, and cellular bioenergetics by 4-hydroxynonenal in primary neurons. Autophagy. 13(11). 1828–1840. 63 indexed citations
9.
Redmann, Matthew, Gloria A. Benavides, Taylor F. Berryhill, et al.. (2016). Inhibition of autophagy with bafilomycin and chloroquine decreases mitochondrial quality and bioenergetic function in primary neurons. Redox Biology. 11. 73–81. 203 indexed citations
10.
11.
Dodson, Matthew, Matthew Redmann, Namakkal S. Rajasekaran, Victor Darley‐Usmar, & Jianhua Zhang. (2015). KEAP1–NRF2 signalling and autophagy in protection against oxidative and reductive proteotoxicity. Biochemical Journal. 469(3). 347–355. 163 indexed citations
12.
Redmann, Matthew, Matthew Dodson, Michaël Boyer‐Guittaut, Victor Darley‐Usmar, & Jianhua Zhang. (2014). Mitophagy mechanisms and role in human diseases. The International Journal of Biochemistry & Cell Biology. 53. 127–133. 118 indexed citations
13.
Giordano, Samantha, Matthew Dodson, Saranya Ravi, et al.. (2014). Bioenergetic adaptation in response to autophagy regulators during rotenone exposure. Journal of Neurochemistry. 131(5). 625–633. 39 indexed citations
14.
Redmann, Matthew, Xiaosen Ouyang, Gloria A. Benavides, et al.. (2013). Novel Contributions of the Lysosomal Pathway to Autophagy, Neuronal Bioenergetics, Oxidative Stress and Neurodegeneration; the Role of Cathepsin D. Free Radical Biology and Medicine. 65. S48–S48. 1 indexed citations
15.
Dodson, Matthew, Qiuli Liang, Michelle S. Johnson, et al.. (2013). Inhibition of glycolysis attenuates 4-hydroxynonenal-dependent autophagy and exacerbates apoptosis in differentiated SH-SY5Y neuroblastoma cells. Autophagy. 9(12). 1996–2008. 51 indexed citations
16.
Zimmermann, Michael, et al.. (1989). [Initial experiences with high-dosage afterloading short-term therapy combined with hyperthermia in non-operated cervix cancer].. PubMed. 30(4). 386–90. 2 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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