Patrick C. Bradshaw

3.5k total citations
47 papers, 2.7k citations indexed

About

Patrick C. Bradshaw is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Patrick C. Bradshaw has authored 47 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 24 papers in Physiology and 9 papers in Clinical Biochemistry. Recurrent topics in Patrick C. Bradshaw's work include Mitochondrial Function and Pathology (21 papers), Alzheimer's disease research and treatments (10 papers) and Metabolism and Genetic Disorders (9 papers). Patrick C. Bradshaw is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), Alzheimer's disease research and treatments (10 papers) and Metabolism and Genetic Disorders (9 papers). Patrick C. Bradshaw collaborates with scholars based in United States, China and Japan. Patrick C. Bradshaw's co-authors include Neil Copes, Douglas R. Pfeiffer, Jeddidiah W. D. Griffin, Clare Edwards, Natasa Dragicevic, John Canfield, Gary W. Arendash, William M. Curtis, Dennis W. Jung and Chuanhai Cao and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Patrick C. Bradshaw

47 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick C. Bradshaw United States 25 1.4k 1000 356 233 222 47 2.7k
Н. Г. Колосова Russia 32 1.7k 1.2× 1.2k 1.2× 171 0.5× 177 0.8× 287 1.3× 216 3.2k
Alba Naudí Spain 36 2.0k 1.4× 1.3k 1.3× 449 1.3× 309 1.3× 84 0.4× 76 3.3k
Igor Rebrin United States 26 1.4k 1.0× 549 0.5× 305 0.9× 221 0.9× 143 0.6× 44 2.3k
Samuel E. Schriner United States 16 1.3k 0.9× 592 0.6× 486 1.4× 144 0.6× 112 0.5× 24 2.0k
Nancy J. Linford United States 18 1.5k 1.1× 778 0.8× 637 1.8× 116 0.5× 209 0.9× 20 2.8k
Alex Bokov United States 23 1.3k 0.9× 1.0k 1.0× 1.0k 2.9× 74 0.3× 341 1.5× 38 2.7k
Samuel T. Henderson United States 23 1.8k 1.3× 1.6k 1.6× 1.3k 3.8× 303 1.3× 531 2.4× 32 3.8k
Antonella Tramutola Italy 31 1.1k 0.8× 1.2k 1.2× 57 0.2× 90 0.4× 81 0.4× 63 2.7k
Rina Recchioni Italy 22 931 0.7× 611 0.6× 116 0.3× 89 0.4× 576 2.6× 70 2.4k
Jeremy M. Van Raamsdonk Canada 33 2.4k 1.7× 618 0.6× 1.1k 3.1× 93 0.4× 239 1.1× 60 3.9k

Countries citing papers authored by Patrick C. Bradshaw

Since Specialization
Citations

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

Fields of papers citing papers by Patrick C. Bradshaw

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick C. Bradshaw. 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 Patrick C. Bradshaw. The network helps show where Patrick C. Bradshaw may publish in the future.

Co-authorship network of co-authors of Patrick C. Bradshaw

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick C. Bradshaw. A scholar is included among the top collaborators of Patrick C. Bradshaw 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 Patrick C. Bradshaw. Patrick C. Bradshaw 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.
Bradshaw, Patrick C., et al.. (2024). The Role of Cardiolipin in Brain Bioenergetics, Neuroinflammation, and Neurodegeneration. Molecular Neurobiology. 62(6). 7022–7040. 5 indexed citations
2.
Veech, Richard L., Michael King, Robert J. Pawlosky, et al.. (2019). The “great” controlling nucleotide coenzymes. IUBMB Life. 71(5). 565–579. 39 indexed citations
3.
Griffin, Jeddidiah W. D. & Patrick C. Bradshaw. (2019). Effects of a high protein diet and liver disease in an in silico model of human ammonia metabolism. Theoretical Biology and Medical Modelling. 16(1). 11–11. 18 indexed citations
4.
Griffin, Jeddidiah W. D. & Patrick C. Bradshaw. (2018). In silico prediction of novel residues involved in amyloid primary nucleation of human I56T and D67H lysozyme. SHILAP Revista de lepidopterología. 18(1). 9–9. 7 indexed citations
5.
Delic, Vedad, Jeddidiah W. D. Griffin, Yumeng Zhang, et al.. (2017). Individual Amino Acid Supplementation Can Improve Energy Metabolism and Decrease ROS Production in Neuronal Cells Overexpressing Alpha-Synuclein. NeuroMolecular Medicine. 19(2-3). 322–344. 22 indexed citations
6.
7.
8.
Edwards, Clare, John Canfield, Neil Copes, et al.. (2015). Mechanisms of amino acid-mediated lifespan extension in Caenorhabditis elegans. BMC Genetics. 16(1). 8–8. 164 indexed citations
9.
Edwards, Clare, et al.. (2014). D-beta-Hydroxybutyrate Extends Lifespan in. Digital Commons - University of South Florida (University of South Florida). 6(8). 621. 29 indexed citations
10.
Edwards, Clare, et al.. (2013). Malate and Fumarate Extend Lifespan in Caenorhabditis elegans. PLoS ONE. 8(3). e58345–e58345. 79 indexed citations
11.
Dragicevic, Natasa, Vedad Delic, Chuanhai Cao, et al.. (2012). Caffeine increases mitochondrial function and blocks melatonin signaling to mitochondria in Alzheimer's mice and cells. Neuropharmacology. 63(8). 1368–1379. 65 indexed citations
12.
Zhu, Yuyan, Huayan Hou, Kavon Rezai‐Zadeh, et al.. (2011). CD45 Deficiency Drives Amyloid-β Peptide Oligomers and Neuronal Loss in Alzheimer's Disease Mice. Journal of Neuroscience. 31(4). 1355–1365. 70 indexed citations
13.
Dragicevic, Natasa, Neil Copes, Jingji Jin, et al.. (2011). Melatonin treatment restores mitochondrial function in Alzheimer’s mice: a mitochondrial protective role of melatonin membrane receptor signaling. Journal of Pineal Research. 51(1). 75–86. 152 indexed citations
14.
Dragicevic, Natasa, Malgorzata Mamcarz, Yuyan Zhu, et al.. (2010). Mitochondrial Amyloid-β Levels are Associated with the Extent of Mitochondrial Dysfunction in Different Brain Regions and the Degree of Cognitive Impairment in Alzheimer's Transgenic Mice. Journal of Alzheimer s Disease. 20(s2). S535–S550. 168 indexed citations
15.
Kujoth, Gregory C., Patrick C. Bradshaw, Suraiya Haroon, & Tomas A. Prolla. (2007). The Role of Mitochondrial DNA Mutations in Mammalian Aging. PLoS Genetics. 3(2). e24–e24. 142 indexed citations
16.
Bradshaw, Patrick C. & Douglas R. Pfeiffer. (2006). Loss of NAD(H) from swollen yeast mitochondria. BMC Biochemistry. 7(1). 3–3. 10 indexed citations
17.
Bradshaw, Patrick C. & David C. Samuels. (2005). A computational model of mitochondrial deoxynucleotide metabolism and DNA replication. American Journal of Physiology-Cell Physiology. 288(5). C989–C1002. 24 indexed citations
18.
Jung, Dennis W., Patrick C. Bradshaw, Monica L. Litsky, & Douglas R. Pfeiffer. (2003). Ca2+ transport in mitochondria from yeast expressing recombinant aequorin. Analytical Biochemistry. 324(2). 258–268. 15 indexed citations
19.
Mannella, Carmen A., Douglas R. Pfeiffer, Patrick C. Bradshaw, et al.. (2001). Topology of the Mitochondrial Inner Membrane: Dynamics and Bioenergetic Implications. IUBMB Life. 52(3-5). 93–100. 194 indexed citations
20.
Bradshaw, Patrick C., Dennis W. Jung, & Douglas R. Pfeiffer. (2001). Free Fatty Acids Activate a Vigorous Ca2+:2H+ Antiport Activity in Yeast Mitochondria. Journal of Biological Chemistry. 276(44). 40502–40509. 21 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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