Michael W. J. Cleeter

4.0k total citations · 2 hit papers
24 papers, 3.2k citations indexed

About

Michael W. J. Cleeter is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Michael W. J. Cleeter has authored 24 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Neurology. Recurrent topics in Michael W. J. Cleeter's work include Mitochondrial Function and Pathology (11 papers), ATP Synthase and ATPases Research (10 papers) and Metabolism and Genetic Disorders (5 papers). Michael W. J. Cleeter is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), ATP Synthase and ATPases Research (10 papers) and Metabolism and Genetic Disorders (5 papers). Michael W. J. Cleeter collaborates with scholars based in United Kingdom, United States and Australia. Michael W. J. Cleeter's co-authors include Anthony H.V. Schapira, Jonathan M. Cooper, Victor Darley‐Usmar, Salvador Moncada, Anne Chomyn, Giuseppe Attardi, Russell F. Doolittle, C I Ragan, Sarah J. Tabrizi and Jan‐Willem Taanman and has published in prestigious journals such as Nature, Science and Journal of Biological Chemistry.

In The Last Decade

Michael W. J. Cleeter

24 papers receiving 3.2k citations

Hit Papers

Reversible inhibition of cytochrome c oxidase, the termin... 1985 2026 1998 2012 1994 1985 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael W. J. Cleeter United Kingdom 17 2.0k 938 732 636 446 24 3.2k
Frank N. Gellerich Germany 35 2.8k 1.4× 984 1.0× 689 0.9× 427 0.7× 646 1.4× 92 4.0k
Casper Caspersen United States 15 1.4k 0.7× 1.1k 1.2× 458 0.6× 366 0.6× 330 0.7× 18 2.6k
Ephraïm Yavin Israel 36 2.3k 1.2× 764 0.8× 932 1.3× 413 0.6× 255 0.6× 146 4.4k
Leonhard S. Wolfe Canada 28 1.5k 0.8× 1.3k 1.4× 660 0.9× 368 0.6× 170 0.4× 38 3.3k
Phillip W. Dickson Australia 32 1.7k 0.8× 484 0.5× 916 1.3× 277 0.4× 184 0.4× 77 3.7k
Brian M. Polster United States 34 2.6k 1.3× 787 0.8× 540 0.7× 314 0.5× 265 0.6× 60 3.9k
Nickolay Brustovetsky United States 35 2.5k 1.3× 536 0.6× 1.2k 1.7× 344 0.5× 383 0.9× 66 3.4k
Manus W. Ward Ireland 33 2.3k 1.2× 687 0.7× 1.1k 1.5× 173 0.3× 210 0.5× 60 3.3k
Angela Messina Italy 34 2.7k 1.4× 814 0.9× 542 0.7× 288 0.5× 421 0.9× 84 3.8k
Ove Eriksson Finland 30 1.7k 0.9× 484 0.5× 395 0.5× 220 0.3× 255 0.6× 62 2.7k

Countries citing papers authored by Michael W. J. Cleeter

Since Specialization
Citations

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

Fields of papers citing papers by Michael W. J. Cleeter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael W. J. Cleeter. 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 Michael W. J. Cleeter. The network helps show where Michael W. J. Cleeter may publish in the future.

Co-authorship network of co-authors of Michael W. J. Cleeter

This figure shows the co-authorship network connecting the top 25 collaborators of Michael W. J. Cleeter. A scholar is included among the top collaborators of Michael W. J. Cleeter 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 Michael W. J. Cleeter. Michael W. J. Cleeter 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.
Kilpatrick, Bethan S., Joana Magalhães, Michelle Beavan, et al.. (2015). Endoplasmic reticulum and lysosomal Ca2+ stores are remodelled in GBA1-linked Parkinson disease patient fibroblasts. Cell Calcium. 59(1). 12–20. 64 indexed citations
2.
Cleeter, Michael W. J., Kai‐Yin Chau, Caroline Gluck, et al.. (2012). Glucocerebrosidase inhibition causes mitochondrial dysfunction and free radical damage. Neurochemistry International. 62(1). 1–7. 167 indexed citations
3.
Cleeter, Michael W. J., Jonathan M. Cooper, & Anthony H.V. Schapira. (2001). Nitric oxide enhances MPP+ inhibition of complex I. FEBS Letters. 504(1-2). 50–52. 16 indexed citations
4.
Tabrizi, Sarah J., Michael W. J. Cleeter, John H. Xuereb, et al.. (1999). Biochemical abnormalities and excitotoxicity in Huntington's disease brain. Annals of Neurology. 45(1). 25–32. 370 indexed citations
5.
Schapira, Anthony H.V., Muxin Gu, Jan‐Willem Taanman, et al.. (1998). Mitochondria in the etiology and pathogenesis of parkinson's disease. Annals of Neurology. 44(S1). S89–98. 192 indexed citations
6.
Schapira, Anthony H.V., et al.. (1997). Complex I function in familial and sporadic dystonia. Annals of Neurology. 41(4). 556–559. 28 indexed citations
7.
Cleeter, Michael W. J., Jonathan M. Cooper, Victor Darley‐Usmar, Salvador Moncada, & Anthony H.V. Schapira. (1994). Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide. FEBS Letters. 345(1). 50–54. 1021 indexed citations breakdown →
8.
Poole, Robert K., Lyndall Hatch, Michael W. J. Cleeter, et al.. (1993). Cytochrome bd biosynthesis in Escherichia coli: the sequences of the cydC and cydD genes suggest that they encode the components of an ABC membrane transporter. Molecular Microbiology. 10(2). 421–430. 66 indexed citations
9.
Howitt, Susan M., Michael W. J. Cleeter, Lyndall Hatch, & G B Cox. (1993). Functional stability of the a-subunit of the F0F1-ATPase from Escherichia coli is affected by mutations in three proline residues. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1144(1). 17–21. 6 indexed citations
10.
Schapira, Anthony H.V., A. Hartley, Michael W. J. Cleeter, & Jonathan M. Cooper. (1993). Free radicals and mitochondrial dysfunction in Parkinson's disease. Biochemical Society Transactions. 21(2). 367–370. 30 indexed citations
11.
Cleeter, Michael W. J., Jonathan M. Cooper, & Anthony H.V. Schapira. (1992). Irreversible Inhibition of Mitochondrial Complex I by 1‐Methyl‐4‐Phenylpyridinium: Evidence for Free Radical Involvement. Journal of Neurochemistry. 58(2). 786–789. 298 indexed citations
12.
Frostell, Åsa, I. Mendel-Hartvig, B.Dean Nelson, et al.. (1988). Mitochondrial Autoantigens in Primary Biliary. Scandinavian Journal of Immunology. 28(6). 645–652. 5 indexed citations
13.
Cleeter, Michael W. J., et al.. (1988). Transmembrane organization of mitochondrial NADH dehydrogenase as revealed by radiochemical labelling and cross-linking. Biochemical Journal. 256(2). 529–535. 13 indexed citations
14.
Chomyn, Anne, et al.. (1988). The site of synthesis of the iron-sulfur subunits of the flavoprotein and iron-protein fractions of human NADH dehydrogenase.. Journal of Biological Chemistry. 263(31). 16395–16400. 29 indexed citations
15.
Moreadith, Randall W., Michael W. J. Cleeter, C I Ragan, Mark L. Batshaw, & Albert L. Lehninger. (1987). Congenital deficiency of two polypeptide subunits of the iron-protein fragment of mitochondrial complex I.. Journal of Clinical Investigation. 79(2). 463–467. 33 indexed citations
17.
Chomyn, Anne, et al.. (1986). URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase Subunit. Science. 234(4776). 614–618. 287 indexed citations
18.
Cleeter, Michael W. J., C I Ragan, Randall W. Moreadith, & Albert L. Lehninger. (1985). Selective deficiency of some subunits of mitochondrial NADH dehydrogenase in an infant with congenital lactic acidosis. Biochemical Society Transactions. 13(4). 731–732. 5 indexed citations
19.
Chomyn, Anne, Paolo Mariottini, Michael W. J. Cleeter, et al.. (1985). Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase. Nature. 314(6012). 592–597. 447 indexed citations breakdown →
20.
Cleeter, Michael W. J. & C I Ragan. (1985). The polypeptide composition of the mitochondrial NADH: ubiquinone reductase complex from several mammalian species. Biochemical Journal. 230(3). 739–746. 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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