Thomas M. Makris

5.7k total citations · 1 hit paper
65 papers, 4.6k citations indexed

About

Thomas M. Makris is a scholar working on Inorganic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Thomas M. Makris has authored 65 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Inorganic Chemistry, 32 papers in Molecular Biology and 25 papers in Pharmacology. Recurrent topics in Thomas M. Makris's work include Metal-Catalyzed Oxygenation Mechanisms (41 papers), Pharmacogenetics and Drug Metabolism (24 papers) and Porphyrin Metabolism and Disorders (10 papers). Thomas M. Makris is often cited by papers focused on Metal-Catalyzed Oxygenation Mechanisms (41 papers), Pharmacogenetics and Drug Metabolism (24 papers) and Porphyrin Metabolism and Disorders (10 papers). Thomas M. Makris collaborates with scholars based in United States, Germany and Canada. Thomas M. Makris's co-authors include Stephen G. Sligar, Ilia G. Denisov, Ilme Schlichting, Job L. Grant, Brian M. Hoffman, Roman Davydov, Chun H. Hsieh, John D. Lipscomb, Kirsty J. McLean and Andrew W. Munro and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Thomas M. Makris

65 papers receiving 4.5k 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.

Structure and Chemistry of Cytochrome P450

2005 1.7k citations Thomas M. Makris et al. profile →

Peers

Thomas M. Makris

PHARM

ONCOL

Michael T. Green United States

Eric D. Coulter United States

Pankaz K. Sharma India

Mark P. Roach United States

Rudi Fasan United States

Osami Shoji Japan

Jonathan Rittle United States

Ronald E. White United States

Tomasz Borowski Poland

Jared C. Lewis United States

Michael T. Green United States

Thomas M. Makris

3.8k ×1.4

1.9k ×1.0

869 ×0.6

PHARM

1.6k ×1.4

1.2k ×1.5

ONCOL

Citations per year, relative to Thomas M. Makris Thomas M. Makris (= 1×) peers Michael T. Green

Countries citing papers authored by Thomas M. Makris

Since Specialization

Citations

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

Fields of papers citing papers by Thomas M. Makris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas M. Makris. 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 Thomas M. Makris. The network helps show where Thomas M. Makris may publish in the future.

Co-authorship network of co-authors of Thomas M. Makris

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas M. Makris. A scholar is included among the top collaborators of Thomas M. Makris 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 Thomas M. Makris. Thomas M. Makris 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

Swartz, Paul, et al.. (2025). The Heme Oxygenase-Like Diiron Enzyme HrmI Reveals Altered Regulatory Mechanisms for Dioxygen Activation and Substrate N-Oxygenation. Journal of the American Chemical Society. 147(33). 30210–30221. 1 indexed citations

Swartz, Paul, et al.. (2024). Assembly of a Heterobimetallic Fe/Mn Cofactor in the para-Aminobenzoate Synthase Chlamydia Protein Associating with Death Domains (CADD) Initiates Long-Range Radical Hole-Hopping. Biochemistry. 63(22). 3020–3029. 3 indexed citations

Li, Xiaojun, et al.. (2023). A Ferric-Superoxide Intermediate Initiates P450-Catalyzed Cyclic Dipeptide Dimerization. Journal of the American Chemical Society. 145(35). 19256–19264. 23 indexed citations

Manley, Olivia M., et al.. (2023). Excision of a Protein-Derived Amine for p-Aminobenzoate Assembly by the Self-Sacrificial Heterobimetallic Protein CADD. Biochemistry. 62(22). 3276–3282. 5 indexed citations

Generoso, Wesley Cardoso, Suman Das, Amanda S. Souza, et al.. (2023). Dimer-assisted mechanism of (un)saturated fatty acid decarboxylation for alkene production. Proceedings of the National Academy of Sciences. 120(22). e2221483120–e2221483120. 15 indexed citations

Manley, Olivia M., Allison K. Stewart, Leonard B. Collins, et al.. (2022). Self-sacrificial tyrosine cleavage by an Fe:Mn oxygenase for the biosynthesis of para -aminobenzoate in Chlamydia trachomatis. Proceedings of the National Academy of Sciences. 119(39). e2210908119–e2210908119. 17 indexed citations

Manley, Olivia M., et al.. (2021). BesC Initiates C–C Cleavage through a Substrate-Triggered and Reactive Diferric-Peroxo Intermediate. Journal of the American Chemical Society. 143(50). 21416–21424. 32 indexed citations

Metavarayuth, Kamolrat, Otega A. Ejegbavwo, Michael L. Myrick, et al.. (2020). Direct Identification of Mixed-Metal Centers in Metal–Organic Frameworks: Cu₃(BTC)₂ Transmetalated with Rh²⁺ Ions. The Journal of Physical Chemistry Letters. 11(19). 8138–8144. 27 indexed citations

Manley, Olivia M., Ruixi Fan, Yisong Guo, & Thomas M. Makris. (2019). Oxidative Decarboxylase UndA Utilizes a Dinuclear Iron Cofactor. Journal of the American Chemical Society. 141(22). 8684–8688. 58 indexed citations

10.

Goode, Robert J. A., et al.. (2019). The Diiron Monooxygenase CmlA from Chloramphenicol Biosynthesis Allows Reconstitution of β-Hydroxylation during Glycopeptide Antibiotic Biosynthesis. ACS Chemical Biology. 14(12). 2932–2941. 14 indexed citations

11.

Kader, Safaa, Mehri Monavarian, Danial Barati, et al.. (2019). Plasmin-Cleavable Nanoparticles for On-Demand Release of Morphogens in Vascularized Osteogenesis. Biomacromolecules. 20(8). 2973–2988. 14 indexed citations

12.

Zhang, Libo, et al.. (2018). Enhanced Arylamine N-Oxygenase Activity of Polymer–Enzyme Assemblies by Facilitating Electron-Transferring Efficiency. Biomacromolecules. 19(3). 918–925. 6 indexed citations

13.

Wybouw, Nicky, Tomasz Borowski, Thomas Van Leeuwen, et al.. (2018). Structural and functional characterization of an intradiol ring-cleavage dioxygenase from the polyphagous spider mite herbivore Tetranychus urticae Koch. Insect Biochemistry and Molecular Biology. 107. 19–30. 10 indexed citations

14.

Hsieh, Chun H., et al.. (2018). Dioxygen Activation by the Biofuel-Generating Cytochrome P450 OleT. ACS Catalysis. 8(10). 9342–9352. 32 indexed citations

15.

Mentink‐Vigier, Frédéric, Thomas M. Makris, Malcolm D. E. Forbes, et al.. (2017). Persistent Radicals of Self‐assembled Benzophenone bis‐Urea Macrocycles: Characterization and Application as a Polarizing Agent for Solid‐state DNP MAS Spectroscopy. Chemistry - A European Journal. 23(34). 8315–8319. 10 indexed citations

16.

Hsieh, Chun H., et al.. (2017). The Enigmatic P450 Decarboxylase OleT Is Capable of, but Evolved To Frustrate, Oxygen Rebound Chemistry. Biochemistry. 56(26). 3347–3357. 62 indexed citations

17.

Khivantsev, Konstantin, Alessandro Biancardi, Mahdi Fathizadeh, et al.. (2017). Catalytic N−H Bond Activation and Breaking by a Well‐Defined Co^II₁O₄ Site of a Heterogeneous Catalyst. ChemCatChem. 10(4). 736–742. 9 indexed citations

18.

Makris, Thomas M., et al.. (2017). Recruitment and Regulation of the Non-ribosomal Peptide Synthetase Modifying Cytochrome P450 Involved in Nikkomycin Biosynthesis. ACS Chemical Biology. 12(5). 1316–1326. 10 indexed citations

19.

Smith, Mark D., et al.. (2017). Activation of C–H Bonds of Alkyl- and Arylnitriles by the TaCl₅–PPh₃ Lewis Pair. Inorganic Chemistry. 56(19). 11798–11803. 14 indexed citations

20.

Hsieh, Chun H. & Thomas M. Makris. (2016). Expanding the substrate scope and reactivity of cytochrome P450 OleT. Biochemical and Biophysical Research Communications. 476(4). 462–466. 30 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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