Thomas Tomasiak

867 total citations
19 papers, 680 citations indexed

About

Thomas Tomasiak is a scholar working on Molecular Biology, Oncology and Nutrition and Dietetics. According to data from OpenAlex, Thomas Tomasiak has authored 19 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Oncology and 5 papers in Nutrition and Dietetics. Recurrent topics in Thomas Tomasiak's work include Drug Transport and Resistance Mechanisms (7 papers), Trace Elements in Health (5 papers) and Protein Structure and Dynamics (4 papers). Thomas Tomasiak is often cited by papers focused on Drug Transport and Resistance Mechanisms (7 papers), Trace Elements in Health (5 papers) and Protein Structure and Dynamics (4 papers). Thomas Tomasiak collaborates with scholars based in United States, Germany and United Kingdom. Thomas Tomasiak's co-authors include Robert M. Stroud, Janet Finer-Moore, Richard D. Cannon, Joel D. A. Tyndall, Brian C. Monk, Joseph D. O’Connell, Jeffrey G. McDonald, Franziska U. Huschmann, Mikhail V. Keniya and Gary Cecchini and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Thomas Tomasiak

17 papers receiving 676 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Tomasiak United States 11 393 162 135 86 69 19 680
Agnes Rinaldo-Matthis Sweden 18 670 1.7× 101 0.6× 91 0.7× 99 1.2× 109 1.6× 35 1.0k
Sachin Surade United Kingdom 14 485 1.2× 68 0.4× 185 1.4× 49 0.6× 87 1.3× 18 672
J. Wielens Australia 14 516 1.3× 98 0.6× 137 1.0× 56 0.7× 82 1.2× 17 740
Luís Fernando Saraiva Macedo Timmers Brazil 16 558 1.4× 52 0.3× 214 1.6× 97 1.1× 156 2.3× 68 908
Florence Leroux France 15 502 1.3× 117 0.7× 263 1.9× 138 1.6× 200 2.9× 42 876
Franziska U. Huschmann Germany 9 431 1.1× 58 0.4× 95 0.7× 65 0.8× 111 1.6× 12 704
Elena Arutyunova Canada 17 447 1.1× 110 0.7× 390 2.9× 65 0.8× 130 1.9× 30 1.0k
Claudia Jessen‐Trefzer Germany 13 497 1.3× 71 0.4× 205 1.5× 103 1.2× 189 2.7× 24 734
Gabriela Mustata United States 14 351 0.9× 49 0.3× 101 0.7× 82 1.0× 102 1.5× 17 592
S.K. Palaninathan United States 16 762 1.9× 182 1.1× 197 1.5× 90 1.0× 219 3.2× 17 1.3k

Countries citing papers authored by Thomas Tomasiak

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Tomasiak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Tomasiak

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

All Works

19 of 19 papers shown
1.
Khandelwal, Nitesh, et al.. (2025). Structural Basis for Oxidized Glutathione Recognition by Yeast Cadmium Factor 1. Journal of the American Chemical Society. 147(30). 26139–26148.
2.
Thaker, Tarjani, et al.. (2024). The N-terminal signature motif on the transporter MCT1 is critical for CD147-mediated trafficking. Journal of Biological Chemistry. 300(6). 107333–107333.
3.
Khandelwal, Nitesh & Thomas Tomasiak. (2024). Structural basis for autoinhibition by the dephosphorylated regulatory domain of Ycf1. Nature Communications. 15(1). 2389–2389. 5 indexed citations
4.
Galgiani, John N., Lisa F. Shubitz, Marc J. Orbach, et al.. (2022). Vaccines to Prevent Coccidioidomycosis: A Gene-Deletion Mutant of Coccidioides Posadasii as a Viable Candidate for Human Trials. Journal of Fungi. 8(8). 838–838. 12 indexed citations
5.
Khandelwal, Nitesh, et al.. (2022). The structural basis for regulation of the glutathione transporter Ycf1 by regulatory domain phosphorylation. Nature Communications. 13(1). 1278–1278. 30 indexed citations
6.
Khandelwal, Nitesh, et al.. (2021). A Conserved Motif in Intracellular Loop 1 Stabilizes the Outward-Facing Conformation of TmrAB. Journal of Molecular Biology. 433(16). 166834–166834. 5 indexed citations
7.
Thaker, Tarjani, Smriti Mishra, Wenchang Zhou, et al.. (2021). Asymmetric drug binding in an ATP-loaded inward-facing state of an ABC transporter. Nature Chemical Biology. 18(2). 226–235. 19 indexed citations
8.
Thaker, Tarjani, et al.. (2020). The role of novel COQ8B mutations in glomerulopathy and related kidney defects. American Journal of Medical Genetics Part A. 185(1). 60–67. 4 indexed citations
9.
Noll, A., Christoph Thomas, Ahmad Reza Mehdipour, et al.. (2017). Crystal structure and mechanistic basis of a functional homolog of the antigen transporter TAP. Proceedings of the National Academy of Sciences. 114(4). E438–E447. 64 indexed citations
10.
Tomasiak, Thomas, Prashant K. Singh, Victoria Yankovskaya, et al.. (2017). New crystal forms of the integral membrane Escherichia coli quinol:fumarate reductase suggest that ligands control domain movement. Journal of Structural Biology. 202(1). 100–104. 8 indexed citations
12.
Monk, Brian C., Thomas Tomasiak, Mikhail V. Keniya, et al.. (2014). Architecture of a single membrane spanning cytochrome P450 suggests constraints that orient the catalytic domain relative to a bilayer. Proceedings of the National Academy of Sciences. 111(10). 3865–3870. 226 indexed citations
13.
Kim, Jung‐Min, Shenping Wu, Thomas Tomasiak, et al.. (2014). Subnanometre-resolution electron cryomicroscopy structure of a heterodimeric ABC exporter. Nature. 517(7534). 396–400. 97 indexed citations
14.
Tomasiak, Thomas, et al.. (2014). General qPCR and Plate Reader Methods for Rapid Optimization of Membrane Protein Purification and Crystallization Using Thermostability Assays. Current Protocols in Protein Science. 77(1). 29.11.1–29.11.14. 15 indexed citations
15.
Singh, Prashant K., et al.. (2013). Plasticity of the Quinone-binding Site of the Complex II Homolog Quinol:Fumarate Reductase. Journal of Biological Chemistry. 288(34). 24293–24301. 10 indexed citations
16.
Bensing, Barbara A., Yan Q. Xiong, Bruce J. Melancon, et al.. (2011). A Structural Model for Binding of the Serine-Rich Repeat Adhesin GspB to Host Carbohydrate Receptors. PLoS Pathogens. 7(7). e1002112–e1002112. 72 indexed citations
17.
Tomasiak, Thomas, Tara L. Archuleta, Juni Andréll, et al.. (2010). Geometric Restraint Drives On- and Off-pathway Catalysis by the Escherichia coli Menaquinol:Fumarate Reductase. Journal of Biological Chemistry. 286(4). 3047–3056. 21 indexed citations
18.
Tomasiak, Thomas, Elena Maklashina, Gary Cecchini, & T.M. Iverson. (2008). A Threonine on the Active Site Loop Controls Transition State Formation in Escherichia coli Respiratory Complex II. Journal of Biological Chemistry. 283(22). 15460–15468. 26 indexed citations
19.
Tomasiak, Thomas, Gary Cecchini, & T.M. Iverson. (2007). Succinate as Donor; Fumarate as Acceptor. EcoSal Plus. 2(2). 7 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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