M. Groll

18.5k total citations · 2 hit papers
254 papers, 14.5k citations indexed

About

M. Groll is a scholar working on Molecular Biology, Oncology and Pharmacology. According to data from OpenAlex, M. Groll has authored 254 papers receiving a total of 14.5k indexed citations (citations by other indexed papers that have themselves been cited), including 216 papers in Molecular Biology, 87 papers in Oncology and 35 papers in Pharmacology. Recurrent topics in M. Groll's work include Ubiquitin and proteasome pathways (119 papers), Peptidase Inhibition and Analysis (85 papers) and Glycosylation and Glycoproteins Research (60 papers). M. Groll is often cited by papers focused on Ubiquitin and proteasome pathways (119 papers), Peptidase Inhibition and Analysis (85 papers) and Glycosylation and Glycoproteins Research (60 papers). M. Groll collaborates with scholars based in Germany, United States and Switzerland. M. Groll's co-authors include Robert Huber, Matthias Bochtler, Lars Ditzel, E.M. Huber, H.D. Bartunik, Jan Löwe, Daniela Stock, Ljudmila Borissenko, Wolfgang Heinemeyer and Luis Moroder and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

M. Groll

243 papers receiving 14.3k citations

Hit Papers

Structure of 20S proteasome from yeast at 2.4Å resolution 1997 2026 2006 2016 1997 2000 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Groll Germany 61 12.2k 4.2k 2.3k 1.5k 1.4k 254 14.5k
M.E.M. Noble United Kingdom 63 9.9k 0.8× 2.9k 0.7× 2.9k 1.3× 1.5k 1.0× 556 0.4× 144 13.7k
William G. Bornmann United States 66 7.7k 0.6× 3.6k 0.9× 687 0.3× 2.9k 1.9× 799 0.6× 167 14.7k
Bruce C. Baguley New Zealand 64 9.1k 0.7× 4.3k 1.0× 1.1k 0.5× 3.8k 2.5× 297 0.2× 384 15.0k
Alan Eastman United States 61 9.0k 0.7× 5.2k 1.2× 1.1k 0.5× 1.4k 0.9× 346 0.2× 185 12.5k
Mirosław Cygler Canada 59 10.2k 0.8× 717 0.2× 2.1k 0.9× 1.4k 0.9× 451 0.3× 246 13.8k
Ross L. Stein United States 41 5.8k 0.5× 2.1k 0.5× 1.1k 0.5× 795 0.5× 774 0.5× 131 8.1k
Peter E. Czabotar Australia 47 8.9k 0.7× 2.1k 0.5× 794 0.4× 621 0.4× 1.2k 0.8× 98 11.8k
Faustino Mollinedo Spain 55 5.8k 0.5× 1.1k 0.3× 1.5k 0.7× 979 0.6× 725 0.5× 207 9.6k
James C. Powers United States 54 5.7k 0.5× 2.6k 0.6× 741 0.3× 2.2k 1.4× 591 0.4× 197 10.8k
Robert M. Immormino United States 18 9.2k 0.8× 919 0.2× 1.1k 0.5× 603 0.4× 808 0.6× 34 12.7k

Countries citing papers authored by M. Groll

Since Specialization
Citations

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

Fields of papers citing papers by M. Groll

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Groll

This figure shows the co-authorship network connecting the top 25 collaborators of M. Groll. A scholar is included among the top collaborators of M. Groll 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 M. Groll. M. Groll 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
2.
Klassen, R. Bryan, et al.. (2025). A Luminescence-Based Screening Platform for Lanthanide-Binding Peptides and Proteins. ACS Chemical Biology. 20(12). 2897–2906.
3.
Bernard, Charles, Carine Lombard, Ville R. I. Kaila, et al.. (2025). Molecular basis for azetidine-2-carboxylic acid biosynthesis. Nature Communications. 16(1). 1348–1348. 5 indexed citations
4.
Li, Heng, et al.. (2025). Structure-Guided Engineering of a Bacterial Sesterterpene Synthase for Sesterviridene Diversification. Journal of the American Chemical Society. 147(38). 34901–34909.
5.
Су, Ли, E.M. Huber, Edna Bode, et al.. (2024). Isofunctional but Structurally Different Methyltransferases for Dithiolopyrrolone Diversification. Angewandte Chemie International Edition. 63(49). e202410799–e202410799. 2 indexed citations
6.
Staudt, Nicole, et al.. (2023). Characterization of the cystargolide biosynthetic gene cluster and functional analysis of the methyltransferase CysG. Journal of Biological Chemistry. 300(1). 105507–105507. 3 indexed citations
7.
Chen, Shuyu, Manuel Hitzenberger, Stephan M. Hacker, et al.. (2023). A Chemical Proteomic Strategy Reveals Inhibitors of Lipoate Salvage in Bacteria and Parasites. Angewandte Chemie International Edition. 62(31). e202304533–e202304533. 4 indexed citations
8.
Shi, Yi‐Ming, Yan‐Ni Shi, Shabbir Ahmed, et al.. (2022). Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteria. Nature Chemistry. 14(6). 701–712. 70 indexed citations
9.
Ishida, Keishi, et al.. (2022). Pathogenic bacteria remodel central metabolic enzyme to build a cyclopropanol warhead. Nature Chemistry. 14(8). 884–890. 21 indexed citations
10.
Molloy, Evelyn M., et al.. (2022). A Specialized Polythioamide‐Binding Protein Confers Antibiotic Self‐Resistance in Anaerobic Bacteria. Angewandte Chemie International Edition. 61(37). e202206168–e202206168. 2 indexed citations
11.
Scherlach, Kirstin, Daniel H. Scharf, Axel A. Brakhage, et al.. (2021). Strukturelle und mechanistische Einblicke in die Bildung der C‐S‐Bindungen in Gliotoxin. Angewandte Chemie. 133(25). 14307–14314. 1 indexed citations
12.
Hortschansky, Peter, Matthias Misslinger, Fabio Gsaller, et al.. (2020). Structural basis of HapEP88L-linked antifungal triazole resistance in Aspergillus fumigatus. Life Science Alliance. 3(7). e202000729–e202000729. 18 indexed citations
13.
Zhou, Qiuqin, et al.. (2020). Structural snapshots of the minimal PKS system responsible for octaketide biosynthesis. Nature Chemistry. 12(8). 755–763. 36 indexed citations
14.
Fischer, Johannes, Anand N. P. Radhakrishnan, Meina Liu, et al.. (2019). Robust and Versatile Host Protein for the Design and Evaluation of Artificial Metal Centers. ACS Catalysis. 9(12). 11371–11380. 10 indexed citations
15.
DuBay, Kateri H., Katharina Iwan, Laura Osorio‐Planes, et al.. (2018). A Predictive Approach for the Optical Control of Carbonic Anhydrase II Activity. ACS Chemical Biology. 13(3). 793–800. 21 indexed citations
16.
Groll, M., Henry Nguyen, Sreekumar Vellalath, & Daniel Romo. (2018). (−)-Homosalinosporamide A and Its Mode of Proteasome Inhibition: An X-ray Crystallographic Study. Marine Drugs. 16(7). 240–240. 6 indexed citations
17.
Haas, Hubertus, et al.. (2018). Iron Scavenging in Aspergillus Species: Structural and Biochemical Insights into Fungal Siderophore Esterases. Angewandte Chemie International Edition. 57(44). 14624–14629. 14 indexed citations
18.
Karan, Ram, S. Bäder, Annika Frank, et al.. (2017). Identification and Experimental Characterization of an Extremophilic Brine Pool Alcohol Dehydrogenase from Single Amplified Genomes. ACS Chemical Biology. 13(1). 161–170. 21 indexed citations
19.
Cui, Haissi, et al.. (2017). Structural Elucidation of a Nonpeptidic Inhibitor Specific for the Human Immunoproteasome. ChemBioChem. 18(6). 523–526. 20 indexed citations
20.
Dick, Tobias P., Alexander K. Nussbaum, Martin Deeg, et al.. (1998). Contribution of Proteasomal β-Subunits to the Cleavage of Peptide Substrates Analyzed with Yeast Mutants. Journal of Biological Chemistry. 273(40). 25637–25646. 209 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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