Marcel Frese

1.5k total citations
70 papers, 1.2k citations indexed

About

Marcel Frese is a scholar working on Molecular Biology, Plant Science and Pharmacology. According to data from OpenAlex, Marcel Frese has authored 70 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 23 papers in Plant Science and 20 papers in Pharmacology. Recurrent topics in Marcel Frese's work include Microbial Natural Products and Biosynthesis (17 papers), Natural product bioactivities and synthesis (13 papers) and Marine Sponges and Natural Products (11 papers). Marcel Frese is often cited by papers focused on Microbial Natural Products and Biosynthesis (17 papers), Natural product bioactivities and synthesis (13 papers) and Marine Sponges and Natural Products (11 papers). Marcel Frese collaborates with scholars based in Germany, Egypt and Cameroon. Marcel Frese's co-authors include Norbert Sewald, Mohamed Shaaban, Hannah Minges, Christian Schnepel, Ahmed S. Abdel‐Razek, Abdelaaty Hamed, Hans‐Georg Stammler, Mohamed Ismail, Tilman Kottke and Negera Abdissa and has published in prestigious journals such as Journal of Biological Chemistry, Angewandte Chemie International Edition and PLoS ONE.

In The Last Decade

Marcel Frese

69 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marcel Frese Germany 21 602 425 316 164 154 70 1.2k
James T. Payne United States 12 530 0.9× 320 0.8× 234 0.7× 81 0.5× 55 0.4× 14 871
Shanteri Singh United States 22 1.2k 2.0× 490 1.2× 492 1.6× 161 1.0× 146 0.9× 58 1.6k
Jeanette E. Stok Australia 19 590 1.0× 224 0.5× 235 0.7× 67 0.4× 92 0.6× 40 1.2k
Ping Wu China 23 697 1.2× 307 0.7× 544 1.7× 180 1.1× 357 2.3× 98 1.6k
J. Rúben Gómez Castellanos United Kingdom 12 637 1.1× 245 0.6× 141 0.4× 53 0.3× 99 0.6× 17 1.0k
Ulrike Garscha Germany 26 646 1.1× 313 0.7× 460 1.5× 42 0.3× 114 0.7× 62 1.5k
Dong Liang China 24 1.1k 1.8× 449 1.1× 249 0.8× 77 0.5× 573 3.7× 125 1.9k
Jean‐François Gallard France 19 429 0.7× 311 0.7× 183 0.6× 133 0.8× 160 1.0× 61 998
Chin‐Yuan Chang Taiwan 18 696 1.2× 253 0.6× 510 1.6× 150 0.9× 43 0.3× 58 1.2k
Akimasa Miyanaga Japan 24 1.2k 2.0× 535 1.3× 776 2.5× 515 3.1× 244 1.6× 80 2.0k

Countries citing papers authored by Marcel Frese

Since Specialization
Citations

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

Fields of papers citing papers by Marcel Frese

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcel Frese

This figure shows the co-authorship network connecting the top 25 collaborators of Marcel Frese. A scholar is included among the top collaborators of Marcel Frese 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 Marcel Frese. Marcel Frese 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.
Mas‐Claret, Eduard, Moses K. Langat, Marcel Frese, et al.. (2024). Cytotoxic clerodane diterpenoids from the roots of Casearia barteri Mast.. RSC Advances. 14(32). 23109–23117. 4 indexed citations
2.
Abebe, Abiy, et al.. (2024). In Vitro Antibacterial Activity, Molecular Docking, and ADMET Analysis of Phytochemicals from Roots of Dovyalis abyssinica. Molecules. 29(23). 5608–5608. 2 indexed citations
3.
Bitchagno, Gabin Thierry M., Marcel Frese, Bruno Ndjakou Lenta, et al.. (2023). Bioguided Fractionation and Isolation of an Antiplasmodial Saponin from the Roots of Nauclea xanthoxylon (A.Chev.) Aubrév. (Rubiaceae). Chemistry & Biodiversity. 20(4). e202200271–e202200271. 2 indexed citations
4.
Frese, Marcel, Jean Claude Ndom, Moses K. Langat, et al.. (2023). Coumarinolignoid and Indole Alkaloids from the Roots of the Hybrid Plant Citrus × paradisi Macfad (Rutaceae). Molecules. 28(3). 1078–1078.
5.
Lenta, Bruno Ndjakou, Fabrice Fekam Boyom, Norbert Sewald, et al.. (2022). Chemical Constituents of Macaranga occidentalis, Antimicrobial and Chemophenetic Studies. Molecules. 27(24). 8820–8820. 4 indexed citations
6.
Frese, Marcel, Ahmed H. Halawa, Maha M. Soltan, et al.. (2021). Metal-free domino amination-Knoevenagel condensation approach to access new coumarins as potent nanomolar inhibitors of VEGFR-2 and EGFR. Green Chemistry Letters and Reviews. 14(4). 578–599. 10 indexed citations
7.
Bitchagno, Gabin Thierry M., Hans‐Georg Stammler, Marcel Frese, et al.. (2021). Furanocoumarins from the twigs of Ficus chlamydocarpa (Moraceae). Phytochemistry Letters. 47. 38–41. 3 indexed citations
8.
Happi, Gervais Mouthé, Marcel Frese, Siméon F. Kouam, et al.. (2021). A new phenylpropanoid glucoside from Psorospermum tenuifolium Kotschy (Hypericaceae). Town Planning Review. 5(1). 31–36. 3 indexed citations
9.
Frese, Marcel, et al.. (2021). L-Carnitine Production Through Biosensor-Guided Construction of the Neurospora crassa Biosynthesis Pathway in Escherichia coli. Frontiers in Bioengineering and Biotechnology. 9. 671321–671321. 2 indexed citations
10.
Hamed, Abdelaaty, Marcel Frese, Tatiana Syrovets, et al.. (2020). Synthesis of novel feruloyl dipeptides with proapoptotic potential against different cancer cell lines. Bioorganic Chemistry. 97. 103678–103678. 8 indexed citations
11.
Azébazé, Anatole Guy Blaise, et al.. (2020). Chemical Constituents of Nauclea vanderguchtii. Natural Product Sciences. 26(2). 144–150. 1 indexed citations
12.
Wibberg, Daniel, et al.. (2020). Draft genome sequence of Streptomyces tunisialbus DSM 105760T. Archives of Microbiology. 202(7). 2013–2017. 2 indexed citations
13.
Happi, Gervais Mouthé, Hans‐Georg Stammler, Beate Neumann, et al.. (2020). Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae). Phytochemistry. 181. 112537–112537. 20 indexed citations
14.
Happi, Gervais Mouthé, Mohamed Ismail, Siméon F. Kouam, et al.. (2020). Ergostane-type steroids from the Cameroonian ‘white tiama’ Entandrophragma angolense. Steroids. 156. 108584–108584. 20 indexed citations
15.
Esposito, Simone, Giulio Auciello, Edith Monteagudo, et al.. (2019). Synthesis and Biological Evaluation of RGD–Cryptophycin Conjugates for Targeted Drug Delivery. Pharmaceutics. 11(4). 151–151. 28 indexed citations
16.
Joncour, Vadim Le, Daniela Modena, Paolo Pagani, et al.. (2019). Octreotide Conjugates for Tumor Targeting and Imaging. Pharmaceutics. 11(5). 220–220. 22 indexed citations
17.
Ismail, Mohamed, Lea Schroeder, Marcel Frese, et al.. (2019). Straightforward Regeneration of Reduced Flavin Adenine Dinucleotide Required for Enzymatic Tryptophan Halogenation. ACS Catalysis. 9(2). 1389–1395. 41 indexed citations
18.
Minges, Hannah, et al.. (2018). Structure-based switch of regioselectivity in the flavin-dependent tryptophan 6-halogenase Thal. Journal of Biological Chemistry. 294(7). 2529–2542. 51 indexed citations
19.
Ismail, Mohamed, et al.. (2018). Novel unit B cryptophycin analogues as payloads for targeted therapy. Beilstein Journal of Organic Chemistry. 14. 1281–1286. 12 indexed citations
20.
Frese, Marcel & Norbert Sewald. (2014). Enzymatic Halogenation of Tryptophan on a Gram Scale. Angewandte Chemie International Edition. 54(1). 298–301. 123 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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