Ingrid Schuberth

1.2k total citations
36 papers, 984 citations indexed

About

Ingrid Schuberth is a scholar working on Molecular Biology, Organic Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Ingrid Schuberth has authored 36 papers receiving a total of 984 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 26 papers in Organic Chemistry and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Ingrid Schuberth's work include Cancer therapeutics and mechanisms (17 papers), Chemical Synthesis and Analysis (16 papers) and Carbohydrate Chemistry and Synthesis (13 papers). Ingrid Schuberth is often cited by papers focused on Cancer therapeutics and mechanisms (17 papers), Chemical Synthesis and Analysis (16 papers) and Carbohydrate Chemistry and Synthesis (13 papers). Ingrid Schuberth collaborates with scholars based in Germany, Hungary and Italy. Ingrid Schuberth's co-authors include Lutz F. Tietze, Felix Major, Birgit Krewer, Kersten M. Gericke, Heiko Schuster, Frauke Alves, Kianga Schmuck, Lutz F. Tietze, Ulrich Bothe and Michael Müller and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and International Journal of Molecular Sciences.

In The Last Decade

Ingrid Schuberth

36 papers receiving 971 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ingrid Schuberth Germany 23 623 544 117 109 86 36 984
Jean‐Pierre Gesson France 21 852 1.4× 637 1.2× 94 0.8× 138 1.3× 39 0.5× 90 1.4k
Mark G. Saulnier United States 21 954 1.5× 807 1.5× 121 1.0× 80 0.7× 34 0.4× 49 1.7k
Dean Stamos United States 21 598 1.0× 704 1.3× 97 0.8× 104 1.0× 41 0.5× 30 1.4k
Anthony B. Mauger United States 17 621 1.0× 645 1.2× 41 0.4× 180 1.7× 40 0.5× 43 1.1k
Glenn J. McGarvey United States 20 1.4k 2.3× 811 1.5× 55 0.5× 103 0.9× 84 1.0× 42 1.7k
Laurent Bialy Germany 15 467 0.7× 656 1.2× 70 0.6× 82 0.8× 21 0.2× 23 975
Zhu‐Jun Yao China 25 1.3k 2.0× 634 1.2× 30 0.3× 193 1.8× 50 0.6× 96 1.8k
Carmen M. Baldino United States 19 1.0k 1.6× 462 0.8× 32 0.3× 80 0.7× 78 0.9× 33 1.3k
Suwei Dong China 21 986 1.6× 1.1k 2.0× 125 1.1× 78 0.7× 35 0.4× 63 1.5k
Paul M. Scola United States 17 1.0k 1.6× 417 0.8× 35 0.3× 176 1.6× 18 0.2× 33 1.4k

Countries citing papers authored by Ingrid Schuberth

Since Specialization
Citations

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

Fields of papers citing papers by Ingrid Schuberth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Schuberth

This figure shows the co-authorship network connecting the top 25 collaborators of Ingrid Schuberth. A scholar is included among the top collaborators of Ingrid Schuberth 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 Ingrid Schuberth. Ingrid Schuberth 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.
Wirth, Tanja, et al.. (2013). The Two Faces of Potent Antitumor Duocarmycin‐Based Drugs: A Structural Dissection Reveals Disparate Motifs for DNA versus Aldehyde Dehydrogenase 1 Affinity. Angewandte Chemie International Edition. 52(27). 6921–6925. 22 indexed citations
2.
Tietze, Lutz F., et al.. (2012). Synthesis, Biological Evaluation, and Live Cell Imaging of Novel Fluorescent Duocarmycin Analogs. Chemistry & Biodiversity. 9(11). 2559–2570. 2 indexed citations
3.
Tietze, Lutz F., et al.. (2012). Photoactivatable Prodrugs of Highly Potent Duocarmycin Analogues for a Selective Cancer Therapy. Chemistry - A European Journal. 19(5). 1726–1731. 17 indexed citations
4.
Tietze, Lutz F., Kianga Schmuck, Heiko Schuster, Michael Müller, & Ingrid Schuberth. (2011). Synthesis and Biological Evaluation of Prodrugs Based on the Natural Antibiotic Duocarmycin for Use in ADEPT and PMT. Chemistry - A European Journal. 17(6). 1922–1929. 23 indexed citations
5.
Tietze, Lutz F., et al.. (2010). Glycosidic Prodrugs of Highly Potent Bifunctional Duocarmycin Derivatives for Selective Treatment of Cancer. Angewandte Chemie International Edition. 49(40). 7336–7339. 45 indexed citations
6.
Schuster, Heiko, Birgit Krewer, Jana Hof, et al.. (2010). Synthesis of the first spacer containing prodrug of a duocarmycin analogue and determination of its biological activity. Organic & Biomolecular Chemistry. 8(8). 1833–1833. 25 indexed citations
7.
Thorn, Andrea, et al.. (2009). A comprehensive view on 4-methyl-2-quinazolinamine, a new microbial alkaloid from Streptomyces of TCM plant origin. The Journal of Antibiotics. 62(8). 439–444. 9 indexed citations
8.
Tietze, Lutz F., Birgit Krewer, Michael Müller, et al.. (2008). Asymmetric Synthesis and Biological Evaluation of Glycosidic Prodrugs for a Selective Cancer Therapy. ChemMedChem. 3(12). 1946–1955. 23 indexed citations
9.
Tietze, Lutz F., Heiko Schuster, Kianga Schmuck, Ingrid Schuberth, & Frauke Alves. (2008). Duocarmycin-based prodrugs for cancer prodrug monotherapy. Bioorganic & Medicinal Chemistry. 16(12). 6312–6318. 46 indexed citations
10.
Tietze, Lutz F., et al.. (2007). Novel strategies for the synthesis of anthrapyran antibiotics: discovery of a new antitumor agent and total synthesis of (S)-espicufolin. Organic & Biomolecular Chemistry. 5(8). 1191–1191. 42 indexed citations
11.
Tietze, Lutz F., Felix Major, Ingrid Schuberth, et al.. (2007). Selective Treatment of Cancer: Synthesis, Biological Evaluation and Structural Elucidation of Novel Analogues of the Antibiotic CC‐1065 and the Duocarmycins. Chemistry - A European Journal. 13(16). 4396–4409. 33 indexed citations
12.
Tietze, Lutz F., Birgit Krewer, Holm Frauendorf, Felix Major, & Ingrid Schuberth. (2006). Investigation of Reactivity and Selectivity of DNA‐Alkylating Duocarmycin Analogues by High‐Resolution Mass Spectrometry. Angewandte Chemie International Edition. 45(39). 6570–6574. 22 indexed citations
13.
Tietze, Lutz F., Felix Major, & Ingrid Schuberth. (2006). Antitumor‐Wirkstoffe: Entwicklung hochpotenter glycosidischer Duocarmycin‐Analoga für eine selektive Krebstherapie. Angewandte Chemie. 118(39). 6724–6727. 29 indexed citations
14.
Tietze, Lutz F., Felix Major, & Ingrid Schuberth. (2006). Antitumor Agents: Development of Highly Potent Glycosidic Duocarmycin Analogues for Selective Cancer Therapy. Angewandte Chemie International Edition. 45(39). 6574–6577. 59 indexed citations
15.
Tietze, Lutz F., Ulrich Griesbach, Ingrid Schuberth, et al.. (2003). Novel Carboranyl C‐Glycosides for the Treatment of Cancer by Boron Neutron Capture Therapy. Chemistry - A European Journal. 9(6). 1296–1302. 46 indexed citations
16.
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18.
Tietze, Lutz F., et al.. (2001). Highly Selective Glycosylated Prodrugs of Cytostatic CC-1065 Analogues for Antibody-Directed Enzyme Tumor Therapy. ChemBioChem. 2(10). 758–758. 32 indexed citations
19.
Kirschning, Andreas, et al.. (2000). Syntheses and biological evaluation of new glyco-modified angucyclin-antibiotics. Bioorganic & Medicinal Chemistry. 8(9). 2347–2354. 22 indexed citations
20.
Tietze, Lutz F., Ulrich Bothe, & Ingrid Schuberth. (2000). Preparation of a New Carboranyl Lactoside for the Treatment of Cancer by Boron Neutron Capture Therapy: Synthesis and Toxicity of Fluoro Carboranyl Glycosides for in vivo19F-NMR Spectroscopy. Chemistry - A European Journal. 6(5). 836–842. 24 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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