Lothar Heinisch

811 total citations
42 papers, 635 citations indexed

About

Lothar Heinisch is a scholar working on Organic Chemistry, Molecular Biology and Plant Science. According to data from OpenAlex, Lothar Heinisch has authored 42 papers receiving a total of 635 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 22 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Lothar Heinisch's work include Synthesis and Characterization of Heterocyclic Compounds (10 papers), Synthesis and biological activity (10 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (10 papers). Lothar Heinisch is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (10 papers), Synthesis and biological activity (10 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (10 papers). Lothar Heinisch collaborates with scholars based in Germany, Austria and Czechia. Lothar Heinisch's co-authors include Ute Möllmann, Dorothe Ankel‐Fuchs, A. Bauernfeind, Thilo Köhler, Thomas Stoiber, Rolf Reissbrodt, Urs A. Ochsner, Bart Ghysels, Sandra Matthijs and Michael L. Vasil and has published in prestigious journals such as Journal of Medicinal Chemistry, Antimicrobial Agents and Chemotherapy and Inorganic Chemistry.

In The Last Decade

Lothar Heinisch

40 papers receiving 603 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lothar Heinisch Germany 11 308 189 183 120 114 42 635
Manuka Ghosh United States 15 314 1.0× 271 1.4× 137 0.7× 121 1.0× 139 1.2× 21 654
Takeshi Murata Japan 16 327 1.1× 281 1.5× 167 0.9× 49 0.4× 117 1.0× 56 854
Ana Amoroso Belgium 14 302 1.0× 157 0.8× 135 0.7× 142 1.2× 104 0.9× 33 704
Kathy Johns Canada 6 415 1.3× 376 2.0× 120 0.7× 49 0.4× 101 0.9× 7 795
Judith A. Kelly United States 14 364 1.2× 297 1.6× 118 0.6× 48 0.4× 95 0.8× 18 750
Shantanu Karkare United Kingdom 7 725 2.4× 141 0.7× 176 1.0× 116 1.0× 54 0.5× 8 979
R. Herman Belgium 15 349 1.1× 219 1.2× 86 0.5× 176 1.5× 148 1.3× 24 752
Lisandro H. Otero Argentina 13 484 1.6× 168 0.9× 128 0.7× 145 1.2× 69 0.6× 42 894
Annie Martel France 16 390 1.3× 58 0.3× 111 0.6× 60 0.5× 91 0.8× 32 788
A. Rosselet Switzerland 7 215 0.7× 210 1.1× 71 0.4× 34 0.3× 112 1.0× 17 485

Countries citing papers authored by Lothar Heinisch

Since Specialization
Citations

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

Fields of papers citing papers by Lothar Heinisch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lothar Heinisch

This figure shows the co-authorship network connecting the top 25 collaborators of Lothar Heinisch. A scholar is included among the top collaborators of Lothar Heinisch 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 Lothar Heinisch. Lothar Heinisch 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.
Waisser, Karel, et al.. (2011). New S-benzylisothiosemicarbazones with antimycobacterial activity. Folia Microbiologica. 56(1). 10–12. 3 indexed citations
2.
3.
Möllmann, Ute, Lothar Heinisch, A. Bauernfeind, Thilo Köhler, & Dorothe Ankel‐Fuchs. (2009). Siderophores as drug delivery agents: application of the “Trojan Horse” strategy. BioMetals. 22(4). 615–624. 217 indexed citations
4.
Marchand, Christophe, John A. Beutler, Scott R. Budihas, et al.. (2007). Madurahydroxylactone Derivatives as Dual Inhibitors of Human Immunodeficiency Virus Type 1 Integrase and RNase H. Antimicrobial Agents and Chemotherapy. 52(1). 361–364. 33 indexed citations
5.
Waisser, Karel, Lothar Heinisch, M Slosárek, & Jan Janota. (2006). New antimycobacterial 2,3-dihydro-1-alkylindole-2-thiones. Folia Microbiologica. 51(1). 25–6. 8 indexed citations
6.
Waisser, Karel, Lothar Heinisch, M Slosárek, & Jan Janota. (2005). New antimycobacterialS-alkylisothiosemicarbazones. Folia Microbiologica. 50(6). 479–81. 7 indexed citations
7.
Ghysels, Bart, Urs A. Ochsner, Lothar Heinisch, et al.. (2005). ThePseudomonas aeruginosa pirAgene encodes a second receptor for ferrienterobactin and synthetic catecholate analogues. FEMS Microbiology Letters. 246(2). 167–174. 70 indexed citations
8.
Heinisch, Lothar, et al.. (2003). Catecholates and mixed catecholate hydroxamates as artificial siderophores for mycobacteria. BioMetals. 17(1). 53–64. 10 indexed citations
9.
Heinisch, Lothar, et al.. (2002). New synthetic catecholate-type siderophores with triamine backbone. BioMetals. 15(2). 133–144. 11 indexed citations
10.
Jütten, Peter, et al.. (2002). A novel type of nonsteroidal estrone sulfatase inhibitors. Bioorganic & Medicinal Chemistry Letters. 12(10). 1339–1342. 27 indexed citations
11.
Fritsche, Gernot, et al.. (2002). Effects of Synthetic Siderophores on Proliferation ofPlasmodium falciparumin Infected Human Erythrocytes. Antimicrobial Agents and Chemotherapy. 46(6). 2010–2013. 7 indexed citations
12.
Schnabelrauch, Matthias, et al.. (2001). New artificial siderophores based on a monosaccharide scaffold. BioMetals. 14(1). 1–11. 9 indexed citations
13.
Schnabelrauch, Matthias, et al.. (2000). New synthetic catecholate-type siderophores based on amino acids and dipeptides. BioMetals. 13(4). 333–348. 14 indexed citations
14.
Heinisch, Lothar, Ernst Roemer, Peter Jütten, et al.. (1999). Semisynthetic Derivatives of Madurahydroxylactone and Their Antibacterial Activities.. The Journal of Antibiotics. 52(11). 1029–1041. 16 indexed citations
15.
Schnabelrauch, Matthias, Daniel Ayuk Mbi Egbe, Lothar Heinisch, Rolf Reissbrodt, & Ute Möllmann. (1998). Novel catecholate-type siderophore analogs based on a myo-inositol scaffold. BioMetals. 11(3). 243–251. 4 indexed citations
16.
Heinisch, Lothar, et al.. (1992). [Synthesis and antibacterial activity of benzoylaminoacyl-penicillins and related compounds with and without acylated catechol substituents].. PubMed. 42(5). 668–73. 4 indexed citations
17.
Heinisch, Lothar. (1988). Synthese neuer substituierter Pyrazolo‐[3,4‐e]‐1,2,4‐triazine. Journal für praktische Chemie. 330(1). 57–64.
18.
Heinisch, Lothar, et al.. (1977). [Synthesis and antiviral effect of N-heterocyclic formylisothiosemicarbazones].. PubMed. 32(12). 752–6. 2 indexed citations
19.
Jacob, H.‐E. & Lothar Heinisch. (1977). Wirkung von substituierten Isatinisothiosemicarbazonen auf die Bakterienvermehrung. Zeitschrift für allgemeine Mikrobiologie. 17(8). 647–650. 1 indexed citations
20.
Heinisch, Lothar. (1970). 3‐Amino‐s‐triazolo [4,3‐a]pyridine aus 2‐Halogenpyridinen und Thiosemicarbazid. Zeitschrift für Chemie. 10(5). 188–188. 3 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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