Hans Peter Märki

897 total citations
20 papers, 734 citations indexed

About

Hans Peter Märki is a scholar working on Molecular Biology, Organic Chemistry and Computational Theory and Mathematics. According to data from OpenAlex, Hans Peter Märki has authored 20 papers receiving a total of 734 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 4 papers in Organic Chemistry and 4 papers in Computational Theory and Mathematics. Recurrent topics in Hans Peter Märki's work include Chemical Synthesis and Analysis (4 papers), Computational Drug Discovery Methods (4 papers) and Peroxisome Proliferator-Activated Receptors (4 papers). Hans Peter Märki is often cited by papers focused on Chemical Synthesis and Analysis (4 papers), Computational Drug Discovery Methods (4 papers) and Peroxisome Proliferator-Activated Receptors (4 papers). Hans Peter Märki collaborates with scholars based in Switzerland, Germany and China. Hans Peter Märki's co-authors include Bernd Kuhn, Paul Hadváry, Jörg Benz, Markus Meyer, Alfred Binggeli, Daniel Bur, A. Ruf, Uwe Grether, Peter Mohr and Hans Hilpert and has published in prestigious journals such as Journal of the American Chemical Society, FEBS Letters and Journal of Medicinal Chemistry.

In The Last Decade

Hans Peter Märki

20 papers receiving 718 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans Peter Märki Switzerland 14 474 182 119 113 105 20 734
Henrietta Dehmlow Switzerland 15 621 1.3× 197 1.1× 65 0.5× 84 0.7× 122 1.2× 21 969
Alfred Binggeli Switzerland 10 325 0.7× 102 0.6× 83 0.7× 102 0.9× 38 0.4× 10 509
Marc M. Kurtz United States 17 750 1.6× 389 2.1× 47 0.4× 95 0.8× 152 1.4× 36 1.3k
Bruce G. Szczepankiewicz United States 19 904 1.9× 386 2.1× 80 0.7× 102 0.9× 64 0.6× 32 1.4k
Figueroa‐Valverde Lauro Mexico 13 185 0.4× 175 1.0× 160 1.3× 39 0.3× 43 0.4× 127 632
James R. Tata United States 21 637 1.3× 606 3.3× 412 3.5× 99 0.9× 133 1.3× 62 1.7k
Claudio F. Sturino Canada 18 355 0.7× 644 3.5× 76 0.6× 32 0.3× 166 1.6× 29 1.1k
Jürgen Maibaum Switzerland 16 376 0.8× 221 1.2× 191 1.6× 138 1.2× 66 0.6× 24 731
Jean‐Jacques Godfroid France 15 323 0.7× 298 1.6× 38 0.3× 30 0.3× 97 0.9× 33 797
Robert T. Fischer United States 17 665 1.4× 94 0.5× 74 0.6× 29 0.3× 80 0.8× 20 965

Countries citing papers authored by Hans Peter Märki

Since Specialization
Citations

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

Fields of papers citing papers by Hans Peter Märki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans Peter Märki. 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 Hans Peter Märki. The network helps show where Hans Peter Märki may publish in the future.

Co-authorship network of co-authors of Hans Peter Märki

This figure shows the co-authorship network connecting the top 25 collaborators of Hans Peter Märki. A scholar is included among the top collaborators of Hans Peter Märki 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 Hans Peter Märki. Hans Peter Märki 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.
Martin, Rainer E., Johannes Lehmann, Johannes D. Aebi, et al.. (2016). Synthesis of annulated pyridines as inhibitors of aldosterone synthase (CYP11B2). Organic & Biomolecular Chemistry. 14(25). 5922–5927. 28 indexed citations
2.
Neidhart, Werner, Tanja Schulz‐Gasch, A. Ruf, et al.. (2015). Challenges and Rewards in Medicinal Chemistry Targeting Cardiovascular and Metabolic Diseases. CHIMIA International Journal for Chemistry. 69(7-8). 407–407. 1 indexed citations
3.
Martin, Rainer E., Johannes D. Aebi, Bernd Kuhn, et al.. (2015). Discovery of 4-Aryl-5,6,7,8-tetrahydroisoquinolines as Potent, Selective, and Orally Active Aldosterone Synthase (CYP11B2) Inhibitors: In Vivo Evaluation in Rodents and Cynomolgus Monkeys. Journal of Medicinal Chemistry. 58(20). 8054–8065. 35 indexed citations
4.
Dutzler, Raimund, Beat Ernst, Matthias A. Hediger, et al.. (2010). Channels and Transporters. CHIMIA International Journal for Chemistry. 64(9). 662–662. 5 indexed citations
5.
Grether, Uwe, Agnès Bénardeau, Jörg Benz, et al.. (2009). Design and Biological Evaluation of Novel, Balanced Dual PPARα/γ Agonists. ChemMedChem. 4(6). 951–956. 25 indexed citations
6.
Bénardeau, Agnès, Jörg Benz, Alfred Binggeli, et al.. (2009). Aleglitazar, a new, potent, and balanced dual PPARα/γ agonist for the treatment of type II diabetes. Bioorganic & Medicinal Chemistry Letters. 19(9). 2468–2473. 85 indexed citations
7.
Neidhart, Werner, Hans Peter Märki, & Peter Möhr. (2009). Frontiers in Medicinal Chemistry – Joint German-Swiss Meeting on Medicinal Chemistry: Heidelberg, Germany, March 15–18, 2009. CHIMIA International Journal for Chemistry. 63(9). 573–573. 1 indexed citations
8.
Kuhn, Bernd, Hans Hilpert, Jörg Benz, et al.. (2006). Structure-based design of indole propionic acids as novel PPARα/γ co-agonists. Bioorganic & Medicinal Chemistry Letters. 16(15). 4016–4020. 64 indexed citations
9.
Dehmlow, Henrietta, Ralf Thoma, A. Ruf, et al.. (2005). Oxidosqualene Cyclase (OSC) Inhibitors for the Treatment of Dyslipidemia. CHIMIA International Journal for Chemistry. 59(3). 72–72. 3 indexed citations
10.
11.
Carcache, David A., Paul Seiler, François Diederich, et al.. (2003). Development of a New Class of Inhibitors for the Malarial Aspartic Protease Plasmepsin II Based on a Central 7‐Azabicyclo[2.2.1]heptane Scaffold. Helvetica Chimica Acta. 86(6). 2173–2191. 21 indexed citations
12.
Carcache, David A., François Diederich, Arnulf Dorn, et al.. (2003). A New Class of Inhibitors for the Malarial Aspartic Protease Plasmepsin II Based on a Central 11‐Azatricyclo[6.2.1.02,7]undeca‐2,4,6‐triene Scaffold. Helvetica Chimica Acta. 86(6). 2192–2209. 16 indexed citations
13.
Carcache, David A., Christoph A. Binkert, Daniel Bur, et al.. (2002). De Novo Design, Synthesis, and In Vitro Evaluation of a New Class of Nonpeptidic Inhibitors of the Malarial Enzyme Plasmepsin II. ChemBioChem. 3(11). 1137–1141. 32 indexed citations
14.
Vieira, Eric, Alfred Binggeli, Volker Breu, et al.. (1999). Substituted piperidines - highly potent renin inhibitors due to induced fit adaptation of the active site. Bioorganic & Medicinal Chemistry Letters. 9(10). 1397–1402. 79 indexed citations
15.
Güller, Rolf, Alfred Binggeli, Volker Breu, et al.. (1999). Piperidine-renin inhibitors compounds with improved physicochemical properties. Bioorganic & Medicinal Chemistry Letters. 9(10). 1403–1408. 52 indexed citations
16.
Märki, Hans Peter, et al.. (1992). Identification of the active‐site serine in human pancreatic lipase by chemical modification with tetrahydrolipstatin. FEBS Letters. 299(1). 111–115. 82 indexed citations
17.
Märki, Hans Peter, Yvo Crameri, Henri Ramuz, et al.. (1988). Optically Pure Isoproterenol Analogues With Side Chains Containing an Amide Bond: Synthesis and biological properties. Helvetica Chimica Acta. 71(2). 320–336. 14 indexed citations
18.
Heathcock, Clayton H., Michael C. Pirrung, Steven D. Young, et al.. (1984). Acyclic stereoselection. 23. Lactaldehyde enolate equivalents. Journal of the American Chemical Society. 106(26). 8161–8174. 45 indexed citations
19.
Märki, Hans Peter & Conrad Hans Eugster. (1981). Synthese von diastereo‐ und enantio‐selektiv deuterierten β,ε‐, β,β‐, β,γ‐ und γ,γ‐Carotinen. Helvetica Chimica Acta. 64(5). 1257–1287. 13 indexed citations
20.
Märki, Hans Peter & Conrad Hans Eugster. (1980). Synthesis and chiroptical properties of (1R,1′R)-[16,16,16,16′,16′,16′-2H6]-β,β-carotene. Journal of the Chemical Society Chemical Communications. 527–528. 2 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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