Heinrich Sticht

15.7k total citations
290 papers, 9.2k citations indexed

About

Heinrich Sticht is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Heinrich Sticht has authored 290 papers receiving a total of 9.2k indexed citations (citations by other indexed papers that have themselves been cited), including 175 papers in Molecular Biology, 50 papers in Immunology and 47 papers in Genetics. Recurrent topics in Heinrich Sticht's work include Cytomegalovirus and herpesvirus research (36 papers), Herpesvirus Infections and Treatments (30 papers) and Protein Structure and Dynamics (28 papers). Heinrich Sticht is often cited by papers focused on Cytomegalovirus and herpesvirus research (36 papers), Herpesvirus Infections and Treatments (30 papers) and Protein Structure and Dynamics (28 papers). Heinrich Sticht collaborates with scholars based in Germany, United States and Switzerland. Heinrich Sticht's co-authors include Anselm H. C. Horn, Paul Rösch, Manfred Marschall, Kristian Schweimer, Anita Rauch, André Reis, Nadine Homeyer, Harald Lanig, Jens Milbradt and Heike Meiselbach and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Heinrich Sticht

286 papers receiving 9.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heinrich Sticht Germany 53 5.1k 1.5k 1.4k 1.1k 906 290 9.2k
María A. Juliano Brazil 47 4.8k 0.9× 1.4k 0.9× 806 0.6× 635 0.6× 736 0.8× 376 9.1k
Luiz Juliano Brazil 53 5.3k 1.0× 1.9k 1.3× 1.1k 0.8× 636 0.6× 832 0.9× 389 11.2k
Martina Schnölzer Germany 54 5.6k 1.1× 707 0.5× 1.3k 0.9× 572 0.5× 537 0.6× 174 9.0k
Angela Bachi Italy 56 7.4k 1.4× 663 0.5× 1.6k 1.2× 732 0.7× 772 0.9× 200 11.2k
Joshua LaBaer United States 46 6.9k 1.3× 684 0.5× 917 0.7× 734 0.7× 637 0.7× 200 10.1k
Maria Panico United Kingdom 56 6.1k 1.2× 681 0.5× 1.8k 1.3× 858 0.8× 802 0.9× 144 10.8k
Ulf Landegren Sweden 51 10.1k 2.0× 690 0.5× 1.3k 0.9× 1.4k 1.2× 604 0.7× 192 14.3k
Connie R. Jiménez Netherlands 56 4.8k 0.9× 1.1k 0.7× 655 0.5× 536 0.5× 446 0.5× 240 8.6k
Gergely L. Lukács Canada 61 6.6k 1.3× 941 0.6× 819 0.6× 1.5k 1.3× 938 1.0× 198 12.3k
Ileana M. Cristea United States 56 5.6k 1.1× 2.6k 1.8× 2.0k 1.4× 757 0.7× 461 0.5× 190 9.4k

Countries citing papers authored by Heinrich Sticht

Since Specialization
Citations

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

Fields of papers citing papers by Heinrich Sticht

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heinrich Sticht

This figure shows the co-authorship network connecting the top 25 collaborators of Heinrich Sticht. A scholar is included among the top collaborators of Heinrich Sticht 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 Heinrich Sticht. Heinrich Sticht 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.
Beierlein, Frank, Anselm H. C. Horn, Heinrich Sticht, Andriy Mokhir, & Petra Imhof. (2024). In Silico Study of Camptothecin-Based Pro-Drugs Binding to Human Carboxylesterase 2. Biomolecules. 14(2). 153–153. 1 indexed citations
2.
Breitinger, Ulrike, et al.. (2023). Patch-clamp studies and cell viability assays suggest a distinct site for viroporin inhibitors on the E protein of SARS-CoV-2. Virology Journal. 20(1). 142–142. 7 indexed citations
3.
Horn, Anselm H. C., et al.. (2023). Computational Analysis of Histamine Protonation Effects on H1R Binding. Molecules. 28(9). 3774–3774. 2 indexed citations
4.
Zanoni, Paolo, Katharina Steindl, Heinrich Sticht, et al.. (2023). The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohort. European Journal of Human Genetics. 31(7). 784–792. 6 indexed citations
5.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
6.
Schafer, Simon T., et al.. (2022). Smaller, Stronger, More Stable: Peptide Variants of a SARS-CoV-2 Neutralizing Miniprotein. International Journal of Molecular Sciences. 23(11). 6309–6309. 11 indexed citations
7.
Joset, Pascal, et al.. (2022). Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies. European Journal of Human Genetics. 31(8). 953–961. 6 indexed citations
8.
Grätz, Lukas, Maximilian F. Schmidt, Anselm H. C. Horn, et al.. (2021). N-Terminus to Arginine Side-Chain Cyclization of Linear Peptidic Neuropeptide Y Y4 Receptor Ligands Results in Picomolar Binding Constants. Journal of Medicinal Chemistry. 64(22). 16746–16769. 13 indexed citations
9.
Müller, Regina, Friedrich Hahn, Peter Lischka, et al.. (2021). Properties of Oligomeric Interaction of the Cytomegalovirus Core Nuclear Egress Complex (NEC) and Its Sensitivity to an NEC Inhibitory Small Molecule. Viruses. 13(3). 462–462. 14 indexed citations
10.
Socher, Eileen, Lukas Heger, Friedrich Paulsen, et al.. (2021). Mutations in the B.1.1.7 SARS-CoV-2 Spike Protein Reduce Receptor-Binding Affinity and Induce a Flexible Link to the Fusion Peptide. Biomedicines. 9(5). 525–525. 25 indexed citations
11.
Gregor, Anne, et al.. (2020). Loss of PHF6 leads to aberrant development of human neuron-like cells. Scientific Reports. 10(1). 19030–19030. 3 indexed citations
12.
Sharafutdinov, Irshad, et al.. (2020). Campylobacter jejuni Serine Protease HtrA Cleaves the Tight Junction Component Claudin-8. Frontiers in Cellular and Infection Microbiology. 10. 590186–590186. 31 indexed citations
13.
Miao, Yinglong, et al.. (2020). Agonist Binding and G Protein Coupling in Histamine H2 Receptor: A Molecular Dynamics Study. International Journal of Molecular Sciences. 21(18). 6693–6693. 12 indexed citations
14.
Marschall, Manfred, Julia Tillmanns, Frank Neipel, et al.. (2020). Nuclear Egress Complexes of HCMV and Other Herpesviruses: Solving the Puzzle of Sequence Coevolution, Conserved Structures and Subfamily-Spanning Binding Properties. Viruses. 12(6). 683–683. 23 indexed citations
15.
Horn, Anselm H. C., et al.. (2018). Interaction of Glycolipids with the Macrophage Surface Receptor Mincle – a Systematic Molecular Dynamics Study. Scientific Reports. 8(1). 5374–5374. 14 indexed citations
16.
Rech, Jürgen, Axel J. Hueber, Norbert Blank, et al.. (2017). Evidence for genetic overlap between adult onset Still’s disease and hereditary periodic fever syndromes. Rheumatology International. 38(1). 111–120. 21 indexed citations
17.
Kraner, Max, et al.. (2017). Probing the potential of CnaB-type domains for the design of tag/catcher systems. PLoS ONE. 12(6). e0179740–e0179740. 23 indexed citations
18.
Hutterer, Corina, Stuart T. Hamilton, Isabel Zeitträger, et al.. (2016). The chemical class of quinazoline compounds provides a core structure for the design of anticytomegaloviral kinase inhibitors. Antiviral Research. 134. 130–143. 41 indexed citations
19.
Pasutto, Francesca, Lucia Mauri, Bernt Popp, et al.. (2015). Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma. Gene. 568(1). 76–80. 7 indexed citations
20.
Templin, Christian, Jelena R. Ghadri, Jean‐Sébastien Rougier, et al.. (2011). Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). European Heart Journal. 32(9). 1077–1088. 140 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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