Peter Lorenz

3.4k total citations
73 papers, 2.6k citations indexed

About

Peter Lorenz is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Peter Lorenz has authored 73 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 17 papers in Radiology, Nuclear Medicine and Imaging and 10 papers in Genetics. Recurrent topics in Peter Lorenz's work include Monoclonal and Polyclonal Antibodies Research (17 papers), Glycosylation and Glycoproteins Research (9 papers) and RNA Research and Splicing (9 papers). Peter Lorenz is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (17 papers), Glycosylation and Glycoproteins Research (9 papers) and RNA Research and Splicing (9 papers). Peter Lorenz collaborates with scholars based in Germany, United States and China. Peter Lorenz's co-authors include Walter Pyerin, Hans‐Jürgen Thiesen, Saleh Ibrahim, Manfred Kunz, Gerd Gross, Rainer Pepperkok, Wilhelm Ansorge, Julia Schultz, Dirk Koczan and Peter Ruschpler and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Peter Lorenz

70 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Lorenz Germany 26 1.7k 432 358 321 297 73 2.6k
Hui Ge United States 27 3.3k 1.9× 252 0.6× 311 0.9× 583 1.8× 227 0.8× 47 4.0k
Michael Haase Germany 23 2.2k 1.3× 457 1.1× 546 1.5× 474 1.5× 154 0.5× 57 3.3k
Rosaria Orlandi Italy 27 1.5k 0.9× 385 0.9× 599 1.7× 180 0.6× 706 2.4× 61 2.7k
Jan Hein van Dierendonck Netherlands 19 1.3k 0.8× 321 0.7× 590 1.6× 243 0.8× 172 0.6× 39 2.4k
Yuichiro Shimizu Japan 27 1.3k 0.8× 228 0.5× 279 0.8× 347 1.1× 176 0.6× 54 2.3k
Milena Paglierani Italy 32 1.6k 0.9× 724 1.7× 1.1k 3.2× 381 1.2× 173 0.6× 105 3.7k
Deena M. Leslie Pedrioli Switzerland 20 1.6k 0.9× 584 1.4× 335 0.9× 143 0.4× 114 0.4× 29 2.2k
M. Cristine Charlesworth United States 31 1.5k 0.9× 197 0.5× 153 0.4× 501 1.6× 199 0.7× 66 3.1k
Akiko Furuya Japan 26 1.9k 1.1× 247 0.6× 424 1.2× 332 1.0× 115 0.4× 65 3.0k
William H. Brissette United States 18 1.5k 0.9× 363 0.8× 687 1.9× 141 0.4× 187 0.6× 25 3.4k

Countries citing papers authored by Peter Lorenz

Since Specialization
Citations

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

Fields of papers citing papers by Peter Lorenz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Lorenz

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Lorenz. A scholar is included among the top collaborators of Peter Lorenz 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 Peter Lorenz. Peter Lorenz 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
2.
Hecker, Michael, Brit Fitzner, Alexander Winkelmann, et al.. (2022). Implication of genetic variants in primary microRNA processing sites in the risk of multiple sclerosis. EBioMedicine. 80. 104052–104052. 6 indexed citations
3.
Opuni, Kwabena F.M., et al.. (2020). ITEM-THREE analysis of a monoclonal anti-malaria antibody reveals its assembled epitope on the pfMSP119 antigen. Journal of Biological Chemistry. 295(44). 14987–14997. 8 indexed citations
4.
Lorenz, Peter, et al.. (2020). Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice. Journal of Molecular Neuroscience. 71(11). 2237–2248. 8 indexed citations
5.
Thiesen, Hans‐Jürgen, et al.. (2019). DUF3669, a “domain of unknown function” within ZNF746 and ZNF777, oligomerizes and contributes to transcriptional repression. BMC Molecular and Cell Biology. 20(1). 60–60. 12 indexed citations
6.
Patro, Rob, Raquel Norel, Robert J. Prill, et al.. (2016). A computational method for designing diverse linear epitopes including citrullinated peptides with desired binding affinities to intravenous immunoglobulin. BMC Bioinformatics. 17(1). 155–155. 2 indexed citations
7.
Ruijter, Jan M., Peter Lorenz, Jari M. Tuomi, Michael Hecker, & Maurice J.B. van den Hoff. (2014). Fluorescent-increase kinetics of different fluorescent reporters used for qPCR depend on monitoring chemistry, targeted sequence, type of DNA input and PCR efficiency. Microchimica Acta. 181(13-14). 1689–1696. 62 indexed citations
8.
Mikkat, Stefan, Peter Lorenz, Christian Scharf, et al.. (2010). MS characterization of qualitative protein polymorphisms in the spinal cords of inbred mouse strains. PROTEOMICS. 10(5). 1050–1062. 13 indexed citations
10.
Ruschpler, Peter, Peter Lorenz, Wolfram Eichler, et al.. (2003). High CXCR3 expression in synovial mast cells associated with CXCL9 and CXCL10 expression in inflammatory synovial tissues of patients with rheumatoid arthritis. Arthritis Research & Therapy. 5(5). R241–52. 182 indexed citations
11.
Lorenz, Peter, Marcus Bantscheff, Saleh Ibrahim, Hans‐Jürgen Thiesen, & Michael O. Glocker. (2003). Proteome Analysis of Diseased Joints from Mice Suffering from Collagen-Induced Arthritis. Clinical Chemistry and Laboratory Medicine (CCLM). 41(12). 1622–32. 25 indexed citations
12.
Booms, Patrick, Frank Tiecke, Seval Türkmen, et al.. (2002). TGGE screening of the entireFBN1coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies. Human Mutation. 20(3). 197–208. 52 indexed citations
13.
Berlau, J., Peter Lorenz, Josef Makovitzky, et al.. (2001). Analysis of aqueous humour proteins of eyes with and without pseudoexfoliation syndrome. Graefe s Archive for Clinical and Experimental Ophthalmology. 239(10). 743–746. 30 indexed citations
14.
Lorenz, Peter, Dirk Koczan, & Hans‐Jürgen Thiesen. (2001). Transcriptional Repression Mediated by the KRAB Domain of the Human C2H2 Zinc Finger Protein Kox1/ZNF10 Does Not Require Histone Deacetylation. Biological Chemistry. 382(4). 637–44. 27 indexed citations
16.
Bunge, Susanna, Cordula Steglich, Peter Lorenz, et al.. (1994). Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,xxy male heterozygous for a missense point mutation. Prenatal Diagnosis. 14(9). 777–780. 5 indexed citations
18.
Pohl, Christoph, Christoph Renner, Martin Schwonzen, et al.. (1992). Anti‐idiotype vaccine against Hodgkin's lymphoma: Induction of B‐ and T‐cell immunity across species barriers against cd30 antigen by murine monoclonal internal image antibodies. International Journal of Cancer. 50(6). 958–967. 17 indexed citations
19.
Pepperkok, Rainer, Peter Lorenz, Rolf Jakobi, Wilhelm Ansorge, & Walter Pyerin. (1991). Cell growth stimulation by EGF: Inhibition through antisense-oligodeoxynucleotides demonstrates important role of casein kinase II. Experimental Cell Research. 197(2). 245–253. 75 indexed citations
20.
Lorenz, Peter, R Bollmann, Marco Mächler, et al.. (1991). False‐negative prenatal exclusion of Wiskott‐Aldrich syndrome by measurement of fetal platelet count and size. Prenatal Diagnosis. 11(11). 819–825. 4 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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