Peter Propping

628 total citations
16 papers, 483 citations indexed

About

Peter Propping is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Peter Propping has authored 16 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Peter Propping's work include Genomic variations and chromosomal abnormalities (3 papers), Receptor Mechanisms and Signaling (3 papers) and Congenital limb and hand anomalies (2 papers). Peter Propping is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Receptor Mechanisms and Signaling (3 papers) and Congenital limb and hand anomalies (2 papers). Peter Propping collaborates with scholars based in Germany, United States and United Kingdom. Peter Propping's co-authors include Markus M. Nöthen, Klaus Zerres, Sven Cichon, Sabine Normann, Ingmar Blümcke, Johannes Schramm, Waltraut Friedl, Siegfried Uhlhaas, Wolfgang Maier and Markus M. N�then and has published in prestigious journals such as Journal of Neurochemistry, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Peter Propping

16 papers receiving 472 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 Propping Germany 12 240 200 99 89 57 16 483
R. M. Collins United States 14 295 1.2× 171 0.9× 101 1.0× 35 0.4× 15 0.3× 16 598
P. Pekkarinen Finland 9 195 0.8× 190 0.9× 38 0.4× 63 0.7× 34 0.6× 13 681
Amy L. Clark United States 10 230 1.0× 79 0.4× 233 2.4× 25 0.3× 20 0.4× 13 513
Mar O’Callaghan Spain 12 273 1.1× 98 0.5× 80 0.8× 42 0.5× 3 0.1× 26 489
Franck Louis France 9 358 1.5× 270 1.4× 113 1.1× 16 0.2× 61 1.1× 10 696
Tzu‐Jou Wang Taiwan 12 131 0.5× 51 0.3× 179 1.8× 99 1.1× 39 0.7× 20 495
Th. de Barsy Belgium 18 320 1.3× 83 0.4× 117 1.2× 130 1.5× 4 0.1× 43 853
Dagan Harris Israel 16 306 1.3× 225 1.1× 44 0.4× 273 3.1× 27 0.5× 24 946
Cynthia Camarillo United States 14 344 1.4× 121 0.6× 55 0.6× 49 0.6× 21 0.4× 20 610

Countries citing papers authored by Peter Propping

Since Specialization
Citations

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

Fields of papers citing papers by Peter Propping

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Propping

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Propping. A scholar is included among the top collaborators of Peter Propping 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 Propping. Peter Propping is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Müller, Daniel J., Harald Krauß, Magdalena Groß, et al.. (2001). Caught in the trio trap? Potential selection bias inherent to association studies usings parent‐offspring trios. American Journal of Medical Genetics. 105(4). 351–353. 18 indexed citations
2.
Haug, Karsten, Kerstin Hallmann, Steve Horvath, et al.. (2000). No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy. Epilepsy Research. 42(1). 57–62. 8 indexed citations
3.
Propping, Peter, et al.. (2000). Adult syndrome allelic to limb mammary syndrome (LMS)?. American Journal of Medical Genetics. 90(2). 179–182. 23 indexed citations
4.
Bosse, Kristin, Regina C. Betz, Young‐Ae Lee, et al.. (2000). Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36. The American Journal of Human Genetics. 67(2). 492–497. 32 indexed citations
5.
Haug, Karsten, Thomas Sander, Kerstin Hallmann, et al.. (2000). Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy. Epilepsy Research. 39(2). 127–132. 5 indexed citations
6.
Franke, Petra, Markus M. N�then, Helge Neidt, et al.. (1999). Human ?-opioid receptor gene and susceptibility to heroin and alcohol dependence. American Journal of Medical Genetics. 88(5). 462–464. 51 indexed citations
7.
Kruse, Roland, Siegfried Uhlhaas, Klaus Keller, et al.. (1999). Peutz-Jeghers syndrome: Four novel inactivating germline mutations in theSTK11 gene. Human Mutation. 13(3). 257–258. 18 indexed citations
8.
N�then, Markus M., Margot Albus, Ernst Franzek, et al.. (1998). Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies. American Journal of Medical Genetics. 81(1). 18–23. 13 indexed citations
9.
Blümcke, Ingmar, Sven Cichon, Sabine Normann, et al.. (1998). Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain. Molecular Brain Research. 59(1). 90–92. 86 indexed citations
10.
11.
Deckert, Jürgen, Markus M. Nöthen, Simone Schuffenhauer, et al.. (1997). Mapping of the human adenosine A 2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region. Human Genetics. 99(3). 326–328. 31 indexed citations
12.
Erdmann, Jeanette, Daphne Shimron‐Abarbanell, Viji Shridhar, et al.. (1997). Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1). Molecular Membrane Biology. 14(3). 133–135. 5 indexed citations
13.
Propping, Peter & Markus M. Nöthen. (1995). Genetic variation of CNS receptors - a new perspective for pharmacogenetics. Pharmacogenetics. 5(5). 318–325. 32 indexed citations
14.
Dawson, Elisabeth, E. Parfitt, Lionel Lim, et al.. (1995). Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23‐24.1. American Journal of Medical Genetics. 60(2). 94–102. 80 indexed citations
15.
Propping, Peter & Klaus Zerres. (1993). ADULT‐syndrome: An autosomal‐dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. American Journal of Medical Genetics. 45(5). 642–648. 53 indexed citations
16.
Hebebrand, Johannes, et al.. (1987). Further Characterization of the Avian Benzodiazepine Receptor Subunits Including Phylo‐and Ontogenetic Aspects. Journal of Neurochemistry. 49(6). 1888–1893. 19 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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