Peter Propping

34.5k total citations · 3 hit papers
329 papers, 16.1k citations indexed

About

Peter Propping is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Peter Propping has authored 329 papers receiving a total of 16.1k indexed citations (citations by other indexed papers that have themselves been cited), including 125 papers in Molecular Biology, 85 papers in Genetics and 68 papers in Pathology and Forensic Medicine. Recurrent topics in Peter Propping's work include Genetic factors in colorectal cancer (64 papers), Bipolar Disorder and Treatment (41 papers) and Neurotransmitter Receptor Influence on Behavior (39 papers). Peter Propping is often cited by papers focused on Genetic factors in colorectal cancer (64 papers), Bipolar Disorder and Treatment (41 papers) and Neurotransmitter Receptor Influence on Behavior (39 papers). Peter Propping collaborates with scholars based in Germany, United States and Belgium. Peter Propping's co-authors include Markus M. Nöthen, Waltraut Friedl, Ortrud K. Steinlein, Samuel F. Berkovic, Sven Cichon, Marcella Rietschel, Elisabeth Mangold, Erik G. Jönsson, Stefan Aretz and Reiner Caspari and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Peter Propping

322 papers receiving 15.5k citations

Hit Papers

A Potassium Channel Mutation in Neonatal Human Epilepsy 1995 2026 2005 2015 1998 1995 1999 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A Potassium Channel Mutation in Neonatal Human Epilepsy
    1998 854 citations Peter Propping, Ortrud K. Steinlein et al. profile →
  2. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
    1995 843 citations Ortrud K. Steinlein, Peter Propping et al. profile →
  3. Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers
    1999 588 citations Markus M. Nöthen, Peter Propping et al. profile →

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 68 6.0k 4.3k 3.7k 3.3k 3.1k 329 16.1k
Howard J. Edenberg United States 76 7.8k 1.3× 4.0k 0.9× 4.1k 1.1× 4.8k 1.4× 1.1k 0.4× 425 19.3k
Alison Goate United States 91 12.2k 2.0× 5.4k 1.2× 4.3k 1.1× 1.6k 0.5× 4.2k 1.4× 431 30.4k
Tatiana Foroud United States 76 7.1k 1.2× 4.7k 1.1× 4.5k 1.2× 2.0k 0.6× 1.5k 0.5× 405 20.1k
Eitan Friedman Israel 64 6.1k 1.0× 3.1k 0.7× 5.1k 1.4× 1.7k 0.5× 1.1k 0.4× 484 17.1k
David A. Greenberg United States 90 11.1k 1.8× 9.0k 2.1× 5.4k 1.4× 982 0.3× 2.3k 0.8× 435 30.5k
Guy A. Rouleau Canada 89 14.3k 2.4× 7.7k 1.8× 5.5k 1.5× 1.1k 0.3× 2.3k 0.7× 659 33.5k
Lindsay A. Farrer United States 71 7.4k 1.2× 3.1k 0.7× 4.4k 1.2× 886 0.3× 4.3k 1.4× 425 23.6k
Margaret A. Pericak‐Vance United States 63 7.0k 1.2× 2.4k 0.6× 2.8k 0.8× 1.3k 0.4× 1.5k 0.5× 340 18.4k
Jeffery M. Vance United States 70 12.8k 2.1× 7.0k 1.6× 4.4k 1.2× 819 0.2× 3.6k 1.2× 298 29.0k
Laura Almasy United States 67 4.9k 0.8× 1.7k 0.4× 6.3k 1.7× 1.2k 0.4× 1.6k 0.5× 373 18.3k

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

20 of 20 papers shown
1.
Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2007). High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome. Journal of Medical Genetics. 44(11). 702–709. 151 indexed citations
2.
Hoefgen, Barbara, Thomas G. Schulze, Stephanie Ohlraun, et al.. (2005). The power of sample size and homogenous sampling: Association between the 5-HTTLPR serotonin transporter polymorphism and major depressive disorder. Biological Psychiatry. 57(3). 247–251. 124 indexed citations
3.
Schumacher, Johannes, Rami Abou Jamra, Tim Becker, et al.. (2005). Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression. Biological Psychiatry. 58(4). 307–314. 247 indexed citations
4.
Schumacher, Julia, Inke R. Koenig, Marco Zucchelli, et al.. (2005). Independent evidence for the VMP/DCDC2/KAAG1 gene locus on chromosomal region 6p22 as susceptibility factor for dyslexia. American Journal of Medical Genetics. 114–114. 2 indexed citations
5.
Jamra, Rami Abou, Johannes Schumacher, Astrid Golla, et al.. (2003). Family‐based association studies of α‐adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 126B(1). 79–81. 5 indexed citations
6.
Freudenberg, Johannes & Peter Propping. (2002). A similarity-based method for genome-wide prediction ofdisease-relevant human genes. Bioinformatics. 18(suppl_2). S110–S115. 177 indexed citations
7.
Schulze, Thomas G., Johannes Schumacher, Daniel J. Müller, et al.. (2001). Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia. American Journal of Medical Genetics. 105(6). 498–501. 53 indexed citations
8.
Cichon, Sven, J Schumacher, Thomas G. Schulze, et al.. (2001). The NOTCH4 locus and schizophrenia: Analyses in the german and palestinian Arab population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 105(7). 3 indexed citations
9.
Honnefelder, Ludger & Peter Propping. (2001). Was wissen wir, wenn wir das menschliche Genom kennen?. 2 indexed citations
10.
Rietschel, Marcella, Margot Albus, Ernst Franzek, et al.. (2000). Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls. American Journal of Medical Genetics. 96(3). 310–311. 11 indexed citations
11.
Stassen, Hans H., et al.. (2000). Non-genetic pathologic developments of brain-wave patterns in MZ twins. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 96(4). 1 indexed citations
12.
Schulze, Thomas G., Johannes Schumacher, D Müller, et al.. (2000). Novel 5′-regulatory region polymorphism of the 5ht2c-receptor gene: no association with clozapine-response. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 96(4). 540–541. 1 indexed citations
13.
Bokhoven, Hans van, John A. McGrath, Jacopo Celli, et al.. (2000). P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.. The American Journal of Human Genetics. 67(4). 41–41. 6 indexed citations
14.
Jungck, Matthias, W. Friedl, & Peter Propping. (1999). Erblich bedingte gastrointestinale Tumorerkrankungen. Der Internist. 40(5). 502–512. 1 indexed citations
15.
Cichon, Sven, Ina R. Vogt, Axel M. Hillmer, et al.. (1998). Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia. Human Molecular Genetics. 7(11). 1671–1679. 114 indexed citations
16.
Steinlein, Ortrud K., Jürgen Deckert, Markus M. Nöthen, et al.. (1997). Neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and panic disorder: An association study. American Journal of Medical Genetics. 74(2). 199–201. 32 indexed citations
17.
Deckert, Jürgen, Marcella Rietschel, Dieter B. Wildenauer, et al.. (1996). Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia. Journal of Neural Transmission. 103(12). 1447–1455. 32 indexed citations
18.
Deckert, Jürgen, Markus M. Nöthen, Stephen P. Bryant, et al.. (1995). Human Adenosine A1 Receptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 1q31-32.1 Using a Silent Polymorphism in the Coding Region. Biochemical and Biophysical Research Communications. 214(2). 614–621. 5 indexed citations
19.
Caspari, Reiner, Waltraut Friedl, Marion Mandl, et al.. (1995). Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. Human Molecular Genetics. 4(3). 337–340. 283 indexed citations
20.
Bouchard, Thomas J. & Peter Propping. (1993). Twins as a tool of behavioral genetics : report of the Dahlem Workshop on What Are the Mechanisms Mediating the Genetic and Environmental Determinants of Behavior? Twins as a Tool of Behavioral Genetics, held in Berlin , 17-22 May 1992. John Wiley eBooks. 5 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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