Peter Propping
Impact in
- Cellular and Molecular Neuroscience top 0.2%
- Neurotransmitter Receptor Influence on Behavior
- Neuroscience and Neuropharmacology Research
- Biological Psychiatry top 0.5%
Papers in
-
- Receptor Mechanisms and Signaling 33
- Ion channel regulation and function 20
- Genetics 87
- Genetics and Neurodevelopmental Disorders 34
- Genetic Associations and Epidemiology 21
- Co-authors
- Markus M. Nöthen (135 shared papers)Waltraut Friedl (86 shared papers)Ortrud K. Steinlein (7 shared papers)Samuel F. Berkovic (3 shared papers)Sven Cichon (71 shared papers)Marcella Rietschel (65 shared papers)Elisabeth Mangold (24 shared papers)Stefan Aretz (19 shared papers)
- Journals
- Human Genetics (26 papers)Psychiatric Genetics (20 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (14 papers)Molecular Psychiatry (12 papers)Human Molecular Genetics (12 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Peter Propping
336 papers receiving 16.6k citations
Peter Propping's Hit Papers
Peers
Comparison fields: 5 of 168
- Cellular and Molecular Neuroscience 4.3k
- Biological Psychiatry 527
- Psychiatry and Mental health 2.9k
- Pathology and Forensic Medicine 3.3k
- Genetics 3.7k
Countries citing papers authored by Peter Propping
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
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-authors
The 25 scholars most cited alongside Peter Propping, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 349 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy Hit paper breakdown → | 1995 | 913 |
| 2 | A Potassium Channel Mutation in Neonatal Human Epilepsy Hit paper breakdown → | 1998 | 898 |
| 3 | Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers Hit paper breakdown → | 1999 | 616 |
| 4 | Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder Hit paper breakdown → | 1999 | 515 |
| 5 | A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Hit paper breakdown → | 2007 | 502 |
| 6 | 1979 | 324 | |
| 7 | 1997 | 314 | |
| 8 | 1995 | 305 | |
| 9 | 2005 | 255 | |
| 10 | 2004 | 251 | |
| 11 | 2009 | 246 | |
| 12 | Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. | 1996 | 216 |
| 13 | 2005 | 193 | |
| 14 | 2005 | 189 | |
| 15 | 2002 | 182 | |
| 16 | 1998 | 179 | |
| 17 | 2000 | 179 | |
| 18 | 1994 | 178 | |
| 19 | 1996 | 168 | |
| 20 | 2007 | 167 |
About Peter Propping
Peter Propping is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 349 papers that have together received 17.5k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (66 papers), Bipolar Disorder and Treatment (42 papers), Neurotransmitter Receptor Influence on Behavior (39 papers), Genetics and Neurodevelopmental Disorders (34 papers), Receptor Mechanisms and Signaling (33 papers), Cancer Genomics and Diagnostics (29 papers), Genetic Associations and Epidemiology (21 papers) and Ion channel regulation and function (20 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.3k citations), Biological Psychiatry (527 citations), Psychiatry and Mental health (2.9k citations), Pathology and Forensic Medicine (3.3k citations) and Genetics (3.7k citations). Peter Propping has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Markus M. Nöthen, Waltraut Friedl, Ortrud K. Steinlein, Samuel F. Berkovic, Sven Cichon, Marcella Rietschel, Elisabeth Mangold, Stefan Aretz, Erik G. Jönsson and Reiner Caspari. Their work appears in journals such as Human Genetics, Psychiatric Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Molecular Psychiatry and Human Molecular Genetics.
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.