Peter Propping

413 papers receiving 26.0k citations

Peter Propping's Hit Papers

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs 2013 · 1.8k citations
1.8k0+10+20Years since publication50010001.5k

Peers

Peter Propping
Comparison fields: 5 of 180
  • Biological Psychiatry 988
  • Psychiatry and Mental health 5.0k
  • Genetics 8.6k
  • Cellular and Molecular Neuroscience 5.1k
  • Pathology and Forensic Medicine 3.9k
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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-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.

Border = papers with Peter Propping Line = papers co-authored together Peter Propping links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 430 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Hit paper breakdown →
20131775
2
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
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20111099
3
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
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1995940
4
A Potassium Channel Mutation in Neonatal Human Epilepsy
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1998933
5
Identification of loci associated with schizophrenia by genome-wide association and follow-up
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2008907
6 1999622
7
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
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2007569
8 1999525
9 2003499
10 2009393
11 2009365
12 1979328
13 1995319
14 1997316
15 2012287
16 2014274
17 2009264
18 2004259
19 2005257
20 2012242

About Peter Propping

Peter Propping is a scholar working on Genetics, Psychiatry and Mental health, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Molecular Biology, having authored 430 papers that have together received 27.3k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (79 papers), Bipolar Disorder and Treatment (54 papers), Genetics and Neurodevelopmental Disorders (48 papers), Neurotransmitter Receptor Influence on Behavior (43 papers), Genetic Associations and Epidemiology (42 papers), Receptor Mechanisms and Signaling (34 papers), Cancer Genomics and Diagnostics (31 papers) and Genomic variations and chromosomal abnormalities (24 papers). The work is most often cited by research in Biological Psychiatry (988 citations), Psychiatry and Mental health (5.0k citations), Genetics (8.6k citations), Cellular and Molecular Neuroscience (5.1k citations) and Pathology and Forensic Medicine (3.9k citations). Peter Propping has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Markus Maria Nöthen, Waltraut Friedl, Ortrud K. Steinlein, Sven Cichon, Samuel Frank Berkovic, Marcella Rietschel, Elisabeth Mangold, Stefan Aretz, Reiner Caspari and Erik Gunnar Jönsson. Their work appears in journals such as Human Genetics, Psychiatric Genetics, Molecular Psychiatry, The American Journal of Human Genetics and American Journal of Medical Genetics Part B Neuropsychiatric 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.

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