Peter Propping

34.5k citations

329 papers · 16.1k · 3 hit papers · h-index 68

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

Molecular Biology 125
- Receptor Mechanisms and Signaling 32
Genetics 85
- Genetics and Neurodevelopmental Disorders 33
- Genetic Associations and Epidemiology 21

Co-authors: Markus M. Nöthen (128 shared papers)Waltraut Friedl (84 shared papers)Ortrud K. Steinlein (7 shared papers)Samuel F. Berkovic (3 shared papers)Sven Cichon (66 shared papers)Marcella Rietschel (61 shared papers)Elisabeth Mangold (24 shared papers)Erik G. Jönsson (15 shared papers)
Journals: Human Genetics (24 papers)Psychiatric Genetics (19 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (14 papers)Molecular Psychiatry (12 papers)Human Molecular Genetics (11 papers)
Partner nations: Germany United States Belgium

In The Last Decade

Peter Propping

322 papers receiving 15.5k citations

Peter Propping's Hit Papers

align trajectories log scale

Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers 1999 · 588 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1999 Molecular Psychiatry
1998 Science
1995 Nature Genetics

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 329 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Potassium Channel Mutation in Neonatal Human Epilepsy Science ·Christian Biervert, Björn C. Schroeder, Christian Kubisch, Samuel F. Berkovic, Peter Propping, Thomas J. Jentsch, Ortrud K. Steinlein Hit paper breakdown →	1998	854
2	A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy Nature Genetics ·Ortrud K. Steinlein, John C. Mulley, Peter Propping, Robyn H. Wallace, Hilary A. Phillips, Grant R. Sutherland, Ingrid E. Scheffer, Samuel F. Berkovic Hit paper breakdown →	1995	843
3	Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers Molecular Psychiatry ·Erik G. Jönsson, Markus M. Nöthen, F Grünhage, Lars Farde, Yoshifumi Nakashima, Peter Propping, Göran C. Sedvall Hit paper breakdown →	1999	588
4	Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder Human Molecular Genetics ·J. Deckert, Marco Catalano, Yana V. Syagailo, Monica Bosi, Olga Okladnova, Daniela Di Bella, Markus M. Nöthen, Pietro Maffei, Petra Franke, J. Fritze, W. Maier, Peter Propping, H. Beckmann, Laura Bellodi, Klaus‐Peter Lesch	1999	482
5	A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Molecular Psychiatry ·Amber E. Baum, Nirmala Akula, Michael Cabanero, Imer Cardona, Winston Corona, Brygida Klemens, Thomas G. Schulze, Sven Cichon, Marcella Rietschel, Markus M. Nöthen, Alexander Georgi, J Schumacher, Markus Schwarz, Rami Abou Jamra, Susanne Höfels, Peter Propping, Jaya M. Satagopan, Sevilla D. Detera‐Wadleigh, John Hardy, Francis J. McMahon	2007	474
6	The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variants Human Genetics ·F. Vogel, E. Schalt, J. Kr�ger, Peter Propping, K. F. Lehnert	1979	296
7	An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Human Molecular Genetics ·Ortrud K. Steinlein, Andrés Magnússon, Jens Stoodt, Sonia Bertrand, Sigrid Weiland, Samuel F. Berkovic, Karl O. Nakken, Peter Propping, Daniel Bertrand	1997	295
8	Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444 Human Molecular Genetics ·Reiner Caspari, S Olschwang, Waltraut Friedl, Marion Mandl, Cécile Boisson, T. Böker, Albert J. Augustin, Martina Kadmon, Gabriela Möslein, Gilles Thomas, Peter Propping	1995	283
9	Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression Biological Psychiatry ·Johannes Schumacher, Rami Abou Jamra, Tim Becker, Stephanie Ohlraun, Norman Klopp, Elisabeth B. Binder, Thomas G. Schulze, Monika Deschner, Christine Schmäl, Susanne Höfels, Astrid Zobel, Thomas Illig, Peter Propping, (unknown), Marcella Rietschel, Markus M. Nöthen, Sven Cichon	2005	247
10	Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder Molecular Psychiatry ·J Schumacher, R Abon Jamra, Jan Freudenberg, Tim Becker, Stephanie Ohlraun, A Otte, Monja Tullius, S. Kovalenko, Ann Van Den Bogaert, W. Maier, Marcella Rietschel, Peter Propping, Markus M. Nöthen, Sven Cichon	2004	234
11	Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis Gastroenterology ·Stefanie Vogt, Natalie Jones, Daria Christian, Christoph Engel, Maartje Nielsen, Astrid Kaufmann, Verena Steinke, Hans F. A. Vasen, Peter Propping, Julian R. Sampson, Frederik J. Hes, Stefan Aretz	2009	229
12	Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. PubMed ·Martin Ruttledge, Anne Andermann, Catherine M. Phelan, Jaime O. Claudio, Fei‐Yu Han, Nathalie Chrétien, Shyam Rangaratnam, Mia MacCollin, Priscilla Short, Dilys M. Parry, Virginia V. Michels, Vincent M. Riccardi, Rosanna Weksberg, Katsumasa Kitamura, J M Bradburn, Bertil Hall, Peter Propping, Guy A. Rouleau	1996	196
13	Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia The American Journal of Human Genetics ·Johannes Schumacher, Heidi Anthoni, Faten Dahdouh, Inke R. König, Axel M. Hillmer, Nadine Kluck, Malou Manthey, Ellen Plume, Andreas Warnke, Helmut Remschmidt, Jutta Hülsmann, Sven Cichon, Cecilia M. Lindgren, Peter Propping, Marco Zucchelli, Andreas Ziegler, Myriam Peyrard‐Janvid, Gerd Schulte‐Körne, Markus M. Nöthen, Juha Kere	2005	180
14	A similarity-based method for genome-wide prediction ofdisease-relevant human genes Bioinformatics ·Johannes Freudenberg, Peter Propping	2002	177
15	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome Human Mutation ·Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl	2005	174
16	Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria The American Journal of Human Genetics ·Roland Kruse, Arno Rütten, Christof Lamberti, Hamid Reza Hosseiny–Malayeri, Yaping Wang, Corina Ruelfs, Matthias Jungck, Micaela Mathiak, Thomas Ruzicka, Wolfgang Hartschuh, Michele Bisceglia, Waltraut Friedl, Peter Propping	1998	168
17	Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B Nature Genetics ·Michael Oldridge, Ana María Fortuna, Monika Maringa, Peter Propping, Sahar Mansour, C. Pollitt, Thomas M. DeChiara, Robert B. Kimble, David M. Valenzuela, George D. Yancopoulos, Andrew O.M. Wilkie	2000	163
18	The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease The American Journal of Human Genetics ·Ann Van Den Bogaert, Johannes Schumacher, Thomas G. Schulze, A Otte, Stephanie Ohlraun, S. S. Kovalenko, Tim Becker, Jan Freudenberg, Erik G. Jönsson, Marja Mattila‐Evenden, Göran C. Sedvall, Piotr M. Czerski, Paweł Kapelski, Joanna Hauser, Wolfgang Maier, Marcella Rietschel, Peter Propping, Markus M. Nöthen, Sven Cichon	2003	159
19	Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer The Lancet ·Reiner Caspari, Waltraut Friedl, Marion Mandl, Peter Propping, Gabriela Möslein, Martina Kadmon, Gundi Timmermanns, Michael Knapp, Jacobasch Kh, K. W. Ecker, D. Kreiβler-Haag	1994	158
20	Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia Human Genetics ·Jeanette Erdmann, Daphne Shimron‐Abarbanell, Marcella Rietschel, Margot Albus, Wolfgang Maier, Judith Körner, Brigitta Bondy, Kevin Chen, Jean C. Shih, Michael Knapp, Peter Propping, Markus M. Nöthen	1996	158

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 329 papers that have together received 16.1k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (64 papers), Bipolar Disorder and Treatment (41 papers), Neurotransmitter Receptor Influence on Behavior (39 papers), Genetics and Neurodevelopmental Disorders (33 papers), Receptor Mechanisms and Signaling (32 papers), Cancer Genomics and Diagnostics (30 papers), Genetic Associations and Epidemiology (21 papers) and Neuroscience and Neuropharmacology Research (19 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.3k citations), Biological Psychiatry (511 citations), Psychiatry and Mental health (3.1k 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 Belgium. Frequent 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. 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.

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Peter Propping

Peter Propping's Hit Papers

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Fields of papers citing papers by Peter Propping

All Works

About Peter Propping

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