Lutz Priebe
Impact in
- Biological Psychiatry top 5%
- Tryptophan and brain disorders
- Behavioral Neuroscience top 10%
- Stress Responses and Cortisol
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 3
- Genetic Associations and Epidemiology 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 2
- Co-authors
- Markus M. Nöthen (8 shared papers)Sven Cichon (9 shared papers)Per Hoffmann (7 shared papers)Lena Backlund (1 shared paper)Mikael Landén (1 shared paper)Carl M. Sellgren (1 shared paper)Pernilla Nikamo (1 shared paper)Lil Träskman‐Bendz (1 shared paper)
- Journals
- Psychiatric Genetics (2 papers)PLoS ONE (2 papers)Clinical Epigenetics (1 paper)Endocrine Research (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Lutz Priebe
13 papers receiving 368 citations
Peers
Comparison fields: 5 of 57
- Biological Psychiatry 95
- Behavioral Neuroscience 55
- Genetics 170
- Psychiatry and Mental health 89
- Urology 15
Countries citing papers authored by Lutz Priebe
This map shows the geographic impact of Lutz Priebe'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 Lutz Priebe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lutz Priebe more than expected).
Fields of papers citing papers by Lutz Priebe
This network shows the impact of papers produced by Lutz Priebe. 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 Lutz Priebe. The network helps show where Lutz Priebe may publish in the future.
Co-authors
The 25 scholars most cited alongside Lutz Priebe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 90 | |
| 2 | 2011 | 63 | |
| 3 | 2015 | 58 | |
| 4 | 1995 | 43 | |
| 5 | 2008 | 22 | |
| 6 | 2013 | 20 | |
| 7 | 2013 | 16 | |
| 8 | 2013 | 16 | |
| 9 | 2010 | 15 | |
| 10 | 2013 | 12 | |
| 11 | 2011 | 11 | |
| 12 | 2012 | 5 | |
| 13 | 2014 | 2 |
About Lutz Priebe
Lutz Priebe is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Surgery, having authored 13 papers that have together received 373 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (2 papers), Bipolar Disorder and Treatment (2 papers), Congenital heart defects research (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Neuroscience and Neuropharmacology Research (2 papers). The work is most often cited by research in Biological Psychiatry (95 citations), Behavioral Neuroscience (55 citations), Genetics (170 citations), Psychiatry and Mental health (89 citations) and Urology (15 citations). Lutz Priebe has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Markus M. Nöthen, Sven Cichon, Per Hoffmann, Lena Backlund, Mikael Landén, Carl M. Sellgren, Pernilla Nikamo, Lil Träskman‐Bendz, Göran Engberg and Martin Schalling. Their work appears in journals such as Psychiatric Genetics, PLoS ONE, Clinical Epigenetics, Endocrine Research and European Journal of Human 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.