Lutz Priebe
Impact in
- Biological Psychiatry top 5%
- Tryptophan and brain disorders
- Behavioral Neuroscience top 10%
- Stress Responses and Cortisol
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- 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)Mikael Landén (1 shared paper)Martin Schalling (1 shared paper)Göran Engberg (1 shared paper)Marquis P. Vawter (1 shared paper)Urban Ösby (1 shared paper)
- Journals
- PLoS ONE (2 papers)Psychiatric Genetics (2 papers)European Journal of Pediatrics (1 paper)Clinical Epigenetics (1 paper)Schizophrenia Research (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Lutz Priebe
13 papers receiving 372 citations
Peers
Comparison fields: 5 of 53
- Biological Psychiatry 92
- Behavioral Neuroscience 43
- Psychiatry and Mental health 77
- Genetics 149
- Molecular Biology 148
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 | 65 | |
| 3 | 2015 | 59 | |
| 4 | 1995 | 44 | |
| 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 377 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Bipolar Disorder and Treatment (2 papers), Neuroscience and Neuropharmacology Research (2 papers), Congenital heart defects research (2 papers) and Adolescent and Pediatric Healthcare (1 paper). The work is most often cited by research in Biological Psychiatry (92 citations), Behavioral Neuroscience (43 citations), Psychiatry and Mental health (77 citations), Genetics (149 citations) and Molecular Biology (148 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, Mikael Landén, Martin Schalling, Göran Engberg, Marquis P. Vawter, Urban Ösby, Lil Träskman‐Bendz and Pernilla Nikamo. Their work appears in journals such as PLoS ONE, Psychiatric Genetics, European Journal of Pediatrics, Clinical Epigenetics and Schizophrenia Research.
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.