Peter Lichtner
Impact in
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- RNA regulation and disease 10
- Congenital heart defects research 5
- Genetics 27
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Thomas Meitinger (46 shared papers)Jens Tetens (5 shared papers)Georg Thaller (3 shared papers)Claudia N. Keilhauer (3 shared papers)Sheila Fisher (3 shared papers)Lars G. Fritsche (2 shared papers)Andrea Rivera (2 shared papers)Bernhard H. F. Weber (2 shared papers)
- Journals
- Movement Disorders (9 papers)The American Journal of Human Genetics (6 papers)European Journal of Human Genetics (5 papers)Anesthesiology (4 papers)Neurology (4 papers)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Peter Lichtner
99 papers receiving 5.3k citations
Peter Lichtner's Hit Papers
Peers
Comparison fields: 5 of 138
- Ophthalmology 620
- Neurology 957
- Nephrology 361
- Genetics 1.4k
- Endocrine and Autonomic Systems 263
Countries citing papers authored by Peter Lichtner
This map shows the geographic impact of Peter Lichtner'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 Lichtner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Lichtner more than expected).
Fields of papers citing papers by Peter Lichtner
This network shows the impact of papers produced by Peter Lichtner. 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 Lichtner. The network helps show where Peter Lichtner may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Lichtner, 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 102 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk Hit paper breakdown → | 2005 | 652 |
| 2 | 2000 | 486 | |
| 3 | 2010 | 371 | |
| 4 | 2006 | 304 | |
| 5 | 2005 | 217 | |
| 6 | 2005 | 198 | |
| 7 | 2010 | 165 | |
| 8 | 2006 | 155 | |
| 9 | 2010 | 151 | |
| 10 | 2008 | 144 | |
| 11 | 2004 | 123 | |
| 12 | 1999 | 102 | |
| 13 | 2005 | 100 | |
| 14 | 2000 | 97 | |
| 15 | 2007 | 97 | |
| 16 | 2007 | 85 | |
| 17 | 1998 | 74 | |
| 18 | 2014 | 72 | |
| 19 | 2019 | 66 | |
| 20 | 2015 | 66 |
About Peter Lichtner
Peter Lichtner is a scholar working on Molecular Biology, Genetics, Neurology, Cellular and Molecular Neuroscience and Epidemiology, having authored 102 papers that have together received 5.5k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (19 papers), RNA regulation and disease (10 papers), Neurological diseases and metabolism (9 papers), Restless Legs Syndrome Research (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers) and Dysphagia Assessment and Management (5 papers). The work is most often cited by research in Ophthalmology (620 citations), Neurology (957 citations), Nephrology (361 citations), Genetics (1.4k citations) and Endocrine and Autonomic Systems (263 citations). Peter Lichtner has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Thomas Meitinger, Jens Tetens, Georg Thaller, Claudia N. Keilhauer, Sheila Fisher, Lars G. Fritsche, Andrea Rivera, Bernhard H. F. Weber, Franz R. Seefried and David Habier. Their work appears in journals such as Movement Disorders, The American Journal of Human Genetics, European Journal of Human Genetics, Anesthesiology and Neurology.
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.