Andreas Lux
Impact in
- Genetics top 2%
- Vascular Anomalies and Treatments
-
- Tracheal and airway disorders
- Pulmonary Hypertension Research and Treatments
Papers in
-
- TGF-β signaling in diseases 5
- Connective Tissue Growth Factor Research 3
- RNA modifications and cancer 3
- Advanced biosensing and bioanalysis techniques 2
- Genetics 12
- Vascular Anomalies and Treatments 12
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Douglas A. Marchuk (8 shared papers)Mathias Hafner (7 shared papers)Liliana Attisano (1 shared paper)Ulrich Goessler (2 shared papers)Calvin Vary (3 shared papers)Haneen Sadick (2 shared papers)Karl Hörmann (1 shared paper)Ramin Naim (2 shared papers)
- Journals
- Human Mutation (6 papers)Journal of Biological Chemistry (4 papers)PLoS ONE (2 papers)Journal of Telemedicine and Telecare (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Andreas Lux
26 papers receiving 923 citations
Peers
Comparison fields: 5 of 78
- Genetics 424
- Pulmonary and Respiratory Medicine 314
- Molecular Biology 404
- Hematology 59
- Immunology and Allergy 30
Countries citing papers authored by Andreas Lux
This map shows the geographic impact of Andreas Lux'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 Andreas Lux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Lux more than expected).
Fields of papers citing papers by Andreas Lux
This network shows the impact of papers produced by Andreas Lux. 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 Andreas Lux. The network helps show where Andreas Lux may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Lux, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta1 as well as high ALK1 tissue expression. | 2005 | 128 |
| 2 | 1999 | 128 | |
| 3 | 2006 | 92 | |
| 4 | 1998 | 80 | |
| 5 | 2000 | 58 | |
| 6 | 2004 | 56 | |
| 7 | 2005 | 43 | |
| 8 | 2011 | 40 | |
| 9 | 2006 | 37 | |
| 10 | 2010 | 36 | |
| 11 | 2006 | 35 | |
| 12 | 1998 | 28 | |
| 13 | 1993 | 24 | |
| 14 | 1995 | 21 | |
| 15 | 1998 | 21 | |
| 16 | 2013 | 19 | |
| 17 | 2014 | 18 | |
| 18 | 1994 | 14 | |
| 19 | 2005 | 14 | |
| 20 | 1996 | 13 |
About Andreas Lux
Andreas Lux is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Genetics and Pathology and Forensic Medicine, having authored 28 papers that have together received 939 indexed citations. Recurring topics across this work include Vascular Anomalies and Treatments (12 papers), TGF-β signaling in diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Tracheal and airway disorders (4 papers), Connective Tissue Growth Factor Research (3 papers), RNA modifications and cancer (3 papers), Chromosomal and Genetic Variations (2 papers) and Advanced biosensing and bioanalysis techniques (2 papers). The work is most often cited by research in Genetics (424 citations), Pulmonary and Respiratory Medicine (314 citations), Molecular Biology (404 citations), Hematology (59 citations) and Immunology and Allergy (30 citations). Andreas Lux has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Douglas A. Marchuk, Mathias Hafner, Liliana Attisano, Ulrich Goessler, Calvin Vary, Haneen Sadick, Karl Hörmann, Ramin Naim, Frank Riedel and Carol J. Gallione. Their work appears in journals such as Human Mutation, Journal of Biological Chemistry, PLoS ONE, Journal of Telemedicine and Telecare 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.