Lars‐Erik Wehner
Impact in
- Molecular Biology top 10%
- Protein Tyrosine Phosphatases
- Protein Kinase Regulation and GTPase Signaling
- Congenital heart defects research
-
- Genomics and Rare Diseases
- Genetic and rare skin diseases.
- Vascular Anomalies and Treatments
Papers in
- Genetics 4
- Vascular Anomalies and Treatments 3
- Congenital Ear and Nasal Anomalies 1
-
- Hereditary Neurological Disorders 2
- Co-authors
- Christian Peter Kratz (2 shared papers)Martin Zenker (2 shared papers)Gideon E. Bollag (1 shared paper)Cornelia Klein (1 shared paper)Luciana Musante (1 shared paper)Vera M. Kalscheuer (1 shared paper)Ineke van der Burgt (1 shared paper)Erik A. Sistermans (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)International Journal of Molecular Medicine (1 paper)DNA and Cell Biology (1 paper)Liver Transplantation (1 paper)Nature Genetics (1 paper)
- Partner nations
- GermanyUnited States
In The Last Decade
Lars‐Erik Wehner
10 papers receiving 914 citations
Peers
Comparison fields: 5 of 44
- Molecular Biology 637
- Genetics 164
- Genetics 45
- Hematology 46
- Neurology 39
Countries citing papers authored by Lars‐Erik Wehner
This map shows the geographic impact of Lars‐Erik Wehner'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 Lars‐Erik Wehner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lars‐Erik Wehner more than expected).
Fields of papers citing papers by Lars‐Erik Wehner
This network shows the impact of papers produced by Lars‐Erik Wehner. 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 Lars‐Erik Wehner. The network helps show where Lars‐Erik Wehner may publish in the future.
Co-authors
The 25 scholars most cited alongside Lars‐Erik Wehner, 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 | 2006 | 596 | |
| 2 | 2006 | 167 | |
| 3 | 2007 | 109 | |
| 4 | 2001 | 26 | |
| 5 | 2006 | 15 | |
| 6 | 2005 | 14 | |
| 7 | 2004 | 7 | |
| 8 | 2009 | 6 | |
| 9 | 2004 | 1 | |
| 10 | 2006 | 1 |
About Lars‐Erik Wehner
Lars‐Erik Wehner is a scholar working on Genetics, Cellular and Molecular Neuroscience, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 10 papers that have together received 942 indexed citations. Recurring topics across this work include Vascular Anomalies and Treatments (3 papers), Protein Tyrosine Phosphatases (3 papers), Multiple Sclerosis Research Studies (2 papers), Hereditary Neurological Disorders (2 papers), Viral-associated cancers and disorders (1 paper) and Congenital Ear and Nasal Anomalies (1 paper). The work is most often cited by research in Molecular Biology (637 citations), Genetics (164 citations), Genetics (45 citations), Hematology (46 citations) and Neurology (39 citations). Lars‐Erik Wehner has collaborated with scholars based in Germany and United States. Frequent co-authors include Christian Peter Kratz, Martin Zenker, Gideon E. Bollag, Cornelia Klein, Luciana Musante, Vera M. Kalscheuer, Ineke van der Burgt, Erik A. Sistermans, Anita M. Rauch and Brian L. West. Their work appears in journals such as Journal of Medical Genetics, International Journal of Molecular Medicine, DNA and Cell Biology, Liver Transplantation and Nature 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.