Thomas Voït
Impact in
- Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research
- Virus-based gene therapy research
-
- Cardiomyopathy and Myosin Studies
Papers in
-
- Muscle Physiology and Disorders 61
- RNA Research and Splicing 9
- Nuclear Structure and Function 8
-
- Cardiomyopathy and Myosin Studies 20
- Co-authors
- Uwe Mellies (8 shared papers)R. Ragette (6 shared papers)Helmut Teschler (6 shared papers)Christian Dohna‐Schwake (4 shared papers)Jörg Klepper (10 shared papers)Alice Steinbrecher (3 shared papers)William B. Dobyns (2 shared papers)Hans van Bokhoven (3 shared papers)
- Journals
- Neuromuscular Disorders (38 papers)Neurology (6 papers)Neuropediatrics (6 papers)European Journal of Pediatrics (4 papers)Human Molecular Genetics (4 papers)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Thomas Voït
132 papers receiving 5.6k citations
Thomas Voït's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 975
- Cardiology and Cardiovascular Medicine 1.1k
- Molecular Biology 3.5k
- Physiology 1.0k
- Clinical Biochemistry 268
Countries citing papers authored by Thomas Voït
This map shows the geographic impact of Thomas Voït'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 Thomas Voït with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Voït more than expected).
Fields of papers citing papers by Thomas Voït
This network shows the impact of papers produced by Thomas Voït. 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 Thomas Voït. The network helps show where Thomas Voït may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Voït, 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 139 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome Hit paper breakdown → | 2002 | 572 |
| 2 | 2015 | 260 | |
| 3 | 2010 | 251 | |
| 4 | 2006 | 227 | |
| 5 | 2012 | 188 | |
| 6 | 2009 | 171 | |
| 7 | 2004 | 165 | |
| 8 | 2015 | 143 | |
| 9 | 2014 | 143 | |
| 10 | 2012 | 129 | |
| 11 | 2001 | 125 | |
| 12 | 2005 | 120 | |
| 13 | 2007 | 115 | |
| 14 | 2003 | 115 | |
| 15 | 2012 | 114 | |
| 16 | 2004 | 107 | |
| 17 | 2006 | 95 | |
| 18 | 2004 | 93 | |
| 19 | 2013 | 86 | |
| 20 | 2006 | 78 |
About Thomas Voït
Thomas Voït is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Physiology, Genetics and Genetics, having authored 139 papers that have together received 5.8k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (61 papers), Cardiomyopathy and Myosin Studies (20 papers), Neurogenetic and Muscular Disorders Research (16 papers), Diet and metabolism studies (11 papers), Metabolism and Genetic Disorders (11 papers), Virus-based gene therapy research (10 papers), RNA Research and Splicing (9 papers) and Nuclear Structure and Function (8 papers). The work is most often cited by research in Genetics (975 citations), Cardiology and Cardiovascular Medicine (1.1k citations), Molecular Biology (3.5k citations), Physiology (1.0k citations) and Clinical Biochemistry (268 citations). Thomas Voït has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Uwe Mellies, R. Ragette, Helmut Teschler, Christian Dohna‐Schwake, Jörg Klepper, Alice Steinbrecher, William B. Dobyns, Hans van Bokhoven, Luis Garcı́a and Han G. Brunner. Their work appears in journals such as Neuromuscular Disorders, Neurology, Neuropediatrics, European Journal of Pediatrics 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.