Markus Wolff
Impact in
- Psychiatry and Mental health top 0.5%
- Epilepsy research and treatment
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Papers in
-
- Epilepsy research and treatment 54
- Genetics 10
- Craniofacial Disorders and Treatments 5
- Glioma Diagnosis and Treatment 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Catherine Cassé‐Perrot (2 shared papers)Charlotte Dravet (2 shared papers)Ingeborg Krägeloh‐Mann (5 shared papers)Andreas Brunklaus (1 shared paper)Karin Haas‐Lude (8 shared papers)Martin Staudt (2 shared papers)Sameer M. Zuberi (1 shared paper)Martin U. Schuhmann (6 shared papers)
- Journals
- Neuropediatrics (11 papers)Epilepsia (8 papers)Neurology (5 papers)Nature Genetics (4 papers)European Journal of Paediatric Neurology (3 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Markus Wolff
73 papers receiving 5.2k citations
Markus Wolff's Hit Papers
Peers
Comparison fields: 5 of 94
- Psychiatry and Mental health 3.5k
- Genetics 875
- Pediatrics, Perinatology and Child Health 271
- Cellular and Molecular Neuroscience 286
- Neurology 156
Countries citing papers authored by Markus Wolff
This map shows the geographic impact of Markus Wolff'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 Markus Wolff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Wolff more than expected).
Fields of papers citing papers by Markus Wolff
This network shows the impact of papers produced by Markus Wolff. 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 Markus Wolff. The network helps show where Markus Wolff may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Wolff, 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 77 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders Hit paper breakdown → | 2017 | 460 |
| 2 | 2013 | 355 | |
| 3 | Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Hit paper breakdown → | 2018 | 340 |
| 4 | 2012 | 282 | |
| 5 | 2016 | 253 | |
| 6 | 2015 | 243 | |
| 7 | 2006 | 230 | |
| 8 | 2015 | 225 | |
| 9 | 2017 | 211 | |
| 10 | 2006 | 210 | |
| 11 | 2013 | 206 | |
| 12 | 2013 | 190 | |
| 13 | 2018 | 175 | |
| 14 | 2017 | 137 | |
| 15 | 2002 | 132 | |
| 16 | 2018 | 131 | |
| 17 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 129 |
| 18 | 2018 | 128 | |
| 19 | 2005 | 109 | |
| 20 | 2015 | 92 |
About Markus Wolff
Markus Wolff is a scholar working on Psychiatry and Mental health, Genetics, Genetics, Neurology and Molecular Biology, having authored 77 papers that have together received 5.4k indexed citations. Recurring topics across this work include Epilepsy research and treatment (54 papers), Ion channel regulation and function (7 papers), Craniofacial Disorders and Treatments (5 papers), Glioma Diagnosis and Treatment (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Traumatic Brain Injury and Neurovascular Disturbances (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Pancreatitis Pathology and Treatment (2 papers). The work is most often cited by research in Psychiatry and Mental health (3.5k citations), Genetics (875 citations), Pediatrics, Perinatology and Child Health (271 citations), Cellular and Molecular Neuroscience (286 citations) and Neurology (156 citations). Markus Wolff has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Catherine Cassé‐Perrot, Charlotte Dravet, Ingeborg Krägeloh‐Mann, Andreas Brunklaus, Karin Haas‐Lude, Martin Staudt, Sameer M. Zuberi, Martin U. Schuhmann, Gus A. Baker and Jill Clayton‐Smith. Their work appears in journals such as Neuropediatrics, Epilepsia, Neurology, Nature Genetics and European Journal of Paediatric 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.