Daniela Probst
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 10%
- Neurological disorders and treatments
Papers in
-
- Genetic Neurodegenerative Diseases 4
- Genetics 1
- Mesenchymal stem cell research 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Stefan G. Lechner (1 shared paper)Werner Zwerschke (1 shared paper)Andreas Marius Kaiser (1 shared paper)Monika Mattesich (1 shared paper)Nikolaus Wenger (1 shared paper)Gerhard Pierer (1 shared paper)Maria C. Mitterberger (1 shared paper)
- Journals
- Neurology (2 papers)The Lancet Neurology (1 paper)Journal of Huntington s Disease (1 paper)Stem Cell Research (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomGermanySwitzerland
In The Last Decade
Daniela Probst
6 papers receiving 752 citations
Peers
Comparison fields: 5 of 65
- Cellular and Molecular Neuroscience 467
- Neurology 173
- Molecular Biology 461
- Aging 8
- Genetics 121
Countries citing papers authored by Daniela Probst
This map shows the geographic impact of Daniela Probst'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 Daniela Probst with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Probst more than expected).
Fields of papers citing papers by Daniela Probst
This network shows the impact of papers produced by Daniela Probst. 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 Daniela Probst. The network helps show where Daniela Probst may publish in the future.
Co-authors
The 7 scholars most cited alongside Daniela Probst, 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 | 2012 | 284 | |
| 2 | 2017 | 238 | |
| 3 | 2000 | 130 | |
| 4 | 2012 | 70 | |
| 5 | 2016 | 38 | |
| 6 | 2018 | 23 |
About Daniela Probst
Daniela Probst is a scholar working on Cellular and Molecular Neuroscience, Genetics, Pediatrics, Perinatology and Child Health, Physiology and Genetics, having authored 6 papers that have together received 783 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), Prenatal Screening and Diagnostics (1 paper), Adipokines, Inflammation, and Metabolic Diseases (1 paper), Epigenetics and DNA Methylation (1 paper), Mesenchymal stem cell research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Adipose Tissue and Metabolism (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (467 citations), Neurology (173 citations), Molecular Biology (461 citations), Aging (8 citations) and Genetics (121 citations). Daniela Probst has collaborated with scholars based in United Kingdom, Germany and Switzerland. Frequent co-authors include Stefan G. Lechner, Werner Zwerschke, Andreas Marius Kaiser, Monika Mattesich, Nikolaus Wenger, Gerhard Pierer and Maria C. Mitterberger. Their work appears in journals such as Neurology, The Lancet Neurology, Journal of Huntington s Disease, Stem Cell Research and European Journal of Human 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.