Valentin Sander
Impact in
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- Blood Coagulation and Thrombosis Mechanisms
Papers in
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- Muscle Physiology and Disorders 3
- Genetics 2
- Neurogenetic and Muscular Disorders Research 2
- Genetics and Neurodevelopmental Disorders 1
- Genomics and Rare Diseases 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Tiina Talvik (4 shared papers)Inga Talvik (4 shared papers)Pilvi Ilves (2 shared papers)Rael Laugesaar (1 shared paper)Anneli Kolk (1 shared paper)Tiiu Tomberg (1 shared paper)Andres Piirsoo (2 shared papers)Tiina Kahre (1 shared paper)
- Journals
- Brain and Development (1 paper)Neuropediatrics (1 paper)Clinical Neurophysiology (1 paper)Pediatric Neurology (1 paper)European Journal of Paediatric Neurology (1 paper)
- Partner nations
- EstoniaUnited States
In The Last Decade
Valentin Sander
5 papers receiving 58 citations
Peers
Comparison fields: 5 of 21
- Hematology 20
- Internal Medicine 3
- Neurology 10
- Genetics 7
- Psychiatry and Mental health 7
Countries citing papers authored by Valentin Sander
This map shows the geographic impact of Valentin Sander'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 Valentin Sander with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Valentin Sander more than expected).
Fields of papers citing papers by Valentin Sander
This network shows the impact of papers produced by Valentin Sander. 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 Valentin Sander. The network helps show where Valentin Sander may publish in the future.
Co-authors
The 12 scholars most cited alongside Valentin Sander, 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 | 2010 | 28 | |
| 2 | 2003 | 13 | |
| 3 | 2016 | 11 | |
| 4 | 1999 | 6 | |
| 5 | 2019 | 1 |
About Valentin Sander
Valentin Sander is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cardiology and Cardiovascular Medicine, having authored 5 papers that have together received 59 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Blood Coagulation and Thrombosis Mechanisms (1 paper), Genomics and Rare Diseases (1 paper), Cardiomyopathy and Myosin Studies (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Genetic Neurodegenerative Diseases (1 paper). The work is most often cited by research in Hematology (20 citations), Internal Medicine (3 citations), Neurology (10 citations), Genetics (7 citations) and Psychiatry and Mental health (7 citations). Valentin Sander has collaborated with scholars based in Estonia and United States. Frequent co-authors include Tiina Talvik, Inga Talvik, Pilvi Ilves, Rael Laugesaar, Anneli Kolk, Tiiu Tomberg, Andres Piirsoo, Tiina Kahre, Tiia Reimand and Ulvi Vaher. Their work appears in journals such as Brain and Development, Neuropediatrics, Clinical Neurophysiology, Pediatric Neurology 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.