Sanna Puusepp
Impact in
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- Metabolism and Genetic Disorders
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
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- Muscle Physiology and Disorders 2
- Mitochondrial Function and Pathology 2
- Ion channel regulation and function 1
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- Genetic Neurodegenerative Diseases 2
- Co-authors
- Katrin Õunap (9 shared papers)Eve Õiglane‐Shlik (5 shared papers)Inga Talvik (4 shared papers)Sander Pajusalu (7 shared papers)Karit Reinson (3 shared papers)Tiia Reimand (6 shared papers)Rita Teek (3 shared papers)Ulvi Vaher (2 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)European Journal of Paediatric Neurology (1 paper)Neuromuscular Disorders (1 paper)Neurology Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- EstoniaGermanyNetherlands
In The Last Decade
Sanna Puusepp
8 papers receiving 129 citations
Peers
Comparison fields: 5 of 38
- Clinical Biochemistry 21
- Genetics 68
- Cellular and Molecular Neuroscience 36
- Molecular Biology 81
- Pediatrics, Perinatology and Child Health 17
Countries citing papers authored by Sanna Puusepp
This map shows the geographic impact of Sanna Puusepp'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 Sanna Puusepp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sanna Puusepp more than expected).
Fields of papers citing papers by Sanna Puusepp
This network shows the impact of papers produced by Sanna Puusepp. 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 Sanna Puusepp. The network helps show where Sanna Puusepp may publish in the future.
Co-authors
The 25 scholars most cited alongside Sanna Puusepp, 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 | 2016 | 62 | |
| 2 | 2018 | 30 | |
| 3 | 2015 | 20 | |
| 4 | 2014 | 18 | |
| 5 | 2020 | 11 | |
| 6 | 2015 | 8 | |
| 7 | 2023 | 2 | |
| 8 | 2024 | 1 | |
| 9 | 2025 | 0 |
About Sanna Puusepp
Sanna Puusepp is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Genetics and Neurology, having authored 9 papers that have together received 152 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), Genetic Neurodegenerative Diseases (2 papers), Cardiomyopathy and Myosin Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper), Neurological disorders and treatments (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Clinical Biochemistry (21 citations), Genetics (68 citations), Cellular and Molecular Neuroscience (36 citations), Molecular Biology (81 citations) and Pediatrics, Perinatology and Child Health (17 citations). Sanna Puusepp has collaborated with scholars based in Estonia, Germany and Netherlands. Frequent co-authors include Katrin Õunap, Eve Õiglane‐Shlik, Inga Talvik, Sander Pajusalu, Karit Reinson, Tiia Reimand, Rita Teek, Ulvi Vaher, Tiiu Tomberg and Andres Piirsoo. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Paediatric Neurology, Neuromuscular Disorders, Neurology Genetics and American Journal of Medical Genetics Part A.
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.