Mark Screen
Impact in
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- Neurogenetic and Muscular Disorders Research
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- Cardiomyopathy and Myosin Studies
Papers in ⓘ
- Genetics 2
- Neurogenetic and Muscular Disorders Research 2
- Connective tissue disorders research 1
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- Genetic Neurodegenerative Diseases 3
- Co-authors
- Bjarne Udd (5 shared papers)Peter Hackman (5 shared papers)Anna Vihola (4 shared papers)Per Harald Jonson (3 shared papers)Anni Evilä (3 shared papers)J. Sarparanta (3 shared papers)Juha Kere (1 shared paper)Sara Lehtinen (1 shared paper)
- Journals
- Annals of Neurology (2 papers)Development (1 paper)Neuromuscular Disorders (1 paper)Neuropathology and Applied Neurobiology (1 paper)PLoS ONE (1 paper)
- Partner nations
- FinlandUnited KingdomUnited States
In The Last Decade
Mark Screen
7 papers receiving 251 citations
Peers
Comparison fields: 5 of 41
- Genetics 49
- Cardiology and Cardiovascular Medicine 83
- Molecular Biology 199
- Cellular and Molecular Neuroscience 52
- Neurology 38
Countries citing papers authored by Mark Screen
This map shows the geographic impact of Mark Screen'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 Mark Screen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Screen more than expected).
Fields of papers citing papers by Mark Screen
This network shows the impact of papers produced by Mark Screen. 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 Mark Screen. The network helps show where Mark Screen may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark Screen, 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 | 103 | |
| 2 | 2014 | 63 | |
| 3 | 2008 | 32 | |
| 4 | 2012 | 22 | |
| 5 | 2014 | 16 | |
| 6 | 2014 | 14 | |
| 7 | 2013 | 2 |
About Mark Screen
Mark Screen is a scholar working on Genetics, Cellular and Molecular Neuroscience, Obstetrics and Gynecology, Hematology and Molecular Biology, having authored 7 papers that have together received 252 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Mitochondrial Function and Pathology (2 papers), Reproductive System and Pregnancy (1 paper), Connective tissue disorders research (1 paper), RNA Research and Splicing (1 paper) and Pregnancy and preeclampsia studies (1 paper). The work is most often cited by research in Genetics (49 citations), Cardiology and Cardiovascular Medicine (83 citations), Molecular Biology (199 citations), Cellular and Molecular Neuroscience (52 citations) and Neurology (38 citations). Mark Screen has collaborated with scholars based in Finland, United Kingdom and United States. Frequent co-authors include Bjarne Udd, Peter Hackman, Anna Vihola, Per Harald Jonson, Anni Evilä, J. Sarparanta, Juha Kere, Sara Lehtinen, Wendy Dean and Gabrielle Åhlberg. Their work appears in journals such as Annals of Neurology, Development, Neuromuscular Disorders, Neuropathology and Applied Neurobiology and PLoS ONE.
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.