Martina Plášilová
- Ophthalmology top 5%
- Glaucoma and retinal disorders 2
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- Genetic factors in colorectal cancer 6
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- Cancer Genomics and Diagnostics 4
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- Hearing, Cochlea, Tinnitus, Genetics 1
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- Colorectal Cancer Treatments and Studies 2
- Colorectal Cancer Screening and Detection 2
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- Thyroid Disorders and Treatments 2
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- Genetic Neurodegenerative Diseases 1
- Co-authors
- Eva FerákováL KádasiV. FerákIvaylo StoilovMansoor SarfaraziKarl HeinimannHansjakob MuellerAnna Russell
- Partner nations
- SwitzerlandUnited StatesSlovakia
In The Last Decade
Martina Plášilová
12 papers receiving 333 citations
Peers
Comparison fields: 5 of 46
- Ophthalmology 144
- Pathology and Forensic Medicine 100
- Cancer Research 55
- Radiology, Nuclear Medicine and Imaging 83
- Sensory Systems 17
Countries citing papers authored by Martina Plášilová
This map shows the geographic impact of Martina Plášilová'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 Martina Plášilová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martina Plášilová more than expected).
Fields of papers citing papers by Martina Plášilová
This network shows the impact of papers produced by Martina Plášilová. 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 Martina Plášilová. The network helps show where Martina Plášilová may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Martina Plášilová, 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 | 2015 | 17 | |
| 2 | 2011 | 11 | |
| 3 | 2008 | 13 | |
| 4 | 2006 | 54 | |
| 5 | 2006 | 4 | |
| 6 | 2006 | 13 | |
| 7 | 2005 | 23 | |
| 8 | 2004 | 9 | |
| 9 | 2003 | 1 | |
| 10 | 1999 | 143 | |
| 11 | [Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma]. | 1998 | 7 |
| 12 | 1998 | 43 |
About Martina Plášilová
Martina Plášilová is a scholar working on Pathology and Forensic Medicine, Cancer Research and Ophthalmology, having authored 12 papers that have together received 338 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (4 papers), Colorectal Cancer Treatments and Studies (2 papers), Colorectal Cancer Screening and Detection (2 papers), Glaucoma and retinal disorders (2 papers), Thyroid Disorders and Treatments (2 papers), Genetic Neurodegenerative Diseases (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). The work is most often cited by research in Ophthalmology (144 citations), Pathology and Forensic Medicine (100 citations) and Cancer Research (55 citations). Martina Plášilová has collaborated with scholars based in Switzerland, United States and Slovakia. Frequent co-authors include Eva Feráková, L Kádasi, V. Ferák, Ivaylo Stoilov, Mansoor Sarfarazi, Karl Heinimann, Hansjakob Mueller, Anna Russell, Giancarlo Marra and Saara Ollila. Their work appears in journals such as PLoS ONE, Cancer Research and The Laryngoscope.
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.