V. Ferák
Impact in
- Ophthalmology top 2%
- Glaucoma and retinal disorders
- Retinal Diseases and Treatments
- Genetics top 5%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Yersinia bacterium, plague, ectoparasites research
Papers in
- Genetics 5
- Forensic and Genetic Research 4
- Genetic diversity and population structure 2
- Co-authors
- Eva Feráková (6 shared papers)L Kádasi (5 shared papers)A Genĉík (2 shared papers)Martina Plášilová (2 shared papers)H Poláková (5 shared papers)Ivaylo Stoilov (1 shared paper)Mansoor Sarfarazi (1 shared paper)Toomas Kivisild (2 shared papers)
- Journals
- Human Genetics (4 papers)The American Journal of Human Genetics (3 papers)Human Heredity (2 papers)Legal Medicine (1 paper)Current Biology (1 paper)
- Partner nations
- SlovakiaUnited StatesSwitzerland
In The Last Decade
V. Ferák
21 papers receiving 887 citations
Peers
Comparison fields: 5 of 94
- Ophthalmology 222
- Genetics 442
- Clinical Biochemistry 102
- Sensory Systems 57
- Archeology 100
Countries citing papers authored by V. Ferák
This map shows the geographic impact of V. Ferák'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 V. Ferák with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Ferák more than expected).
Fields of papers citing papers by V. Ferák
This network shows the impact of papers produced by V. Ferák. 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 V. Ferák. The network helps show where V. Ferák may publish in the future.
Co-authors
The 25 scholars most cited alongside V. Ferák, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 209 | |
| 2 | 1999 | 143 | |
| 3 | 2001 | 125 | |
| 4 | 2006 | 120 | |
| 5 | 1982 | 81 | |
| 6 | 2000 | 67 | |
| 7 | High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL). | 2003 | 59 |
| 8 | 1998 | 43 | |
| 9 | 2000 | 25 | |
| 10 | 1969 | 11 | |
| 11 | 1982 | 11 | |
| 12 | 1995 | 9 | |
| 13 | 1968 | 9 | |
| 14 | 1981 | 6 | |
| 15 | 1995 | 4 | |
| 16 | 1980 | 4 | |
| 17 | 1965 | 3 | |
| 18 | 1992 | 3 | |
| 19 | 1994 | 3 | |
| 20 | 2018 | 1 |
About V. Ferák
V. Ferák is a scholar working on Molecular Biology, Genetics, Ophthalmology, Clinical Biochemistry and Hematology, having authored 21 papers that have together received 937 indexed citations. Recurring topics across this work include Forensic and Genetic Research (4 papers), Metabolism and Genetic Disorders (4 papers), Glaucoma and retinal disorders (4 papers), Cystic Fibrosis Research Advances (2 papers), Tracheal and airway disorders (2 papers), Forensic Anthropology and Bioarchaeology Studies (2 papers), Genetic diversity and population structure (2 papers) and Blood groups and transfusion (2 papers). The work is most often cited by research in Ophthalmology (222 citations), Genetics (442 citations), Clinical Biochemistry (102 citations), Sensory Systems (57 citations) and Archeology (100 citations). V. Ferák has collaborated with scholars based in Slovakia, United States and Switzerland. Frequent co-authors include Eva Feráková, L Kádasi, A Genĉík, Martina Plášilová, H Poláková, Ivaylo Stoilov, Mansoor Sarfarazi, Toomas Kivisild, Richard Villems and Jüri Parik. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Human Heredity, Legal Medicine and Current Biology.
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.