A Genĉík
Impact in
- Ophthalmology top 2%
- Glaucoma and retinal disorders
- Retinal Diseases and Treatments
- Intraocular Surgery and Lenses
-
- Retinopathy of Prematurity Studies
- Corneal surgery and disorders
Papers in
-
- Glaucoma and retinal disorders 5
- Ocular Oncology and Treatments 3
- Genetics 8
- BRCA gene mutations in cancer 4
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- V. Ferák (2 shared papers)E Signer (1 shared paper)Raymond Tobler (1 shared paper)William P. Weber (7 shared papers)Nicole Bürki (3 shared papers)J. Torhorst (4 shared papers)M Hrubisko (1 shared paper)Hj. Müller (2 shared papers)
- Journals
- Human Genetics (3 papers)European Journal of Pediatrics (1 paper)Breast Cancer Research and Treatment (1 paper)Clinical Genetics (1 paper)ORL (1 paper)
- Partner nations
- SwitzerlandSlovakiaGermany
In The Last Decade
A Genĉík
26 papers receiving 350 citations
Peers
Comparison fields: 5 of 44
- Ophthalmology 222
- Radiology, Nuclear Medicine and Imaging 150
- Hematology 32
- Genetics 64
- Pathology and Forensic Medicine 31
Countries citing papers authored by A Genĉík
This map shows the geographic impact of A Genĉík'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 A Genĉík with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Genĉík more than expected).
Fields of papers citing papers by A Genĉík
This network shows the impact of papers produced by A Genĉík. 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 A Genĉík. The network helps show where A Genĉík may publish in the future.
Co-authors
The 25 scholars most cited alongside A Genĉík, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance. | 1989 | 109 |
| 2 | 1982 | 81 | |
| 3 | 1984 | 33 | |
| 4 | 1980 | 28 | |
| 5 | 1983 | 15 | |
| 6 | 1980 | 11 | |
| 7 | 1982 | 11 | |
| 8 | Familial occurrence of congenital diaphragmatic defect in three families. | 1982 | 9 |
| 9 | 1990 | 8 | |
| 10 | 1987 | 8 | |
| 11 | 1986 | 7 | |
| 12 | Retinoblastoma and chromosome 13 deletion. | 1982 | 7 |
| 13 | Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation. | 1982 | 5 |
| 14 | 1979 | 5 | |
| 15 | Partial 1p monosomy in a physically and mentally retarded boy. | 1987 | 4 |
| 16 | High incidence of stomach cancer in relatives of patients with malignant lymphoproliferative disorders. | 1987 | 3 |
| 17 | Mohr syndrome in two siblings. | 1983 | 3 |
| 18 | Familial cancer: consequences for the oncological practice. | 1986 | 3 |
| 19 | Familial cancer: genetically determined? (review). | 1983 | 3 |
| 20 | [Dominant lethal test after peroral administration of arsenic (author's transl)]. | 1977 | 3 |
About A Genĉík
A Genĉík is a scholar working on Ophthalmology, Genetics, Molecular Biology, Pathology and Forensic Medicine and Oncology, having authored 26 papers that have together received 364 indexed citations. Recurring topics across this work include Glaucoma and retinal disorders (5 papers), BRCA gene mutations in cancer (4 papers), Genetic factors in colorectal cancer (3 papers), Chromosomal and Genetic Variations (3 papers), Ocular Oncology and Treatments (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Ophthalmology (222 citations), Radiology, Nuclear Medicine and Imaging (150 citations), Hematology (32 citations), Genetics (64 citations) and Pathology and Forensic Medicine (31 citations). A Genĉík has collaborated with scholars based in Switzerland, Slovakia and Germany. Frequent co-authors include V. Ferák, E Signer, Raymond Tobler, William P. Weber, Nicole Bürki, J. Torhorst, M Hrubisko, Hj. Müller, Hansjakob Müller and M Buser. Their work appears in journals such as Human Genetics, European Journal of Pediatrics, Breast Cancer Research and Treatment, Clinical Genetics and ORL.
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.