M. Vitéz
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Urology top 10%
- Urological Disorders and Treatments
Papers in
-
- Congenital limb and hand anomalies 10
- Surgery 6
- Congenital Anomalies and Fetal Surgery 5
- Co-authors
- Andrew E. Czeizel (12 shared papers)Jane Evans (2 shared papers)W. Lenz (7 shared papers)Mária Staub (1 shared paper)Mária Sasvári‐Székely (1 shared paper)A. Czeizel (1 shared paper)Gábor Szabó (1 shared paper)Evans Ja (1 shared paper)
- Journals
- Human Genetics (1 paper)Clinical Genetics (1 paper)Journal of Medical Genetics (1 paper)American Journal of Medical Genetics (5 papers)Orvosi Hetilap (1 paper)
- Partner nations
- HungaryGermanyUnited States
In The Last Decade
M. Vitéz
16 papers receiving 254 citations
Peers
Comparison fields: 5 of 49
- Developmental Biology 97
- Urology 34
- Pediatrics, Perinatology and Child Health 69
- Surgery 109
- Genetics 58
Countries citing papers authored by M. Vitéz
This map shows the geographic impact of M. Vitéz'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 M. Vitéz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Vitéz more than expected).
Fields of papers citing papers by M. Vitéz
This network shows the impact of papers produced by M. Vitéz. 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 M. Vitéz. The network helps show where M. Vitéz may publish in the future.
Co-authors
The 10 scholars most cited alongside M. Vitéz, 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 | 1994 | 80 | |
| 2 | 1992 | 36 | |
| 3 | 1993 | 22 | |
| 4 | 1993 | 21 | |
| 5 | [Holt-Oram syndrome]. | 1991 | 19 |
| 6 | 1981 | 18 | |
| 7 | 1975 | 16 | |
| 8 | Birth prevalence of five congenital abnormalities of medium frequency in Budapest. | 1981 | 14 |
| 9 | 1993 | 11 | |
| 10 | 1993 | 9 | |
| 11 | An aetiological study on 6 to 14 years-old children with severe visual handicap in Hungary. | 1991 | 9 |
| 12 | 1993 | 8 | |
| 13 | Birth prevalence of different congenital limb deficiency types in a revised, population based Hungarian material, 1975-1984. | 1991 | 8 |
| 14 | On the biologic nature of associations: evidence from a study of radial ray deficiencies and associated malformations. | 1993 | 6 |
| 15 | 1987 | 2 | |
| 16 | Etiological study on isolated proximal intercalary type of congenital limb deficiency in Hungary, 1975-1984. | 1992 | 1 |
| 17 | [Split hand/foot abnormalities: classification, pathogenesis, epidemiology]. | 1991 | 0 |
About M. Vitéz
M. Vitéz is a scholar working on Developmental Biology, Surgery, Molecular Biology, Epidemiology and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 280 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (10 papers), Congenital Anomalies and Fetal Surgery (5 papers), Urological Disorders and Treatments (3 papers), Bone fractures and treatments (3 papers), Prenatal Screening and Diagnostics (2 papers), Ophthalmology and Visual Impairment Studies (1 paper), Folate and B Vitamins Research (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Developmental Biology (97 citations), Urology (34 citations), Pediatrics, Perinatology and Child Health (69 citations), Surgery (109 citations) and Genetics (58 citations). M. Vitéz has collaborated with scholars based in Hungary, Germany and United States. Frequent co-authors include Andrew E. Czeizel, Jane Evans, W. Lenz, Mária Staub, Mária Sasvári‐Székely, A. Czeizel, Gábor Szabó, Evans Ja, John M. Opitz and James F. Reynolds. Their work appears in journals such as Human Genetics, Clinical Genetics, Journal of Medical Genetics, American Journal of Medical Genetics and Orvosi Hetilap.
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.