M Osztovics
- Pediatrics, Perinatology and Child Health top 10%
- Genetics
- Molecular Biology
- Plant Science
- Rheumatology
- Co-authors
- P VéghelyiAndrew E. CzeizelJúlia MétnekiG KardosP. E. PolaniM.A. Ferguson‐SmithS CollyerR De Mey
- Topics
- Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (5 papers)Metabolism and Genetic Disorders (4 papers)
- Partner nations
- United StatesHungarySwitzerland
In The Last Decade
M Osztovics
31 papers receiving 187 citations
Peers
Comparison fields: 5 of 58
- Pediatrics, Perinatology and Child Health 99
- Genetics 92
- Molecular Biology 56
- Plant Science 28
- Rheumatology 19
Countries citing papers authored by M Osztovics
This map shows the geographic impact of M Osztovics'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 Osztovics with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Osztovics more than expected).
Fields of papers citing papers by M Osztovics
This network shows the impact of papers produced by M Osztovics. 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 Osztovics. The network helps show where M Osztovics may publish in the future.
Co-authorship network of co-authors of M Osztovics
This figure shows the co-authorship network connecting the top 25 collaborators of M Osztovics. A scholar is included among the top collaborators of M Osztovics based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M Osztovics. M Osztovics is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 10p monosomy, a phenotypic variant. | 1 |
| 2 | Partial deletion of short arm of chromosome 18. | 4 |
| 3 | Unusual chromosome aberrations in 3 children with Down syndrome. | 2 |
| 4 | Ring chromosome 15. | 2 |
| 5 | CYTOGENETIC INVESTIGATION IN 418 COUPLES WITH RECURENT FETAL WASTAGE | 1 |
| 6 | 19 | |
| 7 | Hyperuricaemia associated with 18q deletion. Atypical Lesch-Nyhan syndrome? | 2 |
| 8 | Cases of a Genetic Counselling Clinic. | 1 |
| 9 | National programme for prevention of the recurrence of neural tube defects. | 3 |
| 10 | Nationwide investigation of multiple malformations. | 9 |
| 11 | 17 | |
| 12 | 8 | |
| 13 | 45,X/46,XY/47,XYY mosaicism in a phenotypic female with gonadoblastoma. | 2 |
| 14 | Sex chromosome aberrations in childhood. II. 45,X and 45,X-mosaics. | 1 |
| 15 | [Normal values of palmar and digital dermatoglyphic indices in the Budapest population]. | 1 |
| 16 | 4 | |
| 17 | Dermatoglyphic data in a sample of the population of Budapest. | 2 |
| 18 | [Correlations between the clinical condition and the antiglobulin consumption test in rheumatic fever in childhood]. | 1 |
| 19 | [Data on immunopathological aspects of rheumatic fever in children. I. Experience with the anti-globulin consumption test]. | 1 |
| 20 | Hyperglobulinaemic purpura associated with splenomegalic cirrhosis in childhood. Contributions to the pathogenesis of the disease. | 1 |
About M Osztovics
M Osztovics is a scholar working on Genetics, Anatomy and Clinical Biochemistry, having authored 34 papers that have together received 207 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (99 citations), Developmental Biology (10 citations) and Genetics (92 citations). M Osztovics has collaborated with scholars based in United States, Hungary and Switzerland. Frequent co-authors include P Véghelyi, Andrew E. Czeizel, Júlia Métneki, G Kardos, P. E. Polani, M.A. Ferguson‐Smith, S Collyer, R De Mey, A D Carothers and Z. Papp. Their work appears in journals such as Cellular and Molecular Life Sciences, Journal of Medical Genetics and Human Genetics.
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.