Ingeborg Barišić
About
In The Last Decade
Ingeborg Barišić
77 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 102
- Pediatrics, Perinatology and Child Health 851
- Surgery 710
- Genetics 525
- Molecular Biology 488
- Public Health, Environmental and Occupational Health 328
Countries citing papers authored by Ingeborg Barišić
This map shows the geographic impact of Ingeborg Barišić'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 Ingeborg Barišić with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingeborg Barišić more than expected).
Fields of papers citing papers by Ingeborg Barišić
This network shows the impact of papers produced by Ingeborg Barišić. 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 Ingeborg Barišić. The network helps show where Ingeborg Barišić may publish in the future.
Co-authorship network of co-authors of Ingeborg Barišić
This figure shows the co-authorship network connecting the top 25 collaborators of Ingeborg Barišić. A scholar is included among the top collaborators of Ingeborg Barišić 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 Ingeborg Barišić. Ingeborg Barišić is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 8 | |
| 3 | 3 | |
| 4 | 24 | |
| 5 | 12 | |
| 6 | 22 | |
| 7 | Osteogenesis imperfecta--multi-systemic and life-long disease that affects whole family. | 6 |
| 8 | 22 | |
| 9 | 2 | |
| 10 | 1 | |
| 11 | Mutations in FGFR3 gene in Croatian patients with achondroplasia and hypochondroplasia | 0 |
| 12 | 9 | |
| 13 | Incidence of Down's syndrome in two regions of Croatia - clustering in time and space? | 0 |
| 14 | F508 deletion in Croatian cystic fibrosis patients | 0 |
| 15 | Prvi rezultati primjene nadomjesne enzimske terapije u dvoje bolesnika s mukopolisaharidozom IH | 1 |
| 16 | Ten-year surveillance of congenital anomalies in Northwestern Croatia | 0 |
| 17 | Diagnosis of microdeletion syndromes using the FISH method in Croatia | 0 |
| 18 | Two cases of alleles with complex genotypes among cystic fibrosis patients from Croatia | 2 |
| 19 | Evaluation of genetic causes of mental retardation | 1 |
| 20 | Expand long PCR for fragile X mutation detection | 5 |
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.