L Zergollern
About
In The Last Decade
L Zergollern
22 papers receiving 122 citations
Peers
Comparison fields: 5 of 38
- Genetics 95
- Molecular Biology 44
- Pediatrics, Perinatology and Child Health 39
- Plant Science 30
- Developmental Biology 20
Countries citing papers authored by L Zergollern
This map shows the geographic impact of L Zergollern'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 L Zergollern with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L Zergollern more than expected).
Fields of papers citing papers by L Zergollern
This network shows the impact of papers produced by L Zergollern. 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 L Zergollern. The network helps show where L Zergollern may publish in the future.
Co-authorship network of co-authors of L Zergollern
This figure shows the co-authorship network connecting the top 25 collaborators of L Zergollern. A scholar is included among the top collaborators of L Zergollern 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 L Zergollern. L Zergollern is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | F508 deletion in Croatian cystic fibrosis patients | 0 |
| 2 | 6 | |
| 3 | Berger, W. et al. Isolation of a candidate gene for Norrie disease by positional cloning. Nature Genet. 1, 199-203 | 1 |
| 4 | [The usefulness of the chorionic villi technic in prenatal diagnosis]. | 0 |
| 5 | [The Goltz-Gorlin syndrome in a male child]. | 2 |
| 6 | De novo terminal deletion del(3) (p25 leads to pter). | 3 |
| 7 | [Hemophilia A associated with Down's syndrome]. | 1 |
| 8 | Partial trisomy 15q dist--a new syndrome? | 4 |
| 9 | 21 | |
| 10 | [Trisomy 10p as a result of familial 10/22 translocation]. | 1 |
| 11 | [Proximal and distal partial trisomy 13 in the same family]. | 2 |
| 12 | Skin disorder in an infant with congenital thrombocytopenia and aplasia of the radial bones. | 1 |
| 13 | 14 | |
| 14 | [Athyrosis in Down's syndrome]. | 2 |
| 15 | 1 | |
| 16 | 5 | |
| 17 | [Triploidy--a new syndrome in human medicine]. | 1 |
| 18 | A follow-up on Hanhart's dwarfs of Krk. | 3 |
| 19 | 24 | |
| 20 | 24 |
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.