Catarina Lundin
- Pediatrics, Perinatology and Child Health top 10%
- Public Health, Environmental and Occupational Health
- Genetics
- Molecular Biology
- Hematology
- Co-authors
- Göran AnnerénSven CnattingiusFredrik MertensBertil JohanssonAnn NordgrenErik ForestierMette Klarskov AndersenL. Zech
- Topics
- Genomic variations and chromosomal abnormalities (4 papers)Prenatal Screening and Diagnostics (3 papers)Acute Lymphoblastic Leukemia research (3 papers)
In The Last Decade
Catarina Lundin
17 papers receiving 279 citations
Peers
Comparison fields: 5 of 45
- Pediatrics, Perinatology and Child Health 106
- Public Health, Environmental and Occupational Health 98
- Genetics 98
- Molecular Biology 85
- Hematology 63
Countries citing papers authored by Catarina Lundin
This map shows the geographic impact of Catarina Lundin'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 Catarina Lundin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catarina Lundin more than expected).
Fields of papers citing papers by Catarina Lundin
This network shows the impact of papers produced by Catarina Lundin. 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 Catarina Lundin. The network helps show where Catarina Lundin may publish in the future.
Co-authorship network of co-authors of Catarina Lundin
This figure shows the co-authorship network connecting the top 25 collaborators of Catarina Lundin. A scholar is included among the top collaborators of Catarina Lundin 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 Catarina Lundin. Catarina Lundin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene | 1 |
| 3 | 8 | |
| 4 | 6 | |
| 5 | 16 | |
| 6 | 10 | |
| 7 | 1 | |
| 8 | 11 | |
| 9 | 3 | |
| 10 | 20 | |
| 11 | 13 | |
| 12 | 11 | |
| 13 | 84 | |
| 14 | 42 | |
| 15 | 22 | |
| 16 | 23 | |
| 17 | 11 |
About Catarina Lundin
Catarina Lundin is a scholar working on Developmental Neuroscience, Dermatology and Pathology and Forensic Medicine, having authored 17 papers that have together received 287 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Acute Lymphoblastic Leukemia research (3 papers). The work is most often cited by research in Hematology (63 citations), Pediatrics, Perinatology and Child Health (106 citations) and Genetics (98 citations). Catarina Lundin has collaborated with scholars based in Sweden, Denmark and Finland. Frequent co-authors include Göran Annerén, Sven Cnattingius, Fredrik Mertens, Bertil Johansson, Ann Nordgren, Erik Forestier, Mette Klarskov Andersen, L. Zech, Claes Wadelius and Sverre Heim. Their work appears in journals such as Blood, Fertility and Sterility and Investigative Ophthalmology & Visual Science.
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.