Ellika Sahlin
- Co-authors
- Erik IwarssonMagnus NordenskjöldPeter GustavssonAgne LiedénNikos PapadogiannakisJosephine WincentSusanne GeorgssonMalin Kvarnung
- Topics
- Prenatal Screening and Diagnostics (7 papers)Genomic variations and chromosomal abnormalities (6 papers)Fetal and Pediatric Neurological Disorders (3 papers)
- Partner nations
- SwedenUnited Kingdom
In The Last Decade
Ellika Sahlin
13 papers receiving 188 citations
Peers
Comparison fields: 5 of 48
- Pediatrics, Perinatology and Child Health 82
- Genetics 78
- Molecular Biology 72
- Surgery 26
- Cancer Research 18
Countries citing papers authored by Ellika Sahlin
This map shows the geographic impact of Ellika Sahlin'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 Ellika Sahlin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ellika Sahlin more than expected).
Fields of papers citing papers by Ellika Sahlin
This network shows the impact of papers produced by Ellika Sahlin. 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 Ellika Sahlin. The network helps show where Ellika Sahlin may publish in the future.
Co-authorship network of co-authors of Ellika Sahlin
This figure shows the co-authorship network connecting the top 25 collaborators of Ellika Sahlin. A scholar is included among the top collaborators of Ellika Sahlin 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 Ellika Sahlin. Ellika Sahlin 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 | 7 | |
| 3 | 2 | |
| 4 | 19 | |
| 5 | 3 | |
| 6 | 32 | |
| 7 | 9 | |
| 8 | 10 | |
| 9 | 16 | |
| 10 | 23 | |
| 11 | 17 | |
| 12 | 20 | |
| 13 | 30 |
About Ellika Sahlin
Ellika Sahlin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Urology, having authored 13 papers that have together received 193 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (82 citations), Genetics (78 citations) and Cancer Research (18 citations). Ellika Sahlin has collaborated with scholars based in Sweden and United Kingdom. Frequent co-authors include Erik Iwarsson, Magnus Nordenskjöld, Peter Gustavsson, Agne Liedén, Nikos Papadogiannakis, Josephine Wincent, Susanne Georgsson, Malin Kvarnung, Elisabeth Syk Lundberg and Karin Pettersson. Their work appears in journals such as PLoS ONE, Genomics and Ultrasound in Obstetrics and Gynecology.
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.