Britt‐Marie Anderlid
- Genetics top 2%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 5%
- Cognitive Neuroscience top 10%
- Plant Science top 10%
- Co-authors
- Magnus NordenskjöldElisabeth BlennowJacqueline SchoumansAnn NordgrenAnna LindstrandDaniel NilssonGöran AnnerénSigrid Sahlén
- Topics
- Genomic variations and chromosomal abnormalities (27 papers)Genetics and Neurodevelopmental Disorders (19 papers)Genomics and Rare Diseases (9 papers)
- Partner nations
- SwedenUnited KingdomFrance
In The Last Decade
Britt‐Marie Anderlid
55 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 92
- Genetics 813
- Molecular Biology 607
- Pediatrics, Perinatology and Child Health 209
- Cognitive Neuroscience 200
- Plant Science 179
Countries citing papers authored by Britt‐Marie Anderlid
This map shows the geographic impact of Britt‐Marie Anderlid'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 Britt‐Marie Anderlid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Britt‐Marie Anderlid more than expected).
Fields of papers citing papers by Britt‐Marie Anderlid
This network shows the impact of papers produced by Britt‐Marie Anderlid. 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 Britt‐Marie Anderlid. The network helps show where Britt‐Marie Anderlid may publish in the future.
Co-authorship network of co-authors of Britt‐Marie Anderlid
This figure shows the co-authorship network connecting the top 25 collaborators of Britt‐Marie Anderlid. A scholar is included among the top collaborators of Britt‐Marie Anderlid 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 Britt‐Marie Anderlid. Britt‐Marie Anderlid is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 4 | |
| 3 | 8 | |
| 4 | 21 | |
| 5 | 22 | |
| 6 | 5 | |
| 7 | 5 | |
| 8 | 19 | |
| 9 | 30 | |
| 10 | 20 | |
| 11 | 21 | |
| 12 | 24 | |
| 13 | 19 | |
| 14 | 29 | |
| 15 | 11 | |
| 16 | 3 | |
| 17 | 64 | |
| 18 | 38 | |
| 19 | 107 | |
| 20 | Subtelomeric rearrangements detected by FISH in patients with idiopatic mental retardation | 6 |
About Britt‐Marie Anderlid
Britt‐Marie Anderlid is a scholar working on Developmental Biology, Genetics and Cognitive Neuroscience, having authored 56 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Genomics and Rare Diseases (9 papers). The work is most often cited by research in Genetics (813 citations), Pediatrics, Perinatology and Child Health (209 citations) and Cognitive Neuroscience (200 citations). Britt‐Marie Anderlid has collaborated with scholars based in Sweden, United Kingdom and France. Frequent co-authors include Magnus Nordenskjöld, Elisabeth Blennow, Jacqueline Schoumans, Ann Nordgren, Anna Lindstrand, Daniel Nilsson, Göran Annerén, Sigrid Sahlén, Tommy Stödberg and Maria Pettersson. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics and Experimental Cell Research.
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.