Birgit Carlsson
Impact in
- Molecular Biology top 10%
- RNA modifications and cancer
- Cancer-related gene regulation
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- RNA Research and Splicing
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Blood disorders and treatments
- Genomic variations and chromosomal abnormalities
Papers in
-
- Glutathione Transferases and Polymorphisms 4
- RNA modifications and cancer 3
- Genetics 8
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Niklas Dahl (12 shared papers)Peter Gustavsson (2 shared papers)Joakim Klar (4 shared papers)Hans Matsson (2 shared papers)Dmitri Tentler (3 shared papers)Narla Mohandas (1 shared paper)Irma Dianzani (1 shared paper)Gil Tchernia (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Journal of Inherited Metabolic Disease (2 papers)Biochemical Journal (2 papers)Human Genetics (2 papers)Nature Genetics (1 paper)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Birgit Carlsson
25 papers receiving 1.3k citations
Birgit Carlsson's Hit Papers
Peers
Comparison fields: 5 of 104
- Molecular Biology 838
- Genetics 303
- Biochemistry 67
- Cell Biology 133
- Hematology 64
Countries citing papers authored by Birgit Carlsson
This map shows the geographic impact of Birgit Carlsson'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 Birgit Carlsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Carlsson more than expected).
Fields of papers citing papers by Birgit Carlsson
This network shows the impact of papers produced by Birgit Carlsson. 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 Birgit Carlsson. The network helps show where Birgit Carlsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Carlsson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia Hit paper breakdown → | 1999 | 594 |
| 2 | 2008 | 99 | |
| 3 | 2005 | 94 | |
| 4 | 1999 | 86 | |
| 5 | 2006 | 63 | |
| 6 | 1999 | 43 | |
| 7 | 1975 | 41 | |
| 8 | 1997 | 32 | |
| 9 | 1994 | 32 | |
| 10 | 1974 | 29 | |
| 11 | 2003 | 24 | |
| 12 | 2000 | 24 | |
| 13 | 1980 | 18 | |
| 14 | 2001 | 16 | |
| 15 | 1993 | 16 | |
| 16 | 2005 | 15 | |
| 17 | 2006 | 14 | |
| 18 | 2000 | 12 | |
| 19 | 2009 | 11 | |
| 20 | 1997 | 9 |
About Birgit Carlsson
Birgit Carlsson is a scholar working on Molecular Biology, Genetics, Biochemistry, Cognitive Neuroscience and Rheumatology, having authored 25 papers that have together received 1.3k indexed citations. Recurring topics across this work include Sulfur Compounds in Biology (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Glutathione Transferases and Polymorphisms (4 papers), Autism Spectrum Disorder Research (3 papers), RNA modifications and cancer (3 papers), Folate and B Vitamins Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Molecular Biology (838 citations), Genetics (303 citations), Biochemistry (67 citations), Cell Biology (133 citations) and Hematology (64 citations). Birgit Carlsson has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Niklas Dahl, Peter Gustavsson, Joakim Klar, Hans Matsson, Dmitri Tentler, Narla Mohandas, Irma Dianzani, Gil Tchernia, Thiébaut-Noël Willig and Björn Andersson. Their work appears in journals such as European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Biochemical Journal, Human Genetics and Nature Genetics.
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.