Birgit Carlsson
Impact in
- Molecular Biology top 10%
- RNA modifications and cancer
- Cancer-related gene regulation
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- Epigenetics and DNA Methylation
- Genetics top 10%
- Blood disorders and treatments
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Glutathione Transferases and Polymorphisms 4
- RNA modifications and cancer 3
- Genetics 7
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Niklas Dahl (12 shared papers)Peter Gustavsson (2 shared papers)Joakim Klar (4 shared papers)Dmitri Tentler (3 shared papers)Hans Matsson (2 shared papers)Björn Andersson (1 shared paper)M Pettersson (1 shared paper)Thiébaut-Noël Willig (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)Human Molecular Genetics (1 paper)
- Partner nations
- SwedenUnited StatesGermany
In The Last Decade
Birgit Carlsson
25 papers receiving 1.3k citations
Birgit Carlsson's Hit Papers
Peers
Comparison fields: 5 of 105
- Molecular Biology 834
- Genetics 311
- Biochemistry 77
- Cell Biology 134
- Hematology 72
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 | 623 |
| 2 | 2008 | 114 | |
| 3 | 1999 | 103 | |
| 4 | 2005 | 95 | |
| 5 | 2006 | 66 | |
| 6 | 1999 | 44 | |
| 7 | 1975 | 44 | |
| 8 | 1997 | 37 | |
| 9 | 1974 | 34 | |
| 10 | 1994 | 34 | |
| 11 | 2003 | 27 | |
| 12 | 2000 | 26 | |
| 13 | 1980 | 19 | |
| 14 | 2001 | 18 | |
| 15 | 1993 | 18 | |
| 16 | 2005 | 15 | |
| 17 | 2006 | 14 | |
| 18 | 1992 | 12 | |
| 19 | 2000 | 12 | |
| 20 | 1997 | 11 |
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 1.4k indexed citations. Recurring topics across this work include Sulfur Compounds in Biology (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Glutathione Transferases and Polymorphisms (4 papers), Folate and B Vitamins Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Autism Spectrum Disorder Research (3 papers), RNA modifications and cancer (3 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Molecular Biology (834 citations), Genetics (311 citations), Biochemistry (77 citations), Cell Biology (134 citations) and Hematology (72 citations). Birgit Carlsson has collaborated with scholars based in Sweden, United States and Germany. Frequent co-authors include Niklas Dahl, Peter Gustavsson, Joakim Klar, Dmitri Tentler, Hans Matsson, Björn Andersson, M Pettersson, Thiébaut-Noël Willig, Sarah E. Ball and Gil Tchernia. Their work appears in journals such as European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Biochemical Journal, Human Genetics and Human Molecular 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.