Birgit Carlsson
Impact in
- Genetics top 5%
- Blood disorders and treatments
- Genomic variations and chromosomal abnormalities
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
-
- Metabolism and Genetic Disorders 5
- Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Blood disorders and treatments 2
- Co-authors
- Niklas Dahl (12 shared papers)Peter Gustavsson (2 shared papers)Joakim Klar (4 shared papers)Natalia Draptchinskaia (2 shared papers)Dmitri Tentler (3 shared papers)Hans Matsson (2 shared papers)Narla Mohandas (1 shared paper)Thiébaut-Noël Willig (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Journal of Inherited Metabolic Disease (2 papers)Human Genetics (2 papers)European Journal of Biochemistry (1 paper)Analytical Biochemistry (1 paper)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Birgit Carlsson
24 papers receiving 1.4k citations
Birgit Carlsson's Hit Papers
Peers
Comparison fields: 5 of 97
- Genetics 508
- Clinical Biochemistry 69
- Biochemistry 69
- Hematology 91
- Cell Biology 92
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 24 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 | 657 |
| 2 | 2008 | 114 | |
| 3 | 1999 | 104 | |
| 4 | 2005 | 97 | |
| 5 | 2006 | 69 | |
| 6 | 1975 | 45 | |
| 7 | 1999 | 44 | |
| 8 | 1997 | 38 | |
| 9 | 1994 | 34 | |
| 10 | 1974 | 33 | |
| 11 | 2000 | 27 | |
| 12 | 2003 | 26 | |
| 13 | 1980 | 19 | |
| 14 | 1993 | 18 | |
| 15 | 2001 | 17 | |
| 16 | 2005 | 15 | |
| 17 | 2006 | 14 | |
| 18 | 1992 | 13 | |
| 19 | 1969 | 12 | |
| 20 | 1997 | 11 |
About Birgit Carlsson
Birgit Carlsson is a scholar working on Clinical Biochemistry, Genetics, Biochemistry, Cognitive Neuroscience and Cell Biology, having authored 24 papers that have together received 1.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers), Eicosanoids and Hypertension Pharmacology (2 papers), Sulfur Compounds in Biology (2 papers), Glutathione Transferases and Polymorphisms (2 papers) and Blood disorders and treatments (2 papers). The work is most often cited by research in Genetics (508 citations), Clinical Biochemistry (69 citations), Biochemistry (69 citations), Hematology (91 citations) and Cell Biology (92 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, Natalia Draptchinskaia, Dmitri Tentler, Hans Matsson, Narla Mohandas, Thiébaut-Noël Willig, Irma Dianzani and Björn Andersson. Their work appears in journals such as European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Human Genetics, European Journal of Biochemistry and Analytical Biochemistry.
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.