Peter Gustavsson
Impact in
- Nephrology top 5%
- Parathyroid Disorders and Treatments
- Molecular Biology top 5%
- RNA modifications and cancer
- Cancer-related gene regulation
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- RNA Research and Splicing
Papers in
-
- Cancer-related gene regulation 6
- Epigenetics and DNA Methylation 6
- RNA modifications and cancer 6
- Congenital heart defects research 4
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Niklas Dahl (8 shared papers)Birgit Carlsson (2 shared papers)Thiébaut-Noël Willig (3 shared papers)Irma Dianzani (3 shared papers)Gil Tchernia (3 shared papers)Joakim Klar (3 shared papers)Sarah E. Ball (2 shared papers)Hans Matsson (2 shared papers)
- Journals
- PLoS ONE (3 papers)Human Molecular Genetics (3 papers)Nature Genetics (3 papers)European Journal of Medical Genetics (2 papers)Birth Defects Research Part A Clinical and Molecular Teratology (2 papers)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Peter Gustavsson
35 papers receiving 1.8k citations
Peter Gustavsson's Hit Papers
Peers
Comparison fields: 5 of 85
- Nephrology 134
- Molecular Biology 1.2k
- Genetics 422
- Pediatrics, Perinatology and Child Health 160
- Genetics 81
Countries citing papers authored by Peter Gustavsson
This map shows the geographic impact of Peter Gustavsson'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 Peter Gustavsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Gustavsson more than expected).
Fields of papers citing papers by Peter Gustavsson
This network shows the impact of papers produced by Peter Gustavsson. 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 Peter Gustavsson. The network helps show where Peter Gustavsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Gustavsson, 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 38 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 | 595 |
| 2 | 2000 | 152 | |
| 3 | 1997 | 144 | |
| 4 | 2007 | 115 | |
| 5 | 2005 | 94 | |
| 6 | 1997 | 73 | |
| 7 | 2007 | 66 | |
| 8 | 1998 | 57 | |
| 9 | 2010 | 53 | |
| 10 | 2013 | 45 | |
| 11 | 2016 | 41 | |
| 12 | 2008 | 37 | |
| 13 | 2012 | 37 | |
| 14 | 2013 | 32 | |
| 15 | 2016 | 32 | |
| 16 | 1998 | 30 | |
| 17 | 2010 | 24 | |
| 18 | 1999 | 23 | |
| 19 | 2019 | 21 | |
| 20 | 2014 | 20 |
About Peter Gustavsson
Peter Gustavsson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 38 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Cancer-related gene regulation (6 papers), Epigenetics and DNA Methylation (6 papers), RNA modifications and cancer (6 papers), Congenital heart defects research (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Nephrology (134 citations), Molecular Biology (1.2k citations), Genetics (422 citations), Pediatrics, Perinatology and Child Health (160 citations) and Genetics (81 citations). Peter Gustavsson has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Niklas Dahl, Birgit Carlsson, Thiébaut-Noël Willig, Irma Dianzani, Gil Tchernia, Joakim Klar, Sarah E. Ball, Hans Matsson, M Pettersson and Narla Mohandas. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, Nature Genetics, European Journal of Medical Genetics and Birth Defects Research Part A Clinical and Molecular Teratology.
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.