Per Stenberg
Impact in
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic diversity and population structure
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- RNA Research and Splicing
- Cancer-related gene regulation
- Genomics and Phylogenetic Studies
Papers in
-
- Genomics and Chromatin Dynamics 23
- RNA Research and Splicing 9
- Epigenetics and DNA Methylation 7
- Genomics and Phylogenetic Studies 6
- Genetics 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Co-authors
- Jan Larsson (15 shared papers)Anssi Saura (4 shared papers)Magnus Lundmark (2 shared papers)Anna‐Mia Johansson (11 shared papers)Tatyana G. Kahn (4 shared papers)Philge Philip (8 shared papers)Vincenzo Pirrotta (3 shared papers)Yuri B. Schwartz (4 shared papers)
- Journals
- PLoS Genetics (8 papers)Nucleic Acids Research (5 papers)Scientific Reports (2 papers)Epigenetics & Chromatin (2 papers)Hereditas (2 papers)
- Partner nations
- SwedenUnited StatesFinland
In The Last Decade
Per Stenberg
47 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 100
- Genetics 437
- Molecular Biology 1.1k
- Aging 24
- Insect Science 167
- Plant Science 462
Countries citing papers authored by Per Stenberg
This map shows the geographic impact of Per Stenberg'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 Per Stenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Per Stenberg more than expected).
Fields of papers citing papers by Per Stenberg
This network shows the impact of papers produced by Per Stenberg. 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 Per Stenberg. The network helps show where Per Stenberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Per Stenberg, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 172 | |
| 2 | 2010 | 161 | |
| 3 | 2009 | 82 | |
| 4 | 2016 | 80 | |
| 5 | 2003 | 72 | |
| 6 | 2007 | 60 | |
| 7 | 2017 | 59 | |
| 8 | 2015 | 57 | |
| 9 | 2013 | 52 | |
| 10 | 2007 | 52 | |
| 11 | 2014 | 47 | |
| 12 | 2011 | 47 | |
| 13 | 2012 | 45 | |
| 14 | 2004 | 44 | |
| 15 | 2012 | 39 | |
| 16 | 2013 | 37 | |
| 17 | 2004 | 37 | |
| 18 | 2012 | 32 | |
| 19 | 2020 | 30 | |
| 20 | 2012 | 28 |
About Per Stenberg
Per Stenberg is a scholar working on Molecular Biology, Genetics, Ecology, Plant Science and Ecology, Evolution, Behavior and Systematics, having authored 50 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (23 papers), Chromosomal and Genetic Variations (12 papers), RNA Research and Splicing (9 papers), Epigenetics and DNA Methylation (7 papers), Genomics and Phylogenetic Studies (6 papers), Invertebrate Immune Response Mechanisms (5 papers), Bacteriophages and microbial interactions (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). The work is most often cited by research in Genetics (437 citations), Molecular Biology (1.1k citations), Aging (24 citations), Insect Science (167 citations) and Plant Science (462 citations). Per Stenberg has collaborated with scholars based in Sweden, United States and Finland. Frequent co-authors include Jan Larsson, Anssi Saura, Magnus Lundmark, Anna‐Mia Johansson, Tatyana G. Kahn, Philge Philip, Vincenzo Pirrotta, Yuri B. Schwartz, Richard Bourgon and Katsuhito Ohno. Their work appears in journals such as PLoS Genetics, Nucleic Acids Research, Scientific Reports, Epigenetics & Chromatin and Hereditas.
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.