Christoffer Nellåker
Impact in
- Health Informatics top 5%
- Molecular Biology top 10%
- RNA regulation and disease
- RNA Research and Splicing
- CRISPR and Genetic Engineering
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
Papers in
-
- Molecular Biology Techniques and Applications 3
- Genetics 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Håkan Karlsson (9 shared papers)Chris P. Ponting (5 shared papers)Yuanrong Yao (2 shared papers)Robert H. Yolken (6 shared papers)Jonathan Flint (3 shared papers)David J. Adams (3 shared papers)Thomas Keane (3 shared papers)Liam P. Keegan (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Genome biology (2 papers)BMC Genomics (2 papers)Communications Biology (2 papers)Nature Communications (1 paper)
- Partner nations
- United KingdomUnited StatesSweden
In The Last Decade
Christoffer Nellåker
29 papers receiving 1.7k citations
Christoffer Nellåker's Hit Papers
Peers
Comparison fields: 5 of 118
- Health Informatics 38
- Molecular Biology 1.1k
- Immunology 244
- Genetics 321
- Biological Psychiatry 23
Countries citing papers authored by Christoffer Nellåker
This map shows the geographic impact of Christoffer Nellåker'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 Christoffer Nellåker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christoffer Nellåker more than expected).
Fields of papers citing papers by Christoffer Nellåker
This network shows the impact of papers produced by Christoffer Nellåker. 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 Christoffer Nellåker. The network helps show where Christoffer Nellåker may publish in the future.
Co-authors
The 25 scholars most cited alongside Christoffer Nellåker, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The RNA-Editing Enzyme ADAR1 Controls Innate Immune Responses to RNA Hit paper breakdown → | 2014 | 500 |
| 2 | 2011 | 235 | |
| 3 | 2012 | 140 | |
| 4 | 2012 | 131 | |
| 5 | 2006 | 131 | |
| 6 | 2014 | 101 | |
| 7 | 2006 | 98 | |
| 8 | 2007 | 68 | |
| 9 | 2014 | 48 | |
| 10 | 2022 | 31 | |
| 11 | 2022 | 29 | |
| 12 | 2023 | 28 | |
| 13 | 2011 | 22 | |
| 14 | 2018 | 20 | |
| 15 | 2024 | 16 | |
| 16 | 2006 | 16 | |
| 17 | 2011 | 16 | |
| 18 | 2009 | 15 | |
| 19 | 2018 | 13 | |
| 20 | 2023 | 13 |
About Christoffer Nellåker
Christoffer Nellåker is a scholar working on Molecular Biology, Genetics, Plant Science, Clinical Biochemistry and Physiology, having authored 31 papers that have together received 1.7k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (7 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (3 papers), Molecular Biology Techniques and Applications (3 papers), Cell Image Analysis Techniques (3 papers), Bacterial Identification and Susceptibility Testing (3 papers), interferon and immune responses (2 papers) and Antibiotic Resistance in Bacteria (2 papers). The work is most often cited by research in Health Informatics (38 citations), Molecular Biology (1.1k citations), Immunology (244 citations), Genetics (321 citations) and Biological Psychiatry (23 citations). Christoffer Nellåker has collaborated with scholars based in United Kingdom, United States and Sweden. Frequent co-authors include Håkan Karlsson, Chris P. Ponting, Yuanrong Yao, Robert H. Yolken, Jonathan Flint, David J. Adams, Thomas Keane, Liam P. Keegan, James Brindle and Julia R. Dorin. Their work appears in journals such as Genetics in Medicine, Genome biology, BMC Genomics, Communications Biology and Nature Communications.
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.