Lars Feuk
- Genetics top 0.1%
- Genomic variations and chromosomal abnormalities 33
- Genomics and Rare Diseases 21
- Genetics and Neurodevelopmental Disorders 10
- Genetic Associations and Epidemiology 9
- Cancer Research top 1%
- Cancer-related molecular mechanisms research 8
- Molecular Biology top 1%
- Genomics and Phylogenetic Studies 14
- RNA modifications and cancer 10
- Plant Science top 1%
- Chromosomal and Genetic Variations 12
- Co-authors
- Stephen W. SchererAndrew R. CarsonCharles LeeA. John IafratePatricia K. DonahoeMiguel N. RiveraYing QiMarc Listewnik
- Partner nations
- SwedenUnited StatesCanada
In The Last Decade
Lars Feuk
83 papers receiving 8.6k citations
Hit Papers
Peers
Comparison fields: 5 of 148
- Genetics 5.5k
- Cancer Research 1.2k
- Molecular Biology 4.9k
- Plant Science 1.7k
- Pediatrics, Perinatology and Child Health 828
Countries citing papers authored by Lars Feuk
This map shows the geographic impact of Lars Feuk'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 Lars Feuk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lars Feuk more than expected).
Fields of papers citing papers by Lars Feuk
This network shows the impact of papers produced by Lars Feuk. 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 Lars Feuk. The network helps show where Lars Feuk may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Lars Feuk, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2024 | 2 | |
| 3 | 2024 | 3 | |
| 4 | 2023 | 25 | |
| 5 | 2022 | 113 | |
| 6 | 2020 | 11 | |
| 7 | 2018 | 31 | |
| 8 | 2018 | 58 | |
| 9 | 2018 | 21 | |
| 10 | 2015 | 19 | |
| 11 | 2013 | 20 | |
| 12 | 2012 | 8 | |
| 13 | 2012 | 76 | |
| 14 | 2012 | 31 | |
| 15 | 2011 | 228 | |
| 16 | 2010 | 214 | |
| 17 | Copy number variation: New insights in genome diversitybreakdown → | 2006 | 592 |
| 18 | 2006 | 149 | |
| 19 | 2006 | 113 | |
| 20 | 2004 | 53 |
About Lars Feuk
Lars Feuk is a scholar working on Aging, Genetics and Molecular Biology, having authored 85 papers that have together received 8.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (21 papers), Genomics and Phylogenetic Studies (14 papers), Chromosomal and Genetic Variations (12 papers), RNA modifications and cancer (10 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genetic Associations and Epidemiology (9 papers) and Cancer-related molecular mechanisms research (8 papers). The work is most often cited by research in Genetics (5.5k citations), Cancer Research (1.2k citations) and Molecular Biology (4.9k citations). Lars Feuk has collaborated with scholars based in Sweden, United States and Canada. Frequent co-authors include Stephen W. Scherer, Andrew R. Carson, Charles Lee, A. John Iafrate, Patricia K. Donahoe, Miguel N. Rivera, Ying Qi, Marc Listewnik, Jeffrey R. MacDonald and Ryan K. C. Yuen. Their work appears in journals such as Human Mutation, Human Genetics, Scientific Reports, Genome biology and European Journal of Human 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.