Lars Feuk
Impact in
- Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
-
- Genomics and Phylogenetic Studies 12
- RNA modifications and cancer 8
- Genetics 46
- Genomic variations and chromosomal abnormalities 30
- Genomics and Rare Diseases 21
- Genetic Associations and Epidemiology 9
- Genetics and Neurodevelopmental Disorders 7
- Co-authors
- Stephen W. Scherer (19 shared papers)Andrew R. Carson (4 shared papers)Charles Lee (5 shared papers)A. John Iafrate (1 shared paper)Ying Qi (1 shared paper)Patricia K. Donahoe (1 shared paper)Miguel N. Rivera (1 shared paper)Marc Listewnik (1 shared paper)
- Journals
- Human Mutation (9 papers)Human Genetics (5 papers)Genome biology (4 papers)Scientific Reports (4 papers)Genome Research (3 papers)
- Partner nations
- SwedenUnited StatesCanada
In The Last Decade
Lars Feuk
83 papers receiving 9.0k citations
Lars Feuk's Hit Papers
Peers
Comparison fields: 5 of 149
- Genetics 5.3k
- Cancer Research 1.0k
- Molecular Biology 4.4k
- Plant Science 1.5k
- Pediatrics, Perinatology and Child Health 683
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-authors
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
Showing the 20 most-cited of 86 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Detection of large-scale variation in the human genome Hit paper breakdown → | 2004 | 2215 |
| 2 | Structural variation in the human genome Hit paper breakdown → | 2006 | 1480 |
| 3 | The Database of Genomic Variants: a curated collection of structural variation in the human genome Hit paper breakdown → | 2013 | 855 |
| 4 | Copy number variation: New insights in genome diversity Hit paper breakdown → | 2006 | 636 |
| 5 | 2007 | 300 | |
| 6 | 2011 | 234 | |
| 7 | 2010 | 224 | |
| 8 | 2006 | 206 | |
| 9 | 2012 | 188 | |
| 10 | 2006 | 152 | |
| 11 | 2001 | 150 | |
| 12 | 2008 | 149 | |
| 13 | 2005 | 139 | |
| 14 | 2013 | 131 | |
| 15 | 2001 | 128 | |
| 16 | 2022 | 125 | |
| 17 | 2006 | 124 | |
| 18 | 2005 | 120 | |
| 19 | 2006 | 101 | |
| 20 | 2013 | 86 |
About Lars Feuk
Lars Feuk is a scholar working on Molecular Biology, Genetics, Plant Science, Physiology and Cancer Research, having authored 86 papers that have together received 9.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Genomics and Rare Diseases (21 papers), Chromosomal and Genetic Variations (12 papers), Genomics and Phylogenetic Studies (12 papers), Genetic Associations and Epidemiology (9 papers), RNA modifications and cancer (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Alzheimer's disease research and treatments (7 papers). The work is most often cited by research in Genetics (5.3k citations), Cancer Research (1.0k citations), Molecular Biology (4.4k citations), Plant Science (1.5k citations) and Pediatrics, Perinatology and Child Health (683 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, Ying Qi, Patricia K. Donahoe, Miguel N. Rivera, Marc Listewnik, Jeffrey R. MacDonald and Ryan K. C. Yuen. Their work appears in journals such as Human Mutation, Human Genetics, Genome biology, Scientific Reports and Genome Research.
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.