Lars Feuk
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genetic and phenotypic traits in livestock
- Cognitive Neuroscience top 1%
- Autism Spectrum Disorder Research
Papers in
- Genetics 54
- Genomic variations and chromosomal abnormalities 37
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 8
- Genetic Associations and Epidemiology 7
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- Genomics and Phylogenetic Studies 16
- RNA Research and Splicing 8
- Co-authors
- Stephen W. Scherer (19 shared papers)Andrew R. Carson (4 shared papers)Charles Lee (4 shared papers)Patricia K. Donahoe (1 shared paper)Miguel N. Rivera (1 shared paper)Ying Qi (1 shared paper)Marc L. Listewnik (1 shared paper)Anthony John Iafrate (1 shared paper)
- Journals
- Human Mutation (9 papers)Nature Genetics (6 papers)Human Genetics (5 papers)European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (5 papers)
- Partner nations
- SwedenCanadaUnited States
In The Last Decade
Lars Feuk
101 papers receiving 21k citations
Lars Feuk's Hit Papers
Peers
Comparison fields: 5 of 157
- Genetics 13.1k
- Cognitive Neuroscience 1.8k
- Molecular Biology 3.7k
- Pediatrics, Perinatology and Child Health 718
- Cancer Research 732
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 102 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Global variation in copy number in the human genome Hit paper breakdown → | 2006 | 3358 |
| 2 | Detection of large-scale variation in the human genome Hit paper breakdown → | 2004 | 2288 |
| 3 | Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies Hit paper breakdown → | 2010 | 2169 |
| 4 | Origins and functional impact of copy number variation in the human genome Hit paper breakdown → | 2009 | 1533 |
| 5 | Structural variation in the human genome Hit paper breakdown → | 2006 | 1531 |
| 6 | Structural Variation of Chromosomes in Autism Spectrum Disorder Hit paper breakdown → | 2008 | 1505 |
| 7 | The Diploid Genome Sequence of an Individual Human Hit paper breakdown → | 2007 | 1237 |
| 8 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements Hit paper breakdown → | 2007 | 1148 |
| 9 | The Database of Genomic Variants: a curated collection of structural variation in the human genome Hit paper breakdown → | 2013 | 1005 |
| 10 | Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Hit paper breakdown → | 2010 | 641 |
| 11 | 2009 | 355 | |
| 12 | 2011 | 343 | |
| 13 | 2007 | 312 | |
| 14 | 2010 | 243 | |
| 15 | 2011 | 240 | |
| 16 | 2006 | 214 | |
| 17 | 2012 | 200 | |
| 18 | 2008 | 162 | |
| 19 | 2006 | 159 | |
| 20 | 2006 | 153 |
About Lars Feuk
Lars Feuk is a scholar working on Genetics, Molecular Biology, Physiology, Psychiatry and Mental health and Clinical Biochemistry, having authored 102 papers that have together received 21.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Genomics and Phylogenetic Studies (16 papers), Alzheimer's disease research and treatments (11 papers), Genomics and Rare Diseases (11 papers), RNA Research and Splicing (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic Associations and Epidemiology (7 papers) and Schizophrenia research and treatment (3 papers). The work is most often cited by research in Genetics (13.1k citations), Cognitive Neuroscience (1.8k citations), Molecular Biology (3.7k citations), Pediatrics, Perinatology and Child Health (718 citations) and Cancer Research (732 citations). Lars Feuk has collaborated with scholars based in Sweden, Canada and United States. Frequent co-authors include Stephen W. Scherer, Andrew R. Carson, Charles Lee, Patricia K. Donahoe, Miguel N. Rivera, Ying Qi, Marc L. Listewnik, Anthony John Iafrate, Jeffrey R. MacDonald and Ryan K. C. Yuen. Their work appears in journals such as Human Mutation, Nature Genetics, Human Genetics, European Journal of Human Genetics and The American 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.