Håkon Håkonarson
Impact in
- Genetics top 0.02%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Cognitive Neuroscience top 0.2%
- Functional Brain Connectivity Studies
Papers in
- Genetics 225
- Genetic Associations and Epidemiology 70
- Genomic variations and chromosomal abnormalities 54
- Genetics and Neurodevelopmental Disorders 37
- Genomics and Rare Diseases 34
- Diabetes and associated disorders 25
-
- Congenital heart defects research 30
- Co-authors
- Kai Wang (42 shared papers)Man Li (1 shared paper)Raquel E. Gur (32 shared papers)Ruben C. Gur (27 shared papers)Theodore D. Satterthwaite (24 shared papers)Joseph Glessner (124 shared papers)Kosha Ruparel (25 shared papers)Struan F.A. Grant (67 shared papers)
- Journals
- PLoS ONE (26 papers)Scientific Reports (15 papers)Human Molecular Genetics (14 papers)Frontiers in Genetics (12 papers)Journal of Allergy and Clinical Immunology (12 papers)
- Partner nations
- United StatesChinaIceland
In The Last Decade
Håkon Håkonarson
581 papers receiving 35.8k citations
Håkon Håkonarson's Hit Papers
Peers
Comparison fields: 5 of 206
- Genetics 10.4k
- Cognitive Neuroscience 5.1k
- Cancer Research 3.0k
- Molecular Biology 10.7k
- Physiology 2.8k
Countries citing papers authored by Håkon Håkonarson
This map shows the geographic impact of Håkon Håkonarson'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 Håkon Håkonarson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Håkon Håkonarson more than expected).
Fields of papers citing papers by Håkon Håkonarson
This network shows the impact of papers produced by Håkon Håkonarson. 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 Håkon Håkonarson. The network helps show where Håkon Håkonarson may publish in the future.
Co-authors
The 25 scholars most cited alongside Håkon Håkonarson, 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 608 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data Hit paper breakdown → | 2010 | 9302 |
| 2 | An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data Hit paper breakdown → | 2012 | 1360 |
| 3 | PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Hit paper breakdown → | 2007 | 1203 |
| 4 | Impact of in-scanner head motion on multiple measures of functional connectivity: Relevance for studies of neurodevelopment in youth Hit paper breakdown → | 2012 | 907 |
| 5 | Sex differences in the structural connectome of the human brain Hit paper breakdown → | 2013 | 852 |
| 6 | Rare Variants Create Synthetic Genome-Wide Associations Hit paper breakdown → | 2010 | 641 |
| 7 | Analysing biological pathways in genome-wide association studies Hit paper breakdown → | 2010 | 590 |
| 8 | Age group and sex differences in performance on a computerized neurocognitive battery in children age 8−21. Hit paper breakdown → | 2012 | 393 |
| 9 | 2010 | 350 | |
| 10 | 2013 | 346 | |
| 11 | 2013 | 323 | |
| 12 | 2005 | 322 | |
| 13 | 2009 | 275 | |
| 14 | 2014 | 266 | |
| 15 | 2014 | 240 | |
| 16 | 2011 | 237 | |
| 17 | 2008 | 236 | |
| 18 | 2017 | 231 | |
| 19 | 2015 | 213 | |
| 20 | 2006 | 211 |
About Håkon Håkonarson
Håkon Håkonarson is a scholar working on Genetics, Molecular Biology, Immunology, Surgery and Physiology, having authored 608 papers that have together received 36.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (70 papers), Genomic variations and chromosomal abnormalities (54 papers), Asthma and respiratory diseases (44 papers), Genetics and Neurodevelopmental Disorders (37 papers), Genomics and Rare Diseases (34 papers), Congenital heart defects research (30 papers), Diabetes and associated disorders (25 papers) and IL-33, ST2, and ILC Pathways (21 papers). The work is most often cited by research in Genetics (10.4k citations), Cognitive Neuroscience (5.1k citations), Cancer Research (3.0k citations), Molecular Biology (10.7k citations) and Physiology (2.8k citations). Håkon Håkonarson has collaborated with scholars based in United States, China and Iceland. Frequent co-authors include Kai Wang, Man Li, Raquel E. Gur, Ruben C. Gur, Theodore D. Satterthwaite, Joseph Glessner, Kosha Ruparel, Struan F.A. Grant, Mingyao Li and Daniel H. Wolf. Their work appears in journals such as PLoS ONE, Scientific Reports, Human Molecular Genetics, Frontiers in Genetics and Journal of Allergy and Clinical Immunology.
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.