Håkon Håkonarson

158.8k citations
587 papers · 34.7k indexed · 7 hit papers · h-index 76
  • Genetics top 0.02%
    • Genetic Associations and Epidemiology 80
    • Genomic variations and chromosomal abnormalities 72
    • Genetics and Neurodevelopmental Disorders 50
    • Genomics and Rare Diseases 41
    • Diabetes and associated disorders 27
    • Congenital heart defects research 41
    • RNA modifications and cancer 27
  • Immunology top 0.5%
    • Asthma and respiratory diseases 48

Håkon Håkonarson

560 papers receiving 34.2k citations

Hit Papers

Sex differences in the structural connectome of the human...77820072026201320192.5k5.0k7.5k

Peers

Håkon Håkonarson
Comparison fields: 5 of 201
  • Genetics 11.6k
  • Cognitive Neuroscience 5.5k
  • Cancer Research 3.7k
  • Molecular Biology 12.4k
  • Immunology 2.7k
Replace Shaun Purcell with:
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Citations per field
00.5×2.6×
Shaun Purcell · 1×
Citations per year

Countries citing papers authored by Håkon Håkonarson

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Håkon Håkonarson Line = papers co-authored together Håkon Håkonarson links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
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Genetic Discrimination between LADA and Type 1 Diabetes within the MHC
20181
17 201763
18 201479
19 2009142
20 20046

About Håkon Håkonarson

Håkon Håkonarson is a scholar working on Genetics, Immunology and Molecular Biology, having authored 587 papers that have together received 34.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (80 papers), Genomic variations and chromosomal abnormalities (72 papers), Genetics and Neurodevelopmental Disorders (50 papers), Asthma and respiratory diseases (48 papers), Genomics and Rare Diseases (41 papers), Congenital heart defects research (41 papers), RNA modifications and cancer (27 papers) and Diabetes and associated disorders (27 papers). The work is most often cited by research in Genetics (11.6k citations), Cognitive Neuroscience (5.5k citations) and Cancer Research (3.7k 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, Joseph Glessner, Theodore D. Satterthwaite, 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, Journal of Allergy and Clinical Immunology and Frontiers in 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.

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2026