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Eija Hämäläinen

Observed names: Eija Hamalainen, Hamalainen E, Hamalainen, E., Hämäläinen E, Hämäläinen, Eija
Observed institutions: University of Copenhagen, University of Helsinki, University of Cambridge, Sankt Hans Hospital, Wellcome Sanger Institute, Copenhagen University Hospital, Institute for Molecular Medicine Finland
OpenAlex ID: A5113889960
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
2010 · Verneri Anttila, M Stella Calafato, et al. · Nature Genetics · 400
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease
2020 · Julien Bryois, Nathan G. Skene, et al. · Nature Genetics · 368
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Elucidating the relationship between migraine risk and brain structure using genetic data
2022 · Brittany L Mitchell, Santiago Diaz-Torres, et al. · Brain · 35
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Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
2016 · Padhraig Gormley, Verneri Anttila, et al. · Nature Genetics · 25
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (vol 98, pg 743, 2018)
2018 · Gormley, P., Kurki, M.I., et al. · Leiden Repository (Leiden University) · 20
Machine Diagnostics and Machine Phenotyping of Migraine
2026 · Antonios Danelakis, Håkon Kvisle Abildsnes, et al. · Neurology · 2
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Rare coding variants in ten genes confer substantial risk for schizophrenia
2026 · Kirov, George, Ganna, Andrea, et al. · Carolina Digital Repository (University of North Carolina at Chapel Hill)
Correction: Common variant burden contributes to the familial aggregation of migraine in 1,589 families
2018 · Padhraig Gormley, Mitja Kurki, et al. · Neuron
Works count: 11
Citation count: 850
H-index: 5
I10-index: 5
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