Eija Hämäläinen
occupation: researcher
Articles 15
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Analysis of shared heritability in common disorders of the brain
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Pitfalls in genetic testing: the story of missed SCN1A mutations
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Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
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Genetic analysis for a shared biological basis between migraine and coronary artery disease
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Distribution and medical impact of loss-of-function variants in the Finnish founder population
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Genome-wide meta-analysis identifies new susceptibility loci for migraine
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Genome-wide association analysis identifies susceptibility loci for migraine without aura
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Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
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Metabonomic, transcriptomic, and genomic variation of a population cohort
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Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors
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Consistently replicating locus linked to migraine on 10q22-q23
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A susceptibility locus for migraine with aura, on chromosome 4q24.
Human - wd:Q42539490