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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

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Genome-wide Screen of Otosclerosis in Population Biobanks: 18 Loci and Shared Heritability with Skeletal Structure

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