Thibaud Boutin
0000-0003-4754-1675
4 papers found
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Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation
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