"Jula, Antti" - Selaus tekijän mukaan Artikkelit
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Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation
(2014)
articleThe X chromosome (chrX) represents one potential source for the “missing heritability” for complex phenotypes, which thus far has remained underanalyzed in genome-wide association studies (GWAS). Here we demonstrate the ... -
Common Genetic Variants Associated with Sudden Cardiac Death : The FinSCDgen Study
(2012)
articleBackground Sudden cardiac death (SCD) accounts for up to half of cardiac mortality. The risk of SCD is heritable but the underlying genetic variants are largely unknown. We investigated whether common genetic variants ... -
Cost-effectiveness analysis of guidelines for antihypertensive care in Finland
(2007)
articleBackground Hypertension is one of the major causes of disease burden affecting the Finnish population. Over the last decade, evidence-based care has emerged to complement other approaches to antihypertensive care, often ... -
Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure
(2012)
articleAlthough genome-wide association studies (GWAS) have identified hundreds of complex trait loci, the pathomechanisms of most remain elusive. Studying the genetics of risk factors predisposing to disease is an attractive ...
