Author: Marjo-Riitta Jarvelin

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Preprints

Common maternal and fetal genetic variants show expected polygenic effects on the probability of being born small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Polygenic risk scores applied to a single cohort reveal pleiotropy among hundreds of human phenotypes

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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Large-Scale Genome-Wide Meta Analysis of Polycystic Ovary Syndrome Suggests Shared Genetic Architecture for Different Diagnosis Criteria.

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Machine Learning in Multi-Omics Data to Assess Longitudinal Predictors of Glycaemic Health

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Determinants of accelerated metabolomic and epigenetic ageing in a UK cohort

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Association of pre-pregnancy body mass index with future offspring metabolic profile: findings from three independent European birth cohorts

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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Maternal and fetal genetic contribution to gestational weight gain

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methylSCOPA and META-methylSCOPA: software for the analysis and aggregation of epigenome-wide association studies of multiple correlated phenotypes

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The effect of sex and underlying disease on the genetic association of QT interval and sudden cardiac death

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