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Works
9
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
A first update on mapping the human genetic architecture of COVID-19
Rare coding variants in ten genes confer substantial risk for schizophrenia
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records
Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk
The individual and global impact of copy-number variants on complex human traits
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms
Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults
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