Genomic data-driven framework for drug target discovery in atrial fibrillation Read more about Genomic data-driven framework for drug target discovery in atrial fibrillation
Sex hormones and meningiomas risk: a Mendelian randomization and immunohistochemical analysis Read more about Sex hormones and meningiomas risk: a Mendelian randomization and immunohistochemical analysis
Genetic Validation of ABI3 p.S209F Variant and Its effects On Early Brain Pathology in Asymptomatic Elderly Individuals Read more about Genetic Validation of ABI3 p.S209F Variant and Its effects On Early Brain Pathology in Asymptomatic Elderly Individuals
Removing genetic effects on plasma proteins enhances their utility as disease biomarkers Read more about Removing genetic effects on plasma proteins enhances their utility as disease biomarkers
Multivariate GWAS reveals shared genetic etiology and pleiotropic loci across carcinomas Read more about Multivariate GWAS reveals shared genetic etiology and pleiotropic loci across carcinomas
Integrative Proteome- and Phenome-Wide Assessment Uncovers Causal Protein Drivers and Drug Targets for Heterogeneous Kidney Diseases Read more about Integrative Proteome- and Phenome-Wide Assessment Uncovers Causal Protein Drivers and Drug Targets for Heterogeneous Kidney Diseases
Genetic architecture of 67 oral diseases and their links to systemic diseases Read more about Genetic architecture of 67 oral diseases and their links to systemic diseases
Proteomic landscape of multidimensional aging phenotypes Read more about Proteomic landscape of multidimensional aging phenotypes
Causal effects and mediation pathways of circulating plasma proteins on osteoporosis: a two-sample and two-step Mendelian randomization study Read more about Causal effects and mediation pathways of circulating plasma proteins on osteoporosis: a two-sample and two-step Mendelian randomization study
Multi-omics causal inference of nuclear-encoded mitochondrial genes in autism spectrum disorder Read more about Multi-omics causal inference of nuclear-encoded mitochondrial genes in autism spectrum disorder