Two-sample Mendelian randomization investigating the causal association between endocarditis and osteomyelitis: A validation analysis using UK Biobank and FinnGen databases Read more about Two-sample Mendelian randomization investigating the causal association between endocarditis and osteomyelitis: A validation analysis using UK Biobank and FinnGen databases
Limited overlap between genetic effects on disease susceptibility and disease survival Read more about Limited overlap between genetic effects on disease susceptibility and disease survival
Association between mitochondrial DNA copy number and the risk of Parkinson's disease: a meta-analysis and Mendelian randomization study Read more about Association between mitochondrial DNA copy number and the risk of Parkinson's disease: a meta-analysis and Mendelian randomization study
Multiomic Mendelian randomization analysis of metabolic gene methylation expression and protein levels in lung adenocarcinoma Read more about Multiomic Mendelian randomization analysis of metabolic gene methylation expression and protein levels in lung adenocarcinoma
Association between brain connectivity and renal pathophysiology: a multi-trait Mendelian randomization analysis Read more about Association between brain connectivity and renal pathophysiology: a multi-trait Mendelian randomization analysis
Exploring Causal Relationships Between Kidney Function and the Risk of Senile Cataract and Primary Open-Angle Glaucoma: A Mendelian Randomization Study and Bioinformatics Analyses Read more about Exploring Causal Relationships Between Kidney Function and the Risk of Senile Cataract and Primary Open-Angle Glaucoma: A Mendelian Randomization Study and Bioinformatics Analyses
Genetic liability to meniscus degeneration and its comorbidity patterns: a phenome-wide association study in the UK Biobank Read more about Genetic liability to meniscus degeneration and its comorbidity patterns: a phenome-wide association study in the UK Biobank
FINEMAP-miss: Fine-mapping genome-wide association studies with missing genotype information Read more about FINEMAP-miss: Fine-mapping genome-wide association studies with missing genotype information
Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data from FinnGen and UK Biobank Read more about Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data from FinnGen and UK Biobank
PCSK9 and breast cancer survival: a Mendelian Randomization study Read more about PCSK9 and breast cancer survival: a Mendelian Randomization study