Genetically Predicted Use of Common Analgesics and Risk of Chronic Obstructive Pulmonary Disease: A Bidirectional Mendelian Randomization Study Read more about Genetically Predicted Use of Common Analgesics and Risk of Chronic Obstructive Pulmonary Disease: A Bidirectional Mendelian Randomization Study
Myricetin inhibits proliferation and migration of bladder cancer cells by inhibiting HSP90AA1-mediated AKT phosphorylation Read more about Myricetin inhibits proliferation and migration of bladder cancer cells by inhibiting HSP90AA1-mediated AKT phosphorylation
Integration of Brain Proteomes and Genome-Wide Association Data Identifies GLO1 as a Candidate Causal Gene and Therapeutic Target for Restless Legs Syndrome Read more about Integration of Brain Proteomes and Genome-Wide Association Data Identifies GLO1 as a Candidate Causal Gene and Therapeutic Target for Restless Legs Syndrome
Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors Read more about Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
DNA demethylation of ANXA4 is associated with atrial fibrillation risk through myeloid immune mechanisms: evidence from Mendelian randomization and multi-omics analyses Read more about DNA demethylation of ANXA4 is associated with atrial fibrillation risk through myeloid immune mechanisms: evidence from Mendelian randomization and multi-omics analyses
Causal relationship between oral diseases and hypertension: a Mendelian randomization study Read more about Causal relationship between oral diseases and hypertension: a Mendelian randomization study
Susceptibility Versus Defense: A Spatially Defined Mitochondrial Network in Trigeminal Neuralgia Read more about Susceptibility Versus Defense: A Spatially Defined Mitochondrial Network in Trigeminal Neuralgia
MyoScore: a Genetically Anchored Transcriptomic Scoring System for Quantifying Human Skeletal Muscle Health Read more about MyoScore: a Genetically Anchored Transcriptomic Scoring System for Quantifying Human Skeletal Muscle Health
Using human genetic variation to estimate the effect of lipoprotein(a) lowering on pregnancy outcomes Read more about Using human genetic variation to estimate the effect of lipoprotein(a) lowering on pregnancy outcomes
Clonal haematopoiesis without identified genetic drivers: insights from analyses of 407,512 individuals Read more about Clonal haematopoiesis without identified genetic drivers: insights from analyses of 407,512 individuals