Maternal hypertensive disorders of pregnancy and childhood neurodevelopmental disorders: A two-sample Mendelian randomization Read more about Maternal hypertensive disorders of pregnancy and childhood neurodevelopmental disorders: A two-sample Mendelian randomization
The causal relationship between cathepsins and ankylosing spondylitis: a two-sample Mendelian randomization study Read more about The causal relationship between cathepsins and ankylosing spondylitis: a two-sample Mendelian randomization study
Genome Wide Association Analysis of Two Pore Domain Potassium Channel Gene Regions Reveals Multiple Pain-Associated Signals Read more about Genome Wide Association Analysis of Two Pore Domain Potassium Channel Gene Regions Reveals Multiple Pain-Associated Signals
Accelerated electrocardiographic aging of the heart as a risk determinant for atrial fibrillation: A Mendelian randomization study Read more about Accelerated electrocardiographic aging of the heart as a risk determinant for atrial fibrillation: A Mendelian randomization study
Helicobacter pylori infection is causally associated with extra-gastric tumors: a Mendelian randomization study Read more about Helicobacter pylori infection is causally associated with extra-gastric tumors: a Mendelian randomization study
Characterization of genetic loci associated with allergic conjunctivitis Read more about Characterization of genetic loci associated with allergic conjunctivitis
A two-sample Mendelian randomization study and mediation analysis exploring the link between cathepsins and epilepsy Read more about A two-sample Mendelian randomization study and mediation analysis exploring the link between cathepsins and epilepsy
Integrating polygenic and methylation risk scores for pleural mesothelioma risk stratification Read more about Integrating polygenic and methylation risk scores for pleural mesothelioma risk stratification
Genetic and functional evidence implicates a CRIP3 non-synonymous variant in age-related hearing loss Read more about Genetic and functional evidence implicates a CRIP3 non-synonymous variant in age-related hearing loss
Large-scale genetic analysis of age-related macular degeneration (AMD) drug targets highlights precision therapy opportunities for patients with high polygenic risk Read more about Large-scale genetic analysis of age-related macular degeneration (AMD) drug targets highlights precision therapy opportunities for patients with high polygenic risk