Unraveling the genetic association between obesity-related anthropometric indices and foot deformities in the European population: A two-sample Mendelian randomization study Read more about Unraveling the genetic association between obesity-related anthropometric indices and foot deformities in the European population: A two-sample Mendelian randomization study
Circulating metabolites on dental caries risk: A Mendelian randomization study Read more about Circulating metabolites on dental caries risk: A Mendelian randomization study
Personality disorders and cardiometabolic diseases: A Mendelian randomization study Read more about Personality disorders and cardiometabolic diseases: A Mendelian randomization study
Genetic evidence for causal associations of thrombohemostasis and anticoagulant drug targets with miscarriage Read more about Genetic evidence for causal associations of thrombohemostasis and anticoagulant drug targets with miscarriage
FKBP5 is a Biomarker for Idiopathic Pulmonary Fibrosis based on a Multi-omic Study Integrating xQTLs Read more about FKBP5 is a Biomarker for Idiopathic Pulmonary Fibrosis based on a Multi-omic Study Integrating xQTLs
Genetic correlations among diaphragmatic, femoral, inguinal, ventral, and umbilical hernias and identification of their candidate genes Read more about Genetic correlations among diaphragmatic, femoral, inguinal, ventral, and umbilical hernias and identification of their candidate genes
Identification of immune cells in benign and malignant thymus tumors: a Mendelian randomization study Read more about Identification of immune cells in benign and malignant thymus tumors: a Mendelian randomization study
Bidirectional causal relationships between antibody-mediated immune responses and autoimmune diseases: Insights from Mendelian randomization analysis Read more about Bidirectional causal relationships between antibody-mediated immune responses and autoimmune diseases: Insights from Mendelian randomization analysis
Investigating causal associations between serum metabolites and cataract by Mendelian randomization Read more about Investigating causal associations between serum metabolites and cataract by Mendelian randomization
Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations Read more about Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations