Genome-wide association analysis of plasma lipidome identifies 495 genetic associations Read more about Genome-wide association analysis of plasma lipidome identifies 495 genetic associations
Detecting and Adjusting for Hidden Biases due to Phenotype Misclassification in Genome-Wide Association Studies Read more about Detecting and Adjusting for Hidden Biases due to Phenotype Misclassification in Genome-Wide Association Studies
The genetic architecture and evolution of the human skeletal form Read more about The genetic architecture and evolution of the human skeletal form
A second update on mapping the human genetic architecture of COVID-19 Read more about A second update on mapping the human genetic architecture of COVID-19
Machine learning reveals genetic modifiers of the immune microenvironment of cancer Read more about Machine learning reveals genetic modifiers of the immune microenvironment of cancer
Birth weight, childhood obesity, adulthood obesity and body composition, and gastrointestinal diseases: a Mendelian randomization study Read more about Birth weight, childhood obesity, adulthood obesity and body composition, and gastrointestinal diseases: a Mendelian randomization study
Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function Read more about Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function
Is anxiety a pathway to Alcohol Use Disorders? A phenome-wide association study of the GABRA2 coding variant rs279858 Read more about Is anxiety a pathway to Alcohol Use Disorders? A phenome-wide association study of the GABRA2 coding variant rs279858
Tissue-specific enhancer-gene maps from multimodal single-cell data identify causal disease alleles Read more about Tissue-specific enhancer-gene maps from multimodal single-cell data identify causal disease alleles
Rare coding variants in CHRNB2 reduce the likelihood of smoking Read more about Rare coding variants in CHRNB2 reduce the likelihood of smoking