Signatures of TSPAN8 variants associated with human metabolic regulation and diseases Read more about Signatures of TSPAN8 variants associated with human metabolic regulation and diseases
Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma Read more about Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma
Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility Read more about Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease Read more about A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes Read more about Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population Read more about KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia Read more about GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia
Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging Read more about Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging
Obesity and risk of female reproductive conditions: A Mendelian randomisation study Read more about Obesity and risk of female reproductive conditions: A Mendelian randomisation study
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder Read more about Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder