Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy Read more about Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
Investigating Causality and Shared Genetic Architecture between Neurodegenerative Disorders and Inflammatory Bowel Disease Read more about Investigating Causality and Shared Genetic Architecture between Neurodegenerative Disorders and Inflammatory Bowel Disease
Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma Read more about Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma
SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease Read more about SCGB1D2 inhibits growth of Borrelia burgdorferi and affects susceptibility to Lyme disease
Gene-based association study reveals a distinct female genetic signal in primary hypertension Read more about Gene-based association study reveals a distinct female genetic signal in primary hypertension
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease Read more about A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease
Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks Read more about Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks
A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy Read more about A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy
HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study Read more about HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study
Association of structural variation with cardiometabolic traits in Finns Read more about Association of structural variation with cardiometabolic traits in Finns