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  1. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
  2. Genetically increased circulating FUT3 level leads to reduced risk of idiopathic pulmonary fibrosis: a Mendelian randomisation study
  3. Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study
  4. The Undiagnosed Disease Burden Associated with Alpha-1 Antitrypsin Deficiency Genotypes
  5. Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study
  6. Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes
  7. Vitamin D deficiency is an etiological factor for MS – Yes
  8. Mendelian randomization in multiple sclerosis: A causal role for vitamin D and obesity?
  9. Large differences in adiponectin levels have no clear effect on multiple sclerosis risk: A Mendelian randomization study
  10. Genetic interactions affecting human gene expression identified by variance association mapping