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Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 14:11
  • Read more about Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

A minority of somatically mutated genes in pre-existing fatty liver disease have prognostic importance in the development of NAFLD

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 13:38
  • Read more about A minority of somatically mutated genes in pre-existing fatty liver disease have prognostic importance in the development of NAFLD

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 13:34
  • Read more about A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Mono- and biallelic variant effects on disease at biobank scale

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 13:26
  • Read more about Mono- and biallelic variant effects on disease at biobank scale

Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 13:20
  • Read more about Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes

Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 13:14
  • Read more about Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study

Global Biobank Meta-analysis Initiative: powering genetic discovery across human diseases

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 12:03
  • Read more about Global Biobank Meta-analysis Initiative: powering genetic discovery across human diseases

Polygenic risk score from a multi-ancestry GWAS uncovers susceptibility of heart failure

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 09:47
  • Read more about Polygenic risk score from a multi-ancestry GWAS uncovers susceptibility of heart failure

Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

Submitted by Frida Mäkelä on Fri, 09/30/2022 - 09:26
  • Read more about Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 15:51
  • Read more about Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics

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The University of Helsinki is the organization responsible for the FinnGen research project. The Finnish consortium partners include all Finnish public biobanks and their background organisations, so the project covers the whole of Finland. All partners are listed on this page.

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