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Genetic architecture of lumbar spinal stenosis

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 16:25
  • Read more about Genetic architecture of lumbar spinal stenosis

GLP-1 Receptor Agonists and Risk of Paralytic Ileus: A drug-target Mendelian Randomization Study

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 16:20
  • Read more about GLP-1 Receptor Agonists and Risk of Paralytic Ileus: A drug-target Mendelian Randomization Study

Binge drinking trajectories across adolescence and early adulthood: Associations with genetic influences for dual-systems impulsive personality traits, alcohol consumption, and alcohol use disorder

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 16:08
  • Read more about Binge drinking trajectories across adolescence and early adulthood: Associations with genetic influences for dual-systems impulsive personality traits, alcohol consumption, and alcohol use disorder

Appraisal of the causal effect of Chlamydia trachomatis infection on epithelial ovarian cancer risk: a two-sample Mendelian randomisation study

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 16:01
  • Read more about Appraisal of the causal effect of Chlamydia trachomatis infection on epithelial ovarian cancer risk: a two-sample Mendelian randomisation study

Clonal hematopoiesis is associated with distinct rheumatoid arthritis phenotypes

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 15:27
  • Read more about Clonal hematopoiesis is associated with distinct rheumatoid arthritis phenotypes

Omega-3 fatty acids and intracranial aneurysms: a Mendelian randomization study

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 15:23
  • Read more about Omega-3 fatty acids and intracranial aneurysms: a Mendelian randomization study

Dissecting the genetic and proteomic risk factors for delirium

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 15:19
  • Read more about Dissecting the genetic and proteomic risk factors for delirium

Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 15:13
  • Read more about Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations

Genetic Determinants of Bone Microarchitecture and its Association with Health Outcomes: A Genome-wide Association and Mendelian Randomization Study on Trabecular Bone Score

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 14:55
  • Read more about Genetic Determinants of Bone Microarchitecture and its Association with Health Outcomes: A Genome-wide Association and Mendelian Randomization Study on Trabecular Bone Score

Family-GWAS reveals effects of environment and mating on genetic associations

Submitted by Frida Mäkelä on Fri, 12/13/2024 - 14:42
  • Read more about Family-GWAS reveals effects of environment and mating on genetic associations

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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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