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CCR5-del32 is not deleterious in the homozygous state in humans

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 16:23
  • Read more about CCR5-del32 is not deleterious in the homozygous state in humans

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 16:13
  • Read more about Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus

Quantifying the contribution of Neanderthal introgression to the heritability of complex traits

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 16:08
  • Read more about Quantifying the contribution of Neanderthal introgression to the heritability of complex traits

The genetic architecture of human infectious diseases and pathogen-induced cellular phenotypes

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 16:01
  • Read more about The genetic architecture of human infectious diseases and pathogen-induced cellular phenotypes

Assessing the efficacy and safety of angiotensinogen inhibition using human genetics

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:54
  • Read more about Assessing the efficacy and safety of angiotensinogen inhibition using human genetics

Genome-Wide Polygenic Risk Score Identifies Individuals at Elevated Parkinson’s Disease Risk

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:41
  • Read more about Genome-Wide Polygenic Risk Score Identifies Individuals at Elevated Parkinson’s Disease Risk

Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:38
  • Read more about Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:33
  • Read more about Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

Findings and insights from the genetic investigation of age of first reported occurrence for complex disorders in the UK Biobank and FinnGen

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:28
  • Read more about Findings and insights from the genetic investigation of age of first reported occurrence for complex disorders in the UK Biobank and FinnGen

A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S

Submitted by Frida Mäkelä on Mon, 10/17/2022 - 15:22
  • Read more about A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S

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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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