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Gene-based association study reveals a distinct female genetic signal in primary hypertension

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:38
  • 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

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:26
  • 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

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:23
  • 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

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:15
  • 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

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:13
  • 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

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 13:01
  • Read more about Association of structural variation with cardiometabolic traits in Finns

Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:58
  • Read more about Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease

Genome-wide association study identifies five risk loci for pernicious anemia

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:56
  • Read more about Genome-wide association study identifies five risk loci for pernicious anemia

Mapping the human genetic architecture of COVID-19

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:53
  • Read more about Mapping the human genetic architecture of COVID-19

Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:51
  • Read more about Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

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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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