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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

Signatures of TSPAN8 variants associated with human metabolic regulation and diseases

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:49
  • Read more about Signatures of TSPAN8 variants associated with human metabolic regulation and diseases

Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:47
  • Read more about Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:45
  • Read more about Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease

Submitted by Frida Mäkelä on Thu, 09/29/2022 - 12:44
  • Read more about A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease

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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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