Skip to main content
  • EN
  • FI
  • SV
Login

Main navigation

  • About FinnGen
    • Summary & Goals
      • Goals
      • FinnGen 1-2
      • FinnGen 3 (2023-2027)
    • Consortium
      • Partners
      • Funding
      • Governance
      • Steering Committee Members
      • Scientific Committee Members
      • Teams
      • Collaboration
    • Impact
      • National Impact
      • National Research Network
      • Open Science
      • Research Highlights
    • Why Finland?
      • Biobank Network
      • Legislative Review
      • National Registries
      • Population Genetic History
      • Industry partners
    • Mediabank
  • For Researchers
    • Research Activities
      • Core Analyses
      • Disease Task Forces
      • Expansion Areas
      • Global Initiatives
    • Cohort and Data
      • Register Data
      • Basic Characteristics
      • Clinical Endpoints
      • Genetic Data
      • Laboratory Values
      • Other Phenotype Data
      • Recruitment
      • Other Biological Data
      • Data Available
    • Accessing Data, Results & Tools
      • Access results
      • Computing environment
      • How We Collaborate
      • Partner researchers
      • Public data releases
      • Tools
    • Publications
    • Researcher FAQ
  • For Participants
    • Participation
      • Study Participants
      • Biobanks' Role in FinnGen
      • Biobank Contact Information
      • Recall Studies
      • Questions and answers
    • Data Protection and Security
      • Data Protection
      • Data Security
      • Sample & Data Flow
      • Data Protection Statement
    • Significance
      • Videos
  • News
  • EN
  • FI
  • SV

Links

  • PheWeb
  • Risteys
  • Meta-analysis Pheweb (FG-MVP-UKBB)
  • FinnGen handbook
  • Meta-analysis Pheweb (FG-UKBB)
  • Coding variant browser
  • Endpoint Browser
  • FinnGen GITHUB
  • LAVAA volcano plot
  • Multiple Manhattan Plot
  • Variant Cluster Corrector
  • Variant Cluster Call Corrector
Breadcrumb
  1. Home

Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 18:26
  • Read more about Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.

The Role of Calcium, 25-Hydroxyvitamin D, and Parathyroid Hormone in Irritable Bowel Syndrome: A Bidirectional Two-Sample Mendelian Randomization Study

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 18:16
  • Read more about The Role of Calcium, 25-Hydroxyvitamin D, and Parathyroid Hormone in Irritable Bowel Syndrome: A Bidirectional Two-Sample Mendelian Randomization Study

Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 18:09
  • Read more about Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes

Polygenic prediction of preeclampsia and gestational hypertension

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 18:06
  • Read more about Polygenic prediction of preeclampsia and gestational hypertension

No Evidence to Support a Causal Relationship between Circulating Adiponectin Levels and Ankylosing Spondylitis: A Bidirectional Two-Sample Mendelian Randomization Study

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 18:02
  • Read more about No Evidence to Support a Causal Relationship between Circulating Adiponectin Levels and Ankylosing Spondylitis: A Bidirectional Two-Sample Mendelian Randomization Study

Quantifying the causal impact of biological risk factors on healthcare costs

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 17:56
  • Read more about Quantifying the causal impact of biological risk factors on healthcare costs

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Submitted by Mari Anneli Kaunisto on Mon, 12/05/2022 - 17:52
  • Read more about Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Health effects of milk consumption: phenome-wide Mendelian randomization study

Submitted by Frida Mäkelä on Fri, 11/25/2022 - 15:21
  • Read more about Health effects of milk consumption: phenome-wide Mendelian randomization study

White blood cells and chronic rhinosinusitis: a Mendelian randomization study

Submitted by Frida Mäkelä on Fri, 11/25/2022 - 15:17
  • Read more about White blood cells and chronic rhinosinusitis: a Mendelian randomization study

The causal association between iron status and the risk of autism: A Mendelian randomization study

Submitted by Frida Mäkelä on Fri, 11/25/2022 - 15:15
  • Read more about The causal association between iron status and the risk of autism: A Mendelian randomization study

Pagination

  • First page « First
  • Previous page ‹ Previous
  • …
  • Page 371
  • Page 372
  • Page 373
  • Page 374
  • Current page 375
  • Page 376
  • Page 377
  • Page 378
  • Page 379
  • …
  • Next page Next ›
  • Last page Last »
Subscribe to

Contact us

Contact person
finngen-info@helsinki.fi
Follow us on Bluesky
@finngen.bsky.social

Lead organisations

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.

About the website

Accessibility statement