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

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 14:03
  • Read more about Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

Clonal hematopoiesis is associated with protection from Alzheimer's disease

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 14:01
  • Read more about Clonal hematopoiesis is associated with protection from Alzheimer's disease

Genome-Wide Association Study and Transcriptome of Japanese Patients with Developmental Dysplasia of the Hip Demonstrates an Association with the Ferroptosis Signaling Pathway

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:56
  • Read more about Genome-Wide Association Study and Transcriptome of Japanese Patients with Developmental Dysplasia of the Hip Demonstrates an Association with the Ferroptosis Signaling Pathway

Mendelian Randomization Analysis Provides Insights into the Pathogenesis of Serum Levels of Branched-Chain Amino Acids in Cardiovascular Disease

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:32
  • Read more about Mendelian Randomization Analysis Provides Insights into the Pathogenesis of Serum Levels of Branched-Chain Amino Acids in Cardiovascular Disease

Causal Link between Inflammatory Bowel Disease and Fistula: Evidence from Mendelian Randomization Study

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:30
  • Read more about Causal Link between Inflammatory Bowel Disease and Fistula: Evidence from Mendelian Randomization Study

Celiac Disease Is a Risk Factor for Mature T and NK Cell Lymphoma: A Mendelian Randomization Study

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:28
  • Read more about Celiac Disease Is a Risk Factor for Mature T and NK Cell Lymphoma: A Mendelian Randomization Study

Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:24
  • Read more about Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 13:04
  • Read more about Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures

150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 12:37
  • Read more about 150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility

Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study

Submitted by Frida Mäkelä on Fri, 06/30/2023 - 12:27
  • Read more about Causal relationship between gut microbiota and cancers: a two-sample Mendelian randomisation study

Pagination

  • First page « First
  • Previous page ‹ Previous
  • …
  • Page 339
  • Page 340
  • Page 341
  • Page 342
  • Current page 343
  • Page 344
  • Page 345
  • Page 346
  • Page 347
  • …
  • 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