FinnGen
@finngen.bsky.social
A forerunner in the global landscape of genomics research projects. The study has collected and analysed genome and health data from >500,000 Finnish biobank donors to understand the genetic basis of diseases.
www.finngen.fi
www.finngen.fi
The findings, based on FinnGen and other cohorts, have just been published in the Circulation journal:
www.ahajournals.org/doi/10.1161/...
www.ahajournals.org/doi/10.1161/...
Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade | Circulation
BACKGROUND: Atrial fibrillation and other cardiac arrhythmias pose a major public health burden,
but prevention remains difficult. We investigated a genetic variant that we found
to act like a natural...
www.ahajournals.org
November 26, 2025 at 9:43 AM
The findings, based on FinnGen and other cohorts, have just been published in the Circulation journal:
www.ahajournals.org/doi/10.1161/...
www.ahajournals.org/doi/10.1161/...
The results of the study were published in Nature Genetics: @natgenet.nature.com
www.nature.com/articles/s41...
www.nature.com/articles/s41...
Genome-wide association analyses identify distinct genetic architectures for early-onset and late-onset depression - Nature Genetics
Genome-wide association analyses leveraging Nordic biobanks with longitudinal health registries identify differences in the genetic architectures of early-onset and late-onset major depressive disorde...
www.nature.com
November 20, 2025 at 1:01 PM
The results of the study were published in Nature Genetics: @natgenet.nature.com
www.nature.com/articles/s41...
www.nature.com/articles/s41...
Eero Ala-Mutka - Genetic Architecture and Risk Profile of Alcohol-Related Diseases [Board No. 9272F]
October 17, 2025 at 6:31 PM
Eero Ala-Mutka - Genetic Architecture and Risk Profile of Alcohol-Related Diseases [Board No. 9272F]
Frida Lona-Durazo - Sex-aware causal inference assessment of the immune system in complex neurodegenerative diseases [Board No. 9253F]
October 17, 2025 at 6:31 PM
Frida Lona-Durazo - Sex-aware causal inference assessment of the immune system in complex neurodegenerative diseases [Board No. 9253F]
Yu Fu - Elucidating the X chromosome influence on the female bias in autoimmune diseases [Board No. 9243F]
October 17, 2025 at 6:31 PM
Yu Fu - Elucidating the X chromosome influence on the female bias in autoimmune diseases [Board No. 9243F]
Jaakko Tyrmi - Genome-wide association study of hirsutism highlights androgen-independent pathways [Board No. 9242F]
October 17, 2025 at 6:31 PM
Jaakko Tyrmi - Genome-wide association study of hirsutism highlights androgen-independent pathways [Board No. 9242F]
Anu Pasanen - Identification of genetic factors associated with spontaneous preterm deliveries with and without PPROM [Board No. 9223F]
October 17, 2025 at 6:31 PM
Anu Pasanen - Identification of genetic factors associated with spontaneous preterm deliveries with and without PPROM [Board No. 9223F]
Julia Tomasi - Investigating the role of endolysosomal, autophagy, and mitochondrial pathway genetic burden in Parkinson's Disease [Board No. 9193F]
October 17, 2025 at 6:31 PM
Julia Tomasi - Investigating the role of endolysosomal, autophagy, and mitochondrial pathway genetic burden in Parkinson's Disease [Board No. 9193F]
Sophie Parsa - Assessing generalizability and interpretability of proteomic disease prediction models from 64,907 individuals across three cohorts [Board No. 9155F]
October 17, 2025 at 6:31 PM
Sophie Parsa - Assessing generalizability and interpretability of proteomic disease prediction models from 64,907 individuals across three cohorts [Board No. 9155F]
Nasa Sinnott-Armstrong - Meta-analysis of genetic variants affecting statin response [Board No. 9097F]
October 17, 2025 at 6:31 PM
Nasa Sinnott-Armstrong - Meta-analysis of genetic variants affecting statin response [Board No. 9097F]
Javier Gracia-Tabuenca - Leveraging OHDSI's OMOP-CDM to Harmonize National Health Data for Genetic Research [Board No. 3008F]
October 17, 2025 at 6:31 PM
Javier Gracia-Tabuenca - Leveraging OHDSI's OMOP-CDM to Harmonize National Health Data for Genetic Research [Board No. 3008F]
Zhili Zheng - A novel score tracing familial resemblance over 500 traits in deep pedigrees of seven million non-genotyped and genotyped Finns [Board No. 1003F]
October 17, 2025 at 6:31 PM
Zhili Zheng - A novel score tracing familial resemblance over 500 traits in deep pedigrees of seven million non-genotyped and genotyped Finns [Board No. 1003F]
Chelsea Nguyen - Genetic loci associated with clinically significant acute knee injury in 944,189 cases and comparators [Board No. 9256T]
October 16, 2025 at 3:06 PM
Chelsea Nguyen - Genetic loci associated with clinically significant acute knee injury in 944,189 cases and comparators [Board No. 9256T]
Feiyi Wang - Beyond complexity: multi-source data integration enhances CVD risk prediction in T2D [Board No. 9094T]
October 16, 2025 at 3:06 PM
Feiyi Wang - Beyond complexity: multi-source data integration enhances CVD risk prediction in T2D [Board No. 9094T]
Mervi Aavikko - Cross-cancer genome-wide association analysis of 121,495 cancer cases in FinnGen [Board No. 9069T]
October 16, 2025 at 3:06 PM
Mervi Aavikko - Cross-cancer genome-wide association analysis of 121,495 cancer cases in FinnGen [Board No. 9069T]
Felix Vaura - GWAS of creatinine response to RAAS inhibition in 32,907 Finns identifies regulatory variant near LINC01267 [Board No. 5085T]
October 16, 2025 at 3:06 PM
Felix Vaura - GWAS of creatinine response to RAAS inhibition in 32,907 Finns identifies regulatory variant near LINC01267 [Board No. 5085T]