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Scientific Reports|November 26, 2020
An epigenome-wide association study of metabolic syndrome and its componentsMarja-Liisa Nuotio, Natalia Pervjakova, Anni Joensuu, et al.BMJ Open|May 27, 2026
Pragmatic trial assessing polygenic risk driven statin therapy for cardiovascular disease prevention: study protocol for the EE-PRS trialAve Voit, Aet Elken, Margus Viigimaa, et al.Scientific Reports|September 26, 2020
A data-driven medication score predicts 10-year mortality among aging adultsPaavo Häppölä, Aki S Havulinna, Tõnis Tasa, et al.Diabetes|May 11, 2021
Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk ProfilesRaymond Noordam, Kristi Läll, Roelof A J Smit, et al.Blood|December 8, 2009
DNA methylation for subtype classification and prediction of treatment outcome in patients with childhood acute lymphoblastic leukemiaLili Milani, Anders Lundmark, Anna Kiialainen, et al.Plos One|August 10, 2017
Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infantsKatri Kantojärvi, Johanna Liuhanen, Outi Saarenpää-Heikkilä, et al.Human Molecular Genetics|September 21, 2007
An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseasesVinciane Dideberg, Gudlaug Kristjansdottir, Lili Milani, et al.European Journal of Medical Genetics|July 22, 2018
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variantValtter B Virtanen, Perttu P Salo, Jia Cao, et al.Nature|August 6, 2025
Parent-of-origin effects on complex traits in up to 236,781 individualsRobin J Hofmeister, Théo Cavinato, Roya Karimi, et al.Nature Human Behaviour|April 20, 2023
Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in FinlandTuomo Hartonen, Bradley Jermy, Hanna Sõnajalg, et al.Pageof 19