Search Results - "FinnGen"

Disentangling the link between maternal influences on birth weight and disease risk in 36,211 genotyped mother–child pairs.

Authors: Leinonen, Jaakko T. FinnGen Pirinen, Matti et al.

Source: Communications Biology. 2/12/2024, Vol. 7 Issue 1, p1-9. 9p.

An immunogenetic basis for lung cancer risk.

Authors: Krishna, Chirag Tervi, Anniina Saffern, Miriam et al.

Source: Science (pre-March 2025). 2/23/2024, Vol. 383 Issue 6685, p847-847. 1p. 1 Diagram.

Subjects: Lung cancer, Disease risk factors, Genetic risk score, Human genetic variation, T cell receptors, Homozygosity

Finnish-Enriched SLC26A7 Variant in Congenital Hypothyroidism: Clinical Spectrum, Thyroid Histopathology, and Expression Analysis.

Authors: Niuro, Laura Ojala, Johanna Ravi, Rowmika et al.

Source: Thyroid. Feb2026, Vol. 36 Issue 2, p141-152. 12p.

Polygenic Risk Scores Predict Hypertension Onset and Cardiovascular Risk.

Authors: Vaura, Felix Kauko, Anni Suvila, Karri et al.

Source: Hypertension (0194911X). Apr2021, Vol. 77 Issue 4, p1119-1127.

Monoallelic TYROBP deletion is a novel risk factor for Alzheimer's disease.

Authors: Martiskainen, Henna Willman, Roosa-Maria Harju, Päivi et al.

Source: Molecular Neurodegeneration. 4/29/2025, Vol. 20 Issue 1, p1-22. 22p.

Cross-sectional assessment of telephone- and computer-administered instruments in detection of cognitive impairment.

Authors: Aaltonen, A. Saari, TT. Urjansson, M. et al.

Source: Journal of Clinical & Experimental Neuropsychology. Apr2026, p1-12. 12p. 2 Illustrations.

Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade.

Authors: Wanner, Julian S. Krafft, Maren Niiranen, Teemu et al.

Source: Circulation. 12/16/2025, Vol. 152 Issue 24, p1679-1690. 12p.

NTHL1 is a recessive cancer susceptibility gene.

Authors: Nurmi, Anna K. Pelttari, Liisa M. Kiiski, Johanna I. et al.

Source: Scientific Reports. 11/30/2023, Vol. 13 Issue 1, p1-14. 14p.

A FinnGen pilot clinical recall study for Alzheimer's disease.

Authors: Julkunen, Valtteri Schwarz, Claudia Kalapudas, Juho et al.

Source: Scientific Reports. 11/18/2023, Vol. 13 Issue 1, p1-15. 15p.

Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome.

Authors: Tyrmi, Jaakko S Arffman, Riikka K Pujol-Gualdo, Natàlia et al.

Source: Human Reproduction. Feb2022, Vol. 37 Issue 2, p352-365. 14p.

Use of electronic health record data mining for heart failure subtyping.

Authors: Vuori, Matti A. Kiiskinen, Tuomo Pitkänen, Niina et al.

Source: BMC Research Notes. 9/11/2023, Vol. 16 Issue 1, p1-6. 6p.

The association of a polygenic lifespan score with the risk of common age-related diseases and mortality.

Authors: Tynkkynen, Niko Paavo Koivunen, Kaisa Herranen, Päivi et al.

Source: Journals of Gerontology Series A: Biological Sciences & Medical Sciences. Sep2025, Vol. 80 Issue 9, p1-10. 10p.

Genetic Susceptibility to Acute Viral Bronchiolitis.

Authors: Pasanen, Anu Karjalainen, Minna K Korppi, Matti et al.

Source: Journal of Infectious Diseases. 8/15/2025, Vol. 232 Issue 2, pe193-e202. 10p.

Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.

Authors: Helkkula, Pyry Hassan, Shabbeer Saarentaus, Elmo et al.

Source: Communications Biology. Dec2023, Vol. 6 Issue 1, p1-12. 12p.

Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes.

Authors: Tamlander, Max Mars, Nina Pirinen, Matti et al.

Source: Communications Biology. 2/23/2022, Vol. 5 Issue 1, p1-13. 13p.

Genome‐wide association study of anterior uveitis.

Authors: Koskimäki, Fredrika Ahokas, Oona Consortium, FinnGen et al.

Source: Acta Ophthalmologica (1755375X). Jan2025 Supplement 1, Vol. 103, pN.PAG-N.PAG. 1p.

Genome-Wide Polygenic Score for Muscle Strength Predicts Risk for Common Diseases and Lifespan: A Prospective Cohort Study.

Authors: Herranen, Päivi Koivunen, Kaisa Palviainen, Teemu et al.

Source: Journals of Gerontology Series A: Biological Sciences & Medical Sciences. Apr2024, Vol. 79 Issue 4, p1-8. 8p.

Genome-wide polygenic risk scores for colorectal cancer have implications for risk-based screening.

Authors: Tamlander, Max Jermy, Bradley Seppälä, Toni T. et al.

Source: British Journal of Cancer. Mar2024, Vol. 130 Issue 4, p651-659. 9p.

Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland.

Authors: Hartonen, Tuomo Jermy, Bradley Sõnajalg, Hanna et al.

Source: Nature Human Behaviour. Jul2023, Vol. 7 Issue 7, p1069-1083. 15p.

POLYGENIC RISK SCORES IMPROVE ON FAMILY HISTORY IN HYPERTENSION RISK PREDICTION.

Authors: Vaura, Felix Kauko, Anni FinnGen et al.

Source: Journal of the American College of Cardiology (JACC). 2022 Supplement, Vol. 79 Issue 9, p1463-1463. 1p.