Search Results - "Pirinen, Matti"

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.

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Risk of pneumococcal bacteremia in Kenyan children with glucose-6-phosphate dehydrogenase deficiency.

Authors: Gilchrist, James J. Uyoga, Sophie Pirinen, Matti et al.

Source: BMC Medicine. 6/15/2020, Vol. 18 Issue 1, p1-10. 10p. 1 Chart, 2 Graphs.

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Effect of predicted protein-truncating genetic variants on the human transcriptome.

Authors: Rivas, Manuel A. Pirinen, Matti Conrad, Donald F. et al.

Source: Science (pre-March 2025). 5/8/2015, Vol. 348 Issue 6235, p666-669. 4p.

Accumulating evidence from meta-analyses of prognostic studies on oral cancer: towards biomarker-driven patient selection.

Authors: Almangush, Alhadi Alabi, Rasheed Omobolaji Pirinen, Matti et al.

Source: BMC Cancer. 12/18/2024, Vol. 24 Issue 1, p1-13. 13p.

Lifestyle differences between co-twins are associated with decreased similarity in their internal and external exposome profiles.

Authors: Drouard, Gabin Wang, Zhiyang Heikkinen, Aino et al.

Source: Scientific Reports. 9/11/2024, Vol. 14 Issue 1, p1-12. 12p.

The Outcome after Endovascular and Open Repair of Abdominal Aortic Aneurysms—A Binational Study Conducted between 1998 and 2017.

Authors: Pirinen, Riku Laine, Matti T. Mani, Kevin et al.

Source: Journal of Clinical Medicine. Aug2024, Vol. 13 Issue 15, p4449. 10p.

Exploring machine learning strategies for predicting cardiovascular disease risk factors from multi-omic data.

Authors: Drouard, Gabin Mykkänen, Juha Heiskanen, Jarkko et al.

Source: BMC Medical Informatics & Decision Making. 5/2/2024, Vol. 24 Issue 1, p1-18. 18p.

Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.

Authors: Bahrami, Shahram Hindley, Guy Winsvold, Bendik Slagsvold et al.

Source: Brain: A Journal of Neurology; Jan2022, Vol. 145 Issue 1, p142-153, 12p

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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.

Longitudinal multi-omics study reveals common etiology underlying association between plasma proteome and BMI trajectories in adolescent and young adult twins.

Authors: Drouard, Gabin Hagenbeek, Fiona A. Whipp, Alyce M. et al.

Source: BMC Medicine. 12/21/2023, Vol. 21 Issue 1, p1-21. 21p.

Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.

Authors: Häppölä, Paavo Gormley, Padhraig Nuottamo, Marjo E et al.

Source: Cephalalgia. Apr2022, Vol. 42 Issue 4/5, p345-356. 12p.

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NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.

Authors: Nuottamo, Marjo Eveliina Häppölä, Paavo Artto, Ville et al.

Source: Cephalalgia. Jun2022, Vol. 42 Issue 7, p631-644. 14p.

The fine-scale genetic structure of the British population.

Authors: Leslie, Stephen Winney, Bruce Hellenthal, Garrett et al.

Source: Nature. 3/19/2015, Vol. 519 Issue 7543, p309-314. 6p.

Subjects: Human population genetics, Human genetics, Single nucleotide polymorphisms, Anglo-Saxons, British people