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Human Molecular Genetics|February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisAdriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Human Molecular Genetics|July 29, 2016
Analysis with the exome array identifies multiple new independent variants in lipid lociStavroula Kanoni, Nicholas G D Masca, Kathleen E Stirrups, et al.
Medrxiv : the Preprint Server for Health Sciences|April 14, 2021
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19Lucija Klaric, Jack S Gisby, Artemis Papadaki, et al.
Ebiomedicine|November 17, 2018
Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adultsPriyanka Parmar, Estelle Lowry, Giovanni Cugliari, et al.
International Journal of Epidemiology|May 29, 2015
Adiposity as a cause of cardiovascular disease: a Mendelian randomization studySara Hägg, Tove Fall, Alexander Ploner, et al.
Nature Genetics|October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biologyManuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.
Nature Genetics|November 25, 2014
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissectionStéphanie Debette, Yoichiro Kamatani, Tiina M Metso, et al.
The Journal of Allergy and Clinical Immunology|February 22, 2026
Meta-analysis of genome-wide association studies of food allergy and IgE-sensitizationLisa Maier, Yidan Sun, Jaanika Kronberg, et al.
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