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NPJ Genomic Medicine|December 22, 2017
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlationsSigurgeir Olafsson, Pernilla Stridh, Steffan Daniël Bos, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature|July 18, 2012
A mutation in APP protects against Alzheimer's disease and age-related cognitive declineThorlakur Jonsson, Jasvinder K Atwal, Stacy Steinberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 19, 2008
Enhanced clearance of Abeta in brain by sustaining the plasmin proteolysis cascadeJ Steven Jacobsen, Thomas A Comery, Robert L Martone, et al.
European Journal of Human Genetics : EJHG|August 31, 2021
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population databaseRun Fridriksdottir, Arnar J Jonsson, Brynjar O Jensson, et al.
Circulation. Genomic and Precision Medicine|December 14, 2020
Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLREythor Bjornsson, Kristbjorg Gunnarsdottir, Gisli H Halldorsson, et al.
Nature Communications|November 12, 2024
Sequence variants associated with BMI affect disease risk through BMI itselfGudmundur Einarsson, Gudmar Thorleifsson, Valgerdur Steinthorsdottir, et al.
Blood Cancer Journal|December 2, 2021
Monoclonal gammopathy of undetermined significance and COVID-19: a population-based cohort studySaemundur Rognvaldsson, Elias Eythorsson, Sigrun Thorsteinsdottir, et al.
Clinical Pharmacology and Therapeutics|May 9, 2019
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity ReactionsPaola Nicoletti, Sarah Barrett, Laurence McEvoy, et al.
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