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European Journal of Heart Failure|April 13, 2025
Prediction and prognostic role of left ventricular systolic dysfunction in family screening for dilated cardiomyopathy and non-dilated left ventricular cardiomyopathyEva Del Mestre, Alessia Paldino, Carola Pio Loco Detto Gava, et al.Atherosclerosis|February 28, 2017
Genetic variation within the Y chromosome is not associated with histological characteristics of the atherosclerotic carotid artery or aneurysmal wallSaskia Haitjema, Jessica van Setten, James Eales, et al.Journal of the American College of Cardiology|November 17, 2022
Prognostic Prediction of Genotype vs Phenotype in Genetic CardiomyopathiesAlessia Paldino, Matteo Dal Ferro, Davide Stolfo, et al.Journal of the American Society of Nephrology : JASN|March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisMatthias Olden, Tanguy Corre, Caroline Hayward, et al.Nature Genetics|April 18, 2018
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritabilityPirro G Hysi, Ana M Valdes, Fan Liu, et al.Nature Genetics|June 1, 2019
Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritabilityPirro G Hysi, Ana M Valdes, Fan Liu, et al.Circulation. Genomic and Precision Medicine|July 8, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter RegistryMaria Perotto, Cinzia Radesich, Alessia Paldino, et al.European Journal of Human Genetics : EJHG|January 26, 2019
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traitsJessica van Setten, Niek Verweij, Hamdi Mbarek, et al.Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.Pageof 6