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Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.Nature Medicine|April 3, 2012
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicingWei Guo, Sebastian Schafer, Marion L Greaser, et al.Genome Medicine|January 8, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defectsGregor Dombrowsky, Liselot van der Laan, Ananília Silva, et al.American Journal of Human Genetics|April 8, 2014
Rare variants in NR2F2 cause congenital heart defects in humansSaeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.Plos Genetics|September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.Plos Genetics|July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart diseaseEnrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.Journal of the American College of Cardiology|May 19, 2022
Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic CardiomyopathyGabrielle Norrish, Aoife Cleary, Ella Field, et al.JACC. Heart Failure|September 29, 2022
Acute Myocarditis Associated With Desmosomal Gene VariantsEnrico Ammirati, Francesca Raimondi, Nicolas Piriou, et al.Circulation. Arrhythmia and Electrophysiology|May 2, 2022
Relationship Between Maximal Left Ventricular Wall Thickness and Sudden Cardiac Death in Childhood Onset Hypertrophic CardiomyopathyGabrielle Norrish, Tao Ding, Ella Field, et al.JACC. Advances|July 6, 2025
Sex Differences in Children and Adolescents With Hypertrophic CardiomyopathyGabrielle Norrish, Kimberley Hall, Ella Field, et al.Pageof 5