Associated Papers
Yield on Reinterpretation of Genetic Variants in Pediatric Cardiomyopathy.
Suzuki T et al.
Journal of the American Heart Association, 2025
40932142 (PubMed )
Supplement: JAH3-14-e041298-s001.zip › jah311383-sup-0001-TableS1.xlsx › Table_S1_CMP_variant_list
Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders.
Junttila MJ et al.
Circulation, 2018
Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes.
Pua CJ et al.
Journal of Cardiovascular Translational Research, 2016
26888179 (PubMed )
Supplement: 12265_2016_9673_MOESM1_ESM.xlsx › ST1_List_of_genes
Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity.
Garcia J et al.
Frontiers in Cardiovascular Medicine, 2016
27446933 (PubMed )
Supplement: data_sheet_1.docx
Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death.
Li MH et al.
Human Genomics, 2015
High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study.
Shendre A et al.
Genes and Immunity, 2014
Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.
Erdmann J et al.
Human Mutation, 2000
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