| 37431535 | Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy. | | 2023 |
| 37652022 | The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings. | Am J Hum Genet | 2023 |
| 37629170 | Cardiomyocyte-Restricted Expression of IL11 Causes Cardiac Fibrosis, Inflammation, and Dysfunction. | | 2023 |
| 34380661 | Moderate excess alcohol consumption and adverse cardiac remodelling in dilated cardiomyopathy. | Heart | 2022 |
| 35654493 | Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional Data. | J Am Coll Cardiol | 2022 |
| 36154167 | Genetic Architecture of Acute Myocarditis and the Overlap With Inherited Cardiomyopathy. | Circulation | 2022 |
| 35926050 | Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies. | Science | 2022 |
| 34503678 | Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy. | Journal of the American College of Cardiology | 2021 |
| 33500567 | Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies. | Genet Med | 2021 |
| 34022131 | Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. | Am J Hum Genet | 2021 |
| 33495596 | Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. | Nat Genet | 2021 |
| 33046849 | Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions. | Genet Med | 2021 |
| 34461741 | Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant Cardiomyopathy. | Circ Genom Precis Med | 2021 |
| 34460321 | New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy. | Circulation | 2021 |
| 33110626 | The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort. | npj Genomic Medicine | 2020 |
| 32306808 | Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? | Journal of the American Heart Association | 2020 |
| 32815737 | Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese Patients. | Circ Genom Precis Med | 2020 |
| 30987448 | Genetic Variants Associated With Cancer Therapy-Induced Cardiomyopathy. | Circulation | 2019 |
| 29892087 | A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy. | Genet Med | 2019 |
| 30609406 | Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture. | Am J Hum Genet | 2019 |
| 31284728 | Widespread Translational Control of Fibrosis in the Human Heart by RNA-Binding Proteins. | Circulation | 2019 |
| 30696458 | Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy. | Genome Med | 2019 |
| 31501434 | Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling. | Nat Commun | 2019 |
| 31399586 | WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling. | Nat Commun | 2019 |
| 31251381 | Association of Titin-Truncating Genetic Variants With Life-threatening Cardiac Arrhythmias in Patients With Dilated Cardiomyopathy and Implanted Defibrillators. | JAMA network open | 2019 |
| 31155234 | The Translational Landscape of the Human Heart. | Cell | 2019 |
| 29773157 | Genetic Etiology for Alcohol-Induced Cardiac Toxicity. | Journal of the American College of Cardiology | 2018 |
| 30442290 | Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations. | Journal of the American College of Cardiology | 2018 |
| 29369293 | CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation. | Genetics in Medicine | 2018 |
| 28082330 | Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes. | Eur Heart J | 2017 |
| 28903782 | Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy. | Genome Biol | 2017 |
| 28494986 | Truncating Variants in Titin Independently Predict Early Arrhythmias in Patients With Dilated Cardiomyopathy. | Journal of the American College of Cardiology | 2017 |
| 28518168 | Using high-resolution variant frequencies to empower clinical genome interpretation. | Genet Med | 2017 |
| 29073955 | Phenotype and Clinical Outcomes of Titin Cardiomyopathy. | J Am Coll Cardiol | 2017 |
| 28050600 | Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>. | Cold Spring Harb Mol Case Stud | 2017 |
| 27869827 | Titin-truncating variants affect heart function in disease cohorts and the general population. | Nat Genet | 2017 |
| 27746127 | The Calcineurin Variant CnAβ1 Controls Mouse Embryonic Stem Cell Differentiation by Directing mTORC2 Membrane Localization and Activation. | Cell Chem Biol | 2016 |
| 27437901 | Recovery of Cardiac Function in Cardiomyopathy Caused by Titin Truncation. | JAMA Cardiology | 2016 |
| 26888179 | Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes. | Journal of Cardiovascular Translational Research | 2016 |
| 26535225 | Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia? | Glob Cardiol Sci Pract | 2015 |
| 25589632 | Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease. | Sci Transl Med | 2015 |
| 25889438 | Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients. | Int J Cardiol | 2015 |
| 26175529 | ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart Failure. | Circ Cardiovasc Genet | 2015 |
| 26078397 | Influence of glutathione-S-transferase (GST) inhibition on lung epithelial cell injury: role of oxidative stress and metabolism. | American Journal of Physiology - Lung Cellular and Molecular Physiology | 2015 |
| 26453460 | Review and Updates in Regenerative and Personalized Medicine, Preclinical Animal Models, and Clinical Care in Cardiovascular Medicine. | J Cardiovasc Transl Res | 2015 |
| 24960161 | RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing. | J Clin Invest | 2014 |
| 25516437 | Regulated inositol-requiring protein 1-dependent decay as a mechanism of corin RNA and protein deficiency in advanced human systolic heart failure. | Journal of the American Heart Association | 2014 |
| 24431031 | AMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatment. | Cardiovascular Drugs and Therapy | 2014 |
| 25033200 | Identification of a new target of miR-16, Vacuolar Protein Sorting 4a. | PLoS One | 2014 |
| 24940686 | Effect of AMP-deaminase 3 knock-out in mice on enzyme activity in heart and other organs. | Nucleosides, Nucleotides and Nucleic Acids | 2014 |