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One or more keywords matched the following items that are connected to MacRae, Calum
Item TypeName
Academic Article A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26.
Academic Article Familial atrial fibrillation.
Academic Article Genetic screening and risk assessment in hypertrophic cardiomyopathy.
Academic Article Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.
Academic Article Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy.
Academic Article Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.
Academic Article Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease.
Academic Article The genetics of hypertrophic cardiomyopathy
Academic Article The genetics of cardiomyopathies: what clinicians should know.
Academic Article Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.
Academic Article Clinical screening and genetic testing.
Academic Article Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.
Academic Article Genetics and dilated cardiomyopathy: limitations of candidate gene strategies.
Academic Article Mutations in desmosomal protein genes and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
Academic Article Independent origin of myosin mutations in hypertrophic cardiomyopathy
Academic Article Arrhythmogenic right ventricular cardiomyopathy: moving toward mechanism.
Academic Article Myocardial blood flow and oxygen consumption in patients with Friedreich's ataxia prior to the onset of cardiomyopathy.
Academic Article Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy.
Academic Article The genetics of hypertrophic cardiomyopathy
Academic Article A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.
Academic Article Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
Academic Article Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.
Academic Article Subclinical myocardial damage revealed by CK-MB2 isoform release in hypertrophic cardiomyopathy
Academic Article RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing.
Academic Article Action and the actionability in exome variation.
Academic Article Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
Academic Article Mode of action of cardiac troponin T mutations in familial hypertrophic cardiomyopathy
Academic Article Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish.
Academic Article Splicing and dilated cardiomyopathy one gene to rule them all?
Academic Article The genetics of congestive heart failure.
Academic Article Multiple genetic loci contribute to familial dilated cardiomyopathy
Academic Article Clinical implications of cardiac troponin T mutations that cause familial hypertrophic cardiomyopathy
Academic Article Inherited cardiomyopathies
Academic Article In vivo natriuretic peptide reporter assay identifies chemical modifiers of hypertrophic cardiomyopathy signalling.
Academic Article A dinucleotide repeat polymorphism in the MYBPH gene.
Academic Article Familial dilated cardiomyopathy with conduction disease exhibits both genetic and phenotypic heterogeneity
Academic Article Management strategy in 249 consecutive patients with obstructive hypertrophic cardiomyopathy referred to a dedicated program.
Academic Article An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.
Academic Article Arrhythmogenic right ventricular cardiomyopathy.
Academic Article A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.
Academic Article Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Academic Article Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
Academic Article A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.
Academic Article Familial dilated cardiomyopathy locus maps to chromosome 2q31.
Academic Article Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.
Concept Cardiomyopathies
Concept Cardiomyopathy, Dilated
Concept Cardiomyopathy, Hypertrophic
Academic Article Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Academic Article Clinical screening and genetic testing.
Academic Article Human amyloidogenic light chain proteins result in cardiac dysfunction, cell death, and early mortality in zebrafish.
Academic Article Next-generation genome-wide association studies: time to focus on phenotype?
Academic Article Revisiting risk stratification in hypertrophic cardiomyopathy: do we need to start from scratch?
Academic Article Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy.
Academic Article Mendelian forms of structural cardiovascular disease.
Academic Article Stanniocalcin1 is a key mediator of amyloidogenic light chain induced cardiotoxicity.
Academic Article Reponse to De Leeuw and Houge.
Academic Article The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Academic Article Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.
Academic Article A clinical approach to inherited premature coronary artery disease.
Academic Article Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell-cell adhesion.
Academic Article Summarizing polygenic risks for complex diseases in a clinical whole-genome report.
Academic Article A Critical Need for Clinical Context in the Genomic Era.
Academic Article Arrhythmogenic Cardiomyopathy - New Insights into Disease Mechanisms and Drug Discovery.
Academic Article Central role for GSK3ß in the pathogenesis of arrhythmogenic cardiomyopathy.
Academic Article Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
Academic Article The Design of the Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Trial.
Academic Article A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.
Academic Article Closing the Genotype-Phenotype Loop for Precision Medicine.
Academic Article Rare Diseases Inform Myocardial Phenotypes for Precision Medicine.
Academic Article Screening drugs for myocardial disease in vivo with zebrafish: an expert update.
Academic Article Zebrafish model of amyloid light chain cardiotoxicity: regeneration versus degeneration.
Mentoring - Completed Student Project Integration of in Vitro and in Vivo Models of Arrhythmogenic Cardiomyopathy to Define Pathogenic Mechanisms and Identify Small Molecule Therapies
Academic Article Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents.
Academic Article The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.
Academic Article Baseline Characteristics of the VANISH Cohort.
Academic Article Cyp1 Inhibition Prevents Doxorubicin-Induced Cardiomyopathy in a Zebrafish Heart-Failure Model.
Academic Article Non-invasive Thoracic Impedance Changes in COVID-19 Pulmonary Infection.
Academic Article Valsartan in early-stage hypertrophic cardiomyopathy: a randomized phase 2 trial.
Search Criteria
  • Cardiomyopathies
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.