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One or more keywords matched the following items that are connected to Seidman, Christine
Item TypeName
Academic Article Electrophysiological abnormalities and arrhythmias in alpha MHC mutant familial hypertrophic cardiomyopathy mice.
Academic Article Altered regulatory function of two familial hypertrophic cardiomyopathy troponin T mutants.
Academic Article The management of hypertrophic cardiomyopathy.
Academic Article Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
Academic Article Accelerated cardiomyopathy in mice with overexpression of cardiac G(s)alpha and a missense mutation in the alpha-myosin heavy chain.
Academic Article Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
Academic Article Altered cardiac excitation-contraction coupling in mutant mice with familial hypertrophic cardiomyopathy.
Academic Article Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice
Academic Article Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy.
Academic Article Development of left ventricular hypertrophy in adults in hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations.
Academic Article The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
Academic Article Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.
Academic Article Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene.
Academic Article Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action.
Academic Article Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene.
Academic Article Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function.
Academic Article Molecular genetic studies of familial hypertrophic cardiomyopathy.
Academic Article Contemporary evaluation and management of hypertrophic cardiomyopathy.
Academic Article Altered crossbridge kinetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy.
Academic Article Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
Academic Article Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation.
Academic Article 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Academic Article Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
Academic Article Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.
Academic Article Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban.
Academic Article An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy.
Academic Article Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression.
Academic Article Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
Academic Article Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.
Academic Article Phenotypic diversity in hypertrophic cardiomyopathy.
Academic Article American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines.
Academic Article 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Academic Article Sudden death due to troponin T mutations.
Academic Article Familial hypertrophic cardiomyopathy mice display gender differences in electrophysiological abnormalities.
Academic Article Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene.
Academic Article Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy.
Academic Article Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
Academic Article Myofilament mechanical performance is enhanced by R403Q myosin in mouse myocardium independent of sex.
Academic Article Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.
Academic Article Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.
Academic Article Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.
Academic Article Glycogen storage diseases presenting as hypertrophic cardiomyopathy.
Academic Article Aberrant activation of AMP-activated protein kinase remodels metabolic network in favor of cardiac glycogen storage.
Academic Article Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy.
Academic Article Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.
Academic Article Comparison of two murine models of familial hypertrophic cardiomyopathy.
Academic Article A novel custom resequencing array for dilated cardiomyopathy.
Academic Article Research priorities in hypertrophic cardiomyopathy: report of a Working Group of the National Heart, Lung, and Blood Institute.
Academic Article Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.
Academic Article The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms.
Academic Article Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy.
Academic Article Assessment of diastolic function with Doppler tissue imaging to predict genotype in preclinical hypertrophic cardiomyopathy.
Academic Article Consequences of pressure overload on sarcomere protein mutation-induced hypertrophic cardiomyopathy.
Academic Article The genetic basis for cardiac remodeling.
Academic Article Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics.
Academic Article Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.
Academic Article Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases:hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association.
Academic Article Isolation of a de novo mutant myocardial beta MHC protein in a pedigree with hypertrophic cardiomyopathy.
Academic Article American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines.
Academic Article Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.
Academic Article A contemporary approach to hypertrophic cardiomyopathy.
Academic Article How should hypertrophic cardiomyopathy be classified?: What's in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy.
Academic Article Comparative proteomics profiling of a phospholamban mutant mouse model of dilated cardiomyopathy reveals progressive intracellular stress responses.
Academic Article The PTPN11 gene is not implicated in nonsyndromic hypertrophic cardiomyopathy.
Academic Article Truncations of titin causing dilated cardiomyopathy.
Academic Article A mouse model of familial hypertrophic cardiomyopathy.
Academic Article Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy.
Academic Article Heritable cardiac conduction and myocardial disease: from the clinic to the basic science laboratory and back to the clinic.
Academic Article 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Academic Article 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Academic Article Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.
Academic Article Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.
Academic Article Genetics of hypertrophic cardiomyopathy.
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 Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy.
Academic Article The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model.
Academic Article Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium.
Academic Article Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.
Academic Article Genetic testing for dilated cardiomyopathy in clinical practice.
Academic Article Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function
Academic Article Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: hypertrophic cardiomyopathy, long-QT syndrome, and marfan syndrome : A statement for healthcare professionals from the councils on clinical cardiology, cardiovascular disease in the young, and basic science, american heart association
Academic Article Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
Academic Article Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.
Academic Article A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy.
Academic Article A de novo mutation in alpha-tropomyosin that causes hypertrophic cardiomyopathy.
Academic Article Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
Academic Article A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.
Academic Article Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.
Academic Article Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy.
Academic Article Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-ß.
Academic Article [Using molecular genetics to guide the diagnosis and treatment of hypertrophic cardiomyopathy].
Academic Article Narrative review: harnessing molecular genetics for the diagnosis and management of hypertrophic cardiomyopathy.
Academic Article Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.
Academic Article Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention.
Academic Article Novel locus for an inherited cardiomyopathy maps to chromosome 7.
Academic Article Sarcomere protein gene mutations and inherited heart disease: a beta-cardiac myosin heavy chain mutation causing endocardial fibroelastosis and heart failure.
Academic Article A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.
Academic Article Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy.
Academic Article Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history.
Academic Article 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Developed in collaboration with the American Association for Thoracic Surgery, American Society of Echocardiography, American Society of Nuclear Cardiology, Heart Failure Society of America, Heart Rhythm Society, Society for Cardiovascular Angiography and Interventions, and Society of Tho...
Academic Article Molecular epidemiology of hypertrophic cardiomyopathy.
Academic Article Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
Academic Article Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy.
Academic Article Molecular medicine in the 21st century.
Academic Article Gene mutations in apical hypertrophic cardiomyopathy.
Academic Article Shared genetic causes of cardiac hypertrophy in children and adults.
Academic Article Functional effects of the TMEM43 Ser358Leu mutation in the pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
Academic Article A dinucleotide repeat polymorphism in the MYBPH gene.
Academic Article Pheochromocytoma-induced cardiomyopathy is modulated by the synergistic effects of cell-secreted factors.
Academic Article An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.
Academic Article Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
Academic Article 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Academic Article Hypertrophic cardiomyopathy: translating cellular cross talk into therapeutics.
Academic Article Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.
Academic Article Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy.
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 Heterogeneous myocyte enhancer factor-2 (Mef2) activation in myocytes predicts focal scarring in hypertrophic cardiomyopathy.
Academic Article QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice.
Academic Article Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
Academic Article A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.
Academic Article Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations.
Academic Article Sarcomere gene mutations in hypertrophy and heart failure.
Academic Article Myocardial fibrosis as an early manifestation of hypertrophic cardiomyopathy.
Academic Article Familial dilated cardiomyopathy locus maps to chromosome 2q31.
Academic Article Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.
Academic Article Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly.
Academic Article Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study.
Academic Article Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene.
Concept Cardiomyopathy, Restrictive
Concept Cardiomyopathies
Concept Cardiomyopathy, Hypertrophic, Familial
Concept Cardiomyopathy, Dilated
Concept Cardiomyopathy, Hypertrophic
Academic Article Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.
Academic Article Allele-specific silencing of mutant Myh6 transcripts in mice suppresses hypertrophic cardiomyopathy.
Academic Article Genetics and disease of ventricular muscle.
Academic Article Deep sequence analysis of gene expression identifies osteopontin as a downstream effector of integrin-linked kinase (ILK) in cardiac-specific ILK knockout mice.
Academic Article 5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy.
Academic Article Effects of losartan on left ventricular hypertrophy and fibrosis in patients with nonobstructive hypertrophic cardiomyopathy.
Academic Article The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Academic Article 126 Advanced Assessment of Cardiac Morphology and Prediction of Gene Carriage by CMR in Hypertrophic Cardiomyopathy - The HCMNET/UCL Collaboration.
Academic Article ß-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutations.
Academic Article Echocardiography and cardiac MRI in mutation-negative hypertrophic cardiomyopathy in an older patient: a case defining the need for ICD.
Academic Article Nationwide study on hypertrophic cardiomyopathy in Iceland: evidence of a MYBPC3 founder mutation.
Academic Article Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy.
Academic Article Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic.
Academic Article Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expression.
Academic Article Haploinsufficiency of MYBPC3 exacerbates the development of hypertrophic cardiomyopathy in heterozygous mice.
Academic Article Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
Academic Article Phenotype and prognostic correlations of the converter region mutations affecting the ß myosin heavy chain.
Academic Article HEART DISEASE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy.
Academic Article Cardiomyocyte-enriched protein CIP protects against pathophysiological stresses and regulates cardiac homeostasis.
Academic Article Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Academic Article Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Academic Article A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice.
Academic Article Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.
Academic Article CORRIGENDUM: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Academic Article Corrigendum: Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.
Academic Article A Tension-Based Model Distinguishes Hypertrophic versus Dilated Cardiomyopathy.
Grant GENETIC ANALYSIS OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
Grant SPECIALIZED CENTER OF RESEARCH IN HEART FAILURE
Grant Defining Genetic Architecture and Pathways of DCM
Grant Using Genetics for Early Phenotyping &Prevention of Hypertrophic Cardiomyopathy
Grant Using Genetics For Early Phenotyping & Prevention of Hypertrophic Cardiomyopathy
Academic Article Molecular profiling of dilated cardiomyopathy that progresses to heart failure.
Academic Article Titin-truncating variants affect heart function in disease cohorts and the general population.
Academic Article Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy.
Academic Article Integrative Analysis of PRKAG2 Cardiomyopathy iPS and Microtissue Models Identifies AMPK as a Regulator of Metabolism, Survival, and Fibrosis.
Academic Article Early remodeling of repolarizing K+ currents in the aMHC403/+ mouse model of familial hypertrophic cardiomyopathy.
Academic Article The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet Study.
Academic Article Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
Academic Article Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypes.
Academic Article Integrative Analysis of PRKAG2 Cardiomyopathy iPS and Microtissue Models Identifies AMPK as a Regulator of Metabolism, Survival, and Fibrosis.
Academic Article Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.
Academic Article Fabry Disease in Families With Hypertrophic Cardiomyopathy: Clinical Manifestations in the Classic and Later-Onset Phenotypes.
Grant Genetic Determinants of Chagas Cardiomyopathy
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 Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter.
Academic Article Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.
Academic Article A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy.
Academic Article Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.
Academic Article Association of Variants in BAG3 With Cardiomyopathy Outcomes in African American Individuals.
Academic Article Telomere shortening is a hallmark of genetic cardiomyopathies.
Academic Article The Role of the L-Type Ca2+ Channel in Altered Metabolic Activity in a Murine Model of Hypertrophic Cardiomyopathy.
Academic Article Multilayer Myocardial Mechanics in Genotype-Positive Left Ventricular Hypertrophy-Negative Patients With Hypertrophic Cardiomyopathy.
Academic Article Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe).
Academic Article A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance.
Academic Article Genetic Testing and Counseling for Hypertrophic Cardiomyopathy.
Academic Article Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin.
Academic Article Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies.
Academic Article Genetic Variants Associated With Cancer Therapy-Induced Cardiomyopathy.
Academic Article Response by Ho et al to Letter Regarding Article, "Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights From the Sarcomeric Human Cardiomyopathy Registry (SHaRe)".
Academic Article Novel Therapies for Prevention and Early Treatment of Cardiomyopathies.
Academic Article The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.
Academic Article Yin Yang 1 Suppresses Dilated Cardiomyopathy and Cardiac Fibrosis Through Regulation of Bmp7 and Ctgf.
Academic Article Association of Race With Disease Expression and Clinical Outcomes Among Patients With Hypertrophic Cardiomyopathy.
Academic Article Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review.
Academic Article Scientists on the Spot: Putting a halt to hypertrophic cardiomyopathy.
Academic Article Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy.
Academic Article Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
Academic Article Hypertrophic cardiomyopathy in myosin-binding protein C (MYBPC3) Icelandic founder mutation carriers.
Academic Article Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2-Mediated COVID-19.
Academic Article Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants.
Academic Article BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy.
Academic Article Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in TNNI3 and TNNT2 That Are Common in Chinese Patients.
Academic Article Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy.
Academic Article Associations Between Female Sex, Sarcomere Variants, and Clinical Outcomes in Hypertrophic Cardiomyopathy.
Academic Article Discordant clinical features of identical hypertrophic cardiomyopathy twins.
Academic Article Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Academic Article Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Academic Article Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
Academic Article LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart.
Academic Article Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy.
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.