Euan Ashley
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Professor of Medicine and Genetics at Stanford University
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Euan Ashley's Degrees
- Masters Medicine University of Oxford
- PhD Genetics University of Oxford
Why Is Euan Ashley Influential?
(Suggest an Edit or Addition)According to Wikipedia, Euan Angus Ashley is a Scottish physician, scientist, author, and founder based at Stanford University in California where he is Associate Dean in the School of Medicine and holds the Roger and Joelle Burnell Chair of Genomics and Precision Health. He is known for helping establish the field of medical genomics.
Euan Ashley's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Guidelines for investigating causality of sequence variants in human disease (2014) (1160)
- Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes (2012) (1128)
- Clinical assessment incorporating a personal genome (2010) (692)
- Patient-Specific Induced Pluripotent Stem Cells as a Model for Familial Dilated Cardiomyopathy (2012) (612)
- Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells. (2013) (566)
- Electrocardiographic interpretation in athletes: the ‘Seattle Criteria’ (2013) (496)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- The precision medicine initiative: a new national effort. (2015) (441)
- Does Size Matter?: Clinical Applications of Scaling Cardiac Size and Function for Body Size (2008) (436)
- Artificial Intelligence in Cardiology. (2018) (428)
- Accuracy in Wrist-Worn, Sensor-Based Measurements of Heart Rate and Energy Expenditure in a Diverse Cohort (2016) (414)
- Towards precision medicine (2016) (398)
- Deep Learning Automates the Quantitative Analysis of Individual Cells in Live-Cell Imaging Experiments (2016) (384)
- A long non-coding RNA protects the heart from pathological hypertrophy (2014) (376)
- Clinical interpretation and implications of whole-genome sequencing. (2014) (365)
- Novel Role for the Potent Endogenous Inotrope Apelin in Human Cardiac Dysfunction (2003) (352)
- The endogenous peptide apelin potently improves cardiac contractility and reduces cardiac loading in vivo. (2005) (349)
- Performance comparison of whole-genome sequencing platforms (2011) (310)
- Apelin signaling antagonizes Ang II effects in mouse models of atherosclerosis. (2008) (308)
- Cardiac Neuronal Nitric Oxide Synthase Isoform Regulates Myocardial Contraction and Calcium Handling (2003) (276)
- Video-based AI for beat-to-beat assessment of cardiac function (2020) (262)
- Cost-Effectiveness of Preparticipation Screening for Prevention of Sudden Cardiac Death in Young Athletes (2010) (258)
- Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy (2018) (244)
- Chromatin regulation by Brg1 underlies heart muscle development and disease (2010) (237)
- Challenges in the clinical application of whole-genome sequencing (2010) (231)
- Prevention of sudden cardiac death with implantable cardioverter-defibrillators in children and adolescents with hypertrophic cardiomyopathy. (2013) (229)
- Interpretation of the Electrocardiogram of Young Athletes (2011) (214)
- Plasma concentrations of the novel peptide apelin are decreased in patients with chronic heart failure (2006) (210)
- Impact of cardiorespiratory fitness on the obesity paradox in patients with heart failure. (2013) (209)
- APJ ACTS AS A DUAL RECEPTOR IN CARDIAC HYPERTROPHY (2012) (207)
- Exercise testing in clinical medicine (2000) (204)
- Chromatin regulation by Brg1 underlies heart muscle development and disease (2011) (200)
- Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease (2018) (199)
- A public resource facilitating clinical use of genomes (2012) (197)
- Endogenous regulation of cardiovascular function by apelin-APJ. (2009) (190)
- Feasibility of Obtaining Measures of Lifestyle From a Smartphone App: The MyHeart Counts Cardiovascular Health Study (2017) (182)
- Long-read genome sequencing identifies causal structural variation in a Mendelian disease (2017) (178)
- RNA-Seq identifies novel myocardial gene expression signatures of heart failure. (2015) (175)
- Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts (2019) (174)
- Molecular Transducers of Physical Activity Consortium (MoTrPAC): Mapping the Dynamic Responses to Exercise (2020) (169)
- Normal electrocardiographic findings: recognising physiological adaptations in athletes (2013) (168)
- Cardiac Nitric Oxide Synthase 1 Regulates Basal and &bgr;-Adrenergic Contractility in Murine Ventricular Myocytes (2002) (167)
- Pathway analysis of coronary atherosclerosis. (2005) (163)
- Functional assessment and transplantation of the donor heart after circulatory death. (2016) (158)
- Molecular Choreography of Acute Exercise (2020) (158)
- Early Repolarization in an Ambulatory Clinical Population (2011) (154)
- Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence (2011) (149)
- Effect of Moderate-Intensity Exercise Training on Peak Oxygen Consumption in Patients With Hypertrophic Cardiomyopathy: A Randomized Clinical Trial (2017) (142)
- Apelin prevents aortic aneurysm formation by inhibiting macrophage inflammation. (2009) (141)
- The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease. (2017) (131)
- Cardiovascular disease: The rise of the genetic risk score (2018) (130)
- Abnormal electrocardiographic findings in athletes: recognising changes suggestive of primary electrical disease (2013) (126)
- Abnormal electrocardiographic findings in athletes: recognising changes suggestive of cardiomyopathy (2013) (124)
- Deep learning interpretation of echocardiograms (2020) (121)
- Electrocardiographic predictors of atrial fibrillation. (2009) (118)
- A meta-analysis of the prognostic significance of cardiopulmonary exercise testing in patients with heart failure (2012) (117)
- Medical implications of technical accuracy in genome sequencing (2016) (115)
- Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy (2020) (115)
- A Reference Equation for Normal Standards for VO2 Max: Analysis from the Fitness Registry and the Importance of Exercise National Database (FRIEND Registry). (2017) (114)
- Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations (2014) (107)
- Direct-to-consumer genetic testing for predicting sports performance and talent identification: Consensus statement (2015) (105)
- Gene Coexpression Network Topology of Cardiac Development, Hypertrophy, and Failure (2011) (100)
- Multi-omic profiling reveals widespread dysregulation of innate immunity and hematopoiesis in COVID-19 (2020) (99)
- Genetics and Cardiovascular Disease: A Policy Statement From the American Heart Association (2012) (98)
- The Undiagnosed Diseases Network of the National Institutes of Health: A National Extension. (2015) (93)
- Personalized medicine: hope or hype? (2012) (92)
- Addition of the Electrocardiogram to the Preparticipation Examination of College Athletes (2010) (91)
- De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects (2016) (90)
- Nitric oxide control of cardiac function: is neuronal nitric oxide synthase a key component? (2004) (89)
- Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performance. (2016) (89)
- Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation (2016) (88)
- Prognostic Value of Heart Rate Increase at Onset of Exercise Testing (2007) (87)
- An evidence-based review of the resting electrocardiogram as a screening technique for heart disease. (2001) (84)
- Mobile Health Advances in Physical Activity, Fitness, and Atrial Fibrillation: Moving Hearts. (2018) (84)
- Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study (2017) (84)
- Cardiopulmonary responses and prognosis in hypertrophic cardiomyopathy: a potential role for comprehensive noninvasive hemodynamic assessment. (2015) (82)
- Signature patterns of gene expression in mouse atherosclerosis and their correlation to human coronary disease. (2005) (82)
- Magnetic resonance imaging of progressive cardiomyopathic changes in the db/db mouse. (2007) (80)
- Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy (2018) (80)
- Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy (2018) (77)
- Deep Learning Interpretation of Echocardiograms (2019) (76)
- Is stress cardiomyopathy the underlying cause of ventricular dysfunction associated with brain death? (2010) (74)
- Cardiac Structural and Sarcomere Genes Associated With Cardiomyopathy Exhibit Marked Intolerance of Genetic Variation (2012) (72)
- BMP promotes motility and represses growth of smooth muscle cells by activation of tandem Wnt pathways (2011) (71)
- A Premature Termination Codon Mutation in MYBPC3 Causes Hypertrophic Cardiomyopathy via Chronic Activation of Nonsense-Mediated Decay (2019) (70)
- Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences (2019) (70)
- Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction (2020) (69)
- Physical activity and other health behaviors in adults with hypertrophic cardiomyopathy. (2013) (67)
- DNA Sequencing: Clinical Applications of New DNA Sequencing Technologies (2012) (66)
- Network Analysis of Human In-Stent Restenosis (2006) (66)
- Validation of a Cardiopulmonary Exercise Test Score in Heart Failure (2012) (65)
- The prognostic value of early repolarization with ST-segment elevation in African Americans. (2012) (65)
- Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension. (2014) (64)
- Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank (2017) (63)
- Drug Discovery in a Multidimensional World: Systems, Patterns, and Networks (2010) (61)
- Association of Obesity With Adverse Long-term Outcomes in Hypertrophic Cardiomyopathy. (2019) (59)
- Predominance of normal left ventricular geometry in the male ‘athlete's heart’ (2014) (58)
- Effect of lossy compression of quality scores on variant calling (2015) (58)
- Ventricular arrhythmias during clinical treadmill testing and prognosis. (2008) (58)
- Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease. (2007) (58)
- Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting. (2022) (56)
- Prevalence and clinical correlates of right ventricular dysfunction in patients with hypertrophic cardiomyopathy. (2013) (56)
- Informed Consent. (2017) (55)
- Personalized preventive medicine: genetics and the response to regular exercise in preventive interventions. (2015) (54)
- Effects of respiratory exchange ratio on the prognostic value of peak oxygen consumption and ventilatory efficiency in patients with systolic heart failure. (2013) (53)
- Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis (2017) (53)
- Achieving high-sensitivity for clinical applications using augmented exome sequencing (2015) (52)
- Emerging therapies for the management of decompensated heart failure: from bench to bedside. (2006) (52)
- Hypertrophic Cardiomyopathy as a Cause of Sudden Cardiac Death in the Young: A Meta-Analysis. (2016) (52)
- Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder (2018) (51)
- Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing. (2014) (50)
- Angiotensin-converting enzyme genotype predicts cardiac and autonomic responses to prolonged exercise. (2006) (49)
- Cardiovascular Precision Medicine in the Genomics Era (2018) (49)
- Electrocardiographic arrhythmia risk testing. (2004) (49)
- A reference equation for maximal aerobic power for treadmill and cycle ergometer exercise testing: Analysis from the FRIEND registry (2018) (48)
- Accuracy of Smartphone Camera Applications for Detecting Atrial Fibrillation (2020) (48)
- Opposing cardiovascular roles for the angiotensin and apelin signaling pathways. (2006) (48)
- European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases (2022) (48)
- Apelin Enhances Directed Cardiac Differentiation of Mouse and Human Embryonic Stem Cells (2012) (47)
- Interdisciplinary psychosocial care for families with inherited cardiovascular diseases. (2016) (47)
- Prevalence and Progression of Late Gadolinium Enhancement in Children and Adolescents With Hypertrophic Cardiomyopathy (2018) (46)
- Ventilatory Power: A Novel Index That Enhances Prognostic Assessment of Patients With Heart Failure (2012) (46)
- New insights for the diagnosis and management of right ventricular failure, from molecular imaging to targeted right ventricular therapy (2010) (45)
- Mouse Strain–Specific Differences in Vascular Wall Gene Expression and Their Relationship to Vascular Disease (2004) (45)
- A research roadmap for next-generation sequencing informatics (2016) (45)
- Early somatic mosaicism is a rare cause of long-QT syndrome (2016) (44)
- A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network (2017) (44)
- Systems-Based Approaches to Cardiovascular Biomarker Discovery (2012) (43)
- Telomere shortening is a hallmark of genetic cardiomyopathies (2018) (43)
- Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study (2017) (42)
- Association of Race With Disease Expression and Clinical Outcomes Among Patients With Hypertrophic Cardiomyopathy. (2019) (42)
- A neural network approach to predicting outcomes in heart failure using cardiopulmonary exercise testing. (2014) (42)
- Limitations of Current AHA Guidelines and Proposal of New Guidelines for the Preparticipation Examination of Athletes (2015) (41)
- The concept of ventricular reserve in heart failure and pulmonary hypertension: an old metric that brings us one step closer in our quest for prediction (2011) (40)
- In Situ Optical Mapping of Voltage and Calcium in the Heart (2012) (40)
- Integrated Polygenic Tool Substantially Enhances Coronary Artery Disease Prediction (2021) (39)
- Oxido-reductive regulation of vascular remodeling by receptor tyrosine kinase ROS1. (2014) (39)
- Future Translational Applications From the Contemporary Genomics Era: A Scientific Statement From the American Heart Association (2015) (39)
- A New Era in Clinical Genetic Testing for Hypertrophic Cardiomyopathy (2009) (38)
- Upregulation of the apelin-APJ pathway promotes neointima formation in the carotid ligation model in mouse. (2010) (38)
- Targeting ferroptosis: A novel therapeutic strategy for the treatment of mitochondrial disease-related epilepsy (2019) (37)
- Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation (2017) (36)
- Patterns and prognosis of all components of the J-wave pattern in multiethnic athletes and ambulatory patients. (2014) (36)
- Long-term outcomes of septal reduction for obstructive hypertrophic cardiomyopathy. (2015) (35)
- Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study (2017) (34)
- Randomized Trial of Personal Genomics for Preventive Cardiology: Design and Challenges (2012) (34)
- A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases. (2015) (34)
- Transcriptional profiling of in vitro smooth muscle cell differentiation identifies specific patterns of gene and pathway activation. (2004) (34)
- Mechanisms of exercise intolerance in patients with hypertrophic cardiomyopathy. (2009) (34)
- Exercise capacity and paroxysmal atrial fibrillation in patients with hypertrophic cardiomyopathy (2013) (34)
- Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling (2020) (33)
- Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy. (2018) (33)
- Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy (2021) (33)
- The effect of digital physical activity interventions on daily step count: a randomised controlled crossover substudy of the MyHeart Counts Cardiovascular Health Study. (2019) (33)
- Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study (2019) (32)
- Stable, Covalent Attachment of Laminin to Microposts Improves the Contractility of Mouse Neonatal Cardiomyocytes (2014) (31)
- Using "big data" to dissect clinical heterogeneity. (2015) (31)
- Impact of Demographic Features, Lifestyle, and Comorbidities on the Clinical Expression of Hypertrophic Cardiomyopathy (2017) (31)
- Gender differences in ventricular remodeling and function in college athletes, insights from lean body mass scaling and deformation imaging. (2015) (31)
- Systems Genomics Identifies a Key Role for Hypocretin/Orexin Receptor-2 in Human Heart Failure. (2015) (31)
- Progressive Dyspnea After CABG: Complication of Retained Epicardial Pacing Wires. (2008) (30)
- Patient-Specific Induced Pluripotent Stem Cells Implicate Intrinsic Impaired Contractility in Hypoplastic Left Heart Syndrome. (2020) (30)
- High-Throughput Precision Phenotyping of Left Ventricular Hypertrophy With Cardiovascular Deep Learning (2021) (30)
- SARS-CoV-2 RNAemia Predicts Clinical Deterioration and Extrapulmonary Complications from COVID-19 (2021) (29)
- Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision (2021) (29)
- Insights into Human β-Cardiac Myosin Function from Single Molecule and Single Cell Studies (2009) (28)
- Measurement Precision in the Optimization of Cardiac Resynchronization Therapy (2010) (28)
- EchoNet-Dynamic: a Large New Cardiac Motion Video Data Resource for Medical Machine Learning (2019) (27)
- Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing (2019) (27)
- The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic (2020) (27)
- A guide for the diagnosis of rare and undiagnosed disease: beyond the exome (2022) (26)
- Multi-task deep learning for cardiac rhythm detection in wearable devices (2020) (26)
- Exercise testing scores as an example of better decisions through science. (2002) (26)
- Adding an electrocardiogram to the pre-participation examination in competitive athletes: a systematic review. (2009) (26)
- Sports genetics moving forward: lessons learned from medical research. (2016) (26)
- A Clinical Approach to Inherited Hypertrophy: The Use of Family History in Diagnosis, Risk Assessment, and Management (2013) (26)
- Comparison of left ventricular manual versus automated derived longitudinal strain: implications for clinical practice and research (2016) (26)
- Time trajectories in the transcriptomic response to exercise - a meta-analysis (2021) (26)
- Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy. (2021) (25)
- Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data (2015) (24)
- Apelin and APJ orchestrate complex tissue-specific control of cardiomyocyte hypertrophy and contractility in the hypertrophy-heart failure transition. (2018) (24)
- Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy (2020) (24)
- The right ventricle following ultra-endurance exercise: insights from novel echocardiography and 12-lead electrocardiography (2014) (24)
- Clinical utility of genomic sequencing: a measurement toolkit (2020) (24)
- Next-Generation Sequencing in Cardiovascular Disease: Present Clinical Applications and the Horizon of Precision Medicine. (2017) (23)
- Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries. (2021) (23)
- Temporal Trend of Age at Diagnosis in Hypertrophic Cardiomyopathy (2020) (23)
- Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability (2015) (23)
- Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association (2022) (23)
- Redox regulation of vascular remodeling (2015) (22)
- Alterations in Cardiac Mechanics Following Ultra-Endurance Exercise: Insights from Left and Right Ventricular Area-Deformation Loops. (2016) (22)
- Athletic Remodeling in Female College Athletes, the "Morganroth Hypothesis" Revisited. (2018) (22)
- Effect of Gender on Computerized Electrocardiogram Measurements in College Athletes (2010) (22)
- Prevalence and prognostic role of right ventricular involvement in stress-induced cardiomyopathy. (2015) (22)
- Cardiopulmonary and noninvasive hemodynamic responses to exercise predict outcomes in heart failure. (2013) (22)
- Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences (2018) (21)
- Broad Genetic Testing in a Clinical Setting Uncovers a High Prevalence of Titin Loss-of-Function Variants in Very Early-Onset Atrial Fibrillation. (2019) (21)
- Impact of Septal Reduction on Left Atrial Size and Diastole in Hypertrophic Cardiomyopathy (2016) (21)
- Design and Challenges (2012) (21)
- Associations Between Female Sex, Sarcomere Variants and Clinical Outcomes in Hypertrophic Cardiomyopathy. (2020) (20)
- Better Decisions Through Science: Exercise Testing Scores (2002) (20)
- Load-dependent effects of apelin on murine cardiomyocytes (2017) (20)
- Comparison of QT Interval Measurement Methods and Correction Formulas in Atrial Fibrillation. (2019) (20)
- Systematic Comparison of Digital Electrocardiograms From Healthy Athletes and Patients With Hypertrophic Cardiomyopathy. (2015) (19)
- Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure (2019) (19)
- Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing (2022) (19)
- Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk (2022) (19)
- Cell-intrinsic functional effects of the α-cardiac myosin Arg-403-Gln mutation in familial hypertrophic cardiomyopathy. (2012) (19)
- Characteristics of undiagnosed diseases network applicants: implications for referring providers (2018) (19)
- European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases. (2022) (19)
- Systems biology of heart failure, challenges and hopes (2011) (18)
- Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts (2017) (18)
- Age and double product (systolic blood pressure x heart rate) reserve-adjusted modification of the Duke Treadmill Score nomogram in men. (2008) (18)
- An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (2020) (18)
- Conquering the ECG (2004) (17)
- Mind the Gap: Current Challenges and Future State of Heart Failure Care. (2017) (17)
- Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions (2020) (17)
- Diagnosing coronary artery disease in diabetic patients (2002) (17)
- In Vivo Post–Cardiac Arrest Myocardial Dysfunction Is Supported by Ca2+/Calmodulin-Dependent Protein Kinase II–Mediated Calcium Long-Term Potentiation and Mitigated by Alda-1, an Agonist of Aldehyde Dehydrogenase Type 2 (2016) (17)
- Towards precision medicine in heart failure (2021) (17)
- Deep learning evaluation of biomarkers from echocardiogram videos (2021) (16)
- Rat model of veno-arterial extracorporeal membrane oxygenation (2014) (16)
- Time based versus strain based myocardial performance indices in hypertrophic cardiomyopathy, the merging role of left atrial strain (2018) (16)
- Classifying Drugs by their Arrhythmogenic Risk Using Machine Learning (2019) (16)
- Arti fi cial Intelligence in Cardiology (2018) (16)
- Blood pressure in athletic preparticipation evaluation and the implication for cardiac remodelling (2019) (15)
- Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Due to a Human Myosin Regulatory Light Chain Mutation. (2019) (15)
- Applying current normative data to prognosis in heart failure: The Fitness Registry and the Importance of Exercise National Database (FRIEND). (2018) (15)
- A novel noninvasive method for remote heart failure monitoring: the EuleriAn video Magnification apPLications In heart Failure studY (AMPLIFY) (2019) (15)
- Silencing of MYH7 ameliorates disease phenotypes in human iPSC-Cardiomyocytes. (2020) (15)
- Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review (2019) (15)
- Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation (2020) (15)
- Computerized Q wave dimensions in athletes and hypertrophic cardiomyopathy patients. (2015) (15)
- Additive prognostic value of a cardiopulmonary exercise test score in patients with heart failure and intermediate risk. (2015) (15)
- Latent obstruction and left atrial size are predictors of clinical deterioration leading to septal reduction in hypertrophic cardiomyopathy. (2014) (15)
- How does morphology impact on diastolic function in hypertrophic cardiomyopathy? A single centre experience (2014) (15)
- The genetics of human performance (2021) (15)
- Incremental value of right heart metrics and exercise performance to well-validated risk scores in dilated cardiomyopathy (2018) (15)
- Preoperative cardiac evaluation: mechanisms, assessment, and reduction of risk. (2005) (14)
- The ageing athlete: screening prior to vigorous exertion in asymptomatic adults without known cardiovascular disease (2009) (14)
- The impact of chronic endurance and resistance training upon the right ventricular phenotype in male athletes (2015) (14)
- Clinical evaluation incorporating a personal genome (2010) (14)
- Phenotypic Expression, Natural History and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants. (2021) (14)
- The prognostic significance of heart rate recovery is not dependent upon maximal effort in patients with heart failure. (2013) (14)
- Exploratory insights from the right-sided electrocardiogram following prolonged endurance exercise (2016) (13)
- Better decisions through science: exercise testing scores. (2003) (13)
- A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network. (2018) (13)
- The relationship between minute ventilation and oxygen consumption in heart failure: comparing peak VE/VO₂ and the oxygen uptake efficiency slope. (2012) (12)
- Clinical sites of the Undiagnosed Diseases Network: Unique contributions to genomic medicine and science (2020) (12)
- High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs (2020) (12)
- Value of Strain Imaging and Maximal Oxygen Consumption in Patients With Hypertrophic Cardiomyopathy. (2017) (12)
- Genomics in clinical practice (2014) (12)
- Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases (2021) (12)
- Genetic Analysis in Cardiovascular Disease: A Clinical Perspective (2011) (12)
- A comparison of methods for determining the ventilatory threshold: implications for surgical risk stratification (2017) (12)
- Race differences in ventricular remodeling and function among college football players. (2013) (12)
- Medical Imaging and Machine Learning (2021) (11)
- The Prognostic Utility of Cardiopulmonary Exercise Testing Stands the Test of Time in Patients With Heart Failure (2012) (11)
- Multi-task deep learning for cardiac rhythm detection in wearable devices. (2020) (11)
- Identification of rare-disease genes in diverse undiagnosed cases using whole blood transcriptome sequencing and large control cohorts (2018) (11)
- Stretch-Induced Biased Signaling in Angiotensin II Type 1 and Apelin Receptors for the Mediation of Cardiac Contractility and Hypertrophy (2020) (11)
- Identification of a New Target of miR-16, Vacuolar Protein Sorting 4a (2014) (11)
- Prognostic implications of Q waves and T-wave inversion associated with early repolarization. (2012) (11)
- Association of Titin Variations With Late-Onset Dilated Cardiomyopathy. (2022) (11)
- Unexplained Double‐Chambered Left Ventricle Associated with Contracting Right Ventricular Aneurysm and Right Atrial Enlargement (2014) (11)
- Low-dose growth hormone is cardioprotective in uremia. (2008) (11)
- Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes (2020) (10)
- The Impact of ST Elevation on Athletic Screening (2011) (10)
- Cardiopulmonary Exercise Testing, Impedance Cardiography and Reclassification of Risk in Patients Referred for Heart Failure Evaluation. (2019) (10)
- Left atrial function and phenotypes in asymmetric hypertrophic cardiomyopathy (2017) (10)
- Aldehyde dehydrogenase activator attenuates diabetic cardiomyopathy; a role in improving the quality of resident cardiac stem cells? (2010) (10)
- Defining the limits of athlete's heart: implications for screening in diverse populations. (2010) (10)
- An integrated polygenic and clinical risk tool enhances coronary artery disease prediction (2020) (9)
- Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease (2016) (9)
- Functional and structural analysis of cytokine selective IL6ST defects that cause recessive hyper-IgE syndrome. (2021) (9)
- Contractile reserve and cardiopulmonary exercise parameters in patients with dilated cardiomyopathy, the two dimensions of exercise testing (2017) (9)
- Corrigendum: Performance comparison of whole-genome sequencing platforms (2012) (9)
- Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks (2021) (9)
- A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing (2019) (9)
- Enhancement of beta adrenergic responsiveness in myocytes lacking nitric oxide synthase 1 (2001) (9)
- SARS-CoV-2 RNAaemia predicts clinical deterioration and extrapulmonary complications from COVID-19. (2020) (9)
- HapIso: An Accurate Method for the Haplotype- Specific Isoforms Reconstruction From Long Single-Molecule Reads (2016) (9)
- Prognostic value of capnography during rest and exercise in patients with heart failure. (2012) (9)
- Understanding the echocardiogram (2004) (9)
- Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder. (2020) (9)
- Designing clinically translatable artificial intelligence systems for high-dimensional medical imaging (2021) (8)
- Exercise oscillatory ventilation reflects diminished quality of life and perceived functional capacity in patients with heart failure. (2011) (8)
- The post myocardial infarction exercise test: still worthy after all of these years. (2001) (8)
- Approaching Higher Dimension Imaging Data Using Cluster-Based Hierarchical Modeling in Patients with Heart Failure Preserved Ejection Fraction (2019) (8)
- Deep Learning Prediction of Biomarkers from Echocardiogram Videos (2021) (8)
- Delivering Clinical Grade Sequencing and Genetic Test Interpretation for Cardiovascular Medicine (2017) (8)
- Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays (2019) (8)
- Genetic Reduction in Left Ventricular Protein Kinase C-&agr; and Adverse Ventricular Remodeling in Human Subjects (2018) (8)
- Mono- and Biallelic Protein-Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms (2021) (7)
- Emerging role of the apelin system in cardiovascular homeostasis. (2007) (7)
- Personalized prediction of adverse heart and kidney events using baseline and longitudinal data from SPRINT and ACCORD (2019) (7)
- PROGNOSTIC IMPLICATIONS OF Q WAVES AND T WAVE INVERSION ASSOCIATED WITH EARLY REPOLARIZATION (2012) (7)
- Arrhythmogenic Right Ventricular Cardiomyopathy: Toward a Modern Clinical and Genomic Understanding. (2015) (7)
- Orexin: a Missing Link Between Sleep Disorders and Heart Failure? (2017) (7)
- Exome sequencing identifies de novo pathogenic variants in FBN1 and TRPS1 in a patient with a complex connective tissue phenotype (2017) (7)
- Apelin increases atrial conduction velocity, refractoriness, and prevents inducibility of atrial fibrillation (2020) (7)
- A precision metric for clinical genome sequencing (2016) (7)
- INHERIT (INHibition of the renin angiotensin system in hypertrophic cardiomyopathy and the Effect on hypertrophy—a Randomised Intervention Trial with losartan) (2015) (7)
- A Patient with Sjogren’s Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis (2019) (7)
- Multimodal deep learning enhances diagnostic precision in left ventricular hypertrophy (2021) (7)
- A Balanced Look at the Implications of Genomic (and Other “Omics”) Testing for Disease Diagnosis and Clinical Care (2014) (7)
- Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain (2020) (7)
- A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States (2022) (6)
- Disruption of Protein Quality Control of Human Ether-à-go-go Related Gene K+ Channel Results in Profound Long QT Syndrome. (2021) (6)
- Myocardial NOS1 controls the lusitropic response to beta-adrenergic stimulation in vivo and in vitro (2003) (6)
- Defining genotype-phenotype relationships in patients with hypertrophic cardiomyopathy using cardiovascular magnetic resonance imaging (2019) (6)
- Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation (2020) (6)
- Interpretable AI for beat-to-beat cardiac function assessment (2019) (6)
- Abstract 16842: Obstructive Hypertrophic Cardiomyopathy: Initial Single Ascending Dose Data in Healthy Volunteers and Patients (2016) (6)
- The Next Generation Precision Medical Record - A Framework for Integrating Genomes and Wearable Sensors with Medical Records (2016) (6)
- Smartphone-Based VO2max Measurement With Heart Snapshot in Clinical and Real-world Settings With a Diverse Population: Validation Study (2021) (6)
- Limitations of Electrocardiography for Detecting Left Ventricular Hypertrophy or Concentric Remodeling in Athletes. (2019) (6)
- Taming the genome: towards better genetic test interpretation (2016) (6)
- Abstract 453: Apelin Regulates Cardiac Contractility and Rescues Neurohormonal Heart Failure (2006) (6)
- Navigating Genetic and Phenotypic Uncertainty in Left Ventricular Noncompaction. (2017) (6)
- A method for determining exercise oscillatory ventilation in heart failure: Prognostic value and practical implications. (2017) (5)
- Genetics of Arrhythmia: Disease Pathways Beyond Ion Channels (2008) (5)
- Machine learning-based detection of insertions and deletions in the human genome (2019) (5)
- Hypertrophic cardiomyopathy: can the horse be put back in the barn? (2015) (5)
- Cell-specific chromatin landscape of human coronary artery resolves regulatory mechanisms of disease risk (2021) (5)
- Establishing disease causality for a novel gene variant in familial dilated cardiomyopathy using a functional in-vitro assay of regulated thin filaments and human cardiac myosin (2015) (5)
- Genome Sequencing in Hypertrophic Cardiomyopathy. (2018) (5)
- Reduced phospholamban phosphorylation is responsible for impaired myocardial relaxation in nNOS(-/-) mice (2005) (5)
- Mobile Health Monitoring of Cardiac Status (2020) (5)
- Allele-specific silencing ameliorates restrictive cardiomyopathy due to a human myosin regulatory light chain mutation (2019) (5)
- Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy. (2019) (5)
- Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations (2021) (5)
- Large Q and S waves in lead III on the electrocardiogram distinguish patients with hypertrophic cardiomyopathy from athletes (2018) (5)
- Statistical Methods for AV/VV Optimization (2008) (5)
- Right Ventricular Structure and Function in the Veteran Ultramarathon Runner: Is There Evidence for Chronic Maladaptation? (2018) (5)
- LDC '19: international workshop on longitudinal data collection in human subject studies (2019) (5)
- Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3. (2019) (5)
- Digital Health Applications for Pharmacogenetic Clinical Trials (2020) (4)
- A community overlap strategy reveals central genes and networks in heart failure (2016) (4)
- Learning epistatic polygenic phenotypes with Boolean interactions (2020) (4)
- Influences of rare protein-coding genetic variants on the human plasma proteome in 50,829 UK Biobank participants (2022) (4)
- Temporal dynamics of the multi-omic response to endurance exercise training across tissues (2022) (4)
- Re: A prospective randomized evaluation of VV delay optimization in CRT-D recipients: echocardiographic observations from the RHYTHM II ICD study. (2009) (3)
- Author Correction: Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk (2022) (3)
- Erratum: Insights into Human β-Cardiac Myosin Function from Single Molecule and Single Cell Studies (2011) (3)
- Echocardiographic Assessment of Left Ventricular Remodeling in American Style Footballers (2019) (3)
- Realtime morphological characterization and sorting of unlabeled viable cells using deep learning (2022) (3)
- Pharmacogenetics of Heart Failure: Evidence, Opportunities, and Challenges for Cardiovascular Pharmacogenomics (2008) (3)
- Acetaminophen or Tylenol? A Retrospective Analysis of Medication Digital Communication Practices (2018) (3)
- Frontiers in nephrology: genomic approaches to understanding the molecular basis of atherosclerosis. (2007) (3)
- Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts (2019) (3)
- Statin Use and Ventricular Arrhythmias During Clinical Treadmill Testing (2009) (3)
- Erratum: De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia (The American Journal of Human Genetics (2019) 105(2) (413–424), (S0002929719302393), (10.1016/j.ajhg.2019.06.014)) (2019) (3)
- Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts (2019) (3)
- Targeted Long-Read RNA Sequencing Demonstrates Transcriptional Diversity Driven by Splice-Site Variation in MYBPC3 (2019) (3)
- Denoising of Quality Scores for Boosted Inference and Reduced Storage (2016) (3)
- 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)". (2019) (3)
- Genetic Testing for Cardiovascular Conditions Predisposing to Sudden Death (2016) (3)
- Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy (2021) (3)
- Generation of three induced pluripotent stem cell lines, SCVIi003-A, SCVIi004-A, SCVIi005-A, from patients with ARVD/C caused by heterozygous mutations in the PKP2 gene (2021) (3)
- Direct-to-consumer genetic testing for predicting sports performance and talent identi fi cation: Consensus statement (2015) (3)
- Rapid Genome Sequencing in the Critically Ill. (2019) (2)
- Mono- and bi-allelic protein truncating variants in alpha-actinin 2 cause cardiomyopathy through distinct mechanisms (2020) (2)
- Heart Snapshot: a broadly validated smartphone measure of VO2max for collection of real world data (2020) (2)
- Abstract 16392: Oxido-Reductive Regulation of Human Vascular Remodeling by the Orphan Receptor Tyrosine Kinase Ros1 (2014) (2)
- Human immunodeficiency virus and respiratory (2000) (2)
- Clinical assessment incorporating a personal genome – Authors' reply (2010) (2)
- A NEURAL NETWORK APPROACH TO PREDICTING OUTCOMES IN HEART FAILURE USING CARDIOPULMONARY EXERCISE TESTING (2013) (2)
- Constraint-based analysis for causal discovery in population-based biobanks (2019) (2)
- Pathologic gene network rewiring implicates PPP1R3A as a central cardioprotective factor in pressure overload heart failure (2016) (2)
- Proactive variant effect mapping to accelerate genetic diagnosis for pediatric cardiac arrest (2022) (2)
- Pathological overlap of Arrhythmogenic Right Ventricular Cardiomyopathy and Cardiac Sarcoidosis. (2019) (2)
- Polygenic risk scores for the prediction of cardiometabolic disease. (2022) (2)
- Association Genetics and Cardiovascular Disease : A Policy Statement From the American Heart (2012) (2)
- Abstract 13231: Patient-Specific Induced Pluripotent Stem Cell as a Model for Familial Dilated Cardiomyopathy (2011) (2)
- Impact of the distance from the chest wall to the heart on surface ECG voltage in athletes (2020) (2)
- AMELIE 3: Fully Automated Mendelian Patient Reanalysis at Under 1 Alert per Patient per Year (2021) (2)
- The Accuracy of Smartphone Camera Apps to Detect Atrial Fibrillation: A Systematic Review, Meta-Analysis, Meta-Regression and Modeling Study (2019) (2)
- HapIso: An Accurate Method for the Haplotype- Specific Isoforms Reconstruction From Long Single-Molecule Reads. (2017) (2)
- Extremely elevated lipoprotein(a), combined hyperlipidemia, and premature atherosclerosis in a Chinese family. (2010) (2)
- Whole-Transcriptome Profiling of Human Heart Tissues Reveals the Potential Novel Players and Regulatory Networks in Different Cardiomyopathy Subtypes of Heart Failure. (2021) (2)
- Should the exercise ECG be used to screen for sudden cardiac death? (2009) (2)
- Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD (2022) (2)
- New Insights into the Clinical Exercise Test (2003) (2)
- Perioperative cardiac risk: pathophysiology, assessment and management (2006) (2)
- Better decisions through science—case in point: exercise testing scores (2002) (2)
- Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy (2022) (1)
- Personal genomes Misha Angrist Here is a Human Being: at (2010) (1)
- Computer Applications in the Interpretation of the Exercise Electrocardiogram (2000) (1)
- The Verbosity Epidemic (2008) (1)
- Taming rare variation with known biology in long QT syndrome. (2013) (1)
- INDUCING VARIATIONS IN THE SHORTENING OF SINGLE CARDIOMYOCYTES WITH LOCALIZED MECHANICAL STIMULATION (2013) (1)
- Multidimensional estimation of cardiac arrhythmia potential across space and time (2019) (1)
- Managing mortality Atul Gawande Being Mortal: Medicine a (2014) (1)
- The Effect of Apelin on Single Isolated Cardiac Myocytes from Wild-Type and Apelin / APJ KO Mice (2010) (1)
- DeepBeat: A multi-task deep learning approach to assess signal quality and arrhythmia detection in wearable devices (2020) (1)
- Exercise capacity in patients with hypertrophic cardiomyopathy: non-invasive hemodynamic responses to exercise and association with clinical and imaging variables (2013) (1)
- Impedance Cardiography Is Superior to Echocardiographic Methods for Pacing Interval Optimization (2008) (1)
- Bone Morphogenetic Protein Promotes Motility And Represses Proliferation Of Vascular Smooth Muscle Cells By Tandem Recruitment Of Canonical And Non-canonical Wnt Signaling Pathways (2010) (1)
- WHAT IS THE PROGNOSTIC VALUE OF THE ST DEPRESSION CRITERIA FOR ISCHEMIA RECOMMENDED IN THE UNIVERSAL DEFINITION FOR MYOCARDIAL INFARCTION (2013) (1)
- Abstract 2194: Age and Double Product Reserve-Adjusted Modification of the Duke Treadmill Score Nomogram (2008) (1)
- Cardiac imaging of aortic valve area from 26,142 UK Biobank participants reveal novel genetic associations and shared genetic comorbidity with multiple disease phenotypes (2020) (1)
- A cardiac neuronal nitric oxide synthase isoform regulates contraction and calcium handling in murine ventricular myocytes (2002) (1)
- A non-exercise based V02max prediction using FRIEND dataset with a neural network (2017) (1)
- Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations (2021) (1)
- Machine learning in drug development (2019) (1)
- Mechanical and electrophysiological properties of murine hypertrophied left ventricular myocytes (2001) (1)
- Athletic Remodeling in Female College Athletes: The "Morganroth Hypothesis" Revisited. (2019) (1)
- Cardiopulmonary Exercise Testing With Echocardiography to Assess Recovery in Patients With Ventricular Assist Devices (2021) (1)
- Aneurysm and dissection of the aorta (2004) (1)
- Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (2021) (1)
- The mitochondrial multi-omic response to exercise training across tissues (2023) (1)
- A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases (2021) (1)
- Overrepresentation of Neuronal Development Pathways in Heart Failure Patients Who Dramatically Responded to Pharmaceutical Therapy (2008) (1)
- Prognostic role of exercise echocardiography in patients with hypertrophic cardiomyopathy (2013) (1)
- A DEEP LEARNING ALGORITHM ACCURATELY DETECTS PERICARDIAL EFFUSION ON ECHOCARDIOGRAPHY (2020) (1)
- Multi-dimensional structure function relationships in human β-cardiac myosin from population scale genetic variation (2016) (1)
- Isolated mouse ventricular cells exhibit a negative contraction frequency response (2001) (1)
- Combining digital data and artificial intelligence for cardiovascular health. (2021) (1)
- PAROXYSMAL ATRIAL FIBRILLATION IS ASSOCIATED WITH EXERCISE INTOLERANCE AMONG INDIVIDUALS WITH HYPERTROPHIC CARDIOMYOPATHY (2013) (1)
- A General Framework for Dose Optimization (2009) (1)
- Is Genetic Testing for Heart Disease Right for Me? (2019) (1)
- JAMA Peer Reviewers in 2018. (2019) (1)
- A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics (2016) (1)
- Coronary artery disease (2004) (1)
- The Undiagnosed Diseases Program--Reply. (2016) (1)
- A cardiac nitric oxide synthase 1 regulates contraction and calcium fluxes - a novel mechanism in the autocrine control of cardiac function (2002) (1)
- Interpreting whole-genome sequencing--reply. (2014) (1)
- Rat model of veno-arterial extracorporeal membrane oxygenation (2014) (1)
- The Genomics of Extreme Athletes. The ELITE Study (Exercise at the Limit - Inherited Traits of Endurance). (2016) (1)
- Comparison of the FRIEND and Wasserman‐Hansen Equations in Predicting Outcomes in Heart Failure (2021) (1)
- Causative Variants for Inherited Cardiac Conditions in a Southeast Asian Population Cohort (2022) (1)
- Abstract 16484: The Transcriptional Repressor NR1D2 is Associated With Congenital Heart Disease and Plays an Evolutionarily Conserved Role in Cardiac Development (2015) (1)
- P1833Serial echo-cardiopulmonary exercise test ramping for evaluation of patients with VAD (2018) (1)
- Abstract 16756: Analysis of Cardiomyopathy Using Whole Genome Sequencing (2012) (0)
- IDENTIFYING THE OPTIMAL ECHOCARDIOGRAPHIC VARIABLES TO PREDICT OUTCOME THROUGH CORRELATION MAPPING IN PATIENTS WITH DILATED CARDIOMYOPATHY (2017) (0)
- Abstract 4129: Addition of the Electrocardiogram to the Pre-participation Examination of College Athletes (2008) (0)
- A guide for the diagnosis of rare and undiagnosed disease: beyond the exome (2022) (0)
- Chromatin regulation by Brgl underlies heart muscle development and disease (2011) (0)
- The Independent Predictive Value of Peak Oxygen Consumption, Left ventricular Strain and Atrial Remodelling in Patients With Dilated Cardiomyopathy (2015) (0)
- Abstract 58: Modeling Pathogenesis in Familial Hypertrophic Cardiomyopathy Using Patient-Specific Induced Pluripotent Stem Cells (2012) (0)
- Ongoing Promises and Public Expectations of the HGP (0)
- Abstract 14425: Exome Sequencing Reveals a Low Frequency Variant in BMPER in a Pedigree With Recurrence of Left Ventricular Outflow Tract Obstruction Defects (2016) (0)
- Effect ofModerate-Intensity Exercise Training on Peak Oxygen Consumption in Patients With Hypertrophic Cardiomyopathy A Randomized Clinical Trial (2017) (0)
- COMPARISON OF UNITED STATES AND EUROPEAN CRITERIA FOR HYPERTENSION IN A LARGE COHORT OF COMPETITIVE ATHLETES EXAMINED AS PART OF PRE-PARTICIPATION EVALUATION (2019) (0)
- Abstract 15528: Myocardial Deformation Imaging and Obstruction in Hypertrophic Cardiomyopathy, Insights from Cross-sectional and Post-myectomy Analysis (2014) (0)
- CARDIOPULMONARY RESPONSE TO EXERCISE IN PATIENTS WITH NEUROMUSCULAR DISEASE (2023) (0)
- Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients (2023) (0)
- INTERDISCIPLINARY PERIPARTUM CARE OF THE PATIENT WITH DIASTOLIC HEART FAILURE IN NON-OBSTRUCTIVE HYPERTROPHIC CARDIOMYOPATHY (2017) (0)
- The PrecisionMedicine Initiative ANewNational Effort (2015) (0)
- Figure 1, [Osler's nodes on a finger and foot.]. (2004) (0)
- Abstract 1475: The Apelin-APJ Pathway Is an Endogenous Regulator of Cardiac Function and Is Upregulated in Cardiac Pressure Overload (2008) (0)
- Abstract 15391: The Natural History of Asymptomatic and Mildly Symptomatic Obstructive Hypertrophic Cardiomyopathy: Insights From the Share Registry (2020) (0)
- B-PO01-081 MACHINE LEARNING OF THE ELECTROCARDIOGRAM IDENTIFIES CARDIAC WALL MOTION ABNORMALITIES BEYOND THE Q WAVE (2021) (0)
- Abstract 16018: Genetic variation near HCRTR2 associates with dramatic improvement of heart function in patients with heart failure (2013) (0)
- Abstract 113: Cell-specific Chromatin Landscape Of Human Coronary Artery Resolves Mechanisms Of Disease Risk (2021) (0)
- Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment (2023) (0)
- Abstract 12075: Whole-Genome Sequencing at 10-Days of Life in Perinatal Long-QT Syndrome Yields New Insights Into Disease Pathogenesis (2014) (0)
- Differential response trajectories to acute exercise in blood and muscle (2019) (0)
- Abstract 14837: Patients with Hypertrophic Cardiomyopathy are Less Physically Active than the General Population (2012) (0)
- Abstract 9254: Race Differences in Ventricular Remodeling Among College Football Players: Implications for a Cardiovascular Screening Program (2012) (0)
- PATTERNS AND PROGNOSIS OF ALL COMPONENTS OF EARLY REPOLARIZATION IN ATHLETES AND AMBULATORY PATIENTS (2013) (0)
- Impact of SARS‐Cov‐2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry (2022) (0)
- Quantifying and Improving Clinical-grade Coverage and Accuracy using Augmented Exome Sequencing (2015) (0)
- Book: Personal genomes (2010) (0)
- Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock. (2022) (0)
- Abstract 343: Bayesian Selection of Modifier Genes in Hypertrophic Cardiomyopathy Through Whole Genome Sequencing (2015) (0)
- Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy (2022) (0)
- Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy. (2021) (0)
- Figure 11, [Right axis deviation.]. (2004) (0)
- Clinical Cardiac Hemodynamics (2011) (0)
- SYSTOLIC DYSFUNCTION WITHOUT LV DILATATION IN A COHORT OF PATIENTS WITH LAMIN A/C CARDIOMYOPATHY (2017) (0)
- Abstract 18360: ACTN2 Mutations Are Associated With Cardiomyopathy and Cardiomyocyte Hypertrophy (2016) (0)
- Utility Of Cardiopulmonary Exercise Testing In Chronic Unexplained Dyspnea In A 77 Year Old Female (2021) (0)
- Abstract 20983: Size Based Microfluidic Enrichment of Human Inducedpluripotent Cell-derived Cardiomyocytes (2016) (0)
- Cardiac splicing as a diagnostic and therapeutic target (2023) (0)
- Promise of Precision Medicine--Reply. (2015) (0)
- Summary of Consensus Recommendations from ESC , EHRA , HRS , AHA / ACC , and HFSA on Genetic Testing in Index Patients for Cardiomyopathies and Inherited Arrhythmias (2017) (0)
- ischemiaexpression profile in mouse myocardium after (2015) (0)
- The right ventricle following ultra-endurance exercise: insights from novel echocardiography and 12-lead electrocardiography (2014) (0)
- 20: The Resuscitated DCD Donor Heart Is Functionally Superior to the Brainstem Dead Donor Heart (2009) (0)
- Past Successes of Genetic Findings Familial Hypercholesterolemia and Low-Density Lipoprotein Cholesterol Lowering (2015) (0)
- 594 Intracellular Calcium Handling in the Donor Heart: Comparison between DCD and Brainstem Dead (BSD) Donor Hearts (2011) (0)
- CL-01 Translation of Clinical Proteomics : Opportunities and Challenges (2013) (0)
- Author Correction: Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk (2022) (0)
- Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. (2023) (0)
- PerspectivesPersonal genomesMisha Angrist, Here is a Human Being: at the Dawn of Personal Genomics, HarperCollins (2010), Pp 352. US$26·99., ISBN: 0061628336 (2010) (0)
- RESTING BLOOD PRESSURE IN 2881 ATHLETES AGED 9-35 YEARS OF AGE AND THE RELATION TO SEX, AGE, BODY SIZE, AND AFRO-AMERICAN DESCENT (2019) (0)
- Truncating Variants in the Desmoplakin Gene Cause a Distinct Arrhythmogenic Cardiomyopathy (2019) (0)
- Regional variation in cardiovascular genes enables a tractable genome editing strategy (2022) (0)
- Defining left ventricular remodeling using lean body mass allometry: a UK Biobank study (2023) (0)
- Reviewers for JCTR (2013) (0)
- CORRELATION OF ECHOCARDIOGRAPHIC FINDINGS WITH SYMPTOMS IN HYPERTROPHIC CARDIOMYOPATHY PATIENTS (2019) (0)
- Abstract 13199: Women With Hypertrophic Cardiomyopathy: Obstructed and Underdiagnosed? Results From the International SHaRe Registry (2018) (0)
- Heart Failure Early Repolarization in an Ambulatory Clinical Population (0)
- Title: Sports Genetics Moving Forward -lessons Learned from Medical Research 1 2 Short Running Title: Sports Genetics Moving Forward 3 4 (2016) (0)
- INTEGRATING MYOCARDIAL STRAIN AND EXERCISE PERFORMANCE INTO PROGNOSTICATION OF HYPERTROPHIC CARDIOMYOPATHY (2017) (0)
- Abstract 11178: Electrocardiographic Comparison of Healthy Young Men, Athletes and Patients with Hypertrophic Cardiomyopathy (2012) (0)
- Abstract 469: Genomic Context Predicts Dilated but Not Hypertrophic Cardiomyopathy (2019) (0)
- Report from the Annual Conference of the British Society of Echocardiography, November 2016, Queen Elizabeth II Conference Centre, London (2017) (0)
- Respiratory Gas Kinetics After Maximal Exercise In Patients Referred For Cardiopulmonary Exercise Testing (2021) (0)
- Ring Finger Protein 207 Degrades T613M Kv11.1 Channel (2018) (0)
- Arterial Stent Deployment Results in a Time Dependent Increase in Neointima Formation and Delayed Endothelial Cell Repopulation Compared With Balloon Angioplasty (2009) (0)
- INTEGRATING CORRELATION BASED NETWORKS INTO RISK PROGNOSTICATION OF CARDIOMYOPATHY (2018) (0)
- Table 6, The recommended procedure for starting an angiotensin-converting enzyme inhibitor (ACEI) (2004) (0)
- OUTCOMES OF AFRICAN AMERICAN VS. NON-AFRICAN AMERICAN WOMEN WITH PERIPARTUM CARDIOMYOPATHY: A COMPARISON ANALYSIS BETWEEN CANADIAN AND UNITED STATES COHORTS (2019) (0)
- Predicting Peak VO2 In Clinical Populations With Obesity (2021) (0)
- Table 2, Causes of secondary hypertension (2004) (0)
- Abstract 17106: Determining the Contributing Factors of Heterogeneity in LV Mass: Results From a Collegiate-Level Football Screening Study (2017) (0)
- P3450 Nitric oxide synthase 1 (NOS1) regulates basal and beta-adrenergic left-ventricular contraction and relaxation in vivo (2003) (0)
- Figure 12, [ECG demonstrating left ventricular hypertrophy...]. (2004) (0)
- 215 Independent Determinants of Septal Curvature in Patients with Pulmonary Arterial Hypertension (2012) (0)
- Abstract 16484: Primary Prevention Implantable Cardioverter Defibrillator Utilization for Hypertrophic Cardiomyopathy in US vs Non-US: Findings From the Share Registry (2020) (0)
- Abstract 12623: Complementary Role of Exercise Performance and Right Heart Metrics to the Validated MAGGIC score: Insights From a Network Analysis (2016) (0)
- Clinical Implications of Technical Performance in Medical Genome Sequencing (2016) (0)
- Abstract 13876: Cardiovascular Magnetic Resonance Imaging Elucidates Genotype-Phenotype Relationships in Patients with Hypertrophic Cardiomyopathy (2011) (0)
- Abstract 6234: Cost-Effectiveness Analysis Demonstrates Superiority of Screening Young Athletes with 12-Lead Electrocardiogram versus History and Physical in Preventing Sudden Cardiac Death (2008) (0)
- Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene. (2023) (0)
- Taming the genome: towards better genetic test interpretation (2016) (0)
- Ning Sun Dilated Cardiomyopathy Patient-Specific Induced Pluripotent Stem Cells as a Model for Familial (2012) (0)
- MOLECULAR AUTOPSY FOR SUDDEN CARDIAC DEATH USING WHOLE GENOME SEQUENCING (2011) (0)
- Electrophysiological and mechanical properties of ventricular myocytes isolated from wild-type mice and mice with disruption of the neuronal nitric oxide synthase gene (2001) (0)
- Abstract 311: Machine Learning of the Electrocardiogram to Detect Regional Structural Abnormalities of the Heart (2020) (0)
- 352: Cardiac Resuscitation Following Circulatory Arrest in the Organ Donor Is Associated with Excellent Functional and Metabolic Recovery: Implications for Clinical Heart Transplantation (2010) (0)
- enhances directed cardiac differentiation of mouse and human embryonic stem cells. (2012) (0)
- Mulibrey Nanism and the Real Time Use of Genome and Biobank Engines to Inform Clinical Care in an Ultrarare Disease (2021) (0)
- Abstract 14884: Obesity is a Major Driver of Obstruction and Heart Failure in Hypertrophic Cardiomyopathy: Results From the International Share Registry (2018) (0)
- Abstract 15102: Are T wave Inversions in the Anterior Precordial Leads Benign in African- Americans? (2012) (0)
- INDEPENDENT PROGNOSTIC VALUES OF CLINICAL RISK SCORES, RIGHT VENTRICULAR SYSTOLIC PRESSURE, AND N-TERMINAL PRO-B-TYPE PEPTIDE IN HEART FAILURE WITH PRESERVED EJECTION FRACTION: INSIGHTS FROM SUPERVISED AND UNSUPERVISED MODELS (2019) (0)
- Mind the Gap: The Complete Human Genome Unlocks Benefits for Clinical Genomics. (2022) (0)
- Origin stories Siddhartha Mukherjee The Gene: An Intimat (2016) (0)
- 348 Hearts from DCD Donors Display Excellent Biventricular Function Following Transplantation (2011) (0)
- Video-based AI for beat-to-beat assessment of cardiac function (2020) (0)
- Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank (2018) (0)
- Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure (2019) (0)
- Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks (2021) (0)
- Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy (2019) (0)
- Redox regulation of vascular remodeling (2015) (0)
- Physical activity, sleep and cardiovascular health data for 50,000 individuals from the MyHeart Counts Study (2019) (0)
- Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions (2020) (0)
- Medical implications of technical accuracy in genome sequencing (2016) (0)
- Approaching Higher Dimension Imaging Data Using Cluster-Based Hierarchical Modeling in Patients with Heart Failure Preserved Ejection Fraction (2019) (0)
- NOVEL ALPHA-ACTININ 2 MUTATIONS ARE ASSOCIATED WITH CARDIOMYOPATHY AND HYPERTROPHY IN HUMAN CARDIAC TISSUE AND IPSC-DERIVED CARDIOMYOCYTES (2019) (0)
- Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study (2018) (0)
- Bi-allelic variants in INTS11 are associated with a complex neurological disorder. (2023) (0)
- Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays (2021) (0)
- Mobile Health Study Incorporating Novel Fitness Test. (2022) (0)
- Being Mortal: Medicine and What Matters in the End, Atul Gawande. Metropolitan Books/Henry Holt and Company (2014), 304, US$26·00, ISBN: 9780805095159 (2014) (0)
- The medical device safety act of 2009: clarifying preemption. (2009) (0)
- Challenges Randomized Trial of Personal Genomics for Preventive Cardiology : Design and (2012) (0)
- Abstract 14117: Clinical Characteristics and Cardiovascular Outcomes in Childhood-Onset Hypertrophic Cardiomyopathy (2020) (0)
- A Cardiac Nitric Oxide Synthase 1 Regulates Contraction and Calcium Fluxes – a Novel Mechanism Involved in the Autocrine Control of Cardiac Function (2002) (0)
- Results Baseline Characteristics of the Study Population and Development of the Summed Score (0)
- The genetics of human performance (2021) (0)
- To the Editor: (2009) (0)
- Dissociation of disease phenotype and allele silencing in hypertrophic cardiomyopathy (2019) (0)
- Cardiopulmonary Exercise Testing for Patients With Neuromuscular Disease and Limited Mobility (2023) (0)
- Informing women’s cardiovascular health through genomic analysis of extreme endurance athletes (2015) (0)
- VarSight: prioritizing clinically reported variants with binary classification algorithms (2019) (0)
- Abstract 1433: The Cardioregulatory Peptide Apelin is Preferentially Expressed by Endothelial Cells and Upregulated in Myocardial Disease States (2007) (0)
- Figure 2, [Coronary heart disease risk tables...]. (2004) (0)
- Figure 1, [Contractile proteins in the cardiac...]. (2004) (0)
- Figure 5, [(a) A horizontal section through...]. (2004) (0)
- Re-envisioning community genetics: community empowerment in preventive genomics (2023) (0)
- Adult congenital heart disease (2004) (0)
- Abstract 2368: Long-term Apelin Infusion Rescues Chronic Cardiomyopathy and Potentiates the Effects of ACE-Inhibition (2006) (0)
- What's in a Name? Factors That Influence the Usage of Generic Versus Trade Names for Cardiac Medications Among Healthcare Providers (2018) (0)
- Abstract 10952: Network Analysis Identifies the Orphan Receptor Tyrosine Kinase Ros1 as a Determinant of Glutathione Peroxidase-1 Mediated Vascular Remodeling (2011) (0)
- A Pilot Study of the Integration of a Quantified-self Wearable Device with EMR data in the Acute Postoperative Setting (2016) (0)
- Modulation of atrial electrophysiology and oxidative stress by the endogenous peptide hormone apelin: implications in human atrial fibrillation (2011) (0)
- 158 Racialdifferencesinval122Ileassociatedtransthyretincardiac amyloidosis (2021) (0)
- European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases (2022) (0)
- Abstract 17417: Pathogenic and Likely Pathogenic Missense Variants in Cardiovascular Disease Genes Cluster Around Functional Domains (2020) (0)
- Abstract 15808: Whole Exome Sequencing and Hypertrophic Cardiomyopathy (2011) (0)
- Table 10, The Vaughan-Williams classification of antiarrhythmic drugs (2004) (0)
- Efficacy and Safety of ARRY-371797 in LMNA-Related Dilated Cardiomyopathy: A Phase 2 Study (2022) (0)
- 418 Titin mutations and female sex characterize dilated cardiomyopathy in the elderly (2021) (0)
- Abstract 12364: Addressing Outcome Prediction in Heart Failure Using Contemporary Equations for Maximal Oxygen Consumption (2017) (0)
- Somatic Mosaicism of Novel SCN5A Mutation in Purkinje System (PS) may Underlie 2:1 Block in an Infant with Long QT Syndrome (LQTS) (2016) (0)
- Participation in a national diagnostic research study: assessing the patient experience (2023) (0)
- Figure 13, [ECG demonstrating left bundle branch block.]. (2004) (0)
- Supporting undiagnosed participants when clinical genomics studies end (2022) (0)
- A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative (2018) (0)
- In vivo Post-cardiac arrest myocardial dysfunction is supported by CaMKII-mediated calcium long-term potentiation and mitigated by Alda-1 , an Agonist of Aldehyde Dehydrogenase Type 2 Running Title : Post-cardiac arrest myocardial dysfunction (2016) (0)
- Contractility of Neonatal Cardiomyocytes is Altered with Different Densities of Laminin Covalently Attached to Microposts (2014) (0)
- Quantitative Phosphorylation in ( FACS ) Purified CD 4 T + Human Thymocytes as a Function of IGF-1 Stimulation (2014) (0)
- Table 4, Patterns of syncope (2004) (0)
- GENETIC DETERMINANTS OF DRAMATIC IMPROVEMENT IN LEFT VENTRICULAR FUNCTION IN PATIENTS WITH HEART FAILURE (2011) (0)
- Assessing post-exercise respiratory gas kinetics in clinical sample - a pilot study (2021) (0)
- Abstract 16179: Impact of a Genetic Risk Score for Coronary Artery Disease in Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study (2016) (0)
- Digital Randomized Controlled Trial of Physical Activity Interventions (A Substudy of the MyHeart Counts Cardiovascular Health Study) (2019) (0)
- ANALYZING PROGRESSION OF DISEASE IN HYPERTROPHIC CARDIOMYOPATHY UTILIZING SEQUENTIAL CARDIOPULMONARY EXERCISE TESTING (2022) (0)
- Abstract 2059: Apelin Potently Inhibits Angiotensin and Disease Induced Superoxide Generation and Associated Vascular Remodeling in Vein Grafts (2007) (0)
- The ECGs that will be read around the world — and save lives of sportspeople (2013) (0)
- PREVALENCE AND PATTERNS OF EARLY REPOLARIZATION (2011) (0)
- Abstract 3807: Outcomes of Septal Myectomy and Alcohol Septal Ablation for Obstructive Hypertrophic Cardiomyopathy: The Stanford Experience (2009) (0)
- ADDRESSING REFERENCE ECHOCARDIOGRAPHIC PARAMETERS IN ATHLETIC SCREENING: A COLLEGE FOOTBALL-BASED STUDY FOCUSING ON THE IMPLICATIONS OF RACE AND CORRECTION FOR BODY COMPOSITION (2017) (0)
- Basic Science for Clinicians Dna Sequencing Clinical Applications of New Dna Sequencing Technologies Historical Perspective Next-generation Sequencing Technologies (2012) (0)
- Abstract 14963: Accelerometer-measured Activity in Non-obstructive Hypertrophic Cardiomyopathy: Patient-generated Activity Measures Correlate With, and Are Convolutional Neural Network Predictors of, Clinical Parameters in the MAVERICK-HCM Study (2020) (0)
- Racial differences in val 122 Ile associated transthyretin cardiac amyloidosis (2021) (0)
- Table 2, Prophylactic regimens for dental, oral, respiratory tract, or esophageal procedures (2004) (0)
- Abstract 14355: Mono- and Biallelic Structural Variants in Alpha-actinin 2 Cause Contractile Dysfunction and Cardiomyopathy in Humans (2020) (0)
- MEDICATION COMMUNICATION PRACTICES BETWEEN PROVIDERS IN CARDIOLOGY (2018) (0)
- Abstract 5683: Insights From Network Analysis: Deficiency of Glutathione Peroxidase-1 Increases In-stent Stenosis (2009) (0)
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