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Author Details

Euan A Ashley
Stanford University
1993
352
70
PMIDPaper TitleJournal TitlePublished Year
36112529Mind the Gap: The Complete Human Genome Unlocks Benefits for Clinical Genomics.Clin Chem2023
37478340Right Ventricular Dysfunction Patterns among Patients with COVID-19 in the Intensive Care Unit: A Retrospective Cohort Analysis.Ann Am Thorac Soc2023
37883018Two epilepsy-associated variants in KCNA2 (K<sub>V</sub> 1.2) at position H310 oppositely affect channel functional expression.J Physiol2023
37639473Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.Eur Heart J2023
37461476A 3'UTR Insertion Is a Candidate Causal Variant at the <i>TMEM106B</i> Locus Associated with Increased Risk for FTLD-TDP.medRxiv2023
37391266Wearable technology and the cardiovascular system: the future of patient assessment.Lancet Digit Health2023
37205549Almanac: Retrieval-Augmented Language Models for Clinical Medicine.Res Sq2023
37226762Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry.Circulation2023
37356413Respiratory gas kinetics in patients with congestive heart failure during recovery from peak exercise.Clinics (Sao Paulo)2023
36653465Cardiac splicing as a diagnostic and therapeutic target.Nat Rev Cardiol2023
36478054Polygenic risk scores for the prediction of cardiometabolic disease.Eur Heart J2023
36718638Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty <i>LMNA</i> gene.Future Cardiol2023
36716194Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.Circ Genom Precis Med2023
36617359Defining left ventricular remodeling using lean body mass allometry: a UK Biobank study.Eur J Appl Physiol2023
36515663Efficacy and Safety of ARRY-371797 in <i>LMNA</i>-Related Dilated Cardiomyopathy: A Phase 2 Study.Circ Genom Precis Med2023
36711881The mitochondrial multi-omic response to exercise training across tissues.bioRxiv2023
36642055Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients.Stem Cell Res2023
36136239Mobile Health Study Incorporating Novel Fitness Test.J Cardiovasc Transl Res2023
34634443Disruption of protein quality control of the human ether-à-go-go related gene K<sup>+</sup> channel results in profound long QT syndrome.Heart Rhythm2022
35768727Author Correction: Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk.Nat Genet2022
35347328Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing.Nat Biotechnol2022
35373836European 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.Europace2022
35671065Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy.Circ Genom Precis Med2022
35862132Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.Circulation2022
35590109Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk.Nat Genet2022
36712167Multimodal deep learning enhances diagnostic precision in left ventricular hypertrophy<sup/>.Eur Heart J Digit Health2022
36042219Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy.Nat Commun2022
35902745Supporting undiagnosed participants when clinical genomics studies end.Nat Genet2022
36255281Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registry.ESC Heart Fail2022
35256804A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States.Nat Genet2022
35133172Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock.Circ Genom Precis Med2022
35130036Causative Variants for Inherited Cardiac Conditions in a Southeast Asian Population Cohort.Circ Genom Precis Med2022
35220969A guide for the diagnosis of rare and undiagnosed disease: beyond the exome.Genome Med2022
35138330Association of Titin Variations With Late-Onset Dilated Cardiomyopathy.JAMA Cardiol2022
35195663High-Throughput Precision Phenotyping of Left Ventricular Hypertrophy With Cardiovascular Deep Learning.JAMA Cardiol2022
35020984Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting.N Engl J Med2022
35293152Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD.Hepatol Commun2022
34522035The genetics of human performance.Nat Rev Genet2022
33441555Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks.Nat Commun2021
33771552Functional and structural analysis of cytokine-selective IL6ST defects that cause recessive hyper-IgE syndrome.J Allergy Clin Immunol2021
33769460Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy.Eur Heart J2021
33743362Generation 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.Stem Cell Res2021
33627090Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays.BMC Bioinformatics2021
33517678Whole-Transcriptome Profiling of Human Heart Tissues Reveals the Potential Novel Players and Regulatory Networks in Different Cardiomyopathy Subtypes of Heart Failure.Circ Genom Precis Med2021
33764162Genomic Context Differs Between Human Dilated Cardiomyopathy and Hypertrophic Cardiomyopathy.J Am Heart Assoc2021
33675770Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries.Am J Cardiol2021
33782553Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation.Genet Med2021
34587765Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.Circulation2021
34491319Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy.Eur Heart J2021
34689609Comparison of the FRIEND and Wasserman-Hansen Equations in Predicting Outcomes in Heart Failure.J Am Heart Assoc2021
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Collaborators

Stanford University School of Medicine
Co-authored papers 72
Co-authored papers 47
Co-authored papers 36
Co-authored papers 28
Co-authored papers 28
Co-authored papers 20
Stanford University
Co-authored papers 20
Boston Children's Hospital, Harvard Medical School
Co-authored papers 15
Stanford Medicine Clinical Genomics Program
Co-authored papers 14
Co-authored papers 13
Co-authored papers 13
Stanford University
Co-authored papers 13
Ontario Institute for Cancer Research
Co-authored papers 13
Stanford University
Co-authored papers 11
Stanford University
Co-authored papers 11
Bakar Computational Health Sciences Institute, University of California san francisco
Co-authored papers 9
Stanford University School of Medicine
Co-authored papers 9
Stanford University
Co-authored papers 8
Co-authored papers 8
Smidt Heart Institute, Cedars-Sinai Medical Center
Co-authored papers 8
Stanford University
Co-authored papers 7
Co-authored papers 7
Stanford University
Co-authored papers 7
Brigham and Women's Hospital (Y.K.
Co-authored papers 7
Cardiovascular Institute, University of Colorado
Co-authored papers 6
Harvard Medical School and Cardiovascular Division, Brigham and Women's Hospital
Co-authored papers 6
Stanford University School of Medicine
Co-authored papers 6
Stanford University School of Medicine
Co-authored papers 6
Center for Inherited Cardiovascular Disease, Stanford University School of Medicine
Co-authored papers 6
Co-authored papers 6