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Author Details

Anthony A Philippakis
Broad Institute of Harvard and the Massachusetts Institute of Technology
2004
76
29
PMIDPaper TitleJournal TitlePublished Year
37291427High-throughput RNA isoform sequencing using programmed cDNA concatenation.Nat Biotechnol2024
37950744Natural Language Processing for Adjudication of Heart Failure in a Multicenter Clinical Trial: A Secondary Analysis of a Randomized Clinical Trial.JAMA Cardiol2024
37291427High-throughput RNA isoform sequencing using programmed cDNA concatenation.Nat Biotechnol2024
37950744Natural Language Processing for Adjudication of Heart Failure in a Multicenter Clinical Trial: A Secondary Analysis of a Randomized Clinical Trial.JAMA Cardiol2024
36350676FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Nucleic Acids Res2023
36350676FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Nucleic Acids Res2023
37669985Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.Nat Commun2023
37662283Natural Language Processing for Adjudication of Heart Failure Hospitalizations in a Multi-Center Clinical Trial.medRxiv2023
37561600The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.Annu Rev Biomed Data Sci2023
37550580Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.Nat Methods2023
37278238Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms.Circ Genom Precis Med2023
36650173BMI-adjusted adipose tissue volumes exhibit depot-specific and divergent associations with cardiometabolic diseases.Nat Commun2023
37081215Genetics of myocardial interstitial fibrosis in the human heart and association with disease.Nat Genet2023
36580284Machine Learning to Understand Genetic and Clinical Factors Associated With the Pulse Waveform Dicrotic Notch.Circ Genom Precis Med2023
37019578The Genetic Determinants of Aortic Distention.J Am Coll Cardiol2023
37013830National Human Genome Research Institute Genomic Data Science Analysis, Visualization, and Informatics Lab-Space: Reaching out to Clinicians.Circ Genom Precis Med2023
37192819Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research.J Am Med Inform Assoc2023
36944631Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.Nat Commun2023
37438524A framework for individualized splice-switching oligonucleotide therapy.Nature2023
37377635Exploring the link between Gilbert's syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals.Eur Heart J Open2023
37105979Cross-modal autoencoder framework learns holistic representations of cardiovascular state.Nat Commun2023
37101945Artificial intelligence-enabled classification of hypertrophic heart diseases using electrocardiograms.Cardiovasc Digit Health J2023
37669985Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.Nat Commun2023
37561600The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.Annu Rev Biomed Data Sci2023
37662283Natural Language Processing for Adjudication of Heart Failure Hospitalizations in a Multi-Center Clinical Trial.medRxiv2023
37550580Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.Nat Methods2023
37192819Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research.J Am Med Inform Assoc2023
37019578The Genetic Determinants of Aortic Distention.J Am Coll Cardiol2023
37081215Genetics of myocardial interstitial fibrosis in the human heart and association with disease.Nat Genet2023
37013830National Human Genome Research Institute Genomic Data Science Analysis, Visualization, and Informatics Lab-Space: Reaching out to Clinicians.Circ Genom Precis Med2023
36944631Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.Nat Commun2023
37278238Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms.Circ Genom Precis Med2023
37377635Exploring the link between Gilbert's syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals.Eur Heart J Open2023
37105979Cross-modal autoencoder framework learns holistic representations of cardiovascular state.Nat Commun2023
37438524A framework for individualized splice-switching oligonucleotide therapy.Nature2023
37101945Artificial intelligence-enabled classification of hypertrophic heart diseases using electrocardiograms.Cardiovasc Digit Health J2023
36650173BMI-adjusted adipose tissue volumes exhibit depot-specific and divergent associations with cardiometabolic diseases.Nat Commun2023
36580284Machine Learning to Understand Genetic and Clinical Factors Associated With the Pulse Waveform Dicrotic Notch.Circ Genom Precis Med2023
34743566ECG-Based Deep Learning and Clinical Risk Factors to Predict Atrial Fibrillation.Circulation2022
36046430Deep learning on resting electrocardiogram to identify impaired heart rate recovery.Cardiovasc Digit Health J2022
35396454Cohort design and natural language processing to reduce bias in electronic health records research.NPJ Digit Med2022
35902171Spatially Distinct Genetic Determinants of Aortic Dimensions Influence Risks of Aneurysm and Stenosis.J Am Coll Cardiol2022
35960155One Clinician Is All You Need-Cardiac Magnetic Resonance Imaging Measurement Extraction: Deep Learning Algorithm Development.JMIR Med Inform2022
35896726Silhouette images enable estimation of body fat distribution and associated cardiometabolic risk.NPJ Digit Med2022
35441669STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysis.Bioinformatics2022
36147540Clinical Implementation of Combined Monogenic and Polygenic Risk Disclosure for Coronary Artery Disease.JACC Adv2022
35869152Prediction performance and fairness heterogeneity in cardiovascular risk models.Sci Rep2022
35614072The potential of polygenic scores to improve cost and efficiency of clinical trials.Nat Commun2022
34743566ECG-Based Deep Learning and Clinical Risk Factors to Predict Atrial Fibrillation.Circulation2022
35051367Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak.Cell2022
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Collaborators

Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 28
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Co-authored papers 21
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Center for Computational Health
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The Broad Institute of MIT and Harvard
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Montreal Neurological Institute, McGill University
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Co-authored papers 6
University of Toronto
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University of Leicester
Co-authored papers 6
Wellcome Sanger Institute
Co-authored papers 5
Harvard University
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Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard
Co-authored papers 5
McGill University
Co-authored papers 5
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European Bioinformatics Institute
Co-authored papers 5
Children's Hospital of Eastern Ontario
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Broad Institute of MIT and Harvard
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American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
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Broad Institute of MIT and Harvard
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Foundation Medicine Inc.
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Hinton State Laboratory Institute
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CSC - IT Center for Science Ltd
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Harvard Medical School, Brigham and Women's Hospital
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Patient-Centered Outcomes Research Institute
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Johns Hopkins University School of Medicine
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