Genetic Medicines to Treat Cardiovascular Disease (A2)
      
      
      
      
      
      January 25-28, 2027
       | Keystone Resort, Keystone, CO, United States
      
      
      
         
          Rick Dewey, Litsa G. Kranias and James S. Ware
        
            
      
      
      
          
      
   
            
     
          
    
      
      
        
        
      
        
      
  
      
      
        
                
        
      
      
    
        
      
        
      
  
      
      
        
                
        
      
      
    
        
      
        
      
  
      
      
        
                
        
      
      
    
      
           
      
  
      
        
        
        
          
            | 4:00–8:00 PM | 
            Registration | 
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            | 6:00–8:00 PM | 
            Welcome Mixer | 
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            Tuesday, January 26, 2027
          
           
         
      
        
      
  
      
      
        
                
        
      
      
    
      
           
      
  
        
      
      
        
                
        
      
      
    
      
           
      
  
      
        
        
        
          
            | 8:00–9:00 AM | 
            Welcome and Keynote Address | 
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            |   | 
            Sekar Kathiresan †, Verve Therapeutics The Human Genome as Teacher and Target: Two Decades of Genomic Discovery to Genomic Medicines | 
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            | 9:00–11:15 AM | 
            New Trailheads: Target Identification for Genetic Medicines in CV Disease | 
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            |   | 
            James S. Ware, Imperial College London Large Scale Genomic Discovery of Causal Mechanisms in Heart Failure | 
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            |   | 
            Victoria Parikh †, Stanford University School of Medicine Genotype-Phenotype Correlation in Inherited Cardiovascular Disease | 
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            |   | 
            Rick Dewey, Versant Ventures Target Selection for Genetic Medicines: Biobanks to Human Proof of Concept | 
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            Short Talk(s) Chosen from Abstracts
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            | 9:30–9:50 AM | 
            Coffee Break | 
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            | 11:15–12:15 PM | 
            Panel Discussion 1: Development, Regulatory, Safety, and Ethical Considerations (including long-term and off-target effects of genetic medicines) | 
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            | 11:15–1:00 PM | 
            Poster Setup | 
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            | 11:15–5:00 PM | 
            On Own for Lunch | 
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            | 1:00–10:00 PM | 
            Poster Viewing | 
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            | 2:30–4:30 PM | 
            Symposia Spotlight 1: Emerging Biological Insights Driving the Next Generation of Genetics Medicines for CV Disease | 
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            Short Talks Chosen from Abstracts
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            | 4:30–5:00 PM | 
            Coffee Available | 
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            | 5:00–7:00 PM | 
            Mechanisms and Models: From Variation to Validation | 
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            |   | 
            Cassady Rupert †, Propria LLC Modeling Human Cardiac Biology with Multi-Dimensional Engineered Human Heart Tissues | 
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            |   | 
            Christine E. Seidman †, Harvard Medical School Modeling Cardiovascular Disease: Genetics, Cellular Systems, Human Models | 
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            |   | 
            Litsa G. Kranias, University of Cincinnati PLN Cardiomyopathy: From Bedside to Bench and Back to Bedside | 
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            Short Talk(s) Chosen from Abstracts
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            | 7:00–8:00 PM | 
            Social Hour with Dinner | 
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            Wednesday, January 27, 2027
          
           
         
      
        
      
  
      
      
        
                
        
      
      
    
      
           
      
  
        
      
      
        
                
        
      
      
    
      
           
      
  
      
        
        
        
          
            | 8:00–11:00 AM | 
            Gene Silencing in Cardiovascular Disease and Promising Avenues | 
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            |   | 
            Marianna Fontana †, University College London CRISPR-Cas9 Gene Editing for TTR Amyloid Cardiomyopathy | 
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            |   | 
            Kate A Fitzgerald †, University of Massachusetts Medical School From RNAi Mechanism to Medicine; the Path to a New Class of Genetic Medicines | 
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            |   | 
            Euan A. Ashley †, Stanford University Allele-Specific Silencing in Cardiomyopathy | 
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            |   | 
            Jin Billy Li †, Stanford University Endogenous RNA Editing in CV Disease: Mechanisms and Therapeutic Applications | 
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            Short Talk(s) Chosen from Abstracts
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            | 9:00–9:20 AM | 
            Coffee Break | 
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            | 11:00–1:00 PM | 
            Poster Setup | 
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            | 11:00–5:00 PM | 
            On Own for Lunch | 
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            | 1:00–10:00 PM | 
            Poster Viewing | 
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            | 3:00–4:30 PM | 
            Career Roundtable | 
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            | 4:30–5:00 PM | 
            Coffee Available | 
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            | 5:00–7:00 PM | 
            Therapeutic Gene Augmentation Strategies in CV Disease | 
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            |   | 
            Roger J. Hajjar †, Mass General Brigham Engineering the Failing Heart: Innovations in Cardiac Gene Therapy | 
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            |   | 
            Annemieke Aartsma-Rus †, Leiden University Medical Center Exon Skipping to Restore Gene Expression in Muscle Disease | 
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            Short Talk(s) Chosen from Abstracts
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            | 7:00–8:00 PM | 
            Social Hour with Dinner | 
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            Thursday, January 28, 2027
          
           
         
      
        
      
  
      
      
        
                
        
      
      
    
      
           
      
  
        
      
      
        
                
        
      
      
    
      
           
      
  
      
        
        
        
          
            | 8:00–11:00 AM | 
            Homing for Cures: Cardiomyocyte-Directed Delivery Approaches | 
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            |   | 
            Luk H. Vandenberghe †, Harvard Medical School Engineering Viral Delivery Systems | 
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            |   | 
            James Dahlman †, Georgia Tech / Emory Medical School Lipid Nanoparticles: Past, Present, and Future of RNA Delivery | 
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            |   | 
            William M Flanagan †, Avidity Biosciences, Inc. Antibody-Oligo Conjugates for Striated Muscle-Enriched Delivery | 
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            Short Talk(s) Chosen from Abstracts
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            | 9:00–9:20 AM | 
            Coffee Break | 
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            | 11:00–12:00 PM | 
            Panel Discussion 2: Navigating the Valley of Opportunity: Moving Ideas from Idea to Products for Patients with Academia, Venture Capital, and Pharma | 
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            | 11:00–5:00 PM | 
            On Own for Lunch | 
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            | 2:30–4:30 PM | 
            Symposia Spotlight 2: Emerging Translational Strategies in CV Disease | 
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            |   | 
            Short Talks Chosen from Abstracts
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            | 4:30–5:00 PM | 
            Coffee Available | 
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            | 5:00–6:45 PM | 
            Products to Patients: Therapeutic Development and Trial Design | 
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            |   | 
            Laura F. Michael †, Eli Lilly and Company Lp(a) -  From Genetic Insight to Novel Biology and Breakthrough Therapy | 
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            |   | 
            Pushkal Garg †, Alnylam Pharmaceuticals, Inc. Industry Perspective on Clinical Development of Genetic Therapies | 
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            |   | 
            Gene Bukhman †, Brigham and Women's Hospital Global Health Equity Considerations for New Treatments for CV Disease | 
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            Short Talk(s) Chosen from Abstracts
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            | 6:45–7:00 PM | 
            Meeting Wrap-Up: Outcomes and Future Directions | 
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            | 7:00–8:00 PM | 
            Social Hour with Dinner | 
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            | 8:00–11:00 PM | 
            Entertainment | 
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