Joshua Meisner, MD, PhD

Joshua Meisner
Assistant Professor of Pediatrics
Medical School
Available to mentor
Joshua Meisner, MD, PhD
Joshua Meisner
Assistant Professor
  • About
  • Qualifications
  • Center Memberships
  • Research Overview
  • Recent Publications
  • Manage Your Profile

  • About

    Dr. Meisner is a physician-scientist in Pediatric Cardiology at the University of Michigan. His clinical focus is in cardiovascular genetics collaborating in the hypertrophic cardiomyopathy, muscular dystrophy, cardiovascular genetics and aortopathy, and RASopathy multidisciplinary clinics. He also sees general cardiology and molecular and biochemical cardiology patients in his individual clinics. His translational research laboratory utilizes induced pluripotent stem cell cardiomyocyte (iPSC CM) and innovative mouse models to understanding the of pathophysiology and clinical course that leads to cardiomyopathy in children and young adults secondary to metabolic disorders (e.g. TANGO2 related metabolic encephalopathy and arrhythmia syndrome), growth signaling (e.g. RASopathies), and disruption of the cardiomyocyte contractile apparatus (e.g. MYBPC3 hypertrophic cardiomyopathy).

    Qualifications

    • Pediatric Cardiology Fellowship
      University of Michigan, Pediatric Cardiology, Ann Arbor, United States
      2018 - 2021
      Residency
    • Pediatric Resident
      University of Michigan, Pediatrics, Ann Arbor, United States
      2015 - 2018
      Residency
    • MD, PhD, Biomedical Engineering
      University of Virginia, Charlottesville, Virginia, United States
      2006 - 2015
    • MS, Biomedical Engineering
      Texas A&M University, College Station, Texas, United States
      2005 - 2006
    • BS, Biomedical Engineering
      Texas A&M University, College Station, Texas, United States
      2000 - 2004

    Center Memberships

    • Center Member
      Samuel and Jean Frankel Cardiovascular Center

    Research Overview

    My research interests focus on optimizing the care in pediatric rare disease across the spectrum from clinical research, translational studies, and basic science on the molecular mechanics of disease across the following core pathologies:

    1. The driving mechanisms and translational therapeutics in MYBPC3 related hypertrophic cardiomyopathy
    2. The role of dysfunctional mitochondrial metabolism as a driver of hypertrophic pathophysiology
    3. Molecularly guided therapies for RASopathies
    4. TANGO2 Deficiency Disorder
    5. Optimizing cellular and animal based models of pediatric onset cardiomyopathy

    Recent Publications

    See All Publications
    • Proceeding / Abstract / Poster
      LONGITUDINAL AORTIC ROOT GROWTH AND OUTCOMES IN PEDIATRIC MARFAN SYNDROME COMPARED BY BASELINE DILATION STATUS: A MULTICENTER STUDY FROM CLARITY
      Bita S, Spence C, Espahbodi N, Gwin C, Stephens S, Yetman A, Tierney S, Iannucci G, Sallee D, Nees S, Jones E, Camarda J, Holmes K, Drant S, Prakash S, Tunks R, McBridge K, Renella P, Dilorenzo M, Channing A, Steele J, Milewicz D, Meisner J, Lu J, Quezada Liuti E, Niaz T, Jacob B, Dawson T, Martin-Sheehan J, Soludczyk E, Weigand J, Morris S. 2026 Oct 4;
    • Preprint
      Genomic Engineering of Gene Dosage: A Generalizable Framework for Modeling Haploinsufficiency-Mediated Human Disorders through Splicing Modulation
      Smith ED, Meisner JK, Bullard A, Ward CB, Licata J, Smith C, Kelly CM, LaRochelle ZT, Friedline S, Renberg A, Yucius R, Lange J, Hughes ED, Saunders TL, Freeman ZT, Tsan Y-C, Previs MJ, Kitzman JO, Helms AS. 2026 Sep 22; openRxiv, DOI:10.64898/2026.09.20.753023
    • Journal Article
      Mapping and rewiring the MYBPC3 promoter for rescue of haploinsufficiency driven hypertrophic cardiomyopathy.
      Renberg A, Coppersmith S, Merritt O, Tsan Y-C, Ismail E, Licata J, Sheth M, Gupta R, Kundaje A, Friedline S, Helms HC, Hughes ED, Freeman ZT, Powell G, Ware JS, Meisner J, Smith EM, Tovar A, Engreitz JM, Kitzman J, Helms AS. bioRxiv, 2026 Sep 22; DOI:10.64898/2026.09.20.752987
      PMID: PMC13622176
    • Journal Article
      Targeted Anti-IL-1 Immunomodulatory Therapy in Pediatric Onset PPP1R13L-Related Arrhythmogenic Cardiomyopathy.
      Renberg A, Coppersmith S, Merritt O, Heider A, Helms A, Michniacki T, Luxford J, Josephi-Taylor S, Roberts P, Meisner J. Am J Med Genet A, 2026 Apr 3; DOI:10.1002/ajmg.a.70156
      PMID: 41928611
    • Presentation
      Determining the Mechanical and Metabolic Pathogenesis of MYBPC3 Related Hypertrophic Cardiomyopathy
      Meisner J. 2026 May 8;
    • Proceeding / Abstract / Poster
      A Triple Diagnosis Case Illustrating the Need for Continued Re-Evaluation
      Reeves S, Sloan-Heggen C, Whitt Z, Meisner J, Ames E, Lejman M. 2026 Mar 10;
    • Proceeding / Abstract / Poster
      AAV Gene Replacement Therapy in Mybpc3 Related Hypertrophic Cardiomyopathy Mouse Model Improves Ventricular Function
      Meisner J, Bullard A, Lange J, Friedline S, Previs M, Helms A. 2026 Mar 9;
    • Journal Article
      P407: A triple diagnosis case illustrating the need for continued re-evaluation
      Reeves S, Sloan-Heggen C, Lejman M, Whitt Z, Meisner J, Ames E. Genetics in Medicine Open, 2026 Mar 7; 4: 103901 DOI:10.1016/j.gimo.2026.103901