Employment

• University of Florida

Education

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Publications (17)

• Enhancing AAV9-UFμDys1 Gene Therapy Efficacy Through Immunosuppression in Mice with Pre-Existing Immunity and Enabling Redosing Strategies for Duchenne Muscular Dystrophy
  Human Gene Therapy 2025 1 citation DOI: 10.1177/10430342251385586
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• Correction: RSK phosphorylates SOS1 creating 14-3-3-docking sites and negatively regulating MAPK activation
  Biochemical Journal 2021 0 citations DOI: 10.1042/bj-2012-0938_cor
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• hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies
  Muscle & Nerve 2021 17 citations DOI: 10.1002/mus.27216
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• Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regeneration
  FEBS Open Bio 2020 30 citations DOI: 10.1002/2211-5463.13031
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• AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome
  Molecular Therapy - Methods & Clinical Development 2019 25 citations DOI: 10.1016/j.omtm.2019.01.007
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• Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy
  2019 17 citations DOI: 10.1093/hmg/ddz064
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• The impact of Megf10/Drpr gain-of-function on muscle development in Drosophila
  FEBS Letters 2019 7 citations DOI: 10.1002/1873-3468.13348
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• The impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan
  Physiological Genomics 2018 22 citations DOI: 10.1152/physiolgenomics.00036.2018
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• AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome
  Human Gene Therapy 2018 70 citations DOI: 10.1089/hum.2018.020
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• Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions
  Human Molecular Genetics 2017 51 citations DOI: 10.1093/hmg/ddx189
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