Dustin Gable, MD PhD
Research & Clinical Fellow, Neuromuscular Neurology
Education and Training:​
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Fellowship
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Neuromuscular Medicine, Johns Hopkins Hospital​​​
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Post-doctoral Fellow
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Harvard and Boston Children's Hospital with Dr. Elizabeth Engle​
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Residency
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Child Neurology, Boston Children's Hospital​
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Pediatrics, Boston Combined Residency Program in Pediatrics​​
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Graduate
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MD, Johns Hopkins School of Medicine
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PhD, Johns Hopkins School of Medicine
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Human Genetics​​​
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Undergraduate
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BS, The Ohio State University
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Biomedical Science​
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Previous Positions:​
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PhD candidate
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Johns Hopkins McKusick-Nathans Institute of Genetic Medicine with Dr. Mary Armanios
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Undergraduate Research Assistant​
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​The Ohio State University Department of Cancer Biology and Genetics with Dr. Amanda Toland
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Research Interests:
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Cranial motor nerve and hindbrain development
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Non-coding RNA processing in spinal muscular atrophies
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Genetic therapies in pediatric neuromuscular disorders
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Current Projects:
Selective cranial motor neuron vulnerability and bulbar dysfunction in spinal muscular atrophy
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Small non-coding RNA processing in disorders of motor neuron and hindbrain development
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Hobbies:
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Reading, music concerts and shows, summer softball and volleyball, puzzles, coffee shops
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Contact:
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Publications:
NCBI Bibliography: https://www.ncbi.nlm.nih.gov/myncbi/1zKelktJbysIc7/bibliography/public/​
Chopra M*, Gable DL* Love-Nichols J, Tsao A, Rockowitz S, Sliz P, Barkoudah E, Bastianelli L, Coulter D, Davidson E, DeGusmao C, Fogelman D, Huth K, Marshall P, Nimec D, Sanders S, Shore B, Snyder B, Stone S, Ubeda A, Watkins C, Berde C, Bolton J, Brownstein C, Costigan M, Ebrahimi-Fakhari D, Lai A, O’Donnell A, Paciorkowski A, Pinto A, Pugh J, Rodan L, Roe E, Swanson L, Zhang B, Kruer M, Sahin M, Poduri A, Srivastava S. Mendelian Etiologies Identified with Whole Exome Sequencing in Cerebral Palsy. Ann Clin Transl Neur. 2022;9(2):193-205. PMID: 35076175, PMCID: PMC8862420
*co-first author​
Gable DL, Gaysinskaya V, Atik CC, Conover Talbot, C Jr., Kang B, Stanley SE, Pugh EW, Amat-Codina N, Mirski/Schenk K, Arcasoy MO, Brayton C, Florea L, Armanios M. ZCCHC8, the Nuclear Exosome Targeting Component, Is Mutated in Familial Pulmonary Fibrosis and Is Required for Telomerase RNA Maturation. Genes Dev. 2019;33(19-20):1381-1396. PMID: 31488579, PMCID: PMC6771387
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Stanley SE*, Gable DL*, Wagner CL, Carlile TM, Hanumanthu VS, Podlevsky JD, Khalil SE, DeZern AE, Rojas-Duran MF, Applegate CD, Alder JK, Parry EM, Gilbert WV, Armanios M. Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema. Sci Transl Med. 2016;8(351):351ra107. PMID: 27510903 PMCID: PMC5351811
*co-first author
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