Biography

Medical School: University of Washington

Internship, residency in Internal Medicine: Baltimore City Hospitals (Johns Hopkins Bayview)

Residency in Neurology: Johns Hopkins Hospital

Fellowship in Neuromuscular Disease: Johns Hopkins Hospital

Education

Medical School
University of Washington School of Medicine (1969)
Internship
Baltimore City Hospital (1970), Internal Medicine
Residency
Johns Hopkins Bayview Medical Center (1974), Neurology
Fellowship
Johns Hopkins University School of Medicine (1976), Neuromuscular Disease

Research Interest

  • Exercise physiology
  • Metabolic disorders of muscle
  • Neuromuscular Disease

Publications

Featured Publications LegendFeatured Publications

Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy (MOTOR trial).
Madsen KL, Buch AE, Cohen BH, Falk MJ, Goldsberry A, Goldstein A, Karaa A, Koenig MK, Muraresku CC, Meyer C, O'Grady M, Scaglia F, Shieh PB, Vockley J, Zolkipli-Cunningham Z, Haller RG, Vissing J, Neurology 2020 Jan
No effect of triheptanoin on exercise performance in McArdle disease.
Madsen KL, Laforêt P, Buch AE, Stemmerik MG, Ottolenghi C, Hatem SN, Raaschou-Pedersen DT, Poulsen NS, Atencio M, Luton MP, Ceccaldi A, Haller RG, Quinlivan R, Mochel F, Vissing J, Ann Clin Transl Neurol 2019 Sep
Progressive Exercise Training Improves Maximal Aerobic Capacity in Individuals with Well-Healed Burn Injuries.
Romero SA, Moralez G, Jaffery MF, Huang M, Cramer MN, Romain N, Kouda K, Haller RG, Crandall CG, Am. J. Physiol. Regul. Integr. Comp. Physiol. 2019 Aug
Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiency.
Vissing J, Akman HO, Aasly J, Kahler SG, Bacino CA, DiMauro S, Haller RG Neurology 2018 Aug
Acute loss of iron-sulfur clusters results in metabolic reprogramming and generation of lipid droplets in mammalian cells.
Crooks DR, Maio N, Lane AN, Jarnik M, Higashi RM, Haller RG, Yang Y, Fan TWM, Linehan M, Rouault TA J. Biol. Chem. 2018 Mar
Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.
Rocha MC, Rosa HS, Grady JP, Blakely EL, He L, Romain N, Haller RG, Newman J, McFarland R, Ng YS, Gorman GS, Schaefer AM, Tuppen HA, Taylor RW, Turnbull DM Ann. Neurol. 2017 Dec
Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency.
Preisler N, Cohen J, Vissing CR, Madsen KL, Heinicke K, Sharp LJ, Phillips L, Romain N, Park SY, Newby M, Wyrick P, Mancias P, Galbo H, Vissing J, Haller RG Mol. Genet. Metab. 2017 Aug
Metabolic profiles of exercise in patients with McArdle disease or mitochondrial myopathy.
Delaney NF, Sharma R, Tadvalkar L, Clish CB, Haller RG, Mootha VK Proc. Natl. Acad. Sci. U.S.A. 2017 Jul
Use of antisense oligonucleotides to correct the splicing error in ISCU myopathy patient cell lines.
Holmes-Hampton GP, Crooks DR, Haller RG, Guo S, Freier SM, Monia BP, Rouault TA Hum. Mol. Genet. 2016 Oct
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype.
Alston CL, Compton AG, Formosa LE, Strecker V, Oláhová M, Haack TB, Smet J, Stouffs K, Diakumis P, Ciara E, Cassiman D, Romain N, Yarham JW, He L, De Paepe B, Vanlander AV, Seneca S, Feichtinger RG, Ploski R, Rokicki D, Pronicka E, Haller RG, Van Hove JL, Bahlo M, Mayr JA, Van Coster R, Prokisch H, Wittig I, Ryan MT, Thorburn DR, Taylor RW Am. J. Hum. Genet. 2016 Jul 99 1 217-27

Professional Associations/Affiliations

  • American Academy of Neurology
  • American Neurological Association
  • International Society of Myochemistry
  • Johns Hopkins Medical & Surgical Association