Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex EG Hughes, JL Orthmann-Murphy, AJ Langseth, DE Bergles Nature neuroscience 21 (5), 696-706, 2018 | 499 | 2018 |
Gap junctions couple astrocytes and oligodendrocytes JL Orthmann-Murphy, CK Abrams, SS Scherer Journal of Molecular Neuroscience 35, 101-116, 2008 | 259 | 2008 |
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins JL Orthmann-Murphy, M Freidin, E Fischer, SS Scherer, CK Abrams Journal of Neuroscience 27 (51), 13949-13957, 2007 | 210 | 2007 |
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations JL Orthmann-Murphy, E Salsano, CK Abrams, A Bizzi, G Uziel, ... Brain 132 (2), 426-438, 2009 | 171 | 2009 |
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus–Merzbacher-like disease JL Orthmann-Murphy, AD Enriquez, CK Abrams, SS Scherer Molecular and Cellular Neuroscience 34 (4), 629-641, 2007 | 125 | 2007 |
Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone‐induced demyelination EG Baxi, J DeBruin, J Jin, HJ Strasburger, MD Smith, ... Glia 65 (12), 2087-2098, 2017 | 100 | 2017 |
Remyelination alters the pattern of myelin in the cerebral cortex J Orthmann-Murphy, CL Call, GC Molina-Castro, YC Hsieh, MN Rasband, ... Elife 9, e56621, 2020 | 95 | 2020 |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia: review of clinical manifestations as foundations for therapeutic development S Papapetropoulos, A Pontius, E Finger, V Karrenbauer, DS Lynch, ... Frontiers in neurology 12, 788168, 2022 | 45 | 2022 |
Gap junction disorders of myelinating cells KA Kleopa, J Orthmann-Murphy, I Sargiannidou Reviews in the Neurosciences 21 (5), 397-419, 2010 | 28 | 2010 |
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource RL Koch, C Soler-Alfonso, BT Kiely, A Asai, AL Smith, DS Bali, PB Kang, ... Molecular genetics and metabolism 138 (3), 107525, 2023 | 20 | 2023 |
Temporal trends and yield of clinical diagnostic genetic testing in adult neurology MH Guo, TM Bardakjian, MR Brzozowski, SS Scherer, C Quinn, L Elman, ... American Journal of Medical Genetics Part A 185 (10), 2922-2928, 2021 | 18 | 2021 |
Therapeutic application of monoclonal antibodies in multiple sclerosis JL Orthmann‐Murphy, PA Calabresi Clinical Pharmacology & Therapeutics 101 (1), 52-64, 2017 | 17 | 2017 |
Motor learning and physical exercise in adaptive myelination and remyelination MS Bloom, J Orthmann-Murphy, JB Grinspan ASN neuro 14, 17590914221097510, 2022 | 14 | 2022 |
The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population W Mu, N Schiess, JL Orthmann-Murphy, AW El-Hattab Journal of Neurogenetics 33 (1), 21-26, 2019 | 14 | 2019 |
Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities MA Al Dhaibani, AW El-Hattab, KB Holroyd, J Orthmann-Murphy, ... Journal of neurogenetics 32 (1), 1-5, 2018 | 14 | 2018 |
Pelizaeus-Merzbacher-like disease 1 N Nahhas, A Conant, J Orthmann-Murphy, A Vanderver, G Hobson | 12 | 2019 |
Clinical reasoning: a 70-year-old woman with acute-onset weakness and progressive hemiataxia KC Schreck, JL Orthmann-Murphy, SD Newsome Neurology 87 (22), e264-e268, 2016 | 6 | 2016 |
Disparities in genetic testing for neurologic disorders A Baldwin, J Copeland, M Azage, L Dratch, K Johnson, RA Paul, ... Neurology 102 (6), e209161, 2024 | 5 | 2024 |
Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States LA Adang, JL Bonkowsky, JJ Boelens, E Mallack, R Ahrens-Nicklas, ... Cytotherapy 26 (7), 739-748, 2024 | 4 | 2024 |
Genetic testing in adults with neurologic disorders: Indications, approach, and clinical impacts L Dratch, M Azage, A Baldwin, K Johnson, RA Paul, TM Bardakjian, ... Journal of neurology 271 (2), 733-747, 2024 | 4 | 2024 |