☰

Jennifer L. Orthmann-Murphy, Ph.D. - Publications

Affiliations: 
University of Pennsylvania, Philadelphia, PA, United States 
Area:
Peripheral nerve
Tree Info Grants Similar researchers Related pubs Distance to... Nearest Nobel PubMed Report error

12/22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Baldwin A, Copeland J, Azage M, Dratch L, Johnson K, Paul RA, Amado DA, Baer M, Deik A, Elman LB, Guo M, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, et al. Disparities in Genetic Testing for Neurologic Disorders. Neurology. 102: e209161. PMID 38447117 DOI: 10.1212/WNL.0000000000209161  0.399
2023 Dratch L, Azage M, Baldwin A, Johnson K, Paul RA, Bardakjian TM, Michon SC, Amado DA, Baer M, Deik AF, Elman LB, Gonzalez-Alegre P, Guo MH, Hamedani AG, Irwin DJ, ... ... Orthmann-Murphy J, et al. Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts. Journal of Neurology. PMID 37891417 DOI: 10.1007/s00415-023-12058-6  0.42
2021 Guo MH, Bardakjian TM, Brzozowski MR, Scherer SS, Quinn C, Elman L, Orthmann-Murphy J, Tropea TF, Ellis CA, Gonzalez-Alegre P. Temporal trends and yield of clinical diagnostic genetic testing in adult neurology. American Journal of Medical Genetics. Part A. PMID 34075706 DOI: 10.1002/ajmg.a.62372  0.414
2020 Orthmann-Murphy J, Call CL, Molina-Castro GC, Hsieh YC, Rasband MN, Calabresi PA, Bergles DE. Remyelination alters the pattern of myelin in the cerebral cortex. Elife. 9. PMID 32459173 DOI: 10.7554/Elife.56621  0.646
2020 Orthmann-Murphy J, Call CL, Molina-Castro GC, Hsieh YC, Rasband MN, Calabresi PA, Bergles DE. Author response: Remyelination alters the pattern of myelin in the cerebral cortex Elife. DOI: 10.7554/Elife.56621.Sa2  0.427
2018 Hughes EG, Orthmann-Murphy JL, Langseth AJ, Bergles DE. Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex. Nature Neuroscience. PMID 29556025 DOI: 10.1038/S41593-018-0121-5  0.635
2017 Baxi EG, DeBruin J, Jin J, Strasburger HJ, Smith MD, Orthmann-Murphy JL, Schott JT, Fairchild AN, Bergles DE, Calabresi PA. Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone-induced demyelination. Glia. PMID 28940645 DOI: 10.1002/Glia.23229  0.635
2011 Kleopa KA, Orthmann-Murphy J, Sargiannidou I. Gap junction disorders of myelinating cells. Reviews in the Neurosciences. 21: 397-419. PMID 21280457 DOI: 10.1515/REVNEURO.2010.21.5.397  0.488
2009 Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D. Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain : a Journal of Neurology. 132: 426-38. PMID 19056803 DOI: 10.1093/Brain/Awn328  0.545
2008 Orthmann-Murphy JL, Abrams CK, Scherer SS. Gap junctions couple astrocytes and oligodendrocytes. Journal of Molecular Neuroscience : Mn. 35: 101-16. PMID 18236012 DOI: 10.1007/S12031-007-9027-5  0.622
2007 Orthmann-Murphy JL, Freidin M, Fischer E, Scherer SS, Abrams CK. Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 13949-57. PMID 18094232 DOI: 10.1523/Jneurosci.3395-07.2007  0.558
2007 Orthmann-Murphy JL, Enriquez AD, Abrams CK, Scherer SS. Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease. Molecular and Cellular Neurosciences. 34: 629-41. PMID 17344063 DOI: 10.1016/J.Mcn.2007.01.010  0.559
Low-probability matches (unlikely to be authored by this person)
2017 Al Dhaibani MA, El-Hattab AW, Holroyd KB, Orthmann-Murphy J, Larson VA, Siddiqui KA, Szolics M, Schiess N. Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities. Journal of Neurogenetics. 1-5. PMID 29191078 DOI: 10.1080/01677063.2017.1404057  0.29
2019 Mu W, Schiess N, Orthmann-Murphy JL, El-Hattab AW. The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population. Journal of Neurogenetics. 1-6. PMID 30724636 DOI: 10.1080/01677063.2018.1555249  0.262
2022 Bloom MS, Orthmann-Murphy J, Grinspan JB. Motor Learning and Physical Exercise in Adaptive Myelination and Remyelination. Asn Neuro. 14: 17590914221097510. PMID 35635130 DOI: 10.1177/17590914221097510  0.256
2015 Jenssen BP, Lautz AJ, Orthmann-Murphy JL, Yum SW, Waanders A, Fox E. A 6-Year-Old With Leg Cramps. Pediatrics. 136: 732-9. PMID 26371189 DOI: 10.1542/Peds.2015-0332  0.219
2016 Schreck KC, Orthmann-Murphy JL, Newsome SD. Clinical Reasoning: A 70-year-old woman with acute-onset weakness and progressive hemiataxia. Neurology. 87: e264-e268. PMID 27895250 DOI: 10.1212/Wnl.0000000000003377  0.198
2022 Papapetropoulos S, Pontius A, Finger E, Karrenbauer V, Lynch DS, Brennan M, Zappia S, Koehler W, Schoels L, Hayer SN, Konno T, Ikeuchi T, Lund T, Orthmann-Murphy J, Eichler F, et al. Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development. Frontiers in Neurology. 12: 788168. PMID 35185751 DOI: 10.3389/fneur.2021.788168  0.193
2016 Orthmann-Murphy JL, Calabresi PA. Therapeutic application of monoclonal antibodies in multiple sclerosis. Clinical Pharmacology and Therapeutics. PMID 27804128 DOI: 10.1002/Cpt.547  0.158
2023 Koch RL, Soler-Alfonso C, Kiely BT, Asai A, Smith AL, Bali DS, Kang PB, Landstrom AP, Akman HO, Burrow TA, Orthmann-Murphy JL, Goldman DS, Pendyal S, El-Gharbawy AH, Austin SL, et al. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource. Molecular Genetics and Metabolism. 138: 107525. PMID 36796138 DOI: 10.1016/j.ymgme.2023.107525  0.155
2013 Abrams CK, Orthmann-Murphy J. Connexin Mutations in Pelizaeus-Merzbacher-Like Disease, Oculodentodigital Dysplasia and Related Diseases Gap Junctions in the Brain. 165-187. DOI: 10.1016/B978-0-12-415901-3.00010-4  0.141
2024 Adang LA, Bonkowsky JL, Boelens JJ, Mallack E, Ahrens-Nicklas R, Bernat JA, Bley A, Burton B, Darling A, Eichler F, Eklund E, Emrick L, Escolar M, Fatemi A, Fraser JL, ... ... Orthmann-Murphy J, et al. Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States. Cytotherapy. PMID 38613540 DOI: 10.1016/j.jcyt.2024.03.487  0.127
Hide low-probability matches.