Steven S. Scherer, MD, PhD

Steven S. Scherer, MD, PhD

Penn Medicine Provider

About me

  • Vice Chair for Academic Development, Department of Neurology
  • Emeritus Professor of Neurology

My education and training

  • University of MichiganMedical School
  • University of Pennsylvania Health SystemResidency
  • University of Pennsylvania School of MedicineFellowship

Spoken languages

English
English

Insurance accepted

Please contact the practice and/or the member services department of your insurance company for specific details before receiving services. Providers may participate in some, but not all, products offered by a health plan; providers may also accept plans at some practice locations but not others.

Penn Medicine hospital privileges

  • Hospital of the University of Pennsylvania: Has privileges to treat patients in the hospital.
Dr. Scherer is a Penn Medicine physician.

Qualifications and experience

Treatments and conditions

Research

Publications

Scherer, S.S., K.A. Kleopa, and M.D. Benson Peripheral Neuropathies. , In: Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease, 6th edition,: 2020,345-375


Motley, W.W., S. Züchner, and S.S. Scherer Isoform-specific loss of Dystonin causes hereditary motor and sensory neuropathy. , Neurol. Genet., 6: 2020,e496


Sase S., A.A. Almad, C.A. Boecker, P. Guedes-Dias, J.J. Li, A. Takanohashi, A. Patel, T. McCaffrey, H. Patel, D. Sirdeshpande, J. Curiel, J.S.-H. Liu, Q. Padiath, E.L.F. Holzbaur, S.S. Scherer, A. Vanderver TUBB4A mutations results in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model. , eLife, 9: 2020,e52986


Cortese A., Y. Zhu, A.P. Rebelo, S. Negri, S. Courel, L. Abreu, C.J. Bacon, Y. Bai, D.M. Bis-Brewer, E. Bugiardini, E. Buglo, M.C. Danzi, S.M.E. Feely, A. Athanasiou-Fragkouli, N.A. Haridy, Inherited Neuropathy Consortium, R. Isasi, A. Khan, M. Laura, S. Magri, M. Pipis, C. Pisciotta, E. Powell, A.M. Rossor, P. Saveri, J.E. Sowden, S. Tozza, J. Vandrovcova, J. Dallman, E. Grignani, E. Marchioni, S.S. Scherer, B. Tang, Z. Lin, A. Al-Ajmi, R. Schule, M. Synofzik, T. Maisonobe, T. Stojkovic, M. Auer-Grumbach, M.A. Abdelhamed, S.A. Hamed, R. Zhang, F. Manganelli, L. Santoro, F. Taroni, D. Pareyson, H. Houlden, D.N. Herrmann, M.M. Reilly, M.E. Shy, R.G. Zhai, S. Züchner Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. , Nat Genet., 52: 2020,473-481


Li J.J., N. Sarute, E. Lancaster, G. Otkiran-Clare, B.M. Fagla, S.R. Ross, and S.S. Scherer A recessive Trim2 mutation causes an axonal neuropathy in mice. , Neurobiol. Dis., 140: 2020,104845


163. Fridman, V., S. Sillau, G. Acsadi, C. Bacon, K. Dooley, J. Burns, J. Day, S. Feely, R.S. Finkel, T. Grider, L. Gutmann, D.N. Herrmann, C.A. Kirk, S.A. Knause, M. Laura, R.A. Lewis, J. Li, T.E. Lloyd, I. Moroni, F. Muntoni, E. Pagliano, C. Pisciotta, G. Piscosquito, S. Ramchandren, M. Saporta, R. Sadjadi, R.R. Shy, C.E. Siskind, C.J. Sumner, D. Walk, J. Wilcox, S.W. Yum, S. Züchner, S.S. Scherer, D. Pareyson, M.M. Reilly, M.E Shy A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores. , Neurology, 94: 2020,e884-e896


Tao, F. Beecham, G. W. Rebelo, A. P. Blanton, S. H. Moran, J. J. Lopez-Anido, C. Svaren, J. Abreu, L. Rizzo, D. Kirk, C. A. Wu, X. Feely, S. Verhamme, C. Saporta, M. A. Herrmann, D. N. Day, J. W. Sumner, C. J. Lloyd, T. E. Li, J. Yum, S. W. Taroni, F. Baas, F. Choi, B. O. Pareyson, D. Scherer, S. S. Reilly, M. M. Shy, M. E. Zuchner, S. Inherited Neuropathy Consortium Modifier gene candidates in Charcot-Marie-Tooth Disease type 1A: a case-only genome-wide association study. , J. Neuromuscul. Dis., 6: 2019,201-211


Lee, D. C. Meyer-Schuman, R. Bacon, C. Shy, M. E. Antonellis, A. Scherer, S. S. A recurrent GARS mutation causes distal hereditary motor neuropathy. , J. Peripher. Nerv. Syst., 24: 2019,320-323


Lee, D. C. Dankwa, L. Edmundson, C. Cornblath, D. R. Scherer, S. S. Yield of next-generation neuropathy gene panels in axonal neuropathies. , J. Peripher. Nerv. Syst., 24: 2019,324-329


Bardakjian, T. Scherer, S.S. MT-ATP6 mutation causes a slowly progressive myeloneuropathy. , J. Neuromuscul. Disord., 6: 2019,385-387


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