Findlay Lab

Andrew Findlay, MD

Andrew Findlay is interested in translating pathomechanism into therapeutic strategies for hereditary muscle disorders such as muscular dystrophy and age associated muscle disorders such as sarcopenia.

Principal investigator

Andrew Findlay, MD

Andrew Findlay, MD

Assistant Professor of Neurology

Recent publications

  • Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches
    Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approachesFindlay, A. R., Oct 2024, In: DMM Disease Models and Mechanisms. 17, 10, dmm050720.Research output: Contribution to journal › Review article › peer-review
  • Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1
    Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1Robinson, S. E., Findlay, A. R., Li, S., Wang, F., Schiava, M., Daw, J., Diaz-Manera, J., Chou, T. F. & Weihl, C., Sep 12 2024, In: Neurology: Genetics. 10, 5, e200191.Research output: Contribution to journal › Article › peer-review
  • DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1
    DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1Findlay, A. R., Paing, M. M., Daw, J. A., Haller, M., Bengoechea, R., Pittman, S. K., Li, S., Wang, F., Miller, T. M., True, H. L., Chou, T. F. & Weihl, C. C., Jun 13 2023, In: Molecular Therapy Nucleic Acids. 32, p. 937-948 12 p.Research output: Contribution to journal › Article › peer-review
  • LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials
    LGMDD1 natural history and phenotypic spectrum: Implications for clinical trialsFindlay, A. R., Robinson, S. E., Poelker, S., Seiffert, M., Bengoechea, R. & Weihl, C. C., Feb 2023, In: Annals of Clinical and Translational Neurology. 10, 2, p. 181-194 14 p.Research output: Contribution to journal › Article › peer-review
  • Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure
    Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureWeihl, C. C., Töpf, A., Bengoechea, R., Duff, J., Charlton, R., Garcia, S. K., Domínguez-González, C., Alsaman, A., Hernández-Laín, A., Franco, L. V., Sanchez, M. E. P., Beecroft, S. J., Goullee, H., Daw, J., Bhadra, A., True, H., Inoue, M., Findlay, A. R., Laing, N. & Olivé, M. & 2 others, Ravenscroft, G. & Straub, V., Jan 2023, In: Acta Neuropathologica. 145, 1, p. 127-143 17 p.Research output: Contribution to journal › Article › peer-review
Complete bibliography