Sinéad M. Murphy

Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing

Sinéad M. Murphy, Matilde Laurá, Katherine A. Fawcett et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 368 citations

Reliability of the CMT neuropathy score (second version) in Charcot‐Marie‐Tooth disease

Sinéad M. Murphy, David N. Herrmann, Michael McDermott et al. · Journal of the Peripheral Nervous System · 2011 · 347 citations · Full text

Transcriptional regulator PRDM12 is essential for human pain perception

Ya-Chun Chen, Michaela Auer‐Grumbach, Shinya Matsukawa et al. · Nature Genetics · 2015 · 170 citations · Full text

Pain Syndrome, Signal Transduction, Health Sciences +8

Genetic dysfunction of <i>MT-ATP6</i> causes axonal Charcot-Marie-Tooth disease

Robert D. S. Pitceathly, Sinéad M. Murphy, Ellen Cottenie et al. · Neurology · 2012 · 110 citations · Full text

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

Gabrielle L. Davidson, Sinéad M. Murphy, James M. Polke et al. · Journal of Neurology · 2012 · 101 citations

Mendelian Disorder, Genetic Disorder, Uk Cohort +13