Annia K. Cherryson

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

Garth A. Nicholson, Linda J. Valentijn, Annia K. Cherryson et al. · Nature Genetics · 1994 · 227 citations

Peripheral Nerves, Genetic Disorder, Medicine +9

The gene for hereditary sensory neuropathy type I (HSN–I) maps to chromosome 9q22.1–q22.3

Garth A. Nicholson, Jennifer L. Dawkins, Ian P. Blair et al. · Nature Genetics · 1996 · 120 citations

Molecular Neuroscience, Genetic Disorder, Genetics +7

Analysis of mutations at the neurofibromatosis 1 (NF1) locus.

Meena Upadhyaya, Ming Shen, Annia K. Cherryson et al. · Human Molecular Genetics · 1992 · 73 citations

Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis

Betsy A. Hosler, Garth A. Nicholson, Peter C. Sapp et al. · Neuromuscular Disorders · 1996 · 51 citations

Amyotrophic Lateral Sclerosis, Neurological Disorder, Genetics +8

Mutational studies in X-linked Charcot-Marie-Tooth disease (CMTX)

Annia K. Cherryson, Leone Yeung, Marina Kennerson et al. · The American Journal of Human Genetics · 1994 · 13 citations