S. M. Forrest

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

Sarah England, L. V. B. Nicholson, Mark Johnson et al. · Nature · 1990 · 597 citations

Urology, Medicine, Mild Muscular Dystrophy +5

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

S. M. Forrest, Gareth Cross, Andreas Speer et al. · Nature · 1987 · 196 citations

Kinesiology, Medicine, Degenerative Disease +4

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

S. M. Forrest, Gareth Cross, Tracey Flint et al. · Genomics · 1988 · 178 citations

Mendelian Disorder, Genetic Disorder, Medicine +9

A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20

Melanie A. Knight, Dena Hernández, Scott J. Diede et al. · Human Molecular Genetics · 2008 · 138 citations · Full text

Sca20 Region, Neurodegenerative Diseases, Developmental Biology +15

Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.

Howard R. Slater, J H Shaw, G.W. Dawson et al. · Journal of Medical Genetics · 1994 · 121 citations · Full text

Chromatin, Infertility, Cytogenetics +13