Sherryl A. Taylor

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

Richard H. Myers, Marcy E. MacDonald, Walter J. Koroshetz et al. · Nature Genetics · 1993 · 248 citations

Life Sciences, Genetics, Molecular Genetics +13

Quantitative neuropathological changes in presymptomatic Huntington's disease

Estrella G�mez-Tortosa, Marcy E. MacDonald, Julia C. Friend et al. · Annals of Neurology · 2001 · 166 citations

Life Sciences, Neurology, Neuroscience +12

Paternal transmission of fragile X syndrome

Susan Zeesman, Lonnie Zwaigenbaum, Donald T. Whelan et al. · American Journal of Medical Genetics Part A · 2004 · 81 citations

Life Sciences, Genetics, Molecular Genetics +13

CCMG practice guideline: laboratory guidelines for next-generation sequencing

Stacey Hume, Tanya N. Nelson, Marsha Speevak et al. · Journal of Medical Genetics · 2019 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Mutation of <i>RET</i> codon 768 is associated with the FMTC phenotype

Lara M. Boccia, Jane S. Green, Carol Joyce et al. · Clinical Genetics · 1997 · 44 citations

Medicine, Genetics, Molecular Genetics +17