Margaret H. Abbott

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

S.-H. Li, Gabriele Schilling, W. Scott Young et al. · Neuron · 1993 · 342 citations

Genetic Disorder, Natural Sciences, Disease Gene +8

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran et al. · The American Journal of Human Genetics · 2005 · 276 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10

A type X collagen mutation causes Schmid metaphyseal chondrodysplasia

Matthew L. Warman, Margaret H. Abbott, Suneel Apte et al. · Nature Genetics · 1993 · 267 citations

Mendelian Disorder, Genetic Disorder, Schmid Metaphyseal Chondrodysplasia +5

Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease.

Neal G. Ranen, O. Colin Stine, Margaret H. Abbott et al. · PubMed · 1995 · 241 citations

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15

O.Collin Stine, N. Pleasant, Mary L. Franz et al. · Human Molecular Genetics · 1993 · 232 citations