D. Holmes Morton

Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2

Kevin A. Strauss, Erik G. Puffenberger, Matthew J. Huentelman et al. · New England Journal of Medicine · 2006 · 624 citations

Genetics, Neurotransmission, Social Sciences +17

A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1

Jennifer J. Johnston, Richard I. Kelley, Thomas O. Crawford et al. · The American Journal of Human Genetics · 2000 · 326 citations · Full text

Troponin T1, Genetics, Pathology +2

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Victoria Carlton, Baruch Z. Harris, Erik G. Puffenberger et al. · Nature Genetics · 2003 · 324 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +9

Diagnosis and Treatment of Maple Syrup Disease: A Study of 36 Patients

D. Holmes Morton, Kevin A. Strauss, Erik G. Puffenberger et al. · PEDIATRICS · 2002 · 321 citations

Type I glutaric aciduria, part 1: Natural history of 77 patients

Kevin A. Strauss, Erik G. Puffenberger, D. Holmes Morton · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2003 · 320 citations

Glomerular Disease, Neurological Disorder, Pathology +24