Mark Leppert

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

Nanda A. Singh, Carole Charlier, Dora Stauffer et al. · Nature Genetics · 1998 · 1.2K citations

Channelopathies, Molecular Neuroscience, Hyperpolarization (Biology) +12

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

Amanda K. Ewart, Colleen A. Morris, Donald L. Atkinson et al. · Nature Genetics · 1993 · 1.1K citations

Developmental Biology, Genetic Disorder, Elastin Locus +5

Localization of an ataxia-telangiectasia gene to chromosome 11q22–23

Richard A. Gatti, İzzet Berkel, Elena Boder et al. · Nature · 1988 · 685 citations

Ataxia-telangiectasia Gene, Genetic Disorder, Genetics +4

The Spectrum of Symptoms and QT Intervals in Carriers of the Gene for the Long-QT Syndrome

G. Michael Vincent, Katherine W. Timothy, Mark Leppert et al. · New England Journal of Medicine · 1992 · 624 citations

Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey <i>ras</i> -1 Gene

Mark Keating, Donald L. Atkinson, Christine Dunn et al. · Science · 1991 · 521 citations