Stephen G. Ryan

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Carole Charlier, Nanda A. Singh, Stephen G. Ryan et al. · Nature Genetics · 1998 · 934 citations

Channelopathies, Signal Transduction, Hyperpolarization (Biology) +12

Mutations in the α1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Rita Shiang, Stephen G. Ryan, Yazhen Zhu et al. · Nature Genetics · 1993 · 551 citations

Clinical Disorders, α1 Subunit, Neurobiology Of Disease +12

A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse

Stephen G. Ryan, Marion S. Buckwalter, Joseph W. Lynch et al. · Nature Genetics · 1994 · 191 citations

Spasmodic Mouse, Molecular Physiology, Signal Transduction +9

Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing

Stephen G. Ryan, Phillip F. Chance, Changhua Zou et al. · Nature Genetics · 1997 · 132 citations

Psychiatry, Gender Studies, Sex Differences +7

Mutational analysis of familial and sporadic hyperekplexia

Rita Shiang, Stephen G. Ryan, Yazhen Zhu et al. · Annals of Neurology · 1995 · 127 citations