Ruth M. Shepherd

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

Maria Bitner‐Glindzicz, Keith Lindley, Paul Rutland et al. · Nature Genetics · 2000 · 324 citations

Infantile Hyperinsulinism, Mendelian Disorder, Genetic Disorder +9

Loss of functional KATP channels in pancreatic β–cells causes persistent hyperinsulinemic hypoglycemia of infancy

Charlotte Kane, Ruth M. Shepherd, Paul E. Squires et al. · Nature Medicine · 1996 · 227 citations

Molecular Physiology, Signal Transduction, Persistent Hyperinsulinemic Hypoglycemia +10

Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor

Mark J. Dunne, Charlotte Kane, Ruth M. Shepherd et al. · New England Journal of Medicine · 1997 · 222 citations · Full text

Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade.

Keith Lindley, Mark J. Dunne, Cheikhou Kane et al. · Archives of Disease in Childhood · 1996 · 90 citations · Full text

Glucose-Dependent Modulation of Insulin Secretion and Intracellular Calcium Ions by GKA50, a Glucokinase Activator

Daniel J. Johnson, Ruth M. Shepherd, Debra Gill et al. · Diabetes · 2007 · 88 citations

Intracellular Calcium Ions, Insulin Signaling, Gastrointestinal Peptide Hormone +19