Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene

Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations

(2011) J.-P. Riveline et al.   DIABETES CARE

MODY

(2011) Stefan S. Fajans et al.   DIABETES CARE

No beta cell desensitisation after a median of 68 months on glibenclamide therapy in patients with KCNJ11-associated permanent neonatal diabetes

(2011) D. Iafusco et al.   DIABETOLOGIA

Heterozygous ABCC8 mutations are a cause of MODY

(2011) P. Bowman et al.   DIABETOLOGIA

Exome sequencing as a tool for Mendelian disease gene discovery

(2011) Michael J. Bamshad et al.   NATURE REVIEWS GENETICS

Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

(2010) Trine W Boesgaard et al.   BMC Medical Genetics

Molecular Diagnosis of Neonatal Diabetes Mellitus Using Next-Generation Sequencing of the Whole Exome

(2010) Amélie Bonnefond et al.   PLoS One

The emerging genetics of type 2 diabetes

(2010) Amélie Bonnefond et al.   TRENDS IN MOLECULAR MEDICINE

Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retention

(2009) G. Meur et al.   DIABETES

Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes

(2008) A. Molven et al.   DIABETES

Variable phenotypic spectrum of diabetes mellitus in a family carrying a novelKCNJ11gene mutation

(2008) E. DAmato et al.   DIABETIC MEDICINE

Neonatal Diabetes Mellitus

(2008) Lydia Aguilar-Bryan et al.   ENDOCRINE REVIEWS

Diagnosis and treatment of neonatal diabetes: an United States experience†

(2008) Julie Støy et al.   PEDIATRIC DIABETES

Clinical implications of a molecular genetic classification of monogenic β-cell diabetes

(2008) Rinki Murphy et al.   Nature clinical practice. Endocrinology & metabolism