Flanagan, Sarah E.

Top Publications

Top Publications Authored or Co-Authored by "Flanagan, Sarah E."

• Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families

  Journal of Clinical Endocrinology and Metabolism, Volume 94, No. 11, Year 2009, Citations 135
• SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion

  Diabetologia, Volume 55, No. 9, Year 2012, Citations 117
• Dominant ER stress-inducing WFS1 mutations underlie a genetic syndrome of neonatal/infancy-onset diabetes, congenital sensorineural deafness, and congenital cataracts

  Diabetes, Volume 66, No. 7, Year 2017, Citations 72
• Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia

  Pediatric Diabetes, Volume 13, No. 4, Year 2012, Citations 60
• Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

  Human Molecular Genetics, Volume 23, No. 24, Year 2014, Citations 44