B. N. Cockburn

Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene.

Tom H. Lindner, Claudia Gragnoli, Hiroto Furuta et al. · Journal of Clinical Investigation · 1997 · 81 citations · Full text

Genetics, Pathology, Molecular Genetics +21

Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor‐1α genes in patients with early‐onset Type 2 diabetes mellitus/MODY

Maggie Ng, B. N. Cockburn, Tom H. Lindner et al. · Diabetic Medicine · 1999 · 55 citations

Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1α and glucokinase

Claudia Gragnoli, B. N. Cockburn, F. Chiaramonte et al. · Diabetologia · 2001 · 54 citations · Full text

Metabolic Syndrome, Diabetes Epidemiology, Hepatology +12

Prevalence of the metabolic syndrome in patients with diabetes mellitus

F Al-Saraj, John McDermott, TJ Cawood et al. · Irish Journal of Medical Science (1971 -) · 2009 · 39 citations

Obesity, Metabolic Syndrome, Body Composition +8

Adaptation to hyperglycemia enhances insulin secretion in glucokinase mutant mice.

Séamus Sreenan, B. N. Cockburn, Aaron C. Baldwin et al. · Diabetes · 1998 · 26 citations

Insulin Signaling, Gastrointestinal Peptide Hormone, Metabolic Syndrome +19