Guftar Shaikh

Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss

A Rajab, Daniel Kelberman, Sandra C. de Castro et al. · Human Molecular Genetics · 2008 · 103 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Syndromic Obesity and Diabetes: Changes in Body Composition with Age and Mutation Analysis of ALMS1 in 12 United Kingdom Kindreds with Alstrom Syndrome

Jayne A.L. Minton, Katharine R. Owen, Christopher J. Ricketts et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 99 citations

Medicine, Endocrinology, Genetics +17

Assessment of childhood obesity in secondary care: OSCA consensus statement

Russell Viner, Billy White, Timothy Barrett et al. · Archives of Disease in Childhood Education & Practice · 2012 · 42 citations

Medicine, Child Health, Pediatrics +15

Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

Maik Welzel, Nele Wüstemann, Gunter Ŝimić-Schleicher et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 35 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism

Jayne Houghton, Indraneel Banerjee, Guftar Shaikh et al. · The Journal of Pathology Clinical Research · 2019 · 30 citations · Full text

Medicine, Endocrinology, Genetics +17