| Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism RR Kapoor, SE Flanagan, VB Arya, JP Shield, S Ellard, K Hussain European journal of endocrinology 168 (4), 557-564, 2013 | 247 | 2013 |
| Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia S Senniappan, S Alexandrescu, N Tatevian, P Shah, V Arya, S Flanagan, ... New England Journal of Medicine 370 (12), 1131-1137, 2014 | 143 | 2014 |
| Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management Z Mohamed, VB Arya, K Hussain Journal of clinical research in pediatric endocrinology 4 (4), 169, 2012 | 101 | 2012 |
| Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism VB Arya, S Senniappan, H Demirbilek, S Alam, SE Flanagan, S Ellard, ... PloS one 9 (5), e98054, 2014 | 97 | 2014 |
| The molecular mechanisms, diagnosis and management of congenital hyperinsulinism S Senniappan, VB Arya, K Hussain Indian journal of endocrinology and metabolism 17 (1), 19-30, 2013 | 70 | 2013 |
| Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations H Demirbilek, VB Arya, MN Ozbek, JAL Houghton, RT Baran, M Akar, ... European Journal of Endocrinology 172 (6), 697-705, 2015 | 67 | 2015 |
| Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy H Demirbilek, P Shah, VB Arya, L Hinchey, SE Flanagan, S Ellard, ... The Journal of Clinical Endocrinology & Metabolism 99 (10), 3660-3667, 2014 | 64 | 2014 |
| Hyperinsulinaemic hypoglycaemia VB Arya, Z Mohammed, O Blankenstein, P De Lonlay, K Hussain Hormone and Metabolic Research 46 (03), 157-170, 2014 | 55 | 2014 |
| Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age VB Arya, SE Flanagan, A Kumaran, JP Shield, S Ellard, K Hussain, ... Archives of Disease in Childhood-Fetal and Neonatal Edition 98 (4), F356-F358, 2013 | 55 | 2013 |
| Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations VB Arya, M Guemes, A Nessa, S Alam, P Shah, C Gilbert, S Senniappan, ... European journal of endocrinology 171 (6), 685-695, 2014 | 54 | 2014 |
| Neonatal hypoglycemia VB Arya, S Senniappan, M Guemes, K Hussain The Indian Journal of Pediatrics 81, 58-65, 2014 | 53 | 2014 |
| HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity‐onset diabetes of the young, and incretin response VB Arya, S Rahman, S Senniappan, SE Flanagan, S Ellard, K Hussain Diabetic Medicine 31 (3), e11-e15, 2014 | 41 | 2014 |
| Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients R Padidela, M Fiest, V Arya, VV Smith, M Ashworth, D Rampling, ... European journal of endocrinology 170 (5), 741-747, 2014 | 40 | 2014 |
| Activating AKT2 Mutation: Hypoinsulinemic Hypoketotic Hypoglycemia VB Arya, SE Flanagan, E Schober, B Rami-Merhar, S Ellard, K Hussain The Journal of Clinical Endocrinology & Metabolism 99 (2), 391-394, 2014 | 39 | 2014 |
| Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation P Shah, VB Arya, SE Flanagan, K Morgan, S Ellard, S Senniappan, ... Journal of Pediatric Endocrinology and Metabolism 28 (5-6), 695-699, 2015 | 29 | 2015 |
| Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy VB Arya, Q Aziz, A Nessa, A Tinker, K Hussain International Journal of Pediatric Endocrinology 2014, 1-5, 2014 | 28 | 2014 |
| Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations H Demirbilek, VB Arya, MN Ozbek, A Akinci, M Dogan, F Demirel, ... European journal of endocrinology 170 (6), 885-892, 2014 | 24 | 2014 |
| Efficacy of oral phenobarbitone in term" at risk" neonates in decreasing neonatal hyperbilirubinemia: A randomized double-blinded, placebo controlled trial VB Arya, R Agarwal, VK Paul, AK Deorari Indian pediatrics 41 (4), 327-334, 2004 | 20 | 2004 |
| Xq27.1 Duplication Encompassing SOX3: Variable Phenotype and Smallest Duplication Associated with Hypopituitarism to Date – A Large Case Series of … VB Arya, G Chawla, AKR Nambisan, N Muhi-Iddin, E Vamvakiti, ... Hormone Research in Paediatrics 92 (6), 382-389, 2020 | 16 | 2020 |
| Elemental formula associated hypophosphataemic rickets S Uday, S Sakka, JH Davies, T Randell, V Arya, C Brain, M Tighe, ... Clinical nutrition 38 (5), 2246-2250, 2019 | 16 | 2019 |
Sarah FlanaganProfessor in Genomic Medicine, Wellcome Trust Senior Research FellowVerified email at exeter.ac.uk
