| Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management S Senniappan, B Shanti, C James, K Hussain Journal of inherited metabolic disease 35, 589-601, 2012 | 176 | 2012 |
| 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 | 153 | 2014 |
| 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 |
| Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities D Giri, ML Vignola, A Gualtieri, V Scagliotti, P McNamara, M Peak, M Didi, ... Human molecular genetics 26 (22), 4315-4326, 2017 | 84 | 2017 |
| 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 |
| Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing A Ghosh, H Schlecht, LE Heptinstall, JK Bassett, E Cartwright, SS Bhaskar, ... Archives of Disease in Childhood 102 (11), 1019-1029, 2017 | 62 | 2017 |
| Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control D Giri, D Pintus, G Burnside, A Ghatak, F Mehta, P Paul, S Senniappan BMC research notes 10, 1-5, 2017 | 59 | 2017 |
| 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 |
| Childhood obesity: A review of current and future management options LJ Apperley, J Blackburn, K Erlandson‐Parry, L Gait, P Laing, ... Clinical Endocrinology 96 (3), 288-301, 2022 | 41 | 2022 |
| 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 |
| Mode of clinical presentation and delayed diagnosis of Turner syndrome: a single Centre UK study L Apperley, U Das, R Ramakrishnan, P Dharmaraj, J Blair, M Didi, ... International Journal of Pediatric Endocrinology 2018, 1-6, 2018 | 40 | 2018 |
| Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389 D Yau, TW Laver, A Dastamani, S Senniappan, JAL Houghton, G Shaikh, ... PLoS One 15 (2), e0228417, 2020 | 36 | 2020 |
| Diazoxide‐induced pulmonary hypertension in hyperinsulinaemic hypoglycaemia: Recommendations from a multicentre study in the United Kingdom SC Chen, A Dastamani, D Pintus, D Yau, S Aftab, L Bath, C Swinburne, ... Clinical Endocrinology 91 (6), 770-775, 2019 | 35 | 2019 |
| Pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus (PHID) syndrome is associated with severe chronic inflammation and cardiomyopathy, and … S Senniappan, M Hughes, P Shah, V Shah, JP Kaski, P Brogan, ... Journal of Pediatric Endocrinology and Metabolism 26 (9-10), 877-882, 2013 | 35 | 2013 |
| Use of long-acting somatostatin analogue (lanreotide) in an adolescent with diazoxide-responsive congenital hyperinsulinism and its psychological impact P Shah, SA Rahman, S McElroy, C Gilbert, K Morgan, L Hinchey, ... Hormone Research in Paediatrics 84 (5), 355-360, 2015 | 34 | 2015 |
| Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management D Giri, K Hawton, S Senniappan Journal of Pediatric Endocrinology and Metabolism 35 (3), 279-296, 2022 | 29 | 2022 |
| 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 |
| Continuous Flash Glucose Monitoring in children with Congenital Hyperinsulinism; first report on accuracy and patient experience H Alsaffar, L Turner, Z Yung, M Didi, S Senniappan International Journal of Pediatric Endocrinology 2018, 1-6, 2018 | 27 | 2018 |
| Clinical profile and outcome of infantile onset diabetes mellitus in southern India P Varadarajan, T Sangaralingam, S Senniappan, S Jahnavi, V Radha, ... Indian pediatrics 50, 759-763, 2013 | 20 | 2013 |
