Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene IS Farooqi, JM Keogh, GSH Yeo, EJ Lank, T Cheetham, S O'Rahilly New England Journal of Medicine 348 (12), 1085-1095, 2003 | 2030 | 2003 |
Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency IS Farooqi, GSH Yeo, JM Keogh, S Aminian, SA Jebb, G Butler, ... The Journal of clinical investigation 106 (2), 271-279, 2000 | 1005 | 2000 |
Diagnosis and management of vitamin D deficiency SHS Pearce, TD Cheetham Bmj 340, 2010 | 791 | 2010 |
A POMC variant implicates β-melanocyte-stimulating hormone in the control of human energy balance YS Lee, BG Challis, DA Thompson, GSH Yeo, JM Keogh, ME Madonna, ... Cell metabolism 3 (2), 135-140, 2006 | 287 | 2006 |
Improving the vitamin D status of vitamin D deficient adults is associated with improved mitochondrial oxidative function in skeletal muscle A Sinha, KG Hollingsworth, S Ball, T Cheetham The Journal of Clinical Endocrinology & Metabolism 98 (3), E509-E513, 2013 | 272 | 2013 |
A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1 SHS Pearce, T Cheetham, H Imrie, B Vaidya, ND Barnes, RW Bilous, ... The American Journal of Human Genetics 63 (6), 1675-1684, 1998 | 204 | 1998 |
Human SH2B1 mutations are associated with maladaptive behaviors and obesity ME Doche, EG Bochukova, HW Su, LR Pearce, JM Keogh, E Henning, ... The Journal of clinical investigation 122 (12), 4732-4736, 2012 | 198 | 2012 |
Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers LC Hernández-Ramírez, P Gabrovska, J Dénes, K Stals, G Trivellin, ... The Journal of Clinical Endocrinology & Metabolism 100 (9), E1242-E1254, 2015 | 177 | 2015 |
X-linked acrogigantism syndrome: clinical profile and therapeutic responses A Beckers, MB Lodish, G Trivellin, L Rostomyan, M Lee, FR Faucz, ... Endocrine-related cancer 22 (3), 353-367, 2015 | 176 | 2015 |
Diabetes insipidus PH Baylis, T Cheetham Archives of Disease in Childhood 79 (1), 84-89, 1998 | 172 | 1998 |
A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics LA Allen, JC Achermann, P Pakarinen, TJ Kotlar, IT Huhtaniemi, ... Human Reproduction 18 (2), 251-256, 2003 | 154 | 2003 |
Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility A Sutherland, J Davies, CJ Owen, S Vaikkakara, C Walker, TD Cheetham, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 3338-3341, 2007 | 138 | 2007 |
Catch-up growth and metabolic outcomes in adolescents born preterm ND Embleton, M Korada, CL Wood, MS Pearce, R Swamy, TD Cheetham Archives of disease in childhood 101 (11), 1026-1031, 2016 | 136 | 2016 |
Preterm birth and subsequent insulin sensitivity: a systematic review R Tinnion, J Gillone, T Cheetham, N Embleton Archives of disease in childhood 99 (4), 362-368, 2014 | 133 | 2014 |
Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome CJ Owen, CE Jennings, H Imrie, A Lachaux, NA Bridges, TD Cheetham, ... The Journal of Clinical Endocrinology & Metabolism 88 (12), 6034-6039, 2003 | 133 | 2003 |
Puberty: Normal physiology (brief overview) CL Wood, LC Lane, T Cheetham Best practice & research Clinical endocrinology & metabolism 33 (3), 101265, 2019 | 128 | 2019 |
Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency KS Alatzoglou, JP Turton, D Kelberman, PE Clayton, A Mehta, ... The Journal of Clinical Endocrinology & Metabolism 94 (9), 3191-3199, 2009 | 126 | 2009 |
The effect of cessation of growth hormone (GH) therapy on bone mineral accretion in GH-deficient adolescents at the completion of linear growth WM Drake, PV Carroll, KT Maher, KA Metcalfe, C Camacho-Hubner, ... The Journal of Clinical Endocrinology & Metabolism 88 (4), 1658-1663, 2003 | 117 | 2003 |
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study D Iacovazzo, R Caswell, B Bunce, S Jose, B Yuan, ... Acta neuropathologica communications 4, 1-12, 2016 | 116 | 2016 |
Difficulties in selecting an appropriate neonatal thyroid stimulating hormone (TSH) screening threshold SM Korada, M Pearce, MPW Platt, E Avis, S Turner, H Wastell, ... Archives of disease in childhood 95 (3), 169-173, 2010 | 114 | 2010 |