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T Cheetham
T Cheetham
Unknown affiliation
Verified email at newcastle.ac.uk
Title
Cited by
Cited by
Year
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
20302003
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
10052000
Diagnosis and management of vitamin D deficiency
SHS Pearce, TD Cheetham
Bmj 340, 2010
7912010
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
2872006
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
2722013
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
2041998
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
1982012
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
1772015
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
1762015
Diabetes insipidus
PH Baylis, T Cheetham
Archives of Disease in Childhood 79 (1), 84-89, 1998
1721998
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
1542003
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
1382007
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
1362016
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
1332014
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
1332003
Puberty: Normal physiology (brief overview)
CL Wood, LC Lane, T Cheetham
Best practice & research Clinical endocrinology & metabolism 33 (3), 101265, 2019
1282019
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
1262009
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
1172003
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
1162016
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
1142010
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