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Mark Gurnell
Mark Gurnell
Institute of Metabolic Science & Department of Medicine, University of Cambridge
Verified email at medschl.cam.ac.uk - Homepage
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Cited by
Cited by
Year
Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension
I Barroso, M Gurnell, VEF Crowley, M Agostini, JW Schwabe, MA Soos, ...
Nature 402 (6764), 880-883, 1999
17691999
Human metabolic syndrome resulting from dominant-negative mutations in the nuclear receptor peroxisome proliferator-activated receptor-γ
DB Savage, GD Tan, CL Acerini, SA Jebb, M Agostini, M Gurnell, ...
Diabetes 52 (4), 910-917, 2003
5802003
Second-to-fourth digit ratio predicts success among high-frequency financial traders
JM Coates, M Gurnell, A Rustichini
Proceedings of the national academy of sciences 106 (2), 623-628, 2009
4922009
A mutation in the thyroid hormone receptor alpha gene
E Bochukova, N Schoenmakers, M Agostini, E Schoenmakers, ...
New England Journal of Medicine 366 (3), 243-249, 2012
4162012
Consensus on diagnosis and management of Cushing's disease: a guideline update
M Fleseriu, R Auchus, I Bancos, A Ben-Shlomo, J Bertherat, NR Biermasz, ...
The lancet Diabetes & endocrinology 9 (12), 847-875, 2021
4042021
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
3652021
A dominant-negative peroxisome proliferator-activated receptor γ (PPARγ) mutant is a constitutive repressor and inhibits PPARγ-mediated adipogenesis
M Gurnell, JM Wentworth, M Agostini, M Adams, TN Collingwood, ...
Journal of Biological Chemistry 275 (8), 5754-5759, 2000
3532000
Pitfalls in the measurement and interpretation of thyroid function tests
O Koulouri, C Moran, D Halsall, K Chatterjee, M Gurnell
Best practice & research Clinical endocrinology & metabolism 27 (6), 745-762, 2013
3292013
Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
E Schoenmakers, M Agostini, C Mitchell, N Schoenmakers, L Papp, ...
The Journal of clinical investigation 120 (12), 4220-4235, 2010
3162010
Cortisol shifts financial risk preferences
N Kandasamy, B Hardy, L Page, M Schaffner, J Graggaber, AS Powlson, ...
Proceedings of the National Academy of Sciences 111 (9), 3608-3613, 2014
2962014
The metabolic syndrome: peroxisome proliferator-activated receptor γ and its therapeutic modulation
M Gurnell, DB Savage, VKK Chatterjee, S O’Rahilly
The Journal of Clinical Endocrinology & Metabolism 88 (6), 2412-2421, 2003
2822003
A consensus on the diagnosis and treatment of acromegaly comorbidities: an update
A Giustina, A Barkan, A Beckers, N Biermasz, BMK Biller, C Boguszewski, ...
The Journal of Clinical Endocrinology & Metabolism 105 (4), e937-e946, 2020
2792020
Traumatic brain injury: progress and challenges in prevention, clinical care, and research
AIR Maas, DK Menon, GT Manley, M Abrams, C Åkerlund, N Andelic, ...
The Lancet Neurology 21 (11), 1004-1060, 2022
2752022
Management of primary hypothyroidism: statement by the British Thyroid Association Executive Committee
O Okosieme, J Gilbert, P Abraham, K Boelaert, C Dayan, M Gurnell, ...
Clinical endocrinology 84 (6), 799-808, 2016
2602016
Multidisciplinary management of acromegaly: a consensus
A Giustina, G Barkhoudarian, A Beckers, A Ben-Shlomo, N Biermasz, ...
Reviews in Endocrine and Metabolic Disorders 21, 667-678, 2020
2372020
Evaluation of the Sensitivity and Specificity of 11C-Metomidate Positron Emission Tomography (PET)-CT for Lateralizing Aldosterone Secretion by Conn's Adenomas
TJ Burton, IS Mackenzie, K Balan, B Koo, N Bird, DV Soloviev, ...
The Journal of Clinical Endocrinology & Metabolism 97 (1), 100-109, 2012
2332012
Non-DNA binding, dominant-negative, human PPARγ mutations cause lipodystrophic insulin resistance
M Agostini, E Schoenmakers, C Mitchell, I Szatmari, D Savage, A Smith, ...
Cell metabolism 4 (4), 303-311, 2006
2172006
Effectiveness of metyrapone in treating Cushing's syndrome: a retrospective multicenter study in 195 patients
E Daniel, S Aylwin, O Mustafa, S Ball, A Munir, K Boelaert, V Chortis, ...
The Journal of Clinical Endocrinology & Metabolism 100 (11), 4146-4154, 2015
2082015
Digenic inheritance of severe insulin resistance in a human pedigree
DB Savage, M Agostini, I Barroso, M Gurnell, J Luan, A Meirhaeghe, ...
Nature genetics 31 (4), 379-384, 2002
1852002
Elevated plasma adiponectin in humans with genetically defective insulin receptors
RK Semple, MA Soos, J Luan, CS Mitchell, JC Wilson, M Gurnell, ...
The Journal of Clinical Endocrinology & Metabolism 91 (8), 3219-3223, 2006
1842006
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