| Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants 1958 Birth Cohort Controls: Jones Richard W 18 McArdle Wendy L 18 Ring Susan ... Nature genetics 39 (11), 1329-1337, 2007 | 1452 | 2007 |
| 2013 ETA guideline: management of subclinical hypothyroidism SHS Pearce, G Brabant, LH Duntas, F Monzani, RP Peeters, S Razvi, ... European thyroid journal 2 (4), 215-228, 2013 | 1013 | 2013 |
| 2018 European Thyroid Association guideline for the management of Graves’ hyperthyroidism GJ Kahaly, L Bartalena, L Hegedüs, L Leenhardt, K Poppe, SH Pearce European thyroid journal 7 (4), 167-186, 2018 | 919 | 2018 |
| Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GO L Bartalena, L Baldeschi, A Dickinson, A Eckstein, P Kendall-Taylor, ... European Journal of Endocrinology 158 (3), 273-285, 2008 | 892 | 2008 |
| A common molecular basis for three inherited kidney stone diseases SE Lloyd, SHS Pearce, SE Fisher, K Steinmeyer, B Schwappach, ... Nature 379 (6564), 445-449, 1996 | 834 | 1996 |
| Diagnosis and management of vitamin D deficiency SHS Pearce, TD Cheetham Bmj 340, 2010 | 823 | 2010 |
| Thyroid hormones and cardiovascular disease A Jabbar, A Pingitore, SHS Pearce, A Zaman, G Iervasi, S Razvi Nature Reviews Cardiology 14 (1), 39-55, 2017 | 680 | 2017 |
| A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor SHS Pearce, C Williamson, O Kifor, M Bai, MG Coulthard, M Davies, ... New England Journal of Medicine 335 (15), 1115-1122, 1996 | 652 | 1996 |
| Consensus statement of the European group on Graves' orbitopathy (EUGOGO) on management of Graves' orbitopathy L Bartalena, L Baldeschi, AJ Dickinson, A Eckstein, P Kendall-Taylor, ... Thyroid 18 (3), 333-346, 2008 | 612 | 2008 |
| The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves’ disease MR Velaga, V Wilson, CE Jennings, CJ Owen, S Herington, ... The Journal of Clinical Endocrinology & Metabolism 89 (11), 5862-5865, 2004 | 586 | 2004 |
| FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity M Fanciulli, PJ Norsworthy, E Petretto, R Dong, L Harper, L Kamesh, ... Nature genetics 39 (6), 721-723, 2007 | 579 | 2007 |
| Prevalence and relative risk of other autoimmune diseases in subjects with autoimmune thyroid disease K Boelaert, PR Newby, MJ Simmonds, RL Holder, JD Carr-Smith, ... The American journal of medicine 123 (2), 183. e1-183. e9, 2010 | 572 | 2010 |
| Expression and characterization of inactivating and activating mutations in the human Ca2+ o-sensing receptor M Bai, S Quinn, S Trivedi, O Kifor, SHS Pearce, MR Pollak, K Krapcho, ... Journal of Biological Chemistry 271 (32), 19537-19545, 1996 | 493 | 1996 |
| Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice J Falardeau, WCJ Chung, A Beenken, T Raivio, L Plummer, Y Sidis, ... The Journal of clinical investigation 118 (8), 2822-2831, 2008 | 482 | 2008 |
| Reversal of idiopathic hypogonadotropic hypogonadism T Raivio, J Falardeau, A Dwyer, R Quinton, FJ Hayes, VA Hughes, ... New England Journal of Medicine 357 (9), 863-873, 2007 | 475 | 2007 |
| The influence of age on the relationship between subclinical hypothyroidism and ischemic heart disease: a metaanalysis S Razvi, A Shakoor, M Vanderpump, JU Weaver, SHS Pearce The Journal of Clinical Endocrinology & Metabolism 93 (8), 2998-3007, 2008 | 467 | 2008 |
| Consensus statement on the diagnosis, treatment and follow‐up of patients with primary adrenal insufficiency ES Husebye, B Allolio, W Arlt, K Badenhoop, S Bensing, C Betterle, ... Journal of internal medicine 275 (2), 104-115, 2014 | 454 | 2014 |
| Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism N Pitteloud, R Quinton, S Pearce, T Raivio, J Acierno, A Dwyer, ... The Journal of clinical investigation 117 (2), 457-463, 2007 | 433 | 2007 |
| The incidence of ischemic heart disease and mortality in people with subclinical hypothyroidism: reanalysis of the Whickham Survey cohort S Razvi, JU Weaver, MP Vanderpump, SHS Pearce The Journal of Clinical Endocrinology & Metabolism 95 (4), 1734-1740, 2010 | 404 | 2010 |
| Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism. SH Pearce, D Trump, C Wooding, GM Besser, SL Chew, DB Grant, ... The Journal of clinical investigation 96 (6), 2683-2692, 1995 | 391 | 1995 |
