| Integrated genomic characterization of papillary thyroid carcinoma N Agrawal, R Akbani, BA Aksoy, A Ally, H Arachchi, SL Asa, JT Auman, ... Cell 159 (3), 676-690, 2014 | 2689 | 2014 |
| K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension M Choi, UI Scholl, P Yue, P Björklund, B Zhao, C Nelson-Williams, W Ji, ... Science 331 (6018), 768-772, 2011 | 1113 | 2011 |
| Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism UI Scholl, G Goh, G Stölting, RC De Oliveira, M Choi, JD Overton, ... Nature genetics 45 (9), 1050-1054, 2013 | 636 | 2013 |
| Thyroid cancer T Carling, R Udelsman Annual review of medicine 65 (1), 125-137, 2014 | 401 | 2014 |
| Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing JW Kunstman, CC Juhlin, G Goh, TC Brown, A Stenman, JM Healy, ... Human molecular genetics 24 (8), 2318-2329, 2015 | 369 | 2015 |
| Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism UI Scholl, G Stölting, C Nelson-Williams, AA Vichot, M Choi, E Loring, ... elife 4, e06315, 2015 | 338 | 2015 |
| Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor T Carling, E Szabo, M Bai, P Ridefelt, G Westin, P Gustavsson, S Trivedi, ... The Journal of Clinical Endocrinology & Metabolism 85 (5), 2042-2047, 2000 | 258 | 2000 |
| 25-Hydroxyvitamin D3-1α-Hydroxylase Expression in Normal and Pathological Parathyroid Glands U Segersten, P Correa, M Hewison, P Hellman, H Dralle, T Carling, ... The Journal of Clinical Endocrinology & Metabolism 87 (6), 2967-2972, 2002 | 253 | 2002 |
| American Thyroid Association design and feasibility of a prospective randomized controlled trial of prophylactic central lymph node dissection for papillary thyroid carcinoma T Carling, SE Carty, MM Ciarleglio, DS Cooper, GM Doherty, LT Kim, ... Thyroid 22 (3), 237-244, 2012 | 252 | 2012 |
| Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein–methyltransferase superfamily G Steele-Perkins, W Fang, XH Yang, M Van Gele, T Carling, J Gu, ... Genes & development 15 (17), 2250-2262, 2001 | 251 | 2001 |
| Tissue Distribution of Human gp330/Megalin, a Putative Ca2+-sensing Protein S Lundgren, T Carling, G Hjälm, C Juhlin, J Rastad, U Pihlgren, L Rask, ... Journal of Histochemistry & Cytochemistry 45 (3), 383-392, 1997 | 246 | 1997 |
| Hypermethylation in human cancers of the RIZ1 tumor suppressor gene, a member of a histone/protein methyltransferase superfamily Y Du, T Carling, W Fang, Z Piao, JC Sheu, S Huang Cancer research 61 (22), 8094-8099, 2001 | 242 | 2001 |
| Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors G Goh, UI Scholl, JM Healy, M Choi, ML Prasad, C Nelson-Williams, ... Nature genetics 46 (6), 613-617, 2014 | 238 | 2014 |
| Vitamin D receptor genotypes in primary hyperparathyroidism T Carling, A Kindmark, P Hellman, E Lundgren, S Ljunghall, J Rastad, ... Nature medicine 1 (12), 1309-1311, 1995 | 238 | 1995 |
| Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter T Åkerström, J Crona, A Delgado Verdugo, LF Starker, K Cupisti, ... Public Library of Science 7 (7), e41926, 2012 | 212 | 2012 |
| 4D parathyroid CT as the initial localization study for patients with de novo primary hyperparathyroidism LF Starker, A Mahajan, P Björklund, G Sze, R Udelsman, T Carling Annals of surgical oncology 18, 1723-1728, 2011 | 184 | 2011 |
| Parathyroid surgery in familial hyperparathyroid disorders T Carling, R Udelsman Journal of internal medicine 257 (1), 27-37, 2005 | 182 | 2005 |
| Parathyroid MEN1 Gene Mutations in Relation to Clinical Characteristics of Nonfamilial Primary Hyperparathyroidism T Carling, P Correa, O Hessman, J Hedberg, B Skogseid, D Lindberg, ... The Journal of Clinical Endocrinology & Metabolism 83 (8), 2960-2963, 1998 | 177 | 1998 |
| Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors T Carling, J Rastad, G Åkerström, G Westin The Journal of Clinical Endocrinology & Metabolism 83 (7), 2255-2259, 1998 | 170 | 1998 |
| Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinoma CC Juhlin, G Goh, JM Healy, AL Fonseca, UI Scholl, A Stenman, ... The Journal of Clinical Endocrinology & Metabolism 100 (3), E493-E502, 2015 | 167 | 2015 |
Per HellmanProfessor of surgery, Uppsala UniversityEmail verificata su surgsci.uu.se