| PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron NV Morgan, SK Westaway, JEV Morton, A Gregory, P Gissen, S Sonek, ... Nature genetics 38 (7), 752-754, 2006 | 574 | 2006 |
| Hypoxia upregulates the expression of the NDRG1 gene leading to its overexpression in various human cancers H Cangul BMC genetics 5, 1-11, 2004 | 239 | 2004 |
| Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial … NV Morgan, MR Morris, H Cangul, D Gleeson, A Straatman-Iwanowska, ... PLoS genetics 6 (2), e1000833, 2010 | 207 | 2010 |
| Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization AR Cullinane, A Straatman-Iwanowska, A Zaucker, Y Wakabayashi, ... Nature genetics 42 (4), 303-312, 2010 | 194 | 2010 |
| Molecular mechanisms of nickel carcinogenesis H Cangul, L Broday, K Salnikow, J Sutherland, W Peng, Q Zhang, ... Toxicology letters 127 (1-3), 69-75, 2002 | 143 | 2002 |
| Comprehensive screening of eight known causative genes in congenital hypothyroidism with gland-in-situ AK Nicholas, EG Serra, H Cangul, S Alyaarubi, I Ullah, E Schoenmakers, ... The Journal of Clinical Endocrinology & Metabolism 101 (12), 4521-4531, 2016 | 96 | 2016 |
| Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome H Smith, R Galmes, E Gogolina, A Straatman‐Iwanowska, K Reay, ... Human mutation 33 (12), 1656-1664, 2012 | 94 | 2012 |
| Enhanced expression of a novel protein in human cancer cells: a potential aid to cancer diagnosis H Cangul, K Salnikow, H Yee, D Zagzag, T Commes, M Costa Cell biology and toxicology 18, 87-96, 2002 | 81 | 2002 |
| Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community H Cangul, Z Aycan, A Olivera‐Nappa, H Saglam, NA Schoenmakers, ... Clinical endocrinology 79 (2), 275-281, 2013 | 75 | 2013 |
| Enhanced overexpression of an HIF-1/hypoxia-related protein in cancer cells. H Cangul, K Salnikow, H Yee, D Zagzag, T Commes, M Costa Environmental health perspectives 110 (suppl 5), 783-788, 2002 | 71 | 2002 |
| Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism H Cangul, XH Liao, E Schoenmakers, J Kero, S Barone, P Srichomkwun, ... JCI insight 3 (20), 2018 | 58 | 2018 |
| Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism Z Aycan, H Cangul, M Muzza, VN Bas, L Fugazzola, VK Chatterjee, ... The Journal of Clinical Endocrinology & Metabolism 102 (9), 3085-3090, 2017 | 55 | 2017 |
| Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism H Cangul, NV Morgan, JR Forman, H Saglam, Z Aycan, T Yakut, T Gulten, ... Clinical endocrinology 73 (5), 671-677, 2010 | 52 | 2010 |
| Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism H Cangul, K Boelaert, M Dogan, Y Saglam, M Kendall, TG Barrett, ... Endocrine 45, 206-212, 2014 | 31 | 2014 |
| TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis H Cangul, Z Aycan, H Saglam, JR Forman, S Cetinkaya, O Tarim, E Bober, ... Journal of Pediatric Endocrinology and Metabolism 25 (5-6), 419-426, 2012 | 30 | 2012 |
| Nanoparticle growth and surface chemistry changes in cell-conditioned culture medium M Kendall, NJ Hodges, H Whitwell, J Tyrrell, H Cangul Philosophical Transactions of the Royal Society B: Biological Sciences 370 …, 2015 | 28 | 2015 |
| A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism H Cangul, Z Aycan, M Kendall, VN Bas, Y Saglam, TG Barrett, ER Maher Journal of Pediatric Endocrinology and Metabolism 27 (3-4), 323-327, 2014 | 23 | 2014 |
| Association of urokinase gene 3′-UTR T/C polymorphism with calcium oxalate urolithiasis in children M Ozturk, Y Kordan, H Cangul, HS Dogan, H Kilicarslan, H Vuruskan, ... International urology and nephrology 40, 563-568, 2008 | 23 | 2008 |
| Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation VN Baş, H Cangul, SY Agladioglu, M Kendall, S Cetinkaya, ER Maher, ... Journal of Pediatric Endocrinology and Metabolism 25 (11-12), 1153-1156, 2012 | 22 | 2012 |
| Puberty, stress, and sudden death M Guclu, L Lin, E Erturk, JC Achermann, H Cangul The Lancet 376 (9751), 1512, 2010 | 21 | 2010 |
Eamonn MaherUniversity of CambridgeVerified email at medschl.cam.ac.uk
