| Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatasez-scores in different types of rickets S Turan, B Topcu, İ Gökçe, T Güran, Z Atay, A Omar, T Akçay, A Bereket Journal of clinical research in pediatric endocrinology 3 (1), 7, 2011 | 210 | 2011 |
| Current status of childhood obesity and its associated morbidities in Turkey A Bereket, Z Atay Journal of Clinical Research in Pediatric Endocrinology 4 (1), 1, 2012 | 201 | 2012 |
| Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor T Guran, G Tolhurst, A Bereket, N Rocha, K Porter, S Turan, FM Gribble, ... The Journal of Clinical Endocrinology & Metabolism 94 (10), 3633-3639, 2009 | 168 | 2009 |
| Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort T Guran, F Buonocore, N Saka, MN Ozbek, Z Aycan, A Bereket, F Bas, ... The Journal of Clinical Endocrinology & Metabolism 101 (1), 284-292, 2016 | 162 | 2016 |
| Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend? Z Atay, S Turan, T Guran, A Furman, A Bereket Pediatrics 128 (1), e40-e45, 2011 | 109 | 2011 |
| Current status on obesity in childhood and adolescence: Prevalence, etiology, co-morbidities and management Z Atay, A Bereket Obesity Medicine 3, 1-9, 2016 | 78 | 2016 |
| The prevalence and risk factors of premature thelarche and pubarche in 4‐to 8‐year‐old girls Z Atay, S Turan, T Guran, A Furman, A Bereket Acta Paediatrica 101 (2), e71-e75, 2012 | 77 | 2012 |
| Prevalence of type 1 diabetes mellitus in 6–18‐yr‐old school children living in Istanbul, Turkey E Akesen, S Turan, T Güran, Z Atay, D Save, A Bereket Pediatric diabetes 12 (6), 567-571, 2011 | 60 | 2011 |
| Exome sequencing of a primary ovarian insufficiency cohort reveals common molecular etiologies for a spectrum of disease A Jolly, Y Bayram, S Turan, Z Aycan, T Tos, ZY Abali, B Hacihamdioglu, ... The Journal of Clinical Endocrinology & Metabolism 104 (8), 3049-3067, 2019 | 59 | 2019 |
| Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features A Arman, A Bereket, A Coker, PÖŞ Kiper, T Güran, B Özkan, Z Atay, ... Orphanet journal of rare diseases 9, 1-8, 2014 | 49 | 2014 |
| Effect of BCG vaccine on tuberculin skin tests in 1‐6‐year‐old children A Bozaykut, IO Ipek, MY Ozkars, LP Seren, E Atay, Z Atay Acta Paediatrica 91 (2), 235-238, 2002 | 43 | 2002 |
| Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes T Guran, T Akcay, A Bereket, Z Atay, S Turan, L Haisch, M Konrad, ... Nephrology Dialysis Transplantation 27 (2), 667-673, 2012 | 42 | 2012 |
| The etiology and clinical features of non-CAH gonadotropin-independent precocious puberty: a multicenter study Z Atay, E Yesilkaya, SS Erdeve, S Turan, L Akin, E Eren, E Doger, ... The Journal of Clinical Endocrinology & Metabolism 101 (5), 1980-1988, 2016 | 40 | 2016 |
| Biallelic and monoallelic ESR2 variants associated with 46, XY disorders of sex development D Baetens, T Güran, BB Mendonca, NL Gomes, L De Cauwer, F Peelman, ... Genetics in Medicine 20 (7), 717-727, 2018 | 38 | 2018 |
| GCK gene mutations are a common cause of childhood‐onset MODY (maturity‐onset diabetes of the young) in Turkey B Haliloglu, G Hysenaj, Z Atay, T Guran, S Abalı, S Turan, A Bereket, ... Clinical endocrinology 85 (3), 393-399, 2016 | 36 | 2016 |
| Homozygous Loss-of-function Mutations in SOHLH1 in Patients With Nonsyndromic Hypergonadotropic Hypogonadism Y Bayram, S Gulsuner, T Guran, A Abaci, G Yesil, HU Gulsuner, Z Atay, ... The Journal of Clinical Endocrinology & Metabolism 100 (5), E808-E814, 2015 | 36 | 2015 |
| Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet Z Atay, A Bereket, B Haliloglu, S Abali, T Ozdogan, E Altuncu, L Canaff, ... Bone 64, 102-107, 2014 | 36 | 2014 |
| Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in children S Bas, T Guran, Z Atay, B Haliloglu, S Abalı, S Turan, A Bereket Hormone research in paediatrics 83 (4), 282-287, 2015 | 34 | 2015 |
| An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W) S Turan, C Hughes, Z Atay, T Guran, B Haliloglu, AJL Clark, A Bereket, ... The Journal of Clinical Endocrinology & Metabolism 97 (5), E771-E774, 2012 | 34 | 2012 |
| Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS S Turan, S Thiele, O Tafaj, B Brix, Z Atay, S Abali, B Haliloglu, A Bereket, ... Bone 71, 53-57, 2015 | 33 | 2015 |
