| TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction AK Topaloglu, F Reimann, M Guclu, AS Yalin, LD Kotan, KM Porter, ... Nature genetics 41 (3), 354-358, 2009 | 1035 | 2009 |
| Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism AK Topaloglu, JA Tello, LD Kotan, MN Ozbek, MB Yilmaz, S Erdogan, ... New England Journal of Medicine 366 (7), 629-635, 2012 | 548 | 2012 |
| 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 | 176 | 2016 |
| Incidence of type 1 diabetes mellitus in Turkish children from the southeastern region of the country: a regional report H Demirbilek, MN Özbek, RT Baran Journal of clinical research in pediatric endocrinology 5 (2), 98, 2013 | 86 | 2013 |
| Turner syndrome and associated problems in Turkish children: a multicenter study E Yeşilkaya, A Bereket, F Darendeliler, F Baş, Ş Poyrazoğlu, BK Aydın, ... Journal of Clinical Research in Pediatric Endocrinology 7 (1), 27, 2015 | 78 | 2015 |
| YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress E De Franco, M Lytrivi, H Ibrahim, H Montaser, MN Wakeling, F Fantuzzi, ... The Journal of clinical investigation 130 (12), 6338-6353, 2020 | 71 | 2020 |
| Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations H Demirbilek, VB Arya, MN Ozbek, JAL Houghton, RT Baran, M Akar, ... European Journal of Endocrinology 172 (6), 697-705, 2015 | 69 | 2015 |
| Wolcott–Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature* MN Ozbek, V Senée, S Aydemir, LD Kotan, NO Mungan, B Yuksel, ... Pediatric diabetes 11 (4), 279-285, 2010 | 60 | 2010 |
| Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of age B Yüksel, MN Özbek, NÖ Mungan, F Darendeliler, B Budan, A Bideci, ... Journal of clinical research in pediatric endocrinology 3 (2), 84, 2011 | 58 | 2011 |
| Nutritional megaloblastic anemia in young Turkish children is associated with vitamin B-12 deficiency and psychomotor retardation S Katar, MN Özbek, A Yarams, S Ecer Journal of pediatric hematology/oncology 28 (9), 559-562, 2006 | 53 | 2006 |
| Diyarbakır ilindeki çocuklarda ve adölesanlarda B12 vitamin ve folik asit düzeyleri K Öncel, MN Özbek, H Onur, M Söker, A Ceylan Dicle Tıp Dergisi 33 (3), 163-169, 2006 | 46 | 2006 |
| Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study F Baş, ZO Uyguner, F Darendeliler, Z Aycan, E Cetinkaya, M Berberoğlu, ... Endocrine 49, 479-491, 2015 | 43 | 2015 |
| Clinical and laboratory presentation of typhoid fever A Yaramis, I Yildirim, S Katar, MN Ozbek, I Yalçin, MA Tas, S Hosoglu International Pediatrics 16 (4), 227-231, 2001 | 41 | 2001 |
| Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism F Gürbüz, LD Kotan, E Mengen, Z Şıklar, M Berberoğlu, S Dökmetaş, ... Journal of clinical research in pediatric endocrinology 4 (3), 121, 2012 | 37 | 2012 |
| Clinical and hormonal profiles correlate with molecular characteristics in patients with 11β-hydroxylase deficiency M Yildiz, E Isik, ZY Abali, M Keskin, MN Ozbek, F Bas, SA Ucakturk, ... The Journal of Clinical Endocrinology & Metabolism 106 (9), e3714-e3724, 2021 | 28 | 2021 |
| Genotype and phenotype characteristics in 22 patients with vitamin D-dependent rickets type I S Tahir, H Demirbilek, MN Ozbek, RT Baran, S Tanriverdi, K Hussain Hormone Research in Paediatrics 85 (5), 309-317, 2016 | 28 | 2016 |
| Chest computerized tomography scan findings in 74 children with tuberculous meningitis in southeastern Turkey A Yaramiş, Y Bükte, S Katar, MN Ozbek The Turkish journal of pediatrics 49 (4), 365-369, 2007 | 28 | 2007 |
| Frequency of celiac disease and spontaneous normalization rate of celiac serology in children and adolescent patients with type 1 diabetes E Unal, M Demiral, B Baysal, M Ağın, EG Devecioğlu, H Demirbilek, ... Journal of clinical research in pediatric endocrinology 13 (1), 72, 2021 | 27 | 2021 |
| Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations H Demirbilek, VB Arya, MN Ozbek, A Akinci, M Dogan, F Demirel, ... European journal of endocrinology 170 (6), 885-892, 2014 | 26 | 2014 |
| Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated … H Demirbilek, MN Ozbek, K Demir, LD Kotan, Y Cesur, M Dogan, F Temiz, ... Clinical Endocrinology 82 (3), 429-438, 2015 | 24 | 2015 |
