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Tulay Guran
Tulay Guran
Marmara University Department of Pediatric Endocrinology and Diabetes
Verified email at marmara.edu.tr
Title
Cited by
Cited by
Year
Mutations in CYP24A1 and idiopathic infantile hypercalcemia
KP Schlingmann, M Kaufmann, S Weber, A Irwin, C Goos, U John, ...
New England Journal of Medicine 365 (5), 410-421, 2011
7672011
Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease
E Karaca, T Harel, D Pehlivan, SN Jhangiani, T Gambin, ZC Akdemir, ...
Neuron 88 (3), 499-513, 2015
3032015
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
2102011
Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome
R Prasad, I Hadjidemetriou, A Maharaj, E Meimaridou, F Buonocore, ...
The Journal of clinical investigation 127 (3), 942-953, 2017
1812017
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
1712009
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
1652016
Changes over time in sex assignment for disorders of sex development
Z Kolesinska, SF Ahmed, M Niedziela, J Bryce, M Molinska-Glura, ...
Pediatrics 134 (3), e710-e715, 2014
1342014
Novel associations in disorders of sex development: findings from the I-DSD Registry
K Cox, J Bryce, J Jiang, M Rodie, R Sinnott, M Alkhawari, W Arlt, L Audi, ...
The Journal of Clinical Endocrinology & Metabolism 99 (2), E348-E355, 2014
1192014
Significance of acanthosis nigricans in childhood obesity
T Guran, S Turan, T Akcay, A Bereket
Journal of paediatrics and child health 44 (6), 338-341, 2008
1152008
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
1102011
The long-term outcome of boys with partial androgen insensitivity syndrome and a mutation in the androgen receptor gene
A Lucas-Herald, S Bertelloni, A Juul, J Bryce, J Jiang, M Rodie, R Sinnott, ...
The Journal of Clinical Endocrinology & Metabolism 101 (11), 3959-3967, 2016
1032016
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1
C Bonnard, AC Strobl, M Shboul, H Lee, B Merriman, SF Nelson, ...
Nature genetics 44 (6), 709-713, 2012
882012
Hypercalciuria and recurrent urinary tract infections: incidence and symptoms in children over 5 years of age
NK Biyikli, H Alpay, T Guran
Pediatric nephrology 20, 1435-1438, 2005
872005
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
772012
Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome
E Dikoglu, A Alfaiz, M Gorna, D Bertola, JH Chae, TJ Cho, M Derbent, ...
American journal of medical genetics Part A 167 (7), 1501-1509, 2015
762015
Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
S Turan, C Aydin, A Bereket, T Akcay, T Güran, BA Yaralioglu, M Bastepe, ...
Bone 46 (2), 402-409, 2010
732010
Primary adrenal insufficiency in children: Diagnosis and management
T Kirkgoz, T Guran
Best Practice & Research Clinical Endocrinology & Metabolism 32 (4), 397-424, 2018
702018
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
642019
Content analysis of food advertising in Turkish television
T Guran, S Turan, T Akcay, F Degirmenci, O Avci, A Asan, E Erdil, A Majid, ...
Journal of paediatrics and child health 46 (7‐8), 427-430, 2010
642010
AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity
T Akcay, M Fernandez‐Cancio, S Turan, T Güran, L Audi, A Bereket
Andrology 2 (4), 572-578, 2014
602014
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