Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

T. Güran · SciRah

Researcher profile · Semantic Scholar

T. Güran

Share profile

T. Güran — researcher profile on SciRah

h-index: 19
Works: 58
Citations: 1,626

Most-cited papers

Mutations in CYP24A1 and idiopathic infantile hypercalcemia.
Karl P. Schlingmann, M. Kaufmann, S. Weber, Andrew Irwin +13 more
2011New England Journal of Medicine621 citations Open access
Semantic Scholar
Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatasez-scores in Different Types of Rickets
S. Turan, B. Topçu, I. Gökçe, T. Güran +4 more
2011Journal of Clinical Research in Pediatric Endocrinology159 citations Open access
Semantic Scholar
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1
C. Bonnard, A. Strobl, M. Shboul, Ha-Ne Lee +8 more
2012Nature Genetics82 citations Open access
Semantic Scholar
Identification of a Novel Dentin Matrix Protein-1 (DMP-1) Mutation and Dental Anomalies in a Kindred with Autosomal Recessive Hypophosphatemia
S. Turan, C. Aydın, A. Bereket, T. Akçay +4 more
2009Bone68 citations Open access
Semantic Scholar
Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.
P. Kühnen, S. Turan, Sebastian Fröhler, T. Güran +6 more
2014Journal of Clinical Endocrinology and Metabolism53 citations Open access
Semantic Scholar
Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features
A. Arman, A. Bereket, A. Çoker, P. Kiper +8 more
2014Orphanet Journal of Rare Diseases46 citations Open access
Semantic Scholar
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy
Karl-Peter Schlingmann, F. Jouret, Kuang Shen, A. Nigam +32 more
2021Journal of the American Society of Nephrology38 citations Open access
Semantic Scholar
Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey
A. Abacı, G. Çatlı, Ö. Kırbıyık, N. Şahin +19 more
2018Journal of Endocrinological Investigation34 citations
Semantic Scholar
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development
D. Baetens, T. Güran, B. Mendonca, N. Gomes +16 more
2017Genetics in Medicine32 citations Open access
Semantic Scholar
Critical Points in the Management of Pseudohypoaldosteronism Type 1
T. Güran, S. Değirmenci, I. Bulut, A. Say +2 more
2011Journal of Clinical Research in Pediatric Endocrinology32 citations Open access
Semantic Scholar
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants
T. Güran, B. Tezel, M. Çakır, A. Akıncı +14 more
2020Journal of Clinical Research in Pediatric Endocrinology28 citations Open access
Semantic Scholar
Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.
M. Welzel, L. Akın, A. Büscher, T. Güran +10 more
2013European Journal of Endocrinology28 citations Open access
Semantic Scholar
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey
E. Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, Eda Çelebi Bitkin +26 more
2018Journal of Clinical Research in Pediatric Endocrinology25 citations Open access
Semantic Scholar
Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children
T. Güran
2017Journal of Clinical Research in Pediatric Endocrinology25 citations Open access
Semantic Scholar
Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for Improvement
Martine Cools, Earl Y. Cheng, Joanne Hall, J. Alderson +20 more
2024Hormone Research in Paediatrics24 citations Open access
Semantic Scholar
A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make
S. Çetinkaya, T. Güran, Erdal Kurnaz, Melikşah Keskin +6 more
2017Journal of Clinical Research in Pediatric Endocrinology24 citations Open access
Semantic Scholar
Prevalence of type 1 diabetes mellitus in 6–18‐yr‐old school children living in Istanbul, Turkey
Eda Akesen, S. Turan, T. Güran, Z. Atay +2 more
2011Pediatric Diabetes24 citations Open access
Semantic Scholar
University of Birmingham Genetic disruption of 21-hydroxylase in zebrafish causes interrenal hyperplasia
H. Eachus, A. Zaucker, J. A. Oakes, A. Griffin +10 more
201723 citations
Semantic Scholar
Cranial MRI abnormalities and long-term follow-up of the lesions in 770 girls with Central Precocious Puberty.
Didem Helvacıoğlu, Serap Demircioğlu Turan, T. Güran, Z. Atay +12 more
2021Journal of Clinical Endocrinology and Metabolism20 citations
Semantic Scholar
Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus
S. Abalı, S. Turan, Z. Atay, T. Güran +2 more
2015Pediatric Diabetes20 citations Open access
Semantic Scholar
Stuve–Wiedemann syndrome: Is it underrecognized?
G. Yeşil, A. Lèbre, S. D. Dos Santos, Ömer Güran +3 more
2014American Journal of Medical Genetics. Part A20 citations Open access
Semantic Scholar
The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience
B. Haliloglu, S. Abalı, Fuat Bugrul, Enes Çelik +5 more
2017Journal of Clinical Research in Pediatric Endocrinology19 citations Open access
Semantic Scholar
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
Ş. Savaş-Erdeve, S. Çetinkaya, Z. Y. Abalı, S. Poyrazoglu +11 more
2017Journal of Pediatric Endocrinology & Metabolism (JPEM)18 citations Open access
Semantic Scholar
Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey
S. Poyrazoglu, R. Bundak, Zehra Yavaş Abalı, H. Önal +51 more
2018Journal of Clinical Research in Pediatric Endocrinology16 citations Open access
Semantic Scholar
Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism
M. Weger, B. Weger, Benjamin Görling, Gernot Poschet +8 more
2018EBioMedicine15 citations Open access
Semantic Scholar
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
Z. Şıklar, S. Turan, A. Bereket, F. Baş +32 more
2020Journal of Clinical Research in Pediatric Endocrinology13 citations Open access
Semantic Scholar
A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect
T. Güran, G. Yeşil, Ömer Güran, S. Cesur +4 more
2012Journal of Clinical Research in Pediatric Endocrinology11 citations Open access
Semantic Scholar
Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure
Uta Neumann, A. V. D. van der Linde, Ruth E Krone, N. Krone +25 more
2022European Journal of Endocrinology10 citations Open access
Semantic Scholar
Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia
H. Eachus, A. Zaucker, J. A. Oakes, A. Griffin +10 more
2017Endocrinology10 citations Open access
Semantic Scholar
Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor.
Z. Aycan, Melikşah Keskin, N. G. Lafcı, Ş. Savaş-Erdeve +13 more
2022European Journal of Medical Genetics9 citations Open access
Semantic Scholar
A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review
A. Maharaj, R. Kwong, Jack L Williams, Christopher Smith +12 more
2022Endocrine Connections8 citations Open access
Semantic Scholar
Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years
T. Güran, Didem Helvacıoğlu, Busra Gurpinar Tosun, Zehra Yavaş Abalı +11 more
2023Journal of Clinical Research in Pediatric Endocrinology7 citations Open access
Semantic Scholar
Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency
A. Maharaj, T. Güran, Federica Buonocore, J. Achermann +3 more
2022Journal of the Endocrine Society6 citations Open access
Semantic Scholar
Neonatal adrenal insufficiency: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report
Ş. Yiğit, M. Türkmen, O. Tuncer, E. Taskin +4 more
2018Türk pediatri arşivi6 citations Open access
Semantic Scholar
Antenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency and Congenital Adrenal Hyperplasia Screening in Newborns
Zehra Yavaş Abalı, Erdal Kurnaz, T. Güran
2024Journal of Clinical Research in Pediatric Endocrinology5 citations Open access
Semantic Scholar
Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients
Tarik Kirkgoz, M. Eltan, S. Kaygusuz, Zehra Yavaş Abalı +6 more
2021Journal of Clinical Research in Pediatric Endocrinology5 citations Open access
Semantic Scholar
The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical Cases
T. Güran, E. Yürüker, A. Anık, Muge Atar +12 more
2025Journal of Clinical Research in Pediatric Endocrinology4 citations Open access
Semantic Scholar
Phenotypic Variation and Pubertal Outcomes in Males and Females With 46,XY Partial Gonadal Dysgenesis
R. Tadokoro-Cuccaro, Ieuan A. Hughes, M. Cools, K. K. van de Vijver +51 more
2025Journal of Clinical Endocrinology and Metabolism4 citations Open access
Semantic Scholar
Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency.
L. S. Boogers, H. Brüggenwirth, K. P. Wolffenbuttel, R. Hersmus +18 more
2025European Journal of Endocrinology4 citations Open access
Semantic Scholar
Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings
Ceren Alavanda, Senol Demir, Serçin Güven, M. Eltan +8 more
2024Journal of Clinical Research in Pediatric Endocrinology4 citations Open access
Semantic Scholar
Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route
S. Abalı, Mayuko Tamura, S. Turan, Z. Atay +7 more
2020Journal of Pediatric Endocrinology & Metabolism (JPEM)4 citations
Semantic Scholar
Constitutional Growth Delay Pattern of Growth in Velo−Cardio−Facial Syndrome: Longitudinal follow up and final height of two cases
S. Turan, N. Özdemir, T. Güran, F. Akalın +4 more
2008Journal of Clinical Research in Pediatric Endocrinology4 citations Open access
Semantic Scholar
Evaluating breast ultrasonography as a complementary diagnostic method in girls with central precocious puberty
Erhan Bıyıklı, Didem Helvacıoğlu, Onur Buğdaycı, B. G. Tosun +3 more
2024Pediatric Radiology3 citations Open access
Semantic Scholar
Bone Phenotype is Always Present But Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency
Didem Helvacıoğlu, T. Güran
2023Journal of Clinical Research in Pediatric Endocrinology3 citations Open access
Semantic Scholar
Evaluation of thyroid function and metabolic parameters in obese and overweight children: A prospective case-control study.
Ayşe Tuğba Kartal, A. Bozaykut, Rabia Gönül Sezer, T. Güran
2022Investigación Clínica3 citations Open access
Semantic Scholar
Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy
Busra Gurpinar Tosun, Ahsen Karagözlü Akgül, E. Almus, Sadık Abidoğlu +3 more
2021Journal of Clinical Research in Pediatric Endocrinology2 citations Open access
Semantic Scholar
mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome
Karl P. Schlingmann, F. Jouret, Kuang Shen, A. Nigam +32 more
2021bioRxiv2 citations
Semantic Scholar
A rare cause of chronic hyponatremia in an infant: Answers
G. Mutlu, M. Taşdemir, N. U. Kızılkan, T. Güran +3 more
2019Pediatric nephrology (Berlin, West)2 citations
Semantic Scholar
BMI-SDS Changes During GnRHa Therapy in 150 Girls with Idiopathic Central Precocious Puberty: Follow-up Through Final Height
Didem Helvacıoğlu, B. G. Tosun, Sefa Öğe, S. Turan +4 more
2026Journal of Clinical Research in Pediatric Endocrinology1 citations Open access
Semantic Scholar
The 40th Minute Cortisol Measurement is the Key Time-Point in the Low-Dose Synacthen Stimulation Test: A Large, Assay-Specific Pediatric Validation Study
B. G. Tosun, Hazal Gacemer, Didem Helvacıoğlu, S. Turan +2 more
2026Journal of Clinical Research in Pediatric Endocrinology0 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

S. Turan×20
Invite
S. Turan — researcher profile on SciRah
A. Bereket×19
Invite
A. Bereket — researcher profile on SciRah
Z. Atay×11
Invite
Z. Atay — researcher profile on SciRah
S. Abalı×7
Invite
S. Abalı — researcher profile on SciRah

×7

Invite

F. Baş — researcher profile on SciRah

Didem Helvacıoğlu×7

Invite

Didem Helvacıoğlu — researcher profile on SciRah

Invite

T. Akçay — researcher profile on SciRah

B. Haliloglu×6

Invite

B. Haliloglu — researcher profile on SciRah

S. Çetinkaya×6

Invite

S. Çetinkaya — researcher profile on SciRah

S. Poyrazoglu×6

Invite

S. Poyrazoglu — researcher profile on SciRah

F. Darendeliler×5

Invite

F. Darendeliler — researcher profile on SciRah

Invite

B. G. Tosun — researcher profile on SciRah