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Gülçin Arslan

Observed names: G. Arslan, Gulcin Arslan
ORCID: 0000-0003-4506-2654
Observed ORCID: 0000-0003-4506-2654
OpenAlex ID: A5043445180
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations
2020 · Huseyin Demirbilek, Atilla Cayir, et al. · The Journal of Clinical Endocrinology & Metabolism · 17
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Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7
2021 · S. Acar, S. Gürsoy, et al. · Journal of Endocrinological Investigation · 13
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation
2019 · Özlem Nalbantoğlu, Gülçin Arslan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 10
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Clinical and Genetic Characteristics of Patients with Common and Rare Types of Congenital Adrenal Hyperplasia: Novel variants in STAR and CYP17A1
2021 · Ozge Koprulu, Behzat Ozkan, et al. · SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital · 4
Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review
2022 · Özge Köprülü, Sezer Acar, et al. · The Journal of Pediatric Research · 3
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Investigating the Efficiency of Vitamin D Administration with Buccal Spray in the Treatment of Vitamin D Deficiency in Children and Adolescents
2021 · Özlem Nalbantoğlu, Sezer Acar, et al. · Journal of Clinical Research in Pediatric Endocrinology · 3
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Identification of two AMH gene variants in two unrelated patients with persistent Müllerian duct syndrome: one novel variant
2021 · Sezer Acar, Özlem Nalbantoğlu, et al. · Gynecological Endocrinology · 3
Duplication in the SHOX Gene as a Rare Genetic Cause of Short Stature and/or Skeletal Abnormalities: A Clinical Report and Review of the Literature
2025 · Benay Turan, Gülçin Arslan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 2
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A rare case of skeletal dysplasia: biallelic variant in ACAN gene
2024 · Gülçin Arslan, Filiz Hazan, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
Identification of a novel homozygous NR5A1 variant in a patient with a 46,XY disorders of sex development
2024 · Tarık Kırkgöz, Semra Gürsoy, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
Should the initial dose of long-acting growth hormone therapy somatrogon for pediatric growth hormone deficiency be standard for each child?
2025 · Eren Er, Benay Turan, et al. · Endocrine Abstracts · 1
A novel synonymous homozygous variant [c.2538G>A (p.Thr846Thr)] in TRPM6 in a patient with hypomagnesemia with secondary hypocalcemia
2021 · Sezer Acar, Karl Peter Schlingmann, et al. · Journal of Pediatric Endocrinology and Metabolism · 1
Extensive Plexiform Neurofibroma Presenting as Clitoromegaly in Neurofibromatosis Type 1
2021 · Özlem Nalbantoğlu, Gülçin Arslan, et al. · Journal of Dr Behcet Uz Children s Hospital · 1
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A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation
2020 · Gülçin Arslan, Sezer Acar, et al. · The Journal of Pediatric Research · 1
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Autoimmunepolyendocrinopathy-Candidiasis-Ectodermal Dystrophy: A Case Report
2018 · Tanju Çelik, Özlem Nalbantoğlu, et al. · 57th Annual ESPE · 1
Retrospective Evaluation of the Clinical Characteristics, Laboratory Findings, and Treatment Approaches in Pediatric and Adolescent Patients Diagnosed with Type 2 Diabetes Mellitus: A Single-Center Experience
2026 · Gülçin Arslan, Tarık Kırkgöz, et al. · Pediatric Practice and Research
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Supplemental Material for: Phenotypic Heterogeneity in Schaaf-Yang Syndrome: Early Musculoskeletal Features and Growth Hormone Deficiency with Partial Empty Sella: A Case Report
2026 · figshare admin karger, Gülümay Vural Topaktaş, et al. · Figshare
Phenotypic Heterogeneity in Schaaf-Yang Syndrome: Early Musculoskeletal Features and Growth Hormone Deficiency with Partial Empty Sella: A Case Report
2026 · Gülümay Vural Topaktas, Gülçin Arslan, et al. · Molecular Syndromology
Subclinical myocardial dysfunction assessed by two-dimensional speckle-tracking echocardiography in children and adolescents with prediabetes
2026 · Gülçin Arslan, Müge Nasırlı, et al. · The Annals of Clinical and Analytical Medicine
Evaluating Thyroid Hormone Sensitivity in Euthyroid Children with Asthma: A Retrospective Case–Control Study
2026 · ECE Ocak, Gülçin Arslan, et al. · European Respiratory Journal
Prematurity is associated with altered central thyroid hormone sensitivity
2026 · Gülçin Arslan, Hakan Birinci, et al. · Frontiers in Endocrinology
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Clinical utility of a novel index for predicting metabolic dysfunction-associated steatotic liver disease risk in children
2026 · Gülçin Arslan, Müge Deveci, et al. · European Journal of Pediatrics
Psychiatric and psychosocial characteristics of children with premature adrenarche: a prospective study
2026 · Gülçin Arslan, Tuğçem Şar, et al. · BMC Pediatrics
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Infantile Sotos Syndrome: A Case Presenting with Mental Retardation and Overgrowth
2026 · Ibrahim Ozgun, Gülçin Arslan, et al. · Pediatric Academic Case Reports
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Evaluation of Cytogenetic and Molecular Genetic Tests in Patients with Short Stature
2026 · Gülçin Arslan, Benay Turan, et al. · Molecular Syndromology
Works count: 32
Citation count: 64
H-index: 4
I10-index: 3
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