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Tayfun Çinleti
Observed names:
Cinleti, Tayfun,
Tayfun Cinleti,
Tayfun ÇİNLETİ
Institution:
İzmir Şehir Hastanesi
Observed institutions:
Izmir University,
Dokuz Eylül University,
Sağlık Bilimleri Üniversitesi,
Izmir Tepecik Eğitim ve Araştırma Hastanesi,
İzmir Tınaztepe Üniversitesi,
İzmir Şehir Hastanesi
show all 6
ORCID:
0000-0001-9041-1820
Observed ORCID:
0000-0001-9041-1820
OpenAlex ID:
A5082379436
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality
2021
·
Masamune Sakamoto
, Kazunori Sasaki
, et al.
·
Human Molecular Genetics
·
27
PDF
DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the Literature
2023
·
Özlem Özsoy
, Tayfun Cinleti
, et al.
·
Molecular Syndromology
·
8
PDF
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy
2022
·
Masamune Sakamoto
, Kazuhiro Iwama
, et al.
·
Genetics in Medicine
·
8
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing Panels
2023
·
Gamze Sarıkaya Uzan
, Ceren Yılmaz Uzman
, et al.
·
Molecular Syndromology
·
6
PDF
Dual Diagnosis of Nongoitrous Congenital Hypothyroidism-6 and Snijders Blok-Campeau Syndrome
2024
·
Hatice Yelda Yalçın
, Tayfun Cinleti
, et al.
·
Molecular Syndromology
·
5
PDF
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey
2023
·
Özlem Özsoy
, Tayfun Cinleti
, et al.
·
Acta Neurologica Belgica
·
5
MIRAGE syndrome in a 10-year-old girl with a novel Lys1024Glu missense variant in SAMD9
2023
·
Tayfun Cinleti
, Ali Gülen
, et al.
·
Clinical Dysmorphology
·
5
Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism
2022
·
Gizem Yıldız
, Meral Torun Bayram
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
5
Mediterranean Fever (MEFV) Gene Variants in Kawasaki Disease in Turkish Children: Do They Influence the Disease Course?
2024
·
Serkan Türkuçar
, Tayfun Çinleti
, et al.
·
Journal of Clinical Practice and Research
·
3
PDF
Clinical Heterogeneity in Patients with Long QT Syndrome and Segregation of Single Nucleotide Variants and Clinical Symptoms in 17 Affected Families
2023
·
Elcin Bora
, Ayca Yıldız Bulut
, et al.
·
Molecular Syndromology
·
3
PDF
Initial Next-Generation Sequencing (NGS) Results of Alport Syndrome
2019
·
Altuğ Koç
, Elçin Bora
, et al.
·
Journal of Basic and Clinical Health Sciences
·
3
PDF
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
PDF
Expression of Autophagy-Related Proteins in Microlissencephaly Associated with a Novel Variant in the WDR81 Gene.
2025
·
Hatice Yelda Yalçın
, Ufkay Karabay
, et al.
·
PubMed Central
·
1
PDF
Report of a New Pediatric Patient with the SLC1A4 Variant and a Brief Review of the Literature
2024
·
Hatice Yelda Yalçın
, Tayfun Cinleti
, et al.
·
Journal of Pediatric Neurology
·
1
PDF
Hemoglobin A1C can differentiate subjects with GCK mutations among patients suspected to have MODY
2022
·
Ceren Yılmaz Uzman
, İbrahim Mert Erbaş
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
1
Autoimmune/autoinflammatory syndrome induced by adjuvants after multi-component meningococcal serogroup B vaccination in a 7-year-old girl: a case report
2022
·
Özge Atay
, Suna Asilsoy
, et al.
·
The Turkish Journal of Pediatrics
·
1
PDF
Blended Phenotype of Pelger-Huet Anomaly with Osteochondroma and Autosomal Recessive Deafness with Enlarged Vestibular Aqueduct
2022
·
Tayfun Cinleti
, Ceren Yılmaz Uzman
, et al.
·
Molecular Syndromology
·
1
Is Mean Platelet Volume a Useful Noninvasive Biomarker for Inflammatory Bowel Disease in Childhood?
2020
·
Tayfun Çinleti
, Özlem Bağ
, et al.
·
The Journal of Medical Sciences
·
1
PDF
Etiological Spectrum of Primary Ovarian Insufficiency in a Group of Children and Adolescents: A Tertiary Single-Center Experience
2026
·
Murat Çağlar Karataş
, Özge Köprülü
, et al.
·
Journal of Pediatric and Adolescent Gynecology
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
Usher Syndrome Type 2A and Epileptic Encephalopathy with Spike-Wave Activation in Sleep: A Coincidental Dual Diagnosis? Case Report
2026
·
Hande Gazeteci Tekin
, Fatma Kuşgöz
, et al.
·
Molecular Syndromology
Supplemental Material for: Usher Syndrome Type 2A (USH2A) and EE-SWAS: A Coincidental Dual Diagnosis? Case Report
2026
·
figshare admin karger
, Hande Gazeteci Tekin
, et al.
·
Figshare
Supplementary_materials_DMD.dox
2026
·
Yalçın, Hatice Yelda
, Güzin, Yiğithan
, et al.
·
Zenodo (CERN European Organization for Nuclear Research)
Evaluation of Cytogenetic and Molecular Genetic Tests in Patients with Short Stature
2026
·
Gülçin Arslan
, Benay Turan
, et al.
·
Molecular Syndromology
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Works count:
31
Citation count:
86
H-index:
5
I10-index:
1
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