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Çağrı Doğan

Observed names: C. Dogan, Cagri Dogan, DOGAN, ÇAGRI, ÇAĞRI DOĞAN, Çagri Doğan
Institution: Ordu University
ORCID: 0000-0001-5068-0380
Observed ORCID: 0000-0001-5068-0380
OpenAlex ID: A5034274443
Mutational Spectrum of α- and β-thalassemia in a Single-Center Cohort from the Eastern Black Sea Region of Türkiye: A Cross-sectional Study
2026 · Çağrı Doğan, Aslı Odabaşı Giden · Acta haematologica oncologica Turcica.
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1.18eP HMGCR-related limb-girdle muscular dystrophy: case report
2026 · Gökçen Öz Tunçer, Seren Aydin, et al. · Neuromuscular Disorders
Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort
2026 · Çağrı Doğan, Alper Gezdirici, et al. · Journal of Human Genetics
Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort
2026 · DOGAN, ÇAGRI · Zenodo (CERN European Organization for Nuclear Research)
MEFV variant spectrum and exploratory in silico stratification of uncommon variants in 611 individuals tested for suspected familial Mediterranean fever in the Eastern Black Sea region of Türkiye
2026 · Çağrı Doğan · BMC Genomic Data
Factor V Leiden Mutation in Women with Recurrent Pregnancy Loss: A Single-center Study
2026 · Aslı Odabaşı Giden, Çağrı Doğan · Acta haematologica oncologica Turcica.
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DAAM2 gene variants p.(Asp165Glu) and p.(Asn614ThrfsTer2) in pediatric cryptorchidism: a hypothesis-generating pilot case-control study from the Eastern Black Sea region of Türkiye
2026 · ONUR YALÇIN, ÇAĞRI DOĞAN · TURKISH JOURNAL OF MEDICAL SCIENCES
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De-identified case-level dataset: sequential prenatal genetic testing in 120 consecutive amniocenteses (northeastern Türkiye, 2022–2025)
2026 · DOGAN, ÇAGRI · Zenodo (CERN European Organization for Nuclear Research)
Genotype-phenotype concordance in 21-hydroxylase deficiency: de-identified dataset from a single-centre cohort in the Eastern Black Sea region of Turkiye
2026 · DOGAN, ÇAGRI · Zenodo (CERN European Organization for Nuclear Research)
Genetic spectrum and treatment implications of maturity-onset diabetes of the young in the eastern Black Sea region of Türkiye: a combined adult and pediatric cohort of 296 patients with identification of rare and novel variants
2026 · Çağrı Doğan, Burak Andaç, et al. · Molecular Biology Reports
Diagnostic Yield, Variant Spectrum, and Incidental Findings of Next-Generation Sequencing in Infertility and Early Reproductive Failure: A Single-Center Cohort Study
2026 · DOGAN, ÇAGRI · Zenodo (CERN European Organization for Nuclear Research)
Integrating Artificial Intelligence into Hereditary Cancer Diagnostics: Variant Interpretation, Clinical Correlation, and Novel Gene–Cancer Associations from a WES-Based Panel Cohort
2026 · DOGAN, ÇAGRI · Zenodo (CERN European Organization for Nuclear Research)
Investigation of Beta-2 Adrenergic Receptor Gene Polymorphisms and Their Association with Maternal Hypotension During Cesarean Under Spinal Anesthesia in a Turkish Population
2026 · Anıl Kılınç, Çağrı Doğan, et al. · Trends in Surgical Sciences
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Investigation of HFE Mutations Associated with Hemochromatosis the Case of Ordu Province
2026 · Çağrı Doğan, Aslı Odabaşı Giden, et al. · Gazi Medical Journal
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Analysis of the results of the BRCA1 and BRCA2 genes in early-onset breast cancer patients from the Ordu province
2026 · Cagri Dogan, Cengiz Akosman, et al. · The Atlantic Journal of Medical Science and Research
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Does the MC4R rs17782313 gene polymorphism affect the rate of exercise-induced fat oxidation?
2025 · Mert Sakar, Çağrı Doğan, et al. · Applied Physiology, Nutrition, and Metabolism
The Effect of FTO rs9939609 Gene Polymorphism on Exercise-Induced Fat Oxidation
2025 · Necdet Apaydin, Ahsen Eren, et al. · Research Square
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Genotype–Phenotype Correlation in Patients with Suspected Marfan Syndrome a Single-Center Experience
2025 · Çağrı Doğan, Elif Doğan, et al. · MIDDLE BLACK SEA JOURNAL OF HEALTH SCIENCE
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The Importance of Clinical Findings in the Evaluation of Genetic Testing A Pseudo-Gaucher
2025 · Cagri Dogan, Elif Dogan · ODÜ Tıp Dergisi
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Congenital mirror movements in a family: Outcomes associated with DCC mutations
2025 · Arife Derda Yücel Şen, Kursat Bora Carman, et al. · Journal of Neurogenetics
Fshd / Opmd / Edmd / Dmi
2018 · M. De Antonio, C. Dogan, et al. · Neuromuscular Disorders
Works count: 21
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