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Taner Karakaya

Observed names: KARAKAYA, TANER, Karakaya, Taner, T. Karakaya, TANER KARAKAYA, Taner KARAKAYA
Institution: Samsun University
ORCID: 0000-0002-3437-5324
Observed ORCID: 0000-0002-3437-5324
OpenAlex ID: A5000214730
Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
2022 · Ayberk Turkyilmaz, Ceren Alavanda, et al. · Journal of Assisted Reproduction and Genetics · 17
Tedaviyi Etkileyen Tarama Testleri
2020 · Taner Karakaya, Fatma Sılan, et al. · Çanakkale Onsekiz Mart University AVESIS · 12
Identification of a novel pathogenic variant in CKAP2L and literature review in a child with Filippi syndrome and congenital talipes equinovarus
2021 · Taner Karakaya, Ali Evren Bilgic, et al. · American Journal of Medical Genetics Part A · 7
Evaluation of Full Blood Count–Derived Inflammatory Indices (SII, SIRI, PIV, NLR) in Behçet’s Disease Patients and Healthy Controls
2025 · Recai Aci, Adem Keskin, et al. · OBM Genetics · 6
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Utility of Optical Genome Mapping in Repeat Disorders
2024 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Clinical Genetics · 6
Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease
2022 · Taner Karakaya, Ayberk Turkyilmaz, et al. · Neurogenetics · 6
The New Youngest Case of Grange Syndrome with a Novel Biallelic Pathogenic Variant in YY1AP1
2023 · Taner Karakaya, Ayberk Turkyilmaz, et al. · Molecular Syndromology · 5
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A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels
2022 · Taner Karakaya, Fatma Silan, et al. · Hemoglobin · 4
Targeted gene panel testing in pediatric epilepsy: Diagnostic outcomes and expanding genetic insights
2026 · Aslihan Sanri, Unal Akca, et al. · Brain and Development · 3
The Distribution of Hereditary Risk Factors in Patients with Pulmonary Thromboembolism without Identifiable Acquired Risk Factors
2025 · Savaş Gegin, Taner Karakaya, et al. · Düzce Tıp Fakültesi Dergisi · 3
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Identification of the molecular etiology in rare congenital hemolytic anemias using next‐generation sequencing with exome‐based copy number variant analysis
2024 · Esra Isik, Yesim Aydinok, et al. · European Journal Of Haematology · 3
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Systemic Immune Inflammation Index and Pan-immune Inflammation Value in Predicting Human Leukocyte Antigen-b27 Positivity: a Study on Ankylosing Spondylitis Patients
2024 · Adem Keskin, Taner Karakaya, et al. · Meandros Medical And Dental Journal · 2
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The genetic spectrum of polycystic kidney disease in children
2023 · Ayca Kocaaga, Yesim Özdemir Atikel, et al. · Revista da Associação Médica Brasileira · 2
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Two siblings with GAPO syndrome: a novel missense variant in ANTXR1
2022 · Onur Yildiz, Elifcan Taşdelen, et al. · Clinical Dysmorphology · 2
Copy number variations in patients with idiopathic recurrent pregnancy loss: an arrayCGH approach
2022 · ONUR YILDIZ, FATMA SILAN, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 2
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The frequency of JAK2 V617F mutation and its association with low EPO levels in polycythemia vera patients
2025 · Recai Aci, Adem Keskin, et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 1
Kisspeptin levels in infertile and miscarried women: a cross-sectional study on the relationship with methylenetetrahydrofolate reductase gene polymorphisms and biochemical parameters
2025 · Adem Keskin, Naim Uzun, et al. · Revista da Associação Médica Brasileira · 1
The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report
2018 · Fatma Silan, Romyla Bourouba, et al. · Egyptian Journal of Medical Human Genetics · 1
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Featured Cover
2025 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Clinical Genetics
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Ligneous periodontitis: A molecularly confirmed case of type I plasminogen deficiency
2025 · A. Sarioglu, K. Ugurlu, et al. · Journal of Clinical and Experimental Dentistry
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Author response for "Utility of Optical Genome Mapping in Repeat Disorders"
2024 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Publons reviews and discussion
Author response for "Utility of Optical Genome Mapping in Repeat Disorders"
2024 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Publons reviews and discussion
Molecular profiling of BRCA1 and BRCA2 genes in Turkish patients with early-onset breast cancer
2023 · Taner Karakaya, Ayca Kocaaga · Egyptian Journal of Medical Human Genetics
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Kabızlık ve Üfürümle Tespit Edilen Williams-Beuren Sendromu
2021 · Merve BÜYÜKBAYRAM, Deniz ERİS, et al. · Yüksek İhtisas Üniversitesi Sağlık Bilimleri Dergisi
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HbF veya HbA2 seviyelerinde farklılığı bulunan bireylerde Kruppel-like factor 1 (KLF1) ve Hemoglobin subunit delta (HBD) genlerinde saptanan mutasyonların genotip-fenotip ilişkisinin incelenmesi
2020 · ÖZDEMİR, ÖZTÜRK, SILAN, FATMA, et al. · Çanakkale Onsekiz Mart University AVESIS
Works count: 43
Citation count: 83
H-index: 6
I10-index: 2
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