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Bahtiyar Şahinoğlu

Observed names: Bahtiyar Sahinoglu, Bahtiyar Sahinoğlu, Bahtiyar ŞAHİNOĞLU, Şahinoğlu, Bahtiyar
ORCID: 0000-0002-2208-540X
Observed ORCID: 0000-0002-2208-540X
OpenAlex ID: A5069521549
Autosomal recessive Robinow syndrome with novel ROR2 variants: distinct cases exhibiting the clinical variability
2020 · Emre Kirat, Hatice Mutlu Albayrak, et al. · Clinical Dysmorphology · 8
A New Variant of the IER3IP1 Gene: The First Case of Microcephaly, Epilepsy, and Diabetes Syndrome 1 from Turkey
2022 · Elif Söbü, Gül Demet Kaya Özçora, et al. · Journal of Clinical Research in Pediatric Endocrinology · 7
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Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients
2025 · Gulcin Akinci, Berk Ozyilmaz, et al. · Neuromuscular Disorders · 6
Clinical, laboratory, and molecular characteristics of patients with spondyloenchondrodysplasia: a case series study
2025 · Esra Pekpak Şahinoğlu, Ayse Ceyda Oren, et al. · European Journal of Pediatrics · 5
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
2023 · Çağatay Günay, Duygu Aykol, et al. · Neuropediatrics · 2
Lathosterolosis: a rare cholesterol metabolism disorder with a wide range of clinical variability
2023 · Elif Söbü, Gül Demet Kaya Özçora, et al. · Journal of Pediatric Endocrinology and Metabolism · 2
İnfertil erkek hastalarda karyotip analizi ve Y kromozom mikrodelesyon analiz sonuçları
2021 · Derya KARAER, Bahtiyar ŞAHİNOĞLU, et al. · Pamukkale Medical Journal · 2
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Coexistence of Bloom Syndrome and Kostmann Disease and a Novel Mutation
2023 · Esra Pekpak Sahinoglu, Ayse Ceyda Oren, et al. · Journal of Pediatric Hematology/Oncology · 1
Evaluation of the frequency of MEFV gene variants in patients with a pre-diagnosis of Familial Mediterranean Fever (FMF) in southeast Turkey.
2023 · Derya KARAER, Bahtiyar ŞAHİNOĞLU, et al. · Pamukkale Medical Journal · 1
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The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · BMC Pediatrics
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Additional file 2 of The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · Figshare
Additional file 1 of The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · Figshare
Fragile X in Eastern & Southeastern Anatolia: A 2019–2025 Single-Center Cohort of 306 Male Referrals
2025 · Şahinoğlu, Bahtiyar, Gümüş, Uğur · Zenodo (CERN European Organization for Nuclear Research)
The clinical and genetic spectrum of infantile osteopetrosis: a single-center experience including a novel TCIRG1 mutation
2025 · Esra Pekpak Şahinoğlu, Ayşe Ceyda Ören, et al. · Trends in Pediatrics
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The effect of examining somatic alterations with NGS in patients with solid tumors, on patient management: A single-center experience in Turkey
2024 · Hacı Arak, Bahtiyar Sahinoğlu, et al. · Journal of Oncology Pharmacy Practice
Works count: 15
Citation count: 34
H-index: 4
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