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Author

Fatih Tepgeç

Observed names: Fatih TEPGEÇ, Fatih Tepgec
ORCID: 0000-0001-8413-6949
Observed ORCID: 0000-0001-8413-6949
OpenAlex ID: A5000508943
The Right Temporal Variant of Frontotemporal Dementia Is Not Genetically Sporadic: A Case Series
2021 · Hulya Ulugut Erkoyun, Sven J. van der Lee, et al. · Journal of Alzheimer s Disease · 26
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Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation
2016 · Emel Oguz Akarsu, Pınar Tekturk, et al. · Seizure · 17
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TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features
2021 · Bedia Samanci, Başar Bilgiç, et al. · European Journal of Neurology · 14
Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family
2017 · Emel Koseoglu, Fatih Tepgec, et al. · Nöro Psikiyatri Arşivi · 12
Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey
2021 · Inci Emekli, Fatih Tepgeç, et al. · Parkinsonism & Related Disorders · 7
Frequency of frontotemporal dementia-related gene variants in Turkey
2021 · Sevilhan Artan, Ebru Erzurumluoglu Gokalp, et al. · Neurobiology of Aging · 6
Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation Carriers
2021 · Mine Sezgin, Ani Kicik, et al. · Journal of Parkinson s Disease · 6
Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
2021 · Burcu Sevinç Rüstemoğlu, Bedia Samanci, et al. · Turkish Journal Of Neurology · 4
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A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease
2021 · Gamze Guven, Bedia Samanci, et al. · Neurological Sciences · 2
Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow
2025 · Volkan Karaman, Fatih Tepgeç, et al. · Forensic Science International · 1
The Comparison of Functional Connectivity in Parkinson’s Disease Patients with and without Parkin Gene Mutations
2024 · Merve Çebi, Ulaş Ay, et al. · Nöro Psikiyatri Arşivi · 1
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Kadıkalesi Geç Bizans Dönemi Gömülerinin Mitokondriyel Kökenleri
2022 · Fatih TEPGEÇ, Mehmet GÖRGÜLÜ · Acta Medica Nicomedia · 1
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Gjb2-related Non-syndromic Hearing Loss Variants’ Spectrum and Their Frequency in Turkish Population
2022 · Çağrı Güleç, Ayça Aslanger, et al. · Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi · 1
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Noonan Sendromu’nun Prenatal Tanisinda Ptpn11 Gen Anali̇zleri̇ni̇n Etki̇nli̇ği̇
2021 · Güven Toksoy, Fatih Tepgeç, et al. · Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi · 1
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Corrigendum to “Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow” [Forensic Sci. Int. 380 (2026) 112807]
2026 · Volkan Karaman, Fatih Tepgeç, et al. · Forensic Science International
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Alzheimer’s Disease: From Molecular Mechanisms to Clinical Practices
2024 · Anı Hande Mete, Asuman Gedikbaşı, et al.
Genetic Research in Alzheimer’s Disease
2024 · Fatih Tepgec, Zehra Oya Uyguner
The Mitochondrial Origins of the Hellenistic Individuals of Ayasuluk Hill
2022 · Fatih Tepgeç, Mehmet Görgülü · Experimed
P1‐233: Sporadic Fatal Insomnia In A Young Man
2016 · Hakan I. Gurvit, Başar Bilgiç, et al. · Alzheimer s & Dementia
Works count: 19
Citation count: 99
H-index: 6
I10-index: 4
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