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Akademisyen

FATİH TEPGEÇ

DOKTOR ÖĞRETİM ÜYESİ

ALTINBAŞ ÜNİVERSİTESİ SAĞLIK HİZMETLERİ MESLEK YÜKSEKOKULU TIBBİ HİZMETLER VE TEKNİKLER BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Tıbbi Genetik

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 22
  • Proje 0
  • Kitap 2
  • Bildiri 25
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 9 Q2 0 Q3 1 Q4 4
WoS (JCR) Q1 3 Q2 6 Q3 0 Q4 5
TR Index 6 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 1
Ort. yüzdelik 51.0%
Üst %1 payı 0.0%
Üst %10 payı 5.0%

Makaleler

YÖKSİS ve OpenAlex kaynak ayrımıyla makaleler; quartile ve TR Index ile daraltabilirsiniz.

Dizin filtreleri

Toplam 22 yayın

Scopus (SJR)
WoS (JCR)
TR Index

Makale listesi

  1. 2024 The Comparison of Functional Connectivity in Parkinson’s Disease Patients with and without Parkin Gene Mutations Archives of Neuropsychiatry DOI 10.29399/npa.28719 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 6.4%
  2. 2022 GJB2-RELATED NON-SYNDROMIC HEARING LOSS VARIANTS’ SPECTRUM AND THEIR FREQUENCY IN TURKISH POPULATION Istanbul University DOI 10.26650/IUITFD.1011501 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 35.2%
  3. 2022 The Mitochondrial Origins of the Hellenistic Individuals of Ayasuluk Hill EXPERIMED DOI 10.26650/experimed.1183293 YÖKSİS OpenAlex 25.9%
  4. 2022 Kadıkalesi Geç Bizans Dönemi Gömülerinin Mitokondriyel Kökenleri Acta Medica Nicomedia DOI 10.53446/actamednicomedia.1123713 YÖKSİS TR Index OpenAlex 18.0%
  5. 2021 TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features European Journal of Neurology DOI 10.1111/ene.14908 YÖKSİS SJR Q1 JCR Q1 OpenAlex 67.5%
  6. 2021 Frequency of frontotemporal dementia-related gene variants in Turkey Neurobiology of Aging DOI 10.1016/j.neurobiolaging.2021.05.007 YÖKSİS SJR Q1 JCR Q2 OpenAlex 63.4%
  7. 2021 Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey Parkinsonism & Related Disorders DOI 10.1016/j.parkreldis.2021.10.024 YÖKSİS SJR Q1 JCR Q2 OpenAlex 54.6%
  8. 2021 The Right Temporal Variant of Frontotemporal Dementia Is Not Genetically Sporadic: A Case Series Journal of Alzheimer's Disease DOI 10.3233/JAD-201191 YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.9%
  9. 2021 Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Turkish Journal Of Neurology DOI 10.4274/tnd.2021.91298 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 56.4%
  10. 2021 A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer disease Neurological Sciences DOI 10.1007/s10072-021-05243-w YÖKSİS SJR Q1 JCR Q2 OpenAlex 62.8%
  11. 2021 Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation Carriers Journal of Parkinson's Disease DOI 10.3233/JPD-202295 YÖKSİS SJR Q1 JCR Q2 OpenAlex 62.1%
  12. 2021 NOONAN SENDROMU'NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ İstanbul Tıp Fakültesi Dergisi DOI 10.26650/IUITFD.2020.803356 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 38.2%
  13. 2017 Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family Noro Psikiyatri Arsivi DOI http://www.noropsikiyatriarsivi.com/crossref?doi=10.5152/npa.2017.19484 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 49.3%
  14. 2016 SPORADIC FATAL INSOMNIA IN A YOUNG MAN Alzheimer’s dementia: the journal of the Alzheimer’s Association DOI 10.1016/j.jalz.2016.06.982 YÖKSİS OpenAlex 7.0%
  15. 2025 Qualitative Assessment of DNA Isolation from Fresh, Frozen, and Ancient Human Bone Using a Homogenizer-Assisted Workflow Forensic Science International DOI 10.1016/j.forsciint.2025.112807 YÖKSİS SJR Q1 JCR Q1 OpenAlex 81.0%
  16. 2023 Embracing Monogenic Parkinsons Disease: The MJFF Global Genetic PD Cohort Wiley DOI 10.1002/mds.29288 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 98.2%
  17. 2022 Kadıkalesi Geç Bizans Dönemi Gömülerinin Mitokondriyel Kökenleri Acta Medica Nicomedia DOI https://dergipark.org.tr/en/pub/actamednicomedia/issue/73032/1123713 YÖKSİS
  18. 2016 Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation Seizure DOI https://linkinghub.elsevier.com/retrieve/pii/S1059131116301546 YÖKSİS SJR Q1 JCR Q2

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