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Akademisyen

EBRU ERZURUMLUOĞLU GÖKALP

DOKTOR ÖĞRETİM ÜYESİ

ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Araştırma konuları OpenAlex
Akademik özet YÖKSİS ve OpenAlex ayrı sayılır.
Makale 47
YÖKSİS47 OpenAlex0
Proje 20
Kitap 9
Bildiri 76

Atıf etkisi

OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 39
h-indeks 7 Türkiye yüzdelik dilimi: 74 Büyük işbirlikleri hariç: h 6 · 1 makale Üniversitesinde h-indekse göre 350. / 1.170
i10-indeks
4
Toplam atıf
163
Türkiye’de üst %28
Makale başına
4,2
FWCI
0,84
1,00 = dünya ortalaması
Dünyada üst %1
0
Dünyada üst %10
4

En çok atıf alan makaleleri

  1. Inflammation and regulatory T cell genes are differentially expressed in peripheral blood mononuclear cells of Parkinson’s disease patients 2021 36 atıf
  2. Which Prognostic Marker is Responsible For the Clinical Heterogenity in CLL with 13q Deletion? 2021 17 atıf
  3. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium 2022 17 atıf

h-indeks ve atıflar, bu akademisyenin YÖKSİS makalelerinden OpenAlex’te eşleşenlerin atıf sayılarından hesaplanır (Google Scholar, WoS veya Scopus değildir). Eşleşmeyen makalelerin atıfı dahil değildir.

Alan sıralaması

YÖKSİS ?

Dizin çeyrekleri

?
Scopus (SJR) 35
  • Q1 8
  • Q2 10
  • Q3 15
  • Q4 2
WoS (JCR) 34
  • Q1 2
  • Q2 11
  • Q3 5
  • Q4 16
TR Index TR Index

13 makale

OpenAlex atıf yüzdelik
  • Üst %1 0
  • Üst %10 4
  • Ort. 51.8%
  • n 40
Diğer sayımlar

Scopus (SJR)

  • YÖKSİS satırı 36

WoS (JCR)

  • YÖKSİS satırı 35

TR Index

  • YÖKSİS satırı 14 makale

Makaleler

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

Yayını olan dergiler

36 dergi
Scopus (SJR)
Q1 8 Q2 10 Q3 15 Q4 2
WoS (JCR)
Q1 2 Q2 11 Q3 5 Q4 16
TR Index
13 makale

Makale listesi

  1. 2026 Downregulation of miR-221, miR-143, and miR-22 in Meningioma: Diagnostic Performance in a Single-Center Case–Control Study Turkish Neurosurgery DOI 10.5137/1019-5149.JTN.49747-25.3 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 14.6%
  2. 2026 Evaluation of the Role of miRNAs Expression Profiles in Aneurysm Turkish Neurosurgery DOI 10.5137/1019-5149.JTN.48396-25.2. YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 19.0%
  3. 2026 Resolving Complex Chromosomal Rearrangements and Rare Structural Variants: An Integrated Cytogenomic Analysis of Four Cases Bratislava Medical Journal DOI https://link.springer.com/article/10.1007/s44411-026-00684-1 YÖKSİS SJR Q3 JCR Q2
  4. 2026 MicroRNAs in Aneurysmal Subarachnoid Hemorrhage: A Stage-Specific Model Linking Rupture, Vasospasm, and Outcome Biomedicines DOI 10.3390/biomedicines14061287 YÖKSİS SJR Q1 JCR Q2 OpenAlex 47.8%
  5. 2026 Aquaporin-4 and MicroRNA Expression in Meningiomas: A Tissue-Level Exploratory Analysis Biomedicines DOI 10.3390/biomedicines14051125 YÖKSİS SJR Q1 JCR Q2 OpenAlex 40.1%
  6. 2026 Adult-onset dystonia associated with CHD8 truncating variants: case series and targeted literature review Neurogenetics DOI 10.1007/s10048-026-00910-6 YÖKSİS SJR Q3 JCR Q4 OpenAlex 43.2%
  7. 2025 A Novel De Novo Exceptional Complex Chromosomal Rearrangement Involving 5 Chromosomes Resulting in Neurodevelopmental Delay and Dysmorphism Molecular Syndromology DOI 10.1159/000545465 YÖKSİS SJR Q3 JCR Q4 OpenAlex 80.5%
  8. 2025 The Role of miRNA Expression Profiles in Different Biofluids in Aneurysm Rupture Journal of Korean Neurosurgical Society DOI 10.3340/jkns.2024.0171 YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %10 OpenAlex 90.7%
  9. 2025 FBXO7 Pathogenic Variants in Early‐Onset Parkinsonism: Insights from a Neuroimaging Perspective and Review of the Literature Movement Disorders Clinical Practice DOI 10.1002/mdc3.70269 YÖKSİS SJR Q2 JCR Q2 OpenAlex 69.6%
  10. 2025 Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from Turkey Annals of Saudi Medicine DOI 10.5144/0256-4947.2025.154 YÖKSİS SJR Q3 JCR Q2 OpenAlex üst %10 OpenAlex 96.8%
  11. 2025 Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies Scientific Reports DOI 10.1038/s41598-025-01007-0 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.1%
  12. 2025 Cerebrospinal Fluid MicroRNAs as Early Biomarker Candidates for Predicting Vasospasm Following Aneurysmal Subarachnoid Hemorrhage Genes DOI 10.3390/genes16091025 YÖKSİS SJR Q2 JCR Q2 OpenAlex 71.5%
  13. 2025 Identification of Genetic Changes in Individuals Diagnosed with Autism Spectrum Disorder Using Classical Cytogenetic and FMR1 Sizing PCR Methods Avicenna Anatolian Journal of Medicine DOI 10.5281/zenodo.17507229 YÖKSİS OpenAlex 44.6%
  14. 2025 Evaluation of Genomic Variants in Non-syndromic Congenital Heart Disease in Turkish Pediatric Group Gazi Medical Journal DOI 10.12996/gmj.2025.4414 YÖKSİS OpenAlex 12.9%
  15. 2025 Comparison of conventional karyotype analysis and CMA results with ultrasound findings in pregnancies with normal QF-PCR results Journal of Turkish Society of Obstetric and Gynecology DOI 10.4274/tjod.galenos.2025.10673 YÖKSİS TR Index SJR Q3 OpenAlex üst %10 OpenAlex 90.3%
  16. 2024 Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions? Turkish Journal Of Medical Sciences DOI 10.55730/1300-0144.5837 YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 68.8%
  17. 2024 Interstitial 3p25.3 deletion syndrome: 13 years'-long follow-up of an affected individual. Clinical Dysmorphology YÖKSİS SJR Q3 JCR Q4
  18. 2024 KLL Olgularında NOTCH1 Gen Amplifikasyonu Osmangazi Journal of Medicine DOI 10.20515/otd.1329205 YÖKSİS TR Index OpenAlex 48.8%
  19. 2023 Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus Galenos Yayinevi DOI 10.4274/jcrpe.galenos.2023.2023-5-10 YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 84.5%
  20. 2023 A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndrome BMC Medical Genomics DOI 10.1186/s12920-023-01529-4 YÖKSİS SJR Q2 JCR Q3 OpenAlex 60.1%

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