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akaturk Akademik ölçüm
Akademik özet YÖKSİS ve OpenAlex ayrı sayılır.
Makale 82
YÖKSİS82 OpenAlex0
Proje 21
Kitap 2
Bildiri 164

Atıf etkisi

OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 64
h-indeks 13 Türkiye yüzdelik dilimi: 92 Büyük işbirlikleri hariç: h 12 · 1 makale Üniversitesinde h-indekse göre 106. / 1.170
i10-indeks
14
Toplam atıf
420
Türkiye’de üst %13
Makale başına
6,6
FWCI
0,71
1,00 = dünya ortalaması
Dünyada üst %1
0
Dünyada üst %10
5

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) 60
  • Q1 13
  • Q2 14
  • Q3 24
  • Q4 9
WoS (JCR) 59
  • Q1 9
  • Q2 8
  • Q3 12
  • Q4 30
TR Index TR Index

28 makale

OpenAlex atıf yüzdelik
  • Üst %1 0
  • Üst %10 5
  • Ort. 51.5%
  • n 65
Diğer sayımlar

Scopus (SJR)

  • YÖKSİS satırı 61

WoS (JCR)

  • YÖKSİS satırı 61

TR Index

  • YÖKSİS satırı 29 makale

Makaleler

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

Yayını olan dergiler

57 dergi

Makale listesi

  1. 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%
  2. 2025 Mutant p.Val114Ala Transthyretin-Related Cardiac Amyloidosis with Heart Failure and Right Bundle Branch Block The Anatolian Journal of Cardiology DOI 10.14744/AnatolJCardiol.2025.5150 YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 6.3%
  3. 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 96.1%
  4. 2025 A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia European Journal of Human Genetics DOI 10.1038/s41431-025-01902-0 YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.2%
  5. 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%
  6. 2025 Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrine Syndrome Type 1: A Case Report and Review of the Literature Journal of Clinical Research in Pediatric Endocrinology DOI 10.4274/jcrpe.galenos.2023.2023-9-17 YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 54.0%
  7. 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%
  8. 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%
  9. 2025 A Rare Case of Hereditary Sensory and Autonomic Neuropathy Type 4 in a 3-Year-Old: Clinical and Genetic Findings Turkiye Klinikleri Journal of Pediatrics DOI 10.5336/pediatr.2025-110707 YÖKSİS SJR Q4 OpenAlex 11.2%
  10. 2024 Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2 Molecular Syndromology DOI 10.1159/000540377 YÖKSİS SJR Q3 JCR Q4 OpenAlex 53.6%
  11. 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%
  12. 2024 KLL Olgularında NOTCH1 Gen Amplifikasyonu Osmangazi Journal of Medicine DOI 10.20515/otd.1329205 YÖKSİS TR Index OpenAlex 48.9%
  13. 2023 Evaluation of the Association Between CRNDE Plasma Expression Level, KRAS, NRAS, and BRAF Variants in Patients with advanced CRC Akademi Doktorlar Yayinevi DOI 10.4999/uhod.236797 YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 40.1%
  14. 2023 Genetic Investigations in Turkish Idiopathic Pancreatitis Patients Show Unique Characteristics Turkish Journal of Gastroenterology DOI 10.5152/tjg.2023.22773 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 71.6%
  15. 2023 A genetic polymorphism on chromosome 4q25 (rs17570669_T) may predict atrial fibrillation recurrence after successful electrical cardioversion Oxford University Press (OUP) DOI 10.1093/eurheartj/ehad655.339 YÖKSİS SJR Q1 JCR Q1 OpenAlex 29.0%
  16. 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%
  17. 2023 ERCC8 related Cockayne syndrome type-1: A rare entity diagnosed in a Turkish boy Journal of Surgery and Medicine DOI 10.28982/josam.7380 YÖKSİS OpenAlex 8.7%
  18. 2022 An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3 CYTOGENETIC AND GENOME RESEARCH DOI https://pubmed.ncbi.nlm.nih.gov/34915466/ YÖKSİS SJR Q3 JCR Q4
  19. 2022 The Impact of Cytogenetic Aberrations in the Clonal Evolution of Chronic Myeloid Leukemia: A Single-Center Experience Among 450 Turkish Patients Cohort Study Turkish Journal of Hematology DOI 10.4274/tjh.galenos.2022.2022.0045 YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 49.6%
  20. 2022 Clinical and Molecular Evaluation of MEFV Gene Variants in the Turkish Population: A Study by The National Genetics Consortium FUNCTIONAL & INTEGRATIVE GENOMICS DOI 10.1007/s10142-021-00819-3 2 YÖKSİS kaydı YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%

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