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Academician

GÖKHAN YİGİT

DOKTOR ÖĞRETİM ÜYESİ

KAFKAS ÜNİVERSİTESİ DEDE KORKUT EĞİTİM FAKÜLTESİ YABANCI DİLLER EĞİTİMİ BÖLÜMÜ

  • Ana Dal Eğitim Bilimleri Temel Alanı
  • Yan Dal İngiliz Dili Eğitimi

A quick look at recorded outputs — details below.

  • Articles 18
  • Projects 0
  • Books 0
  • Proceedings 0
  • Patents 0
  • Artistic 0
Scopus (SJR) Q1 11 Q2 4 Q3 0 Q4 1
WoS (JCR) Q1 11 Q2 1 Q3 1 Q4 0
TR Index 1 articles

Field+year+type normalized OpenAlex percentiles — not Clarivate ESI / SciVal.

Top 1% articles 1
Top 10% articles 9
Avg percentile 89.7%
Top 1% share 5.9%
Top 10% share 52.9%

Articles

Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.

Index filters

18 publications total

Scopus (SJR)
Q1 11 Q2 4 Q3 0 Q4 1
WoS (JCR)
Q1 11 Q2 1 Q3 1 Q4 0
TR Index
1 articles

Article list

  1. 2026 The Role of Synthetic Data in Educational Research: A Systematic Review International Journal of Interactive Mobile Technologies DOI 10.3991/ijim.v20i16.62224 YÖKSİS SJR Q2 OpenAlex 87.4%
  2. 2025 Unlocking the Science in English Coursebooks: A Critical Exploration of Scientific Literacy Bartın Üniversitesi Eğitim Fakültesi Dergisi DOI 10.14686/buefad.1284580 YÖKSİS TR Index OpenAlex 89.8%
  3. 2025 Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis The Journal of Clinical Endocrinology & Metabolism DOI 10.1210/clinem/dgaf020 YÖKSİS SJR Q1 JCR Q1 OpenAlex 80.1%
  4. 2025 SEC24C deficiency causes trafficking and glycosylation abnormalities in an epileptic encephalopathy with cataracts and dyserythropoeisis JCI Insight DOI 10.1172/jci.insight.173484 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.0%
  5. 2021 Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state Journal of Medical Genetics DOI 10.1136/jmedgenet-2021-107769 YÖKSİS SJR Q1 JCR Q1 OpenAlex 83.8%
  6. 2021 Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies Genetics in Medicine DOI 10.1038/s41436-021-01260-4 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.7%
  7. 2015 RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome JOURNAL OF CLINICAL INVESTIGATION DOI 10.1172/JCI80102 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 95.4%
  8. 2015 A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I title American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.36955 YÖKSİS SJR Q2 JCR Q3 OpenAlex 84.8%
  9. 2014 Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome The American Journal of Human Genetics DOI 10.1016/j.ajhg.2014.10.008 YÖKSİS SJR Q1 JCR Q1 OpenAlex 87.5%
  10. 2013 title Mutations in the interleukin receptor i IL11RA i cause autosomal recessive Crouzon like craniosynostosis title Molecular Genetics & Genomic Medicine DOI 10.1002/mgg3.28 YÖKSİS SJR Q2 JCR Q2 OpenAlex 82.2%
  11. 2013 A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome Human Genetics DOI 10.1007/s00439-013-1337-9 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.7%
  12. 2012 Attenuated BMP1 Function Compromises Osteogenesis Leading to Bone Fragility in Humans and Zebrafish The American Journal of Human Genetics DOI 10.1016/j.ajhg.2012.02.026 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.3%
  13. 2011 A mutation screen in patients with Kabuki syndrome Human Genetics DOI 10.1007/s00439-011-1004-y YÖKSİS SJR Q2 JCR Q1 OpenAlex top 10% OpenAlex 97.9%
  14. 2010 CEP152 is a genome maintenance protein disrupted in Seckel syndrome Nature Genetics DOI 10.1038/ng.725 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.1%
  15. 2009 ALX4 dysfunction disrupts craniofacial and epidermal development HUMAN MOLECULAR GENETICS DOI 10.1093/hmg/ddp391 YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.7%
  16. 2024 Development of Artificial Intelligence Technologies and Language Learning Artificial Intelligence in Educational Research DOI 10.5281/zenodo.11243867 YÖKSİS OpenAlex 79.3%
  17. 2021 The Influence of L1 on the Acquisition of L2 Collocations: Turkish ELT Students TESL- EJ DOI https://www.tesl-ej.org/wordpress/issues/volume25/ej99/ej99a2/ YÖKSİS SJR Q1
  18. 2018 Perceptions of ELT Students Related to Learner Autonomy in Language Learning International Journal of Higher Education DOI 10.5430/ijhe.v7n4p76 YÖKSİS SJR Q4 OpenAlex top 10% OpenAlex 90.8%

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