Academician
ÇİĞDEM YÜCE KAHRAMAN
DOÇENT
ATATÜRK ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Article counts come from two sources, each shown separately: YÖKSİS (academic declarations) and OpenAlex (open scholarly catalog). Patents and artistic activities are listed under the Works tabs below.
Index quartiles
Scopus (SJR)
28 Total
- Q1 4
- Q2 13
- Q3 5
- Q4 6
Other counts
- YÖKSİS rows 29 Q1 0 Q2 0 Q3 0 Q4 0
WoS (JCR)
26 Total
- Q1 5
- Q2 2
- Q3 13
- Q4 6
Other counts
- YÖKSİS rows 27 Q1 0 Q2 0 Q3 0 Q4 0
TR Index
11 articles
OpenAlex citation percentiles
Top 1% articles
0
Top 10% articles
1
Avg percentile
50.9%
Articles with percentile
35
OpenAlex citation percentile; covered works only (~52%).
What do these indicators mean?
- Q1–Q4: the quartile of the journal in the given index (Scopus/WoS). Q1 = top 25%, Q4 = bottom 25%.
- Top 1% / top 10%: number of works among the top 1% or 10% most-cited worldwide in the same field and year.
- Avg percentile: mean citation percentile of the works (100 = highest).
- Source: index quartiles from Scopus/WoS and TR Index flags; citation percentiles from OpenAlex.
Proceedings
Conference proceedings recorded in YÖKSİS.
Records
- 2021 About Gene Therapy
- 2022 Genetic Analysis Of Mutations In Hematological Malignancies By NextGeneration Sequencing
- 2010 A case with Crouzon syndrome without craniosynostosis.
- 2014 Endotelyal Nitrik Oksit Sentaz (eNOS) Gen Polimorfizmlerinin Varikoselle İlişkisi ve Bu Polimorfizmlerin eNOS Geni mRNA Ekspresyonuna Etkisi. 1
- 2014 Bruck Sendromlu Bir Vaka
- 2019 A novel mutation of a rare genetic condition: Primary hypertrophic osteoarthropathy
- 2019 45,X and SRY positive male with infertility: A case report
- Legius Syndrome with a Preliminary Diagnosis of NF1-like Syndrome: Case Report
- 2024 Kanserde Vazgeçilmez Bir Araç Olan NGS:AML Hastalarında Tespit Edilen Varyantların Değerlendirilmesi
- 2024 A Mother and Daughter with Goltz Syndrome
- 2019 Nutrigenetics, Nutrigenomics and Chronic Diseases
- 2019 A case of Cri du Chat syndrome
- 2022 Novel finding in a patient with 17p13.1 deletion syndrome: a case report
- Kanser Hastalarında MUTYH Geni Varyantlarının Retrospektif Değerlendirilmesi
- 2024 A decade of insights:prenatal cytogenetic diagnosis results of high-risk pregnancies at Atatürk University Medical Genetics Laboratory(ATAGEN)
- 2025 RetrospectiveEvaluationofNGSResultsinPatientswithColorectalPolyposis
- 2025 EvaluationoftheLINC00958/miR-3619-5p/CTNNB1pathwayinpatientswithcolorectalcancer
- 2023 SRY-positive 45, X male with monoorchism and hypospadias
- 2022 Laringeal Skuamöz Hücreli Karsinomlu Hastalarda Cerna Düzenleyici Yolakta Bulunan Uca1/mir-138/cdk6 Ekspresyon Seviyelerinin Değerlendirilmesi
- 2019 Coronal Synostosis Syndrome (Muenke Syndrome)