- Q1 13
- Q2 14
- Q3 24
- Q4 9
Academician
OĞUZ ÇİLİNGİR
PROFESÖR
ESKİŞEHİR OSMANGAZİ ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
- Epigenetics and DNA Methylation8
- Genomic variations and chromosomal abnormalities6
- Chronic Myeloid Leukemia Treatments5
- Cancer-related molecular mechanisms research5
- Acute Myeloid Leukemia Research4
- Chronic Lymphocytic Leukemia Research4
- Inflammasome and immune disorders4
- Prenatal Screening and Diagnostics4
- Hereditary Neurological Disorders3
- Sexual Differentiation and Disorders3
- Genomics and Rare Diseases3
- Glaucoma and retinal disorders3
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
Citation impact
OpenAlex YÖKSİS articles matched in OpenAlex: 64- i10-index
- 14
- Total citations
- 420 Top 13% in Türkiye
- Per article
- 6.6
- FWCI
- 0.71 1.00 = world average
- World top 1%
- 0
- World top 10%
- 5
Most cited articles
h-index and citations are computed from the citation counts of this academic’s YÖKSİS articles matched in OpenAlex (not Google Scholar, WoS or Scopus). Unmatched articles are not included.
Field ranking
YÖKSİS ?-
Main field Sağlık Bilimleri Temel AlanıPoints rank #2,839/ 43,834 top 6.5%Score 48.05 journal 47.8 · OA add 0.25
- Article rank3,427/43,834
- Scopus rank2,189/43,834
- WoS rank2,204/43,834
- YÖKSİS82
- Scopus60
- WoS59
-
Side field Tıbbi GenetikPoints rank #39/ 280 top 13.9%Score 48.05 journal 47.8 · OA add 0.25
- Article rank40/280
- Scopus rank35/280
- WoS rank35/280
- YÖKSİS82
- Scopus60
- WoS59
Index quartiles
?- Q1 9
- Q2 8
- Q3 12
- Q4 30
28 articles
- Top 1% 0
- Top 10% 5
- Avg 51.5%
- n 65
Other counts
Scopus (SJR)
- YÖKSİS rows 61
WoS (JCR)
- YÖKSİS rows 61
TR Index
- YÖKSİS rows 29 articles
Articles
Articles with YÖKSİS and OpenAlex source split; narrow by quartile or TR Index.
Journals with publications
57 journals
- 1305-4953 6
- Turkish Journal of Medical Sciences 4
- 1302-4612 2
- 2456-6373 2
- American Journal of Medical Genetics, Part A 2
- Anatolian Journal of Cardiology 2
- Cancer Genetics 2
- Cytogenetic and Genome Research 2
- European Journal of Human Genetics 2
- JCRPE Journal of Clinical Research in Pediatric Endocrinology 2
- Neurobiology of Aging 2
- Ophthalmic Genetics 2
- Turkish Journal of Gastroenterology 2
- Turkish Journal of Hematology 2
- Turk Onkoloji Dergisi 2
- 1300-056X 1
- 2148-8878 1
- 2168-1589 1
- 2168-1597 1
- 2329-6682 1
- 2602-2079 1
- 2602-3032 1
- 2718-0948 1
- Actas Dermo-Sifiliograficas 1
- Andrologia 1
- Annals of Saudi Medicine 1
- Biomedical Research (India) (discontinued) 1
- British Journal of Dermatology 1
- Cancer Genetics and Cytogenetics 1
- Eurasian Journal of Medicine 1
- European Heart Journal 1
- Experimental and Therapeutic Medicine (discontinued) 1
- Fertility and Sterility 1
- Functional and Integrative Genomics 1
- Gazi Medical Journal 1
- Genes 1
- Hormone Research in Paediatrics 1
- International Journal of Endocrinology 1
- International Journal of Ophthalmology 1
- JAMA Ophthalmology 1
- Journal of Health Science 1
- Journal of Korean Neurosurgical Society 1
- Journal of Neurological Sciences 1
- Journal of Pediatric Endocrinology and Metabolism 1
- Journal of Pediatric Genetics 1
- Journal of Pediatric Neurology 1
- Journal of the Turkish German Gynecology Association 1
- Molecular Biology Reports 1
- Molecular Cytogenetics 1
- Molecular Syndromology 1
- Scientific Reports 1
- Turkish Journal of Pediatrics 1
- Turkiye Klinikleri Journal of Medical Sciences 1
- Turkiye Klinikleri Pediatri 1
- Turk Oftalmoloiji Dergisi 1
- UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi 1
- World Journal of Urology 1
Article list
- 2025 Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.1%
- 2025 Mutant p.Val114Ala Transthyretin-Related Cardiac Amyloidosis with Heart Failure and Right Bundle Branch Block YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 6.3%
- 2025 Chromosomal abnormalities in couples with recurrent pregnancy loss: a 16-year cross-sectional study of 4030 cases from Turkey YÖKSİS SJR Q3 JCR Q2 OpenAlex top 10% OpenAlex 96.1%
- 2025 A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 91.2%
- 2025 The Role of miRNA Expression Profiles in Different Biofluids in Aneurysm Rupture YÖKSİS SJR Q2 JCR Q2 OpenAlex top 10% OpenAlex 90.7%
- 2025 Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrine Syndrome Type 1: A Case Report and Review of the Literature YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 54.0%
- 2025 Cerebrospinal Fluid MicroRNAs as Early Biomarker Candidates for Predicting Vasospasm Following Aneurysmal Subarachnoid Hemorrhage YÖKSİS SJR Q2 JCR Q2 OpenAlex 71.5%
- 2025 Evaluation of Genomic Variants in Non-syndromic Congenital Heart Disease in Turkish Pediatric Group YÖKSİS OpenAlex 12.9%
- 2025 A Rare Case of Hereditary Sensory and Autonomic Neuropathy Type 4 in a 3-Year-Old: Clinical and Genetic Findings YÖKSİS SJR Q4 OpenAlex 11.2%
- 2024 Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2 YÖKSİS SJR Q3 JCR Q4 OpenAlex 53.6%
- 2024 Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions? YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 68.8%
- 2024 KLL Olgularında NOTCH1 Gen Amplifikasyonu YÖKSİS TR Index OpenAlex 48.9%
- 2023 Evaluation of the Association Between CRNDE Plasma Expression Level, KRAS, NRAS, and BRAF Variants in Patients with advanced CRC YÖKSİS TR Index SJR Q4 JCR Q4 OpenAlex 40.1%
- 2023 Genetic Investigations in Turkish Idiopathic Pancreatitis Patients Show Unique Characteristics YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 71.6%
- 2023 A genetic polymorphism on chromosome 4q25 (rs17570669_T) may predict atrial fibrillation recurrence after successful electrical cardioversion YÖKSİS SJR Q1 JCR Q1 OpenAlex 29.0%
- 2023 Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus YÖKSİS TR Index SJR Q2 JCR Q2 OpenAlex 84.5%
- 2023 ERCC8 related Cockayne syndrome type-1: A rare entity diagnosed in a Turkish boy YÖKSİS OpenAlex 8.7%
- 2022 An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3 YÖKSİS SJR Q3 JCR Q4
- 2022 The Impact of Cytogenetic Aberrations in the Clonal Evolution of Chronic Myeloid Leukemia: A Single-Center Experience Among 450 Turkish Patients Cohort Study YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 49.6%
- 2022 Clinical and Molecular Evaluation of MEFV Gene Variants in the Turkish Population: A Study by The National Genetics Consortium YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%