- Q1 13
- Q2 14
- Q3 24
- Q4 9
Akademisyen
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
Atıf etkisi
OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 64- 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
En çok atıf alan makaleleri
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 ?-
Ana dal Sağlık Bilimleri Temel AlanıPuan sırası #2.839/ 43.834 üst %6,5Puan 48,05 dergi 47,8 · OA ek 0,25
- Makale sırası3.427/43.834
- Scopus sırası2.189/43.834
- WoS sırası2.204/43.834
- YÖKSİS82
- Scopus60
- WoS59
-
Yan dal Tıbbi GenetikPuan sırası #39/ 280 üst %13,9Puan 48,05 dergi 47,8 · OA ek 0,25
- Makale sırası40/280
- Scopus sırası35/280
- WoS sırası35/280
- YÖKSİS82
- Scopus60
- WoS59
Dizin çeyrekleri
?- Q1 9
- Q2 8
- Q3 12
- Q4 30
28 makale
- 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
- 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
Makale listesi
- 2025 Investigating the dual role of mitochondrial and nuclear genome variants in pediatric cardiomyopathies YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %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 üst %10 OpenAlex 96.1%
- 2025 A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia YÖKSİS SJR Q1 JCR Q1 OpenAlex üst %10 OpenAlex 91.2%
- 2025 The Role of miRNA Expression Profiles in Different Biofluids in Aneurysm Rupture YÖKSİS SJR Q2 JCR Q2 OpenAlex üst %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%