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Akademisyen

ASLIHAN KİRAZ

DOÇENT

ERCİYES ÜNİVERSİTESİ

Araştırma konuları OpenAlex
Akademik özet YÖKSİS ve OpenAlex ayrı sayılır.
Makale 58
YÖKSİS58 OpenAlex0
Proje 1
Kitap 7
Bildiri 51

Atıf etkisi

OpenAlex YÖKSİS makalelerinden OpenAlex’te eşleşen: 10
h-indeks 6 Türkiye yüzdelik dilimi: 72 Büyük işbirlikleri hariç: h 5 · 1 makale
i10-indeks
6
Toplam atıf
94
Türkiye’de üst %34
Makale başına
9,4
FWCI
0,75
1,00 = dünya ortalaması
Dünyada üst %1
0
Dünyada üst %10
0

En çok atıf alan makaleleri

  1. TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis 2012 18 atıf
  2. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium 2022 17 atıf
  3. Combination of two different homozygote mutations in Pompe disease 2016 16 atıf

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) 49
  • Q1 9
  • Q2 17
  • Q3 19
  • Q4 4
WoS (JCR) 48
  • Q1 4
  • Q2 10
  • Q3 15
  • Q4 19
TR Index TR Index

15 makale

OpenAlex atıf yüzdelik
  • Üst %1 0
  • Üst %10 0
  • Ort. 58.1%
  • n 10
Diğer sayımlar

Scopus (SJR)

  • YÖKSİS satırı 50

WoS (JCR)

  • YÖKSİS satırı 49

Makaleler

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

Yayını olan dergiler

45 dergi
Scopus (SJR)
Q1 9 Q2 17 Q3 19 Q4 4
WoS (JCR)
Q1 4 Q2 10 Q3 15 Q4 19
TR Index
15 makale

Makale listesi

  1. 2025 Brain malformation, neurodevelopmental disorder and epilepsy in a case of two rare genetic diseases: overlapping phenotype Neurogenetics DOI 10.1007/s10048-024-00795-3 YÖKSİS
  2. 2025 A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis Neurogenetics DOI 10.1007/s10048-025-00825-8 YÖKSİS SJR Q3 JCR Q4
  3. 2025 Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases Molecular biology reports DOI 10.1007/s11033-025-11101-1 YÖKSİS SJR Q2 JCR Q3
  4. 2025 Blended Phenotypes of Sexual Development Disorder and Coenzyme Q10 Deficiency, Together with a Sibling with Homozygous Variants in the AHI1 Gene Molecular Syndromology DOI 10.1159/000541717 YÖKSİS SJR Q3 JCR Q4
  5. 2025 A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature American journal of medical genetics. Part A DOI 10.1002/ajmg.a.64072 YÖKSİS SJR Q2 JCR Q4
  6. 2025 The Relationship Between Bone Morphogenic Protein-4 and Visceral-Central Adiposity Pediatric gastroenterology, hepatology & nutrition. DOI 10.5223/pghn.2025.28.5.312 YÖKSİS SJR Q2 JCR Q3
  7. 2024 A Case Series of Three Patients with Cleidocranial Dysplasia: Clinical Presentation and Diagnostic Considerations Cleft Palate Craniofac J. DOI 10.1177/10556656241234742. YÖKSİS SJR Q1 JCR Q3
  8. 2024 Recurrent symptomatic urolithiasis in a patient with cystic fibrosis Pediatric Nephrology DOI 10.1007/s00467-024-06433-2 YÖKSİS SJR Q1 JCR Q1
  9. 2024 Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients JOURNAL OF CLINICAL LABORATORY ANALYSIS DOI 10.1002/jcla.24997 YÖKSİS SJR Q1 JCR Q2
  10. 2024 Effect of radiation dose rates and cisplatin on cytogenetic damage in rats receiving head neck radiotherapy Journal of Cancer Research and Therapeutics DOI 10.4103/jcrt.jcrt_2006_22 YÖKSİS SJR Q2 JCR Q4 OpenAlex 48.1%
  11. 2024 The increased chromosomal DNA damage in patients with Familial Mediterranean Fever Biotechnic & Histochemistry DOI 10.1080/10520295.2024.2383960 YÖKSİS SJR Q2 JCR Q4
  12. 2023 Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia JOURNAL OF MEDICAL VIROLOGY DOI 10.1002/jmv.28457. YÖKSİS SJR Q1 JCR Q1
  13. 2023 Osteopontin as an early predictor of atherosclerosis in attack-free Familial Mediterranean fever patients Medicine (Baltimore) DOI 10.1097/MD.0000000000035137. YÖKSİS SJR Q3 JCR Q2
  14. 2023 Detection of Novel NF1 Variants with Next-Generation DNA Sequencing Technology and Genotype-Phenotype Characteristics of Neurofibromatosis Erciyes Medical Journal DOI 10.14744/etd.2022.90023 YÖKSİS TR Index SJR Q4 JCR Q3
  15. 2023 Are MUC5B and TERT mutations genetic risk factors for pulmonary fibrosis in individuals with severe COVID-19? Tuberculosis and Thorax DOI 10.5578/tt.20239905. YÖKSİS TR Index SJR Q3 JCR Q4
  16. 2022 Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in theTurkish population Journal of Medical Virology DOI 10.1002/jmv.27976 YÖKSİS SJR Q1 JCR Q1 OpenAlex 82.1%
  17. 2022 A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu‐Boycott‐Innes syndrome American Journal of Medical Genetics Part A DOI 10.1002/ajmg.a.62667 YÖKSİS SJR Q2 JCR Q3
  18. 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 YÖKSİS SJR Q2 JCR Q3 OpenAlex 75.1%
  19. 2022 Polisitemi ile Takipli Hastalarda Genetik Mutasyon Test Sonuçlarının Retrospektif Analizi Journal of Anatolian Medical Research DOI https://dergipark.org.tr/en/download/article-file/2777341 YÖKSİS
  20. 2021 Restrictive cardiomyopathy with ring chromosome 6 anomaly in a child The Anatolian Journal of Cardiology DOI 10.5152/AnatolJCardiol.2021.80820 YÖKSİS TR Index SJR Q3 JCR Q4

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