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Akademisyen

DİDEM ÖZKAN

DOKTOR ÖĞRETİM ÜYESİ

İSTANBUL OKAN ÜNİVERSİTESİ SAĞLIK HİZMETLERİ MESLEK YÜKSEKOKULU TIBBİ HİZMETLER VE TEKNİKLER BÖLÜMÜ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Tıbbi Biyoloji

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

  • Makale 26
  • Proje 0
  • Kitap 0
  • Bildiri 0
  • Patent 0
  • Sanatsal 0
Scopus (SJR) Q1 3 Q2 6 Q3 2 Q4 6
WoS (JCR) Q1 2 Q2 2 Q3 5 Q4 11
TR Index 8 makale

Alan+yıl+tür normalize OpenAlex yüzdelik — Clarivate ESI / SciVal değildir.

Üst %1 makale 0
Üst %10 makale 1
Ort. yüzdelik 37.9%
Üst %1 payı 0.0%
Üst %10 payı 5.6%

Makaleler

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

Dizin filtreleri

Toplam 26 yayın

Makale listesi

  1. 2022 Angiotensinogen (AGT) Gene Screening and Nutrigenetic Approaches in Patients Diagnosed with Hypertension Turkish Journal of Clinics and Laboratory DOI 10.18663/tjcl.1137153 YÖKSİS TR Index OpenAlex 16.9%
  2. 2021 Identification of novel TUBB1 variants in patients with macrothrombocytopenia TURKISH JOURNAL OF MEDICAL SCIENCES DOI 10.3906/sag-2003-259 YÖKSİS TR Index SJR Q3 JCR Q3 OpenAlex 55.1%
  3. 2020 Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population ACTA HAEMATOLOGICA DOI 10.1159/000505174 YÖKSİS SJR Q2 JCR Q4 OpenAlex 54.2%
  4. 2020 Analysis of Protein C Inhibitor/ SERPINA5 Turkish Journal of Clinics and Laboratory DOI 10.18663/tjcl.645392 YÖKSİS TR Index OpenAlex 41.6%
  5. 2019 Asbestos-related Diseases in Turkey: Caused Not Only by Naturally Occurring Fibers but Also by Industrial Exposures American Journal of Respiratory and Critical Care Medicine DOI 10.1164/rccm.201810-1922LE YÖKSİS SJR Q1 JCR Q1 OpenAlex 63.2%
  6. 2018 A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia The Egptian Journal of Medical Human Genetics DOI 10.1016/j.ejmhg.2017.08.006 YÖKSİS SJR Q4 JCR Q4 OpenAlex 12.0%
  7. 2018 The Investigation of the Apoptose Structural Effects and Mechanism in Leukemic Cells of Sirt1 Inhibitor Sirtinol Open Access Library Journal DOI 10.4236/oalib.1104268. YÖKSİS OpenAlex 0.8%
  8. 2016 Variables determining the development of colistin-associated renal impairment Wiener klinische Wochenschrift DOI 10.1007/s00508-015-0773-z YÖKSİS SJR Q3 JCR Q3 OpenAlex 49.6%
  9. 2022 Molecular profiling of TAM Tyrosine Kinase Receptors and Ligands in Endometrial Carcinoma: An in silico study. Taiwanese Journal of Obsetrics and Gynecology YÖKSİS SJR Q2 JCR Q3
  10. 2022 Beta-lactam antibiotic-induced thrombocytopenia: MYH9 & TUBB1 genes ANNALS OF CLINICAL AND ANALYTICAL MEDICINE DOI 10.4328/ACAM.21174 YÖKSİS JCR Q4 OpenAlex 15.7%
  11. 2022 Pathogenic Ala303Val mutation in the PROS1 gene is associated with the pathogenesis of Deep Vein Thrombosis Erciyes Medical Journal DOI 10.14744/etd.2021.42223 YÖKSİS TR Index SJR Q4 JCR Q3 OpenAlex 63.9%
  12. 2022 Identification Of Circadian-Related Gene Mutation And Expression Patterns In Skin Cancer Sağlık Profesyonelleri Araştırma Dergisi YÖKSİS
  13. 2021 Why Cytoskeletal Associated Proteins are Important in Colorectal Cancer Patients: Molecular & Bioinformatic Analysis Lokman Hekim Health Sciences DOI 10.14744/lhhs.2021.70004 YÖKSİS TR Index OpenAlex 14.5%
  14. 2018 Screening of single nucleotide polymorphism in CD95 (APO-1/FAS) promoter region (G-1377A) in children with acute leukemia The Egyptian Journal of Haematology DOI 10.4103/ejh.ejh_55_17 YÖKSİS JCR Q4 OpenAlex 6.0%
  15. 2018 Screening of EPCR gene mutations in children with acute lymphoblastic leukemia The Egyptian Journal of Haematology DOI 10.4103/ejh.ejh_13_18 YÖKSİS JCR Q4 OpenAlex 20.1%
  16. 2018 Congenital macrothrombocytopenia: is it misdiagnosed? Haemophilia DOI 10.1111/hae.13393 YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.1%
  17. 2015 Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia Platelets YÖKSİS SJR Q2 JCR Q2
  18. 2014 Hemoglobin Lansing (Alpha)[HBA2 CD87 (HIS GLU)(C A)] in a Turkish individual resulting from another nucleotide substitution Turkish Journal of Hematology YÖKSİS TR Index SJR Q4 JCR Q4
  19. 2014 C0182: First Observation of De Novo MYH9 Gene Mutation in a Patient with Macrothrombocytopenia Thrombosis Research DOI 10.1016/S0049-3848(14)50256-3 YÖKSİS
  20. 2013 MUTATION ANALYSIS IN TURKISH RARE BLOOD DISORDERS HAEMATOLOGICA YÖKSİS SJR Q1 JCR Q1

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