Akademisyen

MALİK EJDER YILDIRIM

PROFESÖR

SİVAS CUMHURİYET ÜNİVERSİTESİ TIP FAKÜLTESİ DAHİLİ TIP BİLİMLERİ BÖLÜMÜ

Ana Dal Sağlık Bilimleri Temel Alanı
Yan Dal Tıbbi Genetik

Kayıtlı çıktılara kısa bakış — ayrıntılar aşağıda.

Makale 47
Proje 0
Kitap 4
Bildiri 18
Patent 0
Sanatsal 0

Scopus (SJR) Q1 0 Q2 14 Q3 7 Q4 16

WoS (JCR) Q1 0 Q2 1 Q3 7 Q4 18

TR Index 22 makale

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

Üst %1 makale 0

Üst %10 makale 3

Ort. yüzdelik 41.3%

Üst %1 payı 0.0%

Üst %10 payı 9.4%

Makaleler

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

Makale listesi

2026 A POSSIBLE ASSOCIATION OF ABCB1 (MDR1) GENE rs1045642 VARIANT (SNP) WITH THE DEVELOPMENT OF RENAL GLOMERULAR DISEASES Bozok Tıp Dergisi DOI 10.16919/bozoktip.1758051 YÖKSİS TR Index OpenAlex 57.6%
2025 Methylation profile of CD247 and FOXP3 genes and frequency of certain HLA-DQ haplotypes in Celiac disease Clinics and Research in Hepatology and Gastroenterology DOI 10.1016/j.clinre.2025.102562 YÖKSİS SJR Q2 JCR Q3 OpenAlex 3.8%
2025 The Genetics of Sexual Development Disorders Cumhuriyet Medical Journal DOI 10.7197/cmj.1605185 YÖKSİS TR Index SJR Q4 OpenAlex 3.6%
2024 Genetic and Epigenetic Changes of CDKN2A in Gastric Cancer Cumhuriyet Medical Journal DOI 10.7197/cmj.1443256 YÖKSİS TR Index SJR Q4 OpenAlex 5.8%
2022 A Negative Correlation Between <i>MEFV</i> Mutations and Allergic Diseases The Journal of Pediatric Research DOI 10.4274/jpr.galenos.2021.33407 YÖKSİS TR Index SJR Q3 JCR Q4 OpenAlex 4.5%
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%
2021 Effects of ApaI, FokI, and BsmI gene polymorphisms of the vitamin D receptor on serum vitamin D level in Turkish MS patients with different types and severities of the disease Annals of Medical Research DOI 10.5455/annalsmedres.2021.01.096 YÖKSİS TR Index OpenAlex 20.7%
2020 An Examination of Paraoxonase 1 Gene Polymorphism inCases of Chronic Otitis Media ENT Updates DOI 10.32448/entupdates.594272 YÖKSİS TR Index JCR Q4 OpenAlex 16.0%
2019 Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia ANNALS OF SAUDI MEDICINE DOI 10.5144/0256-4947.2019.382. YÖKSİS SJR Q3 JCR Q4 OpenAlex 75.1%
2019 The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas The Journal of International Advanced Otology DOI 10.5152/iao.2019.5401 YÖKSİS SJR Q2 JCR Q4 OpenAlex 57.2%
2019 The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study Journal of Gynecology Obstetrics and Human Reproduction DOI 10.1016/j.jogoh.2019.05.014. YÖKSİS SJR Q3 JCR Q4 OpenAlex üst %10 OpenAlex 91.3%
2018 Genetic variants in the microRNA machinery gene (Dicer) have a prognostic value in the management of endometrial cancer Journal of Cancer Research and Therapeutics DOI 10.4103/0973-1482.187291 YÖKSİS SJR Q3 JCR Q4 OpenAlex 47.0%
2017 The Association of Plasminogen Activator Inhibitor Type 1 (PAI-1) Level and PAI-1 4G/5G Gene Polymorphism with the Formation and the Grade of Endometrial Cancer Biochemical Genetics DOI 10.1007/s10528-017-9796-7 YÖKSİS SJR Q2 JCR Q3 OpenAlex 61.5%
2016 MCP 1 2518 A G and CCR2 V64I polymorphisms in Turkish patients with lung cancer Journal of Experimental and Clinical Medicine DOI 10.5835/jecm.omu.33.02.006 YÖKSİS SJR Q4 OpenAlex 7.8%
2015 Bcıı RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long term hemodialysis Renal Failure DOI 10.3109/0886022x.2014.982954 YÖKSİS SJR Q2 JCR Q4 OpenAlex 64.0%
2015 Vitamin D deficiency, myopathy and VDR gene polymorphism in a young woman Cumhuriyet Medical Journal DOI 10.7197/cmj.v37i2.5000117146 YÖKSİS TR Index SJR Q4 OpenAlex 3.2%
2015 A female infant case with tetrasomy 18p Cumhuriyet Medical Journal DOI 10.7197/cmj.v37i4.5000117147 YÖKSİS TR Index SJR Q4 OpenAlex 7.9%
2015 Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion Molecular Cytogenetics DOI 10.1186/s13039-015-0195-7 YÖKSİS SJR Q2 JCR Q4 OpenAlex üst %10 OpenAlex 97.7%
2014 Plazminojen aktivatör inhibitor-1 (PAI-1) 4g/4g polimorfizminin gebelik kayıplarıyla ilişkisi Cumhuriyet Medical Journal DOI 10.7197/cmj.v36i3.5000060803 YÖKSİS TR Index SJR Q4 OpenAlex 4.2%
2011 The association between methylene tetrahydrofolate reductase gene polymorphism and lung cancer risk Molecular Biology Reports DOI 10.1007/s11033-010-0194-z YÖKSİS SJR Q2 JCR Q2 OpenAlex 89.6%

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