Get started
Author

Betül Eser

Observed names: B Eser, B. Eser, Betul ESER, Betul Eser, Betül ESER, Betŭl Eser, Eser, Betul
OpenAlex ID: A5083644195
Association of the Polymorphisms of Vitamin D Receptor and Aggrecan Genes with Degenerative Disc Disease
2010 · Betul Eser, Tulin Cora, et al. · Genetic Testing and Molecular Biomarkers · 86
Analysis of Familial Mediterranean Fever Gene Mutations in 202 Patients with Familial Mediterranean Fever
2008 · Mustafa Solak, Handen Yıldız, et al. · Genetic Testing · 40
Association of estrogen receptor alpha and collagen type I alpha 1 gene polymorphisms with bone mineral density in postmenopausal women
2010 · M. O. Erdogan, H. Yıldız, et al. · Osteoporosis International · 39
The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 ( PAI -1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels
2014 · Esin Sogutlu Sari, Alper Yazici, et al. · Cutaneous and Ocular Toxicology · 20
Short aggrecan gene repetitive alleles associated with lumbar degenerative disc disease in Turkish patients
2011 · O. Eser, B. Eser, et al. · Genetics and Molecular Research · 20
PDF
The effects of IL-1A and IL-6 genes polymorphisms on gene expressions, hormonal and biochemical parameters in polycystic ovary syndrome
2016 · Betul Eser, Mine Islimye Taskin, et al. · Journal of Obstetrics and Gynaecology · 19
Effects of MMP-1 and MMP-3 gene polymorphisms on gene expression and protein level in lumbar disc herniation
2016 · B. Eser, O. Eser, et al. · Genetics and Molecular Research · 17
PDF
NUCB2 gene polymorphism and its relationship with nesfatin-1 levels in polycystic ovary syndrome
2015 · Mine Islimye Taskin, Betul Eser, et al. · Gynecological Endocrinology · 15
C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects
2010 · M.O. Erdogan, S.H. Yildiz, et al. · Genetics and Molecular Research · 15
PDF
677C>T and 1298A>C polymorphisms of methylenetetrahydropholate reductase gene and biochemical parameters in Turkish population with spina bifida occulta.
2010 · Betul Eser, Murat Cosar, et al. · PubMed · 14
Evaluation of tool-like receptor-2 and 4 and interleukin-6 gene expressions in Turkish rheumatoid arthritis patients
2016 · Betul Eser, Nilay Sahin · Clinical Rheumatology · 11
Genotyping for Cx26 and Cx30 Mutations in Cases with Congenital Hearing Loss
2008 · Neslihan Evirgen, Mustafa Solak, et al. · Genetic Testing · 11
A case of subcutaneous panniculitis‐like T‐cell lymphoma with haemophagocytosis developing secondary to chemotherapy
2004 · B Eser, F Altuntas, et al. · Journal of the European Academy of Dermatology and Venereology · 8
The effects of polymorphisms of death pathway genes and mitochondrial pathway genes in intervertebral disc degeneration
2016 · Betul Eser, Olcay Eser, et al. · Turkish Neurosurgery · 7
PDF
Lack of association between the methylenetetrahydropholate reductase gene A1298C polymorphism and neural tube defects in a Turkish study group
2016 · S.H. Yildiz, M. Ozdemir Erdogan, et al. · Genetics and Molecular Research · 7
Double Aneuploidy: A Case of Trisomy 21 with XYY
2011 · Betül Eser, Resit Köken, et al. · Electronic Journal of General Medicine · 5
PDF
Intracerebral Hematoma Complicated With Brain Abscess in an Infant -Case Report-
2008 · Olcay ESER, Murat COSAR, et al. · Neurologia medico-chirurgica · 4
PDF
Mineralocorticoid receptor gene-2G/C polymorphism in central serous chorioretinopathy and relation of polymorphism with plasma cortisol levels
2016 · Alper Yazici, Esin Sogutlu Sari, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 3
Ailevi Akdeniz Ateşi Ön Tanısı Alan 165 Olgunun MEFV Geni Mutasyonlarının İncelenmesi
2008 · Mustafa Solak, Handan Yıldız, et al. · Turkiye Klinikleri Tip Bilimleri Dergisi · 3
Two different nucleotide substitutions ofAPCgene in a family with familial adenomatous polyposis
2015 · Betul Eser, Murat Yıldar · Journal of Surgical Case Reports · 2
PDF
A Deletion Mutation of the Connexin 26 (Gjb2) Gene in a Turkish Patient with Vohwinkel Syndrome .
2016 · S Ozturk, I Can, et al. · PubMed · 1
Increased Expression of Matrix Metalloproteinases in Ligamentum Flavum Hypertrophy of the Patients with Lumbar Spinal Stenosis
2016 · Betul Eser, Olcay Eser, et al. · International Journal of Human Genetics
Prenatal Diagnosis of a De Novo Partial Trisomy 17q Case Associated with Increased Nuchal Translucency, Hypoplastic Left Heart Syndrome, Cerebral Anomalies: Case Report
2016 · Mehmet TÜRE, Şebnem ÖZEMRİ SAĞ, et al. · Turkiye Klinikleri Journal of Gynecology and Obstetrics
PDF
Two Different Mutations of Gl13 Gene in Two Different Syndromes.
2016 · S Candan, G Yesil, et al. · PubMed
Cscr中盐皮质激素受体基因-2g/c的多态性及其与血浆皮质醇水平的关系
2016 · Alper Yazıcı, Esin Söğütlü Sarı, et al. · 国际眼科杂志(中文刊）
Works count: 30
Citation count: 347
H-index: 11
I10-index: 12
Year
Topic
Type