Kahraman, Cigdem Yuce

Genetic Polymorphisms and Their Association With Endodontic Postoperative Pain: A Systematic Review

A decade of insights: prenatal cytogenetic diagnosis results of high-risk pregnancies at Ataturk University Medical Genetics laboratory (ATAGEN)

Whole Exome Sequencing in Neurodevelopmental Disorders: A Single Center Study

An Investigation on the Correlation Between Diabetic Foot Infection, Osteomyelitis, Venous Insufficiency, and IL-6 (-174 G>C) and TNF-α (-238 G>A) Gene Polymorphisms

SRY-positive 45, X male with monoorchism and hypospadias

Novel finding in a patient with 17p13.1 deletion syndrome: a case report

Evaluation of Phenotypes and <i>CLDN16</i> Variants in 2 Different Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Families: Phenotypic Differences in Siblings and Phenotypic Similarity in Monozygotic Twins

Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation Sequencing

A new case of Turnpenny-Fry syndrome

Therapeutic Potential of Ferulic Acid in Alzheimer's Disease

Next-Generation Sequencing Panel Test in Myeloid Neoplasms and Evaluation with the Clinical Results

Relationship between the <i>TAS2R38</i> and <i>TAS1R2</i> polymorphisms and the dental status in obese children

Molecular Genetics and Cytotoxic Responses to Titanium Diboride and Zinc Borate Nanoparticles on Cultured Human Primary Alveolar Epithelial Cells

A novel genomic variant in two siblings with very low-density lipoprotein receptor-associated cerebellar hypoplasia

Evaluation of the Relationship between Janus Kinase 2 Mutational Burden and Clinical Findings in Adult Myeloproliferative Neoplasm Patients

Clinical and molecular evaluation of <i>MEFV</i> gene variants in the Turkish population: a study by the National Genetics Consortium

The Assessment of Selected miRNA Profile in Familial Mediterranean Fever

The relationship between NLRP3 rs10159239 and Vaspin rs2236242 gene variants and obstructive sleep apnea

Evaluation of the relationship between pentraxin 3 (PTX3) rs2305619 (281A/G) and rs1840680 (1449A/G) polymorphisms and the clinical course of COVID-19

Is There an Association Between Nasal Polyposis and ADAMTS Genes Expressions?

A Novel Mutation of <i>ATP7B</i> Gene in a Case of Wilson Disease

Glycyl-L-Prolyl-L-Glutamate Pseudotripeptides for Treatment of Alzheimer's Disease