Selma Demir

Edirne, 22030, Turkey

Last Updated: 09/26/2026

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Found 45 publications

Exosomal lncRNAs HOTAIR, HULC, and ANRIL: Decoding the Biomarker Landscape of Sporadic Triple-Negative Breast Cancer.

Exosomal lncRNAs HOTAIR, HULC, and ANRIL: Decoding the Biomarker Landscape of Sporadic Triple-Negative Breast Cancer.

Journal: International journal of molecular sciences

Published: March 23, 2026

Investigation of the Expression Levels of Exosomal miRNAs in the Patients: Myocardial Infarction with Nonobstructive Coronary Arteries.

Investigation of the Expression Levels of Exosomal miRNAs in the Patients: Myocardial Infarction with Nonobstructive Coronary Arteries.

Journal: Molecular syndromology

Published: October 20, 2025

Next-Generation Sequencing Infertility Panel in Turkey: First Results.

Next-Generation Sequencing Infertility Panel in Turkey: First Results.

Journal: Balkan journal of medical genetics : BJMG

Published: March 12, 2025

Investigation of Genetic Aetiology in Intellectual Developmental Disorder with Trio-Whole Exome Sequencing Approach.

Investigation of Genetic Aetiology in Intellectual Developmental Disorder with Trio-Whole Exome Sequencing Approach.

Journal: Noro psikiyatri arsivi

Published: February 13, 2025

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.

Journal: The journal of international advanced otology

Published: August 20, 2024

Investigation of Pogz Gene Variants in Non-Syndromic Autism Spectrum Disorder.

Investigation of Pogz Gene Variants in Non-Syndromic Autism Spectrum Disorder.

Journal: Noro psikiyatri arsivi

Published: September 22, 2023

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.

Journal: Global medical genetics

Published: June 19, 2023

Evaluation of Cardiomyopathy-Related Target Genes by Next-Generation Sequencing Method and Investigation of the Phenotype-Genotype Relationship.

Evaluation of Cardiomyopathy-Related Target Genes by Next-Generation Sequencing Method and Investigation of the Phenotype-Genotype Relationship.

Journal: Molecular syndromology

Published: May 29, 2023

Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

Journal: Balkan medical journal

Published: November 14, 2022

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.

Journal: Global medical genetics

Published: September 08, 2022

Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method.

Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method.

Journal: Global medical genetics

Published: July 18, 2022

The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene.

The efficiency of cinacalcet treatment in delaying parathyroidectomy in a case with neonatal severe hyperparathyroidism caused by homozygous mutation in the CASR gene.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: April 11, 2022

Showing 1-12 of 45

Last Updated: 09/26/2026