Drenushe Zhuri

Edirne, Turkey

Last Updated: 09/26/2026

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Found 14 publications

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

A novel likely pathogenic POFUT1 variant in a Turkish family with Dowling-Degos disease.

A novel likely pathogenic POFUT1 variant in a Turkish family with Dowling-Degos disease.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Published: July 24, 2025

Genomic characterization of patients with colorectal cancer.

Genomic characterization of patients with colorectal cancer.

Journal: Hereditary cancer in clinical practice

Published: February 20, 2025

Clinical and Genetic Aspects of Verheij Syndrome in Two Cases.

Clinical and Genetic Aspects of Verheij Syndrome in Two Cases.

Journal: Molecular syndromology

Published: December 03, 2024

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

A Study of FoxO1, mTOR, miR-21, miR-29b, and miR-98 Expression Levels Regarding Metabolic Syndrome in Acne Vulgaris Patients.

A Study of FoxO1, mTOR, miR-21, miR-29b, and miR-98 Expression Levels Regarding Metabolic Syndrome in Acne Vulgaris Patients.

Journal: Cureus

Published: March 19, 2024

Functional analysis of MMR gene VUS from potential Lynch syndrome patients.

Functional analysis of MMR gene VUS from potential Lynch syndrome patients.

Journal: PloS one

Published: November 03, 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

Homozygous Paternally Inherited ASPA Variant in a Patient with Canavan Disease.

Homozygous Paternally Inherited ASPA Variant in a Patient with Canavan Disease.

Journal: Molecular syndromology

Published: April 19, 2023

A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the CSNK2A1 Gene in a Turkish Patient.

A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the CSNK2A1 Gene in a Turkish Patient.

Journal: Molecular syndromology

Published: December 28, 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

Showing 1-12 of 14

Last Updated: 09/26/2026