Ebru Erzurumluoglu-Gokalp

Eskisehir, Turkey

Last Updated: 09/26/2026

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Found 13 publications

Evaluation of the Role of miRNAs Expression Profiles in Aneurysm.

Evaluation of the Role of miRNAs Expression Profiles in Aneurysm.

Journal: Turkish neurosurgery

Published: January 19, 2026

Comparison of conventional karyotype analysis and CMA results with ultrasound findings in pregnancies with normal QF-PCR results.

Comparison of conventional karyotype analysis and CMA results with ultrasound findings in pregnancies with normal QF-PCR results.

Journal: Turkish journal of obstetrics and gynecology

Published: June 04, 2025

Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions?

Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions?

Journal: Turkish journal of medical sciences

Published: April 25, 2024

Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus

Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus

Journal: Journal of clinical research in pediatric endocrinology

Published: December 06, 2023

An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3.

An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3.

Journal: Cytogenetic and genome research

Published: August 11, 2021

The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.

The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.

Journal: Ophthalmic genetics

Published: August 04, 2021

Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients.

Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients.

Journal: Anatolian journal of cardiology

Published: February 15, 2021

Frequency of frontotemporal dementia-related gene variants in Turkey.

Frequency of frontotemporal dementia-related gene variants in Turkey.

Journal: Neurobiology of aging

Published: January 14, 2021

Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?

Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?

Journal: Molecular cytogenetics

Published: October 08, 2020

A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13,q22,q31) and the relocalization of AML1/ETO fusion gene.

A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13,q22,q31) and the relocalization of AML1/ETO fusion gene.

Journal: Cancer genetics

Published: September 22, 2020

Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey.

Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey.

Journal: International journal of ophthalmology

Published: April 08, 2020

A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency.

A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency.

Journal: American journal of medical genetics. Part A

Published: August 15, 2019

Showing 1-12 of 13

Last Updated: 09/26/2026