Izem O. Sahin

Erciyes, Turkey

Last Updated: 09/26/2026

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Found 15 publications

Investigation of testicular METRNL and RARRES2 expression in non-obstructive azoospermia.

Investigation of testicular METRNL and RARRES2 expression in non-obstructive azoospermia.

Journal: Journal of applied genetics
Published: June 05, 2026

Functional Iron-Transport Genes-TF and TMPRSS6-As Genetic Determinants of Transferrin and Fasting Glucose in a Kazakh Adult Cohort: A Whole-Exome Sequencing Pilot Study.

Functional Iron-Transport Genes-TF and TMPRSS6-As Genetic Determinants of Transferrin and Fasting Glucose in a Kazakh Adult Cohort: A Whole-Exome Sequencing Pilot Study.

Journal: International journal of molecular sciences
Published: May 22, 2026

A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis.

A case series of joubert syndrome evaluated with whole exome sequencing and the utility of optical genome mapping in the diagnosis.

Journal: Neurogenetics
Published: March 07, 2025

Corrigendum to "A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort": [Turkish Journal of Medical Sciences 54 (1) 2024 86-98].

Corrigendum to "A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort": [Turkish Journal of Medical Sciences 54 (1) 2024 86-98].

Journal: Turkish journal of medical sciences
Published: October 01, 2024

Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy.

Molecular analysis of SMN2, NAIP, and GTF2H2 gene deletions and relationships with clinical subtypes of spinal muscular atrophy.

Journal: Journal of neurogenetics
Published: September 25, 2024

The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution.

The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution.

Journal: Functional & integrative genomics
Published: July 02, 2024

Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.

Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.

Journal: Journal of clinical laboratory analysis
Published: September 21, 2023

Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing.

Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing.

Journal: Genes and immunity
Published: June 10, 2023

A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.

A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.

Journal: Turkish journal of medical sciences
Published: February 15, 2023

Case Report: A Novel Mutation Leading to 11-β Hydroxylase Deficiency in a Female Patient.

Case Report: A Novel Mutation Leading to 11-β Hydroxylase Deficiency in a Female Patient.

Journal: Endocrine, metabolic & immune disorders drug targets
Published: April 03, 2022

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

Journal: Functional & integrative genomics
Published: July 09, 2021

Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches.

Current and Future Therapeutic Strategies for Limb Girdle Muscular Dystrophy Type R1: Clinical and Experimental Approaches.

Journal: Pathophysiology : the official journal of the International Society for Pathophysiology
Published: April 21, 2021
Showing 1-12 of 15

Last Updated: 09/26/2026