Esra A. Ates

Cerrahpasa, Turkey

Last Updated: 09/26/2026

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Found 15 publications

Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.

Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.

Journal: Clinical genetics

Published: February 20, 2025

Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.

Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.

Journal: The American journal of cardiology

Published: August 27, 2024

Glyoxal and methylglyoxal formation in chocolate and their bioaccessibility.

Glyoxal and methylglyoxal formation in chocolate and their bioaccessibility.

Journal: Food research international (Ottawa, Ont.)

Published: March 07, 2024

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Journal: Journal of medical virology

Published: December 09, 2022

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability.

Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability.

Journal: Balkan journal of medical genetics : BJMG

Published: October 17, 2022

A Second Family with Myhre Syndrome Caused by the Same Recurrent SMAD4 Pathogenic Variation (p.Arg496Cys).

A Second Family with Myhre Syndrome Caused by the Same Recurrent SMAD4 Pathogenic Variation (p.Arg496Cys).

Journal: Molecular syndromology

Published: April 12, 2022

When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?

When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?

Journal: Archives of endocrinology and metabolism

Published: January 14, 2022

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.

Journal: Journal of assisted reproduction and genetics

Published: September 06, 2021

Genetic and Clinical Characterization of Patients with Maturity-Onset of Diabetes of the Young (MODY): Identification of Novel Variations.

Genetic and Clinical Characterization of Patients with Maturity-Onset of Diabetes of the Young (MODY): Identification of Novel Variations.

Journal: Balkan medical journal

Published: August 31, 2021

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

Correction to: HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Correction to: HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Journal: Acta neurologica Belgica

Published: May 07, 2021

HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.

Journal: Acta neurologica Belgica

Published: December 11, 2020

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Last Updated: 09/26/2026