Publications by authors named "Esra Ates"

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Decoding the Genetic Puzzle of Inherited Retinal Dystrophies: Novel Insights From a Turkish Cohort.
Şenol Demir, Esra Arslan Ateş, Orkun Sevik, Bengisu Sözer, Tuğba Köse

Clin Genet· November 2025

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Assessment of Genetic Variants Linked to Susceptibility to Mechanical Prosthetic Valve Thrombosis.
Semih Kalkan, M Ozan Gürsoy, Ahmet Güner, Semra Gürsoy, Macit Kalçık

Am J Cardiol· January 2025

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Glyoxal and methylglyoxal formation in chocolate and their bioaccessibility.
Elif Ede-Cintesun, Jale Çatak, Esra Ateş, Mustafa Yaman

Food Res Int· August 2024

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Correction to: HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.
Gunes Sager, Ayberk Turkyilmaz, Esra Arslan Ates, Busra Kutlubay

Acta Neurol Belg· October 2023

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A Second Family with Myhre Syndrome Caused by the Same Recurrent Pathogenic Variation (p.Arg496Cys).
Şenol Demir, Ceren Alavanda, Gözde Yeşil, Ayça Dilruba Aslanger, Esra Arslan Ateş

Mol Syndromol· April 2023

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Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.
Aslıhan Kiraz, Ozlem Sezer, Adem Alemdar, Sezin Canbek, Nilgun Duman

J Med Virol· February 2023

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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Munis Dundar, Umut Fahrioglu, Saliha Handan Yildiz, Burcu Bakir-Gungor, Sehime Gulsun Temel, Esra Arslan Ates

Funct Integr Genomics· June 2022

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HACE1, GLRX5, and ELP2 gene variant cause spastic paraplegies.
Gunes Sager, Ayberk Turkyilmaz, Esra Arslan Ates, Busra Kutlubay

Acta Neurol Belg· April 2022

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When do we need to suspect maturity onset diabetes of the young in patients with type 2 diabetes mellitus?
Özlem Üstay, Tuğçe Apaydın, Onur Elbasan, Hamza Polat, Gizem Günhan

Arch Endocrinol Metab· March 2022

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Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.
Ayberk Turkyilmaz, Ceren Alavanda, Esra Arslan Ates, Bilgen Bilge Geckinli, Hamza Polat

J Assist Reprod Genet· March 2022

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Genetic and Clinical Characterization of Patients with Maturity-Onset of Diabetes of the Young (MODY): Identification of Novel Variations.
Esra Arslan Ateş, Özlem Üstay, Hamza Polat, Tuğçe Apaydın, Onur Elbasan

Balkan Med J· September 2021

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Biallelic Mutations in are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family.
Esra Arslan Ateş, Ayberk Turkyilmaz, Kenan Delil, Ceren Alavanda, Mehmet Ali Söylemez

Mol Syndromol· June 2021

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Novel clinical features and pleiotropic effect in three unrelated patients with LMNA variant.
Ayberk Turkyilmaz, Bilgen Bilge Geçkinli, Ceren Alavanda, Esra Arslan Ates, Ahmet Arman

Clin Dysmorphol· January 2021

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Evaluation of the Relationship Between Homocysteine, Parathormone, Vitamin D, and Bone Mineral Densitometry in Recipients of Kidney Transplant.
Bulent Kaya, Esra Ates, Saime Paydas, Yasar Sertdemir, Mustafa Balal

Transplant Proc· September 2019

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Genotype and Anterior Segment Phenotype in a Cohort of Turkish Patients with Lamellar Ichthyosis.
Melis Palamar, Huseyin Onay, Ilgen Ertam, Esra Arslan Ates, Tugrul Dereli

Ophthalmic Genet· April 2016

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