Gozde Y. Sayın
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 11 publications
Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.
Journal: Clinical genetics
Published: April 15, 2026
Awareness and attitudes of pregnant women about prenatal screening and diagnostic tests from Türkiye.
Journal: Journal of community genetics
Published: March 27, 2025
Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures.
Journal: Clinical genetics
Published: November 16, 2023
The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course.
Journal: Nucleosides, nucleotides & nucleic acids
Published: January 28, 2023
The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease.
Journal: European review for medical and pharmacological sciences
Published: January 17, 2023
Phenotypic continuum of NFU1-related disorders.
Journal: Annals of clinical and translational neurology
Published: August 01, 2022
Investigation of genetic and phenotypic heterogeneity in 37 Turkish patients with Kabuki and Kabuki-like phenotype.
Journal: American journal of medical genetics. Part A
Published: December 14, 2021
Functional loss of ubiquitin-specific protease 14 may lead to a novel distal arthrogryposis phenotype.
Journal: Clinical genetics
Published: November 19, 2021
Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients.
Journal: Pathogens and global health
Published: September 27, 2021
Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection.
Journal: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
Published: September 29, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026