Ozge Sonmezler

Adana, Turkey

Last Updated: 09/26/2026

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Found 10 publications

A scalable deep-learning framework for cancer detection using cell-free DNA shallow whole-genome sequencing.

A scalable deep-learning framework for cancer detection using cell-free DNA shallow whole-genome sequencing.

Journal: Science advances

Published: July 10, 2026

Site specific genetic differences in colorectal cancer via Next-Generation-Sequencing using a multigene panel.

Site specific genetic differences in colorectal cancer via Next-Generation-Sequencing using a multigene panel.

Journal: Annali italiani di chirurgia

Published: December 22, 2023

A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.

A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.

Journal: European journal of breast health

Published: March 29, 2023

Pre-operative Neo-adjuvant Chemotherapy Related miRNAs as Key Regulators and Therapeutic Targets in Colorectal Cancer.

Pre-operative Neo-adjuvant Chemotherapy Related miRNAs as Key Regulators and Therapeutic Targets in Colorectal Cancer.

Journal: Current aging science

Published: December 28, 2022

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey.

Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey.

Journal: Breast (Edinburgh, Scotland)

Published: January 19, 2022

Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey.

Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey.

Journal: Genes

Published: December 15, 2020

Clinical Validation of a Novel GeneReader Next Generation Sequencing System for Tumor Specific Mutations and Bioinformatics Variant Analysis.

Clinical Validation of a Novel GeneReader Next Generation Sequencing System for Tumor Specific Mutations and Bioinformatics Variant Analysis.

Journal: Clinical laboratory

Published: November 12, 2020

The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).

The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).

Journal: Scientific reports

Published: October 24, 2020

Integration of Liquid Biopsies into Clinical Laboratory Applications via NGS in Cancer Diagnostics.

Integration of Liquid Biopsies into Clinical Laboratory Applications via NGS in Cancer Diagnostics.

Journal: Clinical laboratory

Published: May 12, 2020

BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history.

BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history.

Journal: The breast journal

Published: August 08, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026