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Expanding the Genotype-Phenotype Correlations and Mutational Spectrum in Inherited Retinal Diseases: Novel and Recurrent Mutations

Curēus (Palo Alto, CA), 2024-02

2024

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Differences in apparent diffusion coefficient histogram analysis according to EGFR mutation status in brain metastasis due to lung adenocarcinoma

Journal of X-ray science and technology, 2023-01, Vol.31 (5), p.1035-1045

2023

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Neurofibromatosis Type 1 Molecular Diagnosis in Turkish Patients

Gazi tıp dergisi, 2020-07, Vol.31 (3), p.406-409

2020

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Evaluation of Oxidant/Antioxidant System, IL-6 and IL-10 Parameters and SOD-Enzyme Activity in Pregnancy with Down Syndrome in Amnion Fluid Analysis

Gazi tıp dergisi, 2022-01, Vol.33 (1), p.53-57

2022

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Non-Invasive Cancer Genotyping: A Single-Center Experience on the Challenges, Limitations, and Methods

Gazi tıp dergisi, 2022-01, Vol.33 (2), p.146-150

2022

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Role of WT1 in Measurable Residual Disease Follow-Up in the Post Allogeneic Stem Cell Transplant Setting

Journal of clinical medicine, 2024-08, Vol.13 (17), p.5145

2024

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Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

Anatolian journal of cardiology, 2022-06, Vol.26 (6), p.460-465

2022

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Comparison of RT-qPCR and RT-Digital PCR for Detection and Quantification of BCR-ABL1 Transcripts in Chronic Myeloid Leukemia

Gazi tıp dergisi, 2019-01, Vol.30 (4A), p.421-424

2019

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Face masks and polycythemia is the standard hemoglobin cutoff valid in the pandemic?

Iraqi Journal of Hematology, 2022-07, Vol.11 (2), p.130

2022

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Evaluation of Clinical Outcome and Mixed Chimerism Follow-up after Allogeneic Hematopoietic Stem Cell Transplantation in Hematological Malignancies

Gazi tıp dergisi, 2020-01, Vol.31 (1), p.52-55

2020

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Comparison of the Diagnostic Accuracy of Next Generation Sequencing and Microarray Resequencing Methods for Detection of BRCA1 and BRCA2 Gene Mutations

Gazi tıp dergisi, 2018-01, Vol.29 (2), p.116-118

2018

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P210 breakpoint is associated with less minimal residual disease compared to p190 breakpoint in acute lymphoblastic leukemia patients with Philadelphia chromosome

Journal of health sciences and medicine : (Turkey), 2020-06, Vol.3 (3), p.307-311

2020

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Spectrum of Variants Detected in Cancer Susceptibility Genes Analyzed in Turkish Pancreatic Cancer Patients

Acta Oncologica Turcica, 2020, Vol.53 (1), p.140-144

2020

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Validation of SMA screening kits with SMN1 gene analysis in a Turkish cohort

Clinica chimica acta, 2024-03, Vol.555, p.117793-117793, Article 117793

2024

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Function of telomere in aging and age related diseases

Environmental toxicology and pharmacology, 2021-07, Vol.85, p.103641, Article 103641

2021

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Multigene panel testing for hereditary breast cancer: An analysis of 70 BRCA-negative Turkish patients

Cumhuriyet tıp dergisi, 2019-09

2019

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Genetic Etiology of Ichthyosis in Turkish Patients: Next-generation Sequencing Identified Seven Novel Mutations

Medeniyet medical journal, 2022-06, Vol.37 (2), p.126-130

2022

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Spectrum of BRCA1/BRCA2 variants in 1419 Turkish breast and ovarian cancer patients: a single center study

Turkish Journal of Biochemistry, 2020-02, Vol.45 (1), p.83-90

2020

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Spectrum of germline cancer susceptibility gene mutations in Turkish colorectal cancer patients: a single center study

TURKISH JOURNAL OF MEDICAL SCIENCES, 2020-06, Vol.50 (4), p.1015-1021

2020

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Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancer

Annals of human genetics, 2024-08

2024

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CALR, JAK2 and MPL Genes Mutations in Myeloproliferative Neoplasms, Single Center Experience

Acta Oncologica Turcica, 2019, Vol.52 (3), p.388-392

2019

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Genetic testing and counseling challenges in personalized breast cancer care: review article with insights from Türkiye

Future oncology (London, England), 2024-05, Vol.20 (15), p.1031-1045

2024

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Comparison of Clinicopathological Characteristics of BRCA1 and BRCA2 Carriers with Breast Cancer: The Role of Ki-67 Index

Journal of oncological science, 2021, Vol.7 (3), p.91-97

2021

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Liquid biopsy: Novel perspectives on the importance and spectrum of PIK3CA, PTEN and RET mutations in solid tumors

Molecular and clinical oncology, 2022-01, Vol.16 (1), Article 1

2022

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Molecular evaluation of mutations in acute myeloid leukemia patients from Turkey: A single-center study

Medicine (Baltimore), 2021-10, Vol.100 (41), p.e27458

2021

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Expanding the Genotype-Phenotype Correlations and Mutational Spectrum in Inherited Retinal Diseases: Novel and Recurrent Mutations

Differences in apparent diffusion coefficient histogram analysis according to EGFR mutation status in brain metastasis due to lung adenocarcinoma

Neurofibromatosis Type 1 Molecular Diagnosis in Turkish Patients

Evaluation of Oxidant/Antioxidant System, IL-6 and IL-10 Parameters and SOD-Enzyme Activity in Pregnancy with Down Syndrome in Amnion Fluid Analysis

Non-Invasive Cancer Genotyping: A Single-Center Experience on the Challenges, Limitations, and Methods

Role of WT1 in Measurable Residual Disease Follow-Up in the Post Allogeneic Stem Cell Transplant Setting

Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

Comparison of RT-qPCR and RT-Digital PCR for Detection and Quantification of BCR-ABL1 Transcripts in Chronic Myeloid Leukemia

Face masks and polycythemia is the standard hemoglobin cutoff valid in the pandemic?

Evaluation of Clinical Outcome and Mixed Chimerism Follow-up after Allogeneic Hematopoietic Stem Cell Transplantation in Hematological Malignancies

Comparison of the Diagnostic Accuracy of Next Generation Sequencing and Microarray Resequencing Methods for Detection of BRCA1 and BRCA2 Gene Mutations

P210 breakpoint is associated with less minimal residual disease compared to p190 breakpoint in acute lymphoblastic leukemia patients with Philadelphia chromosome

Spectrum of Variants Detected in Cancer Susceptibility Genes Analyzed in Turkish Pancreatic Cancer Patients

Validation of SMA screening kits with SMN1 gene analysis in a Turkish cohort

Function of telomere in aging and age related diseases

Multigene panel testing for hereditary breast cancer: An analysis of 70 BRCA-negative Turkish patients

Genetic Etiology of Ichthyosis in Turkish Patients: Next-generation Sequencing Identified Seven Novel Mutations

Spectrum of BRCA1/BRCA2 variants in 1419 Turkish breast and ovarian cancer patients: a single center study

Spectrum of germline cancer susceptibility gene mutations in Turkish colorectal cancer patients: a single center study

Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancer

CALR, JAK2 and MPL Genes Mutations in Myeloproliferative Neoplasms, Single Center Experience

Genetic testing and counseling challenges in personalized breast cancer care: review article with insights from Türkiye

Comparison of Clinicopathological Characteristics of BRCA1 and BRCA2 Carriers with Breast Cancer: The Role of Ki-67 Index

Liquid biopsy: Novel perspectives on the importance and spectrum of PIK3CA, PTEN and RET mutations in solid tumors

Molecular evaluation of mutations in acute myeloid leukemia patients from Turkey: A single-center study

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