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Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes

International journal of immunogenetics, 2019-08, Vol.46 (4), p.232-240

2019

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The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia

Turk oftalmoloji gazetesi, 2020-06, Vol.50 (3), p.143-150

2020

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Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study

Turkish journal of urology, 2020-03, Vol.46 (2), p.95-100

2020

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Assessment of Quality of Life of Chronic Myeloid Leukemia Patients by Using the EORTC QLQ-C30

Turkish journal of haematology, 2017-06, Vol.34 (2), p.197-199

2017

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Targeted fetal cell‐free DNA screening for aneuploidies in 4,594 pregnancies: Single center study

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00678-n/a

2019

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First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss

Turkish archives of otorhinolaryngology, 2019-09, Vol.57 (3), p.140-148

2019

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The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis

The clinical respiratory journal, 2021-02, Vol.15 (2), p.196-202

2021

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Recurrent hydatidiform moles: detection of a new mutation in the NLRP7 gene in the family

International journal of reproduction, contraception, obstetrics and gynecology, 2023-07, Vol.12 (7), p.2251-2254

2023

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cfDNA in exhaled breath condensate (EBC) and contamination by ambient air: toward volatile biopsies

Journal of breath research, 2019-05, Vol.13 (3), p.036006-036006

2019

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Renal–Hepatic–Pancreatic Dysplasia: An Ultra-Rare Ciliopathy with a Novel NPHP3 Genotype

Journal of pediatric genetics (Birmingham, Ala.), 2020-06, Vol.9 (2), p.101-103

2020

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Fetal HLA-G alleles and their effect on miscarriage

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2018-09, Vol.27 (9), p.1233-1237

2018

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QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey

Turkish journal of medical sciences, 2017-01, Vol.47 (1), p.142-147

2017

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Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

Annals of human genetics, 2019-09, Vol.83 (5), p.331-347

2019

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Association between fetal fraction of cell-free DNA and adverse pregnancy outcomes

Archives of gynecology and obstetrics, 2024-08, Vol.310 (2), p.1037-1048

2024

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Self-limited Familial Neonatal Epilepsy due to the c.1589G > A Novel Pathogenic Variant in KCNQ2: A Family Report

Journal of pediatric epilepsy, 2024-03, Vol.13 (1), p.6-10

2024

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Can fetal fractions in the cell-free DNA test predict the onset of fetal growth restriction?

Journal of perinatal medicine, 2020-05, Vol.48 (4), p.395-401

2020

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The Frequency and Management of TP53 Mutation Carriers in Turkish Patients with BRCA-Negative Breast Cancer Under 50 Years of Age

Türk onkoloji dergisi, 2020

özdemir, taha reşid

2020

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Experiences in the molecular genetic and histopathological evaluation of calpainopathies

Neurogenetics, 2022-04, Vol.23 (2), p.103-114

2022

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Molecular genetic evaluation of NLRP 3, MVK and TNFRSF 1A associated periodic fever syndromes

International journal of immunogenetics, 2019-08, Vol.46 (4), p.232-240

2019

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The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15.5 Loci

Journal of pediatric genetics (Birmingham, Ala.), 2020-03, Vol.9 (1), p.009-018

2020

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The Histopathological Findings of High-grade Serous Ovarian Carcinomas in Patients with BRCA Germline Mutations, Single Center Experience

The Anatolian Journal of General Medical Research, 2024-04, p.50-56

2024

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A Single Nucleotide Polymorphism of Follicle-Stimulating Hormone Receptor Gene in Turkish Women with PCOS: A Cross-Sectional Study

Journal of clinical and experimental investigations, 2017-06, Vol.8 (2), p.32

2017

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Renal-Hepatic-Pancreatic Dysplasia: An Ultra-Rare Ciliopathy with a Novel NPHP3 Genotype

Journal of pediatric genetics, 2020, Vol.9 (2), p.101-103

2020

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Assessment of quality of life of chronic myeloid leukemia patients by using the EORTC QLQ-C30

Turkish journal of haematology, 2017, Vol.34 (2), p.197-199

2017

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Epigallocatechin 3-gallate applications on HT-29 and MCF-7 cell lines andevaluation of tumor suppressor gene methylation

Turkish journal of biology, 2015, Vol.39, p.698-704

2015

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Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes

The Role of Heredity and the Prevalence of Strabismus in Families with Accommodative, Partial Accommodative, and Infantile Esotropia

Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study

Assessment of Quality of Life of Chronic Myeloid Leukemia Patients by Using the EORTC QLQ-C30

Targeted fetal cell‐free DNA screening for aneuploidies in 4,594 pregnancies: Single center study

First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss

The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis

Recurrent hydatidiform moles: detection of a new mutation in the NLRP7 gene in the family

cfDNA in exhaled breath condensate (EBC) and contamination by ambient air: toward volatile biopsies

Renal–Hepatic–Pancreatic Dysplasia: An Ultra-Rare Ciliopathy with a Novel NPHP3 Genotype

Fetal HLA-G alleles and their effect on miscarriage

QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey

Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

Association between fetal fraction of cell-free DNA and adverse pregnancy outcomes

Self-limited Familial Neonatal Epilepsy due to the c.1589G > A Novel Pathogenic Variant in KCNQ2: A Family Report

Can fetal fractions in the cell-free DNA test predict the onset of fetal growth restriction?

The Frequency and Management of TP53 Mutation Carriers in Turkish Patients with BRCA-Negative Breast Cancer Under 50 Years of Age

Experiences in the molecular genetic and histopathological evaluation of calpainopathies

Molecular genetic evaluation of NLRP 3, MVK and TNFRSF 1A associated periodic fever syndromes

The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15.5 Loci

The Histopathological Findings of High-grade Serous Ovarian Carcinomas in Patients with BRCA Germline Mutations, Single Center Experience

A Single Nucleotide Polymorphism of Follicle-Stimulating Hormone Receptor Gene in Turkish Women with PCOS: A Cross-Sectional Study

Renal-Hepatic-Pancreatic Dysplasia: An Ultra-Rare Ciliopathy with a Novel NPHP3 Genotype

Assessment of quality of life of chronic myeloid leukemia patients by using the EORTC QLQ-C30

Epigallocatechin 3-gallate applications on HT-29 and MCF-7 cell lines andevaluation of tumor suppressor gene methylation

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