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A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma

Clinical and experimental dermatology, 2020-06, Vol.45 (4), p.508-511

2020

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Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma

Balkan journal of medical genetics, 2021-03, Vol.23 (2), p.59-64

2021

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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

Journal of medical virology, 2023-02, Vol.95 (2), p.e28457-n/a

2023

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Liquid biopsy as a new era in endometrial cancer

Oncologie (Paris, France), 2024-05, Vol.26 (3), p.483-486

2024

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Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C＞T Gene Polymorphism in Differentiated Thyroid Cancers

Asian Pacific journal of cancer prevention : APJCP, 2013, Vol.14 (5), p.3213-3217

2013

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The CYP4502D6 4 and 6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patients

European journal of drug metabolism and pharmacokinetics, 2016-06, Vol.41 (3), p.281-286

2016

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Iron alters Ca2+ homeostasis in doxorubicin‐resistant K562 cells

Clinical and experimental pharmacology & physiology, 2020-07, Vol.47 (7), p.1221-1230

2020

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Novel c.1505_1509dupCTGCC pathogenic variation in a male case with Christianson syndrome

Clinical dysmorphology, 2021-01, Vol.30 (1), p.36

2021

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High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

American journal of human genetics, 2021-10, Vol.108 (10), p.1981-2005

2021

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The Phenotypic Spectrum of Desanto-Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey

Genetic testing and molecular biomarkers, 2024-05, Vol.28 (5), p.213

2024

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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.320-331

2021

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Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

Balkan medical journal, 2023-01, Vol.40 (1), p.13-20

2023

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Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

Balkan medical journal, 2020-09, Vol.37 (5), p.297-298

2020

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Iron alters Ca 2+ homeostasis in doxorubicin-resistant K562 cells

Clinical and experimental pharmacology & physiology, 2020-07, Vol.47 (7), p.1221-1230

2020

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Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report

Molecular syndromology, 2021-03, Vol.12 (1), p.46-51

2021

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Effect of CD38 on the multidrug resistance of human chronic myelogenous leukemia K562 cells to doxorubicin

Oncology letters, 2016-03, Vol.11 (3), p.2290-2296

2016

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Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants

Balkan medical journal, 2021-11, Vol.38 (6), p.341-347

2021

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Customised targeted massively parallel sequencing enables more precisely diagnosis of patients with epilepsy

Internal medicine journal, 2022-07

2022

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The effect of iron on the expression levels of calcium related gene in cisplatin resistant epithelial ovarian cancer cells

Exploration of targeted anti-tumor therapy, 2021, Vol.2 (4), p.309-322

2021

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A Rare β°-Thalassemia Frameshift Mutation in a Turkish Individual: (+T) at Codon 9/10

Erciyes medical journal (Online), 2016-03, Vol.38 (1), p.46-47

2016

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Abstract 11576: Association Between Pre-Operative Right Heart Catheterization Parameters and Outcomes in Isolated Coronary Artery Bypass Grafting

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1)

2022

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Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy

Internal medicine journal, 2022-07, Vol.52 (7), p.1174-1184

2022

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Components of Intracellular Calcium Movements in Cancer Cells: Review

Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi, 2017, Vol.37 (2), p.98-108

YALÇINTEPE GÜNEŞTUTAR, Leman

2017

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THE FREQUENCY OF Y CHROMOSOME MICRODELETIONS AND CYTOGENETIC ABNORMALITIES IN CASES WITH MALE INFERTILITY FROM THRACE REGION: SINGLE CENTER EXPERIENCE/TRAKYA BOLGESI ERKEK INFERTILITE OLGULARINDA Y KROMOZOM MIKRODELESYONLARI VE SITOGENETIK ANOMALILERIN SIKLIGI: TEK MERKEZ DENEYIMI

İstanbul Tıp Fakültesi dergisi = Journal of the Istanbul Faculty of Medicine, 2021-03, Vol.84 (1), p.27

2021

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Identification of a novel KIF11 variant p.(Leu804Thrfs Ter13) in a case with isolated microcephaly

Journal of head & neck physicians and surgeons, 2022-01, Vol.10 (1), p.112-115

2022

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A novel nonsense mutation of the CYLD gene in a Turkish family with multiple familial trichoepithelioma

Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia

Liquid biopsy as a new era in endometrial cancer

Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C＞T Gene Polymorphism in Differentiated Thyroid Cancers

The CYP4502D6 4 and 6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patients

Iron alters Ca2+ homeostasis in doxorubicin‐resistant K562 cells

Novel c.1505_1509dupCTGCC pathogenic variation in a male case with Christianson syndrome

High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

The Phenotypic Spectrum of Desanto-Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey

The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

Iron alters Ca 2+ homeostasis in doxorubicin-resistant K562 cells

Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report

Effect of CD38 on the multidrug resistance of human chronic myelogenous leukemia K562 cells to doxorubicin

Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants

Customised targeted massively parallel sequencing enables more precisely diagnosis of patients with epilepsy

The effect of iron on the expression levels of calcium related gene in cisplatin resistant epithelial ovarian cancer cells

A Rare β°-Thalassemia Frameshift Mutation in a Turkish Individual: (+T) at Codon 9/10

Abstract 11576: Association Between Pre-Operative Right Heart Catheterization Parameters and Outcomes in Isolated Coronary Artery Bypass Grafting

Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy

Components of Intracellular Calcium Movements in Cancer Cells: Review

THE FREQUENCY OF Y CHROMOSOME MICRODELETIONS AND CYTOGENETIC ABNORMALITIES IN CASES WITH MALE INFERTILITY FROM THRACE REGION: SINGLE CENTER EXPERIENCE/TRAKYA BOLGESI ERKEK INFERTILITE OLGULARINDA Y KROMOZOM MIKRODELESYONLARI VE SITOGENETIK ANOMALILERIN SIKLIGI: TEK MERKEZ DENEYIMI

Identification of a novel KIF11 variant p.(Leu804Thrfs Ter13) in a case with isolated microcephaly

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