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Hazal Sezginer Guler

Observed names: Guler, Hazal Sezginer, Güler, Hazal Sezginer, H., SezginerGuler, Hazal SEZGİNER GÜLER, Hazal Sezgi̇ner Güler, Hazal Sezginer Güler
Institution: Trakya University
Observed institution: Trakya University
ORCID: 0000-0003-3993-1374
Observed ORCID: 0000-0003-3993-1374
OpenAlex ID: A5037238117
Functional analysis of MMR gene VUS from potential Lynch syndrome patients
2024 · Marwa Mahdouani, Drenushe Zhuri, et al. · PLoS ONE · 9
Investigation of the Relationship between Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2 and GABRA4 Genes
2021 · Sinem Yalcintepe, Isik Gorker, et al. · Nöro Psikiyatri Arşivi · 6
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A Study of FoxO1, mTOR, miR-21, miR-29b, and miR-98 Expression Levels Regarding Metabolic Syndrome in Acne Vulgaris Patients
2024 · Nazan Akdağ, Engin Atli, et al. · Cureus · 4
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The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method
2023 · Sinem Yalcintepe, Yasemin Karal, et al. · Global Medical Genetics · 4
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First Report of Jacobsen Syndrome with Dextrocardia Diagnosed with del(11)(q24q25)
2022 · Sinem Yalcintepe, Drenushe Zhuri, et al. · Molecular Syndromology · 4
Exosomal lncRNAs HOTAIR, HULC, and ANRIL: Decoding the Biomarker Landscape of Sporadic Triple-Negative Breast Cancer
2026 · Hazal Sezginer Guler, Hakan Gurkan, et al. · International Journal of Molecular Sciences · 3
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Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss
2024 · Drenushe Zhuri, Hazal Sezginer Guler, et al. · The Journal of International Advanced Otology · 3
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Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma
2021 · Sinem Yalcintepe, Hakan Gurkan, et al. · Journal of Kidney Cancer and VHL · 3
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Clinical exome sequencing reveals an important role for clinical diagnosis of intellectual disability with definition of seven novel variants
2023 · Sinem Yalcintepe, Isik Gorker, et al. · Neurology Asia · 2
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Circulating miRNAs as an epigenetic footprint in hypospadias
2026 · Sadettin Yildiz, Hazal Sezginer Guler, et al. · Journal of Pediatric Urology · 1
Screening of Premature Ovarian Insufficiency-Associated Genes in Turkish Patients
2025 · Emine İkbal ATLI, Hakan GÜRKAN, et al. · Namık Kemal Tıp Dergisi · 1
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Evaluation of Cardiomyopathy-Related Target Genes by Next-Generation Sequencing Method and Investigation of the Phenotype-Genotype Relationship
2024 · Hazal Sezginer Guler, Drenushe Zhuri, et al. · Molecular Syndromology · 1
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Homozygous Paternally Inherited ASPA Variant in a Patient with Canavan Disease
2024 · Sinem Yalcintepe, Tuba Maras, et al. · Molecular Syndromology · 1
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Identification of a Novel KIF11 Variant p.(Leu804Thrfs Ter13) in a Case with Isolated Microcephaly
2022 · Sinem Yalcintepe, Hazal Sezginer Guler, et al. · Journal of Head & Neck Physicians and Surgeons · 1
Promoter Methylation and Somatic Mutations in Cancer-Related Genes Are Associated with Hyperprogressive Disease in Patients with Malignant Melanoma and Renal Cell Carcinoma Receiving Anti-PD-1/PD-L1 Immunotherapy
2026 · Adem Deligonul, Mehmet Sarimahmut, et al. · Journal of Clinical Medicine
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Investigation of the Expression Levels of Exosomal miRNAs in the Patients: Myocardial Infarction with Nonobstructive Coronary Arteries
2026 · Sinem Yalcintepe, Servet Altay, et al. · Molecular Syndromology
Supplementary Material for: Investigation the Expression Levels of Exosomal miRNAs in the Patients - Myocardial Infarction with Non-Obstructive Coronary Arteries (MINOCA)
2026 · karger, figshare admin, S., Yalcintepe, et al. · Figshare
No Association Between Autism Spectrum Disorder and Mitochondrial DNA Variants: A Comprehensive Genetic Study in Trakya Population
2026 · Hasan Cem Aykutlu, Engin Atlı, et al. · International Journal of Developmental Neuroscience
Clinical and Genetic Aspects of Verheij Syndrome in Two Cases
2025 · Yade Dilay Kursat, Hazal Sezginer Guler, et al. · Molecular Syndromology
Importance of hereditary variants in ovarian cancer and endometrial cancer
2025 · Zhuri, Drenushe, Demir, Selma, et al. · European Journal of Gynaecological Oncology
Investigation of exosomal long non-coding rnas as biomarkers in triple negative sporadic breast cancer
2025 · Güler, Hazal Sezginer · Trakya University's Institutional Open Access System (Trakya University)
Contribution of Targeted Next Generation Sequencing to Clinical Diagnosis in Myeloid Malignancies: A Single Centre Experience
2025 · Gurkan, Hakan, Atli, Emine Ikbal, et al. · Trakya University's Institutional Open Access System (Trakya University)
Tracing The Genetic Basis of Hypotonia in Whole Exome Sequencing Data: Experinces of Trakya University Genetic Diagnosis Center
2024 · Demir, Selma, Yalcintepe, Sinem, et al. · Trakya University's Institutional Open Access System (Trakya University)
Investigation of the Effect of miR-155, let-7c and miR-433 microRNA Expressions on Congenital Heart Diseases in Down Syndrome Individuals
2024 · Maras, Tuba, Yalcintepe, Sinem, et al. · Trakya University's Institutional Open Access System (Trakya University)
Investigation of variant distribution and frequency in triple negative breast cancer patients living in the Trakya Region of Turkey: A Single Center Experience
2024 · Gurkan, Hakan, Atli, Engin, et al. · Trakya University's Institutional Open Access System (Trakya University)
Works count: 28
Citation count: 43
H-index: 4
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