Author

Drenushe Zhuri

Observed names: D., Zhuri, Drenushe ZHURİ, Drenushe Zhuri̇, Zhuri D, Zhuri, Drenushe, Zhurı, Drenushe

Institution: Trakya University

Observed institution: Trakya University

ORCID: 0000-0002-8370-1990

Observed ORCID: 0000-0002-8370-1990

OpenAlex ID: A5049981905

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype

2022 · Drenushe Zhuri, Hakan Gurkan, et al. · Global Medical Genetics · 12

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The possible role of epigenetics in the etiology of hypospadias

2024 · Yıldız S, Inanç I, et al. · Journal of Pediatric Urology · 9

Functional analysis of MMR gene VUS from potential Lynch syndrome patients

2024 · Marwa Mahdouani, Drenushe Zhuri, et al. · PLoS ONE · 9

A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the CSNK2A1 Gene in a Turkish Patient

2023 · Drenushe Zhuri, Fulya Dusenkalkan, et al. · Molecular Syndromology · 7

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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

Genomic characterization of patients with colorectal cancer

2025 · Marwa Mahdouani, Drenushe Zhuri, et al. · Hereditary Cancer in Clinical Practice · 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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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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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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Liquid biopsy as a new era in endometrial cancer

2024 · Drenushe Zhuri, Sinem Yalcintepe · ONCOLOGIE · 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

Eine neue pathogene Variante des POFUT1 ‐Gens in einer türkischen Familie mit Morbus Dowling‐Degos

2026 · Sezgi Sarikaya Solak, Hülya Mürüvvet Güvendi, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft

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A novel likely pathogenic POFUT1 variant in a Turkish family with Dowling–Degos disease

2026 · Sezgi Sarikaya Solak, Hülya Mürüvvet Güvendi, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft

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

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

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)

Comprehensive molecular profiling of breast cancer subtypes in a Turkish population: Insights from next-generation sequencing analysis

2024 · Zhuri, Drenushe, Atli, Engin, et al. · Trakya University's Institutional Open Access System (Trakya University)

Effects of modifying genes in the spinal muscular atrophy phenotype investigation

2020 · Zhurı, Drenushe · Trakya University's Institutional Open Access System (Trakya University)

Works count: 26

Citation count: 68

H-index: 5

I10-index: 1