日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Evaluation of Cardiomyopathy-Related Target Genes by Next-Generation Sequencing Method and Investigation of the Phenotype-Genotype Relationship

利用新一代测序技术评估心肌病相关靶基因并研究表型-基因型关系

期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000542097
Sezginer Guler, Hazal; Zhuri, Drenushe; Yalcintepe, Sinem; Altay, Servet; Deveci, Murat; Demir, Selma; Gurlertop, Hanefi Yekta; Atli, Engin; Atli, Emine İkbal; Gurkan, Hakan
心血管
心肌病
Sequencing
发表日期：2025
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Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss

利用下一代测序方法研究听力损失中的目标基因并识别新变异

期刊:Journal of International Advanced Otology
影响因子:1
doi:10.5152/iao.2024.22919
Drenushe Zhuri, Hazal Sezginer Guler, Sinem Yalcintepe, Selma Demir, Engin Atli, Emine Ikbal Atli, Hakan Gurkan
发表日期：2024
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The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies

靶向下一代测序在细胞遗传学正常的髓系恶性肿瘤中的应用的重要性

期刊:Mediterranean Journal of Hematology and Infectious Diseases
影响因子:2
doi:10.4084/MJHID.2021.013
Emine Ikbal Atli, Hakan Gurkan, Engin Atli, Hakki Onur Kirkizlar, Sinem Yalcintepe, Selma Demir, Ufuk Demirci, Damla Eker, Cisem Mail, Rasime Kalkan, Ahmet Muzaffer Demir
肿瘤
其它细胞
发表日期：2021
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A Rare Case of Mosaic Unbalanced Non-Robertsonian Translocation Involving Chromosomes 15 and 22 with Congenital Abnormalities in Monozygotic Twins

同卵双胞胎中罕见15号和22号染色体嵌合不平衡非罗伯逊易位先天畸形病例

期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000505004
Emine I Atli, Engin Atli, Sinem Yalcintepe, Hakan Gurkan
信号转导
发表日期：2020
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