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

Genomic and clinical predictors of cardiovascular disease in Familial dyslipidemia: risk stratification in Egyptian adolescents and young adults

家族性血脂异常患者心血管疾病的基因组和临床预测因子：埃及青少年和青年人群的风险分层

期刊:Lipids in Health and Disease
影响因子:4.2
doi:10.1186/s12944-025-02814-0
Metwally, Ammal M; Elaraby, Nesma M; Ezzat, Wafaa M; Dimitry, Mark O; Elshaarawy, Ghada A; Ashaat, Neveen A; Reda, Ashraf; Bendary, Ahmed; Abbas, Mohamed H; El Mawardy, Tarek R; Basha, Walaa A; Kamel, Iman H; Ashaat, Engy A
心血管疾病
心血管
发表日期：2025
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Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants

埃及患者遗传性肾病的遗传病因：新一代测序技术鉴定出六个新的变异

期刊:Molecular and Cellular Pediatrics
影响因子:3.4
doi:10.1186/s40348-025-00203-2
Elaraby, Nesma M; Metwally, Ammal M; Sayed, Sara M; Ashaat, Neveen A; Gamal, Mohammed; Hussen, Dalia Farouk; Abuelela, Soha; Ramadan, Abeer; Kobesiy, Maha M; Shaker, Mai M; Elgebaly, Howida; Elnady, Hala G; Gammal, Mona El; Ashaat, Engy A
Sequencing
发表日期：2025
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Association between GRIK1 rs363598 and intergenic rs360932 variants and susceptibility to autism spectrum disorders in Egyptian children

GRIK1 rs363598 和基因间 rs360932 变异与埃及儿童自闭症谱系障碍易感性的关联

期刊:BMC Pediatrics
影响因子:2
doi:10.1186/s12887-025-06229-9
Bassiony, Heba; Baiomy, Ahmed; Ahmed, Doaa; Elaraby, Nesma M; Ammar, Tamer H A; Ashaat, Engy A
自闭症
神经科学
发表日期：2025
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The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy

全外显子组测序在小脑萎缩相关罕见神经系统疾病谱系诊断中的价值

期刊:Molecular Neurobiology
影响因子:4.3
doi:10.1007/s12035-023-03866-y
Ashaat, Engy A; Ahmed, Hoda A; Elaraby, Nesma M; Fayez, Alaaeldin; Metwally, Ammal M; Mekkawy, Mona K; Hussen, Dalia Farouk; Ashaat, Neveen A; Elhossini, Rasha M; ElAwady, Heba Ahmed; Abdelgawad, Randa H A; Gammal, Mona El; Al Kersh, Mohamed Ahmed; Saleh, Dina Amin
神经科学
发表日期：2024
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Evaluation of tumorigenesis-related miRNAs in breast cancer in Egyptian women: a retrospective, exploratory analysis

埃及女性乳腺癌中肿瘤发生相关miRNA的评估：一项回顾性探索性分析

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-68758-0
Salum, Ghada M; Elaraby, Nesma M; Ahmed, Hoda A; Abd El Meguid, Mai; Fotouh, Basma E; Ashraf, Muhammed; Elhusseny, Yasmine; Dawood, Reham M
miRNA
肿瘤
肿瘤免疫
乳腺癌
发表日期：2024
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Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene

更正：扩展由LSS基因新变异引起的APMR4综合征的表型谱

期刊:Journal of Molecular Neuroscience
影响因子:2.7
doi:10.1007/s12031-024-02233-3
Elaraby, Nesma M; Ahmed, Hoda A; Ashaat, Neveen A; Tawfik, Sameh; Ahmed, Mahmoud K H; Hassib, Nehal F; Ashaat, Engy A
发表日期：2024
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Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients

对埃及再生障碍性贫血患者首次分子分析中鉴定的26个变异体的致病性进行研究

期刊:Journal of Genetic Engineering and Biotechnology
影响因子:2.8
doi:10.1186/s43141-023-00585-8
Sokkar, Mona F; Hamdy, Mona; Erian, Peter Sf; Mosaad, Rehab M; Elaraby, Nesma M; Taher, Mohamed B; El-Sayed, Heba; Al Komy, Mohammed; Eid, Maha M; Mohamed, Amal M; Amr, Khalda S; El-Kamah, Ghada Y
贫血
代谢
发表日期：2023
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First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease.

埃及患者首次LIPA基因突变分析揭示了一种新的变异：沃尔曼病

期刊:Journal of Molecular Neuroscience
影响因子:2.7
doi:10.1007/s12031-023-02139-6
Elaraby Nesma M, Galal Eman Reda, Abdel-Hamid Mohamed, Elbendary Hasnaa M, Elbadry Mohamed, Mekkawy Mona K, Ashaat Neveen A, Mounir Samir M, Ashaat Engy A
其它
发表日期：2023
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Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene and Review of Literature.

扩展由 LSS 基因新变异引起的 APMR4 综合征的表型谱及文献综述

期刊:Journal of Molecular Neuroscience
影响因子:2.7
doi:10.1007/s12031-022-02074-y
Elaraby Nesma M, Ahmed Hoda A, Ashaat Neveen A, Tawfik Sameh, Ahmed Mahmoud K H, Hassib Nehal F, Ashaat Engy A
其它
发表日期：2022
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