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

How Screen Time Affects Greek Schoolchildren's Eating Habits and Functional Food Consumption?-A Cross-Sectional Study

屏幕时间如何影响希腊学龄儿童的饮食习惯和功能性食品消费？——一项横断面研究

期刊:Nutrients
影响因子:5
doi:10.3390/nu17081311
Votsi, Irene Chrysovalantou; Koutelidakis, Antonios Ε
发表日期：2025
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Candidozyma auris Outbreak and Its Effective Control in a General Hospital

耳念珠菌暴发及其在综合医院的有效控制

期刊:Antibiotics-Basel
影响因子:4.6
doi:10.3390/antibiotics14060579
Kontopidou, Flora V; Antonopoulou, Maria; Votsi, Anastasia; Papoutsaki, Vassiliki; Bereri, Vassiliki; Kourkoulou, Evangelia; Rompola, Amalia; Tsokou, Georgia; Pavli, Anna; Koutantelia, Olga Maria; Siopi, Maria; Leventaki, Sevasti; Meletiadis, Joseph; Daikos, George L
发表日期：2025
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The FGF14 GAA repeat expansion is a major cause of ataxia in the Cypriot population

FGF14 GAA重复序列扩增是塞浦路斯人群共济失调的主要原因之一

期刊:Brain Communications
影响因子:4.5
doi:10.1093/braincomms/fcae479
Livanos, Ioannis; Votsi, Christina; Michailidou, Kyriaki; Pellerin, David; Brais, Bernard; Zuchner, Stephan; Pantzaris, Marios; Kleopa, Kleopas A; Zamba Papanicolaou, Eleni; Christodoulou, Kyproula
FGF1
发表日期：2025
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First Report of Co-Occurring FGF14 (SCA27B) and RFC1 (CANVAS) Repeat Expansions in Two of Three Siblings with Late-Onset Cerebellar Ataxia

首次报道三名患有晚发性小脑共济失调的兄弟姐妹中的两名同时存在FGF14（SCA27B）和RFC1（CANVAS）重复序列扩增。

期刊:Cerebellum
影响因子:2.4
doi:10.1007/s12311-025-01921-z
Tsokkos, Tasos; Christodoulou, Kyproula; Votsi, Christina; Georghiou, Anthi; Christofides, Andrea; Constantinou, Astero; Zamba-Papanicolaou, Eleni
FGF1
神经科学
发表日期：2025
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Genetic epidemiology of amyotrophic lateral sclerosis in Cyprus: a population-based study

塞浦路斯肌萎缩侧索硬化症的遗传流行病学：一项基于人群的研究

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-80851-y
Mitsi, Ellie; Votsi, Christina; Koutsou, Pantelitsa; Georghiou, Anthi; Christodoulou, Christiana C; Kleopa, Kleopas; Zamba-Papanicolaou, Eleni; Christodoulou, Kyproula; Nicolaou, Paschalis
发表日期：2024
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RFC1 Repeat Distribution in the Cypriot Population: Study of a Large Cohort of Patients With Undiagnosed Ataxia and Non-Disease Controls

塞浦路斯人群中 RFC1 重复序列分布：一项针对大量未确诊共济失调患者和非疾病对照组的研究

期刊:Neurology-Genetics
影响因子:3.7
doi:10.1212/NXG.0000000000200149
Votsi, Christina; Tomazou, Marios; Nicolaou, Paschalis; Pantzaris, Marios C; Pitsas, Giorgos; Adamou, Archontia; Kleopa, Kleopas A; Zamba-Papanicolaou, Eleni; Christodoulou, Kyproula
发表日期：2024
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Spinal muscular atrophy type I associated with a novel SMN1 splicing variant that disrupts the expression of the functional transcript

型脊髓性肌萎缩症与一种新型 SMN1 剪接变体相关，该变体破坏了功能性转录本的表达。

期刊:Frontiers in Neurology
影响因子:2.8
doi:10.3389/fneur.2023.1241195
Votsi, Christina; Koutsou, Pantelitsa; Ververis, Antonis; Georghiou, Anthi; Nicolaou, Paschalis; Tanteles, George; Christodoulou, Kyproula
神经科学
SMN
肌萎缩症
SMN1
发表日期：2023
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Transcriptomic characterization of tissues from patients and subsequent pathway analyses reveal biological pathways that are implicated in spastic ataxia

对患者组织进行转录组学表征以及后续的通路分析，揭示了与痉挛性共济失调相关的生物学通路。

期刊:Cell and Bioscience
影响因子:6.2
doi:10.1186/s13578-022-00754-1
Kakouri, Andrea C; Votsi, Christina; Oulas, Anastasis; Nicolaou, Paschalis; Aureli, Massimo; Lunghi, Giulia; Samarani, Maura; Compagnoni, Giacomo M; Salani, Sabrina; Di Fonzo, Alessio; Christophides, Thalis; Tanteles, George A; Zamba-Papanicolaou, Eleni; Pantzaris, Marios; Spyrou, George M; Christodoulou, Kyproula
信号转导
发表日期：2022
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A Framework for Efficient N-Way Interaction Testing in Case/Control Studies With Categorical Data

针对病例对照研究中分类数据，构建高效的N维交互作用检验框架

期刊:IEEE Open Journal of Engineering in Medicine and Biology
影响因子:2.9
doi:10.1109/OJEMB.2021.3100416
Aristodimou, Aristos; Antoniades, Athos; Dardiotis, Efthimios; Loizidou, Eleni; Spyrou, George; Votsi, Christina; Kyproula, Christodoulou; Pantzaris, Marios; Grigoriadis, Nikolaos; Hadjigeorgiou, Georgios; Kyriakides, Theodoros; Pattichi, Constantinos
发表日期：2021
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A Novel CLN6 Variant Associated With Juvenile Neuronal Ceroid Lipofuscinosis in Patients With Absence of Visual Loss as a Presenting Feature

一种与幼年神经元蜡样脂褐质沉积症相关的新型CLN6变异体，该病患者无视力丧失的首发症状。

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2021.746101
Nicolaou, Paschalis; Tanteles, George A; Votsi, Christina; Zamba-Papanicolaou, Eleni; Papacostas, Savvas S; Christodoulou, Kyproula; Christou, Yiolanda-Panayiota
神经科学
发表日期：2021
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