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

Comprehensive Evaluation of a 1021-Gene Panel in FFPE and Liquid Biopsy for Analytical and Clinical Use

对 1021 基因检测板在 FFPE 和液体活检中的分析和临床应用进行全面评估

Meintani, Angeliki; Ozdogan, Mustafa; Touroutoglou, Nikolaos; Papazisis, Konstantinos; Boukovinas, Ioannis; Bilir, Cemil; Giassas, Stylianos; Sualp, Tansan; Lacin, Sahin; Dan Corneliu, Jinga; Kosmidis, Paraskevas; Ozatli, Tahsin; Ziogas, Dimitrios; Theochari, Maria; Botsolis, Konstantinos; Kapetsis, George; Tsantikidi, Aikaterini; Florou-Chatzigiannidou, Chrysiida; Maxouri, Styliani; Metaxa-Mariatou, Vasiliki; Grigoriadis, Dimitrios; Papathanasiou, Athanasios; Tsaousis, Georgios N; Kollia, Panagoula; Trougakos, Ioannis; Agathangelidis, Andreas; Papadopoulou, Eirini; Nasioulas, George

Microsatellite Instability Is Insufficiently Used as a Biomarker for Lynch Syndrome Testing in Clinical Practice

微卫星不稳定性在临床实践中作为林奇综合征检测的生物标志物应用不足。

Papadopoulou, Eirini; Rigas, George; Fountzilas, Elena; Boutis, Anastasios; Giassas, Stylianos; Mitsimponas, Nikolaos; Daliani, Danai; Ziogas, Dimitrios C; Liontos, Michalis; Ramfidis, Vasileios; Christophilakis, Charalampos; Matthaios, Dimitris; Floros, Theofanis; Florou-Chatzigiannidou, Chrysiida; Agiannitopoulos, Konstantinos; Meintani, Angeliki; Tsantikidi, Aikaterini; Katseli, Anastasia; Potska, Kevisa; Tsaousis, Georgios; Metaxa-Mariatou, Vasiliki; Nasioulas, George

The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory

遗传性癌症的临床和遗传特征:来自单一临床诊断实验室的经验

Tsoulos, Nikolaos; Agiannitopoulos, Konstantinos; Potska, Kevisa; Katseli, Anastasia; Ntogka, Christina; Pepe, Georgia; Bouzarelou, Dimitra; Papathanasiou, Athanasios; Grigoriadis, Dimitrios; Tsaousis, Georgios N; Gogas, Helen; Troupis, Theodore; Papazisis, Konstantinos; Natsiopoulos, Ioannis; Venizelos, Vassileios; Amarantidis, Kyriakos; Giassas, Stylianos; Papadimitriou, Christos; Fountzilas, Elena; Stathoulopoulou, Maroulio; Koumarianou, Anna; Xepapadakis, Grigorios; Blidaru, Alexandru; Zob, Daniela; Voinea, Oana; Özdoğan, Mustafa; Ergören, Mahmut Çerkez; Hegmane, Alinta; Papadopoulou, Eirini; Nasioulas, George; Markopoulos, Christos

Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing

在接受遗传性癌症检测的患者中,拷贝数变异(CNV)占致病变异的10.8%。

Agiannitopoulos, Konstantinos; Pepe, Georgia; Tsaousis, Georgios N; Potska, Kevisa; Bouzarelou, Dimitra; Katseli, Anastasia; Ntogka, Christina; Meintani, Angeliki; Tsoulos, Nikolaos; Giassas, Stylianos; Venizelos, Vassileios; Markopoulos, Christos; Iosifidou, Rodoniki; Karageorgopoulou, Sofia; Christodoulou, Christos; Natsiopoulos, Ioannis; Papazisis, Konstantinos; Vasilaki-Antonatou, Maria; Kabletsas, Eleftherios; Psyrri, Amanta; Ziogas, Dimitrios; Lalla, Efthalia; Koumarianou, Anna; Anastasakou, Kornilia; Papadimitriou, Christos; Ozmen, Vahit; Tansan, Sualp; Kaban, Kerim; Ozatli, Tahsin; Eniu, Dan Tudor; Chiorean, Angelica; Blidaru, Alexandru; Rinsma, Marrit; Papadopoulou, Eirini; Nasioulas, George