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

Calcium release channel deficiency syndrome in patients diagnosed with idiopathic ventricular fibrillation and decedents classified as sudden unexplained death in the young

钙释放通道缺乏综合征见于被诊断为特发性室颤的患者以及被归类为青年猝死的死者

期刊:Europace
影响因子:7.4
doi:10.1093/europace/euaf303
Giammarino, Lucilla; Neves, Raquel; Tester, David J; Bains, Sahej; Karlinski Vizentin, Vanessa; Bos, J Martijn; Giudicessi, John R; Ackerman, Michael J
发表日期：2026
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AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome

在1型短QT综合征转基因兔模型中，AAV9介导的KCNH2抑制替代基因疗法

期刊:European Heart Journal
影响因子:
doi:10.1093/eurheartj/ehaf660
Nimani, Saranda; Bains, Sahej; Alerni, Nicolò; Ördög, Balázs; Horváth, András; Matas, Lluis; Louradour, Julien; Giammarino, Lucilla; Tester, David J; Beslac, Olgica; Lopez, Ruben; Meier, Stefan; Egle, Manuel; Christoforou, Nicolas; Barbieri, Miriam; Vashanthakumar, Varjany; Perez-Feliz, Stefanie; Parodi, Chiara; Garcia Casalta, Luisana G; Kim, C S John; Zhou, Wei; Ye, Dan; Jurgensen, Jacqulyn; Barry, Michael A; Bego, Mariana; Keyes, Lisa; Owens, Jane; Pinkstaff, Jason; Christoph, Jan; Zehender, Manfred; Brunner, Michael; Heijman, Jordi; Casoni, Daniela; Praz, Fabien; Haeberlin, Andreas; Brooks, Gabriel; Ackerman, Michael J; Odening, Katja E
KCNH2
发表日期：2026
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Variant-Specific Late Gadolinium Enhancement Patterns Influence Clinical Outcomes in LMNA-Related Cardiomyopathy

变异特异性晚期钆增强模式影响LMNA相关性心肌病的临床结局

期刊:Journal of the American Heart Association
影响因子:5.3
doi:10.1161/JAHA.124.041230
Castrichini, Matteo; Garmany, Ramin; Siontis, Konstantinos C; Collins, Jeremy D; Bois, John P; Pereira, Naveen L; Tester, David J; Gluscevic, Martina; Huynh, Trung; Neves, Raquel; Rosenbaum, Andrew N; Ackerman, Michael J; Giudicessi, John R
心血管
心肌病
发表日期：2025
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KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndrome

在患有1型长QT综合征的转基因兔中进行KCNQ1抑制替代基因治疗

期刊:European Heart Journal
影响因子:35.6
doi:10.1093/eurheartj/ehae476
Bains, Sahej; Giammarino, Lucilla; Nimani, Saranda; Alerni, Nicolo; Tester, David J; Kim, C S John; Christoforou, Nicolas; Louradour, Julien; Horváth, András; Beslac, Olgica; Barbieri, Miriam; Matas, Lluis; Hof, Thomas S; Lopez, Ruben; Perez-Feliz, Stefanie; Parodi, Chiara; Garcia Casalta, Luisana G; Jurgensen, Jacqulyn; Barry, Michael A; Bego, Mariana; Keyes, Lisa; Owens, Jane; Pinkstaff, Jason; Koren, Gideon; Zehender, Manfred; Brunner, Michael; Casoni, Daniela; Praz, Fabien; Haeberlin, Andreas; Brooks, Gabriel; Ackerman, Michael J; Odening, Katja E
基因治疗
发表日期：2024
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Elucidation of ALG10B as a Novel Long-QT Syndrome-Susceptibility Gene

阐明ALG10B是一种新型长QT综合征易感基因

期刊:Circulation-Genomic and Precision Medicine
影响因子:5.5
doi:10.1161/CIRCGEN.122.003726
Zhou, Wei; Ye, Dan; Tester, David J; Bains, Sahej; Giudicessi, John R; Haglund-Turnquist, Carla M; Orland, Kate M; January, Craig T; Eckhardt, Lee L; Maginot, Kathleen R; Ackerman, Michael J
发表日期：2023
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Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy

肌切除组织蛋白质组学和磷酸化蛋白质组学分析揭示了肌节性肥厚型心肌病和基因型阴性肥厚型心肌病之间的差异。

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-023-40795-1
Garmany, Ramin; Bos, J Martijn; Dasari, Surendra; Johnson, Kenneth L; Tester, David J; Giudicessi, John R; Dos Remedios, Cristobal; Maleszewski, Joseph J; Ommen, Steve R; Dearani, Joseph A; Ackerman, Michael J
信号转导
心血管
磷酸化
心肌病
发表日期：2023
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Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for KCND3-Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes

阿卡西汀是一种强效的瞬时外向电流阻滞剂，可能是一种治疗KCND3编码的Kv4.3功能获得性相关J波综合征的新型疗法。

期刊:Circulation-Genomic and Precision Medicine
影响因子:5.5
doi:10.1161/CIRCGEN.120.003238
Ye, Dan; Zhou, Wei; Hamrick, Samantha K; Tester, David J; Kim, C S John; Barajas-Martinez, Hector; Hu, Dan; Giudicessi, John R; Antzelevitch, Charles; Ackerman, Michael J
发表日期：2022
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Red herring pathogenic variants: a case report of premature ventricular contraction-triggered ventricular fibrillation with an incidental pathogenic LMNA variant

误导性致病变异：一例由室性早搏触发的室颤病例报告，伴有偶然发现的致病性LMNA变异

期刊:European Heart Journal - Case Reports
影响因子:0.8
doi:10.1093/ehjcr/ytac115
Garmany, Ramin; Neves, Raquel; Ali Ahmed, Fatima; Tester, David J; Cannon, Bryan C; Giudicessi, John R; Ackerman, Michael J
发表日期：2022
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A novel functional variant residing outside the SCN5A-encoded Na(v)1.5 voltage-sensing domain causes multifocal ectopic Purkinje-related premature contractions

位于SCN5A编码的Na(v)1.5电压感应域之外的新型功能变异导致多灶性异位浦肯野细胞相关早搏

期刊:HeartRhythm Case Reports
影响因子:
doi:10.1016/j.hrcr.2021.11.002
Gao, Xiaozhi; Ye, Dan; Zhou, Wei; Tester, David J; Ackerman, Michael J; Giudicessi, John R
细胞生物学
发表日期：2022
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De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca(2+) regulation

儿童猝死病例中新发突变会破坏细胞内Ca(2+)调节。

期刊:Proceedings of the National Academy of Sciences of the United States of America
影响因子:9.1
doi:10.1073/pnas.2115140118
Halvorsen, Matthew; Gould, Laura; Wang, Xiaohan; Grant, Gariel; Moya, Raquel; Rabin, Rachel; Ackerman, Michael J; Tester, David J; Lin, Peter T; Pappas, John G; Maurano, Matthew T; Goldstein, David B; Tsien, Richard W; Devinsky, Orrin
细胞生物学
发表日期：2021
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