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

The impact of common and rare genetic variants on bradyarrhythmia development

常见和罕见基因变异对缓慢性心律失常发展的影响

Weng, Lu-Chen; Rämö, Joel T; Jurgens, Sean J; Khurshid, Shaan; Chaffin, Mark; Hall, Amelia Weber; Morrill, Valerie N; Wang, Xin; Nauffal, Victor; Sun, Yan V; Beer, Dominik; Lee, Simon; Nadkarni, Girish N; Duong, ThuyVy; Wang, Biqi; Czuba, Tomasz; Austin, Thomas R; Yoneda, Zachary T; Friedman, Daniel J; Clayton, Anne; Hyman, Matthew C; Judy, Renae L; Skanes, Allan C; Orland, Kate M; Treu, Timothy M; Oetjens, Matthew T; Alonso, Alvaro; Soliman, Elsayed Z; Lin, Honghuang; Lunetta, Kathryn L; van der Pals, Jesper; Issa, Tariq Z; Nafissi, Navid A; May, Heidi T; Leong-Sit, Peter; Roselli, Carolina; Choi, Seung Hoan; Khan, Habib R; Knight, Stacey; Karlsson Linnér, Richard; Bezzina, Connie R; Ripatti, Samuli; Heckbert, Susan R; Gaziano, J Michael; Loos, Ruth J F; Psaty, Bruce M; Smith, J Gustav; Benjamin, Emelia J; Arking, Dan E; Rader, Daniel J; Shah, Svati H; Roden, Dan M; Damrauer, Scott M; Eckhardt, Lee L; Roberts, Jason D; Cutler, Michael J; Shoemaker, M Benjamin; Haggerty, Christopher M; Cho, Kelly; Palotie, Aarno; Wilson, Peter W F; Ellinor, Patrick T; Lubitz, Steven A

A PAS-targeting hERG1 activator reduces arrhythmic events in Jervell and Lange-Nielsen syndrome patient-derived hiPSC-CMs.

靶向 PAS 的 hERG1 激活剂可减少 Jervell 和 Lange-Nielsen 综合征患者来源的 hiPSC-CM 的心律失常事件

Ukachukwu Chiamaka U, Jimenez-Vazquez Eric N, Salwi Shreya, Goodrich Matthew, Sanchez-Conde Francisco G, Orland Kate M, Jain Abhilasha, Eckhardt Lee L, Kamp Timothy J, Jones David K

Cardiologists' Perceptions of Cardiogenetic Testing and Management

心脏病专家对心脏遗传检测和管理的看法

Tang, W H Wilson; Bui, Quan M; Cirino, Allison L; Dellefave-Castillo, Lisa; Floyd, Brendan J; Guerchicoff, Alejandra; Guerchicoff, Marianna; V Khera, Amit; Knowles, Joshua W; Lafayette, Kristen; P Landstrom, Andrew; Ma, Daria W; Morales, Ana; Orland, Kate M; Pineda-Alvarez, Daniel E; Prakash, Siddharth K; Theriot, Paul; Dempsey, Melissa

Modeling Idiopathic Ventricular Fibrillation Using iPSC Cardiomyocytes and Computational Approaches: A Proof-of-Concept Study

利用诱导多能干细胞来源的心肌细胞和计算方法模拟特发性室颤:概念验证研究

Reilly, Louise; Josvai, Mitchell; Kalluri, Manasa; Anderson, Corey L; Ni, Haibo; Orland, Kate M; Lang, Di; Glukhov, Alexey V; Grandi, Eleonora; Eckhardt, Lee L

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

全基因组关联研究的荟萃分析揭示了室上性心律失常的遗传机制

Weng, Lu-Chen; Khurshid, Shaan; Hall, Amelia Weber; Nauffal, Victor; Morrill, Valerie N; Sun, Yan V; Rämö, Joel T; Beer, Dominik; Lee, Simon; Nadkarni, Girish; Johnson, Renee; Andreasen, Laura; Clayton, Anne; Pullinger, Clive R; Yoneda, Zachary T; Friedman, Daniel J; Hyman, Matthew C; Judy, Renae L; Skanes, Allan C; Orland, Kate M; Jordà, Paloma; Treu, Timothy M; Oetjens, Matthew T; Subbiah, Rajesh; Hartmann, Jacob P; May, Heidi T; Kane, John P; Issa, Tariq Z; Nafissi, Navid A; Leong-Sit, Peter; Dubé, Marie-Pierre; Roselli, Carolina; Choi, Seung Hoan; Tardif, Jean-Claude; Khan, Habib R; Knight, Stacey; Svendsen, Jesper H; Walker, Bruce; Karlsson Linnér, Richard; Gaziano, J Michael; Tadros, Rafik; Fatkin, Diane; Rader, Daniel J; Shah, Svati H; Roden, Dan M; Marcus, Gregory M; Loos, Ruth J F; Damrauer, Scott M; Haggerty, Christopher M; Cho, Kelly; Palotie, Aarno; Olesen, Morten S; Eckhardt, Lee L; Roberts, Jason D; Cutler, Michael J; Shoemaker, M Benjamin; Wilson, Peter W F; Ellinor, Patrick T; Lubitz, Steven A

Dynamic role of hormones on Brugada syndrome phenotype

激素对布鲁加达综合征表型的动态作用

Vrtikapa, Dejan; Krasowski, Ashley A; Orland, Kate M; Eckhardt, Lee L

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

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

Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome

钙释放缺乏综合征相关兰尼碱受体2变异体的临床和功能特征

Roston, Thomas M; Wei, Jinhong; Guo, Wenting; Li, Yanhui; Zhong, Xiaowei; Wang, Ruiwu; Estillore, John Paul; Peltenburg, Puck J; Noguer, Ferran Rosés I; Till, Jan; Eckhardt, Lee L; Orland, Kate M; Hamilton, Robert; LaPage, Martin J; Krahn, Andrew D; Tadros, Rafik; Vinocur, Jeffrey M; Kallas, Dania; Franciosi, Sonia; Roberts, Jason D; Wilde, Arthur A M; Jensen, Henrik K; Sanatani, Shubhayan; Chen, S R Wayne

Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes

长QT综合征KCNH2变异体诱导患者特异性诱导多能干细胞衍生的心肌细胞中hERG1a/1b亚基失衡

Feng, Li; Zhang, Jianhua; Lee, ChangHwan; Kim, Gina; Liu, Fang; Petersen, Andrew J; Lim, Evi; Anderson, Corey L; Orland, Kate M; Robertson, Gail A; Eckhardt, Lee L; January, Craig T; Kamp, Timothy J

Shared Decision Making in Cardiac Electrophysiology Procedures and Arrhythmia Management

心脏电生理手术和心律失常管理中的共同决策

Chung, Mina K; Fagerlin, Angela; Wang, Paul J; Ajayi, Tinuola B; Allen, Larry A; Baykaner, Tina; Benjamin, Emelia J; Branda, Megan; Cavanaugh, Kerri L; Chen, Lin Y; Crossley, George H; Delaney, Rebecca K; Eckhardt, Lee L; Grady, Kathleen L; Hargraves, Ian G; True Hills, Mellanie; Kalscheur, Matthew M; Kramer, Daniel B; Kunneman, Marleen; Lampert, Rachel; Langford, Aisha T; Lewis, Krystina B; Lu, Ying; Mandrola, John M; Martinez, Kathryn; Matlock, Daniel D; McCarthy, Sarah R; Montori, Victor M; Noseworthy, Peter A; Orland, Kate M; Ozanne, Elissa; Passman, Rod; Pundi, Krishna; Roden, Dan M; Saarel, Elizabeth V; Schmidt, Monika M; Sears, Samuel F; Stacey, Dawn; Stafford, Randall S; Steinberg, Benjamin A; Youn Wass, Sojin; Wright, Jennifer M