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

Large-scale functional assessment of variants of the potassium channel Kir2.1: Clinical and comparative insights

大规模钾通道 Kir2.1 变体的功能评估：临床和比较见解

期刊:Journal of Biological Chemistry
影响因子:3.9
doi:10.1016/j.jbc.2025.110985
Anderson, Corey L; Munuwar, Saba; Walters, Janay K; McWilliams, Seamus F; Melnick, Molly; Langer, Emma R; Bereslavskyy, Igor; Milaitis, Maxwell R; Reilly, Louise; Eckhardt, Lee L
发表日期：2026
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The role of iPSC research for insight into inherited arrhythmia conditions

iPSC研究在深入了解遗传性心律失常方面的作用

期刊:Heart Rhythm
影响因子:5.7
doi:10.1016/j.hrthm.2025.03.2005
Josvai, Mitchell B; Anderson, Corey L; Eckhardt, Lee L
发表日期：2025
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hiPSC-derived cardiac fibroblasts dynamically enhance the mechanical function of hiPSC-derived cardiomyocytes on an engineered substrate.

hiPSC衍生的心脏成纤维细胞可动态增强hiPSC衍生的心肌细胞在工程基质上的机械功能

期刊:Frontiers in Bioengineering and Biotechnology
影响因子:4.8
doi:10.3389/fbioe.2025.1546483
Josvai Mitchell, Lawson Jodi, Kanade Harshal, Kalluri Meghana, Anderson Corey L, Zhang Jianhua, Stempien Alana, Eckhardt Lee L, Kamp Timothy J, Crone Wendy C
细胞生物学
心肌炎
发表日期：2025
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Atomic-level investigation of KCNJ2 mutations associated with ventricular arrhythmic syndrome phenotypes

对与室性心律失常综合征表型相关的KCNJ2突变进行原子级研究

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-95062-2
Munawar, Saba; Anderson, Corey L; Reilly, Louise; Woltz, Ryan; Kiani, Yusra Sajid; Chiamvimonvat, Nipavan; Eckhardt, Lee L
发表日期：2025
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Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes

Kv7.1 (KCNQ1) 和 Kv11.1 (KCNH2) 通道功能障碍与长 QT 综合征表型的突变特异性差异

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms23137389
Kekenes-Huskey, Peter M; Burgess, Don E; Sun, Bin; Bartos, Daniel C; Rozmus, Ezekiel R; Anderson, Corey L; January, Craig T; Eckhardt, Lee L; Delisle, Brian P
KCNH2
发表日期：2022
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How Functional Genomics Can Keep Pace With VUS Identification

功能基因组学如何才能与VUS识别保持同步

期刊:Frontiers in Cardiovascular Medicine
影响因子:2.9
doi:10.3389/fcvm.2022.900431
Anderson, Corey L; Munawar, Saba; Reilly, Louise; Kamp, Timothy J; January, Craig T; Delisle, Brian P; Eckhardt, Lee L
发表日期：2022
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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

期刊:Circulation-Arrhythmia and Electrophysiology
影响因子:9.8
doi:10.1161/CIRCEP.120.009343
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
发育与干细胞
ERG
ERG1
干细胞
细胞生物学
KCNH2
发表日期：2021
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A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants

一种用于评估罕见DNA序列变异致病性的蛋白质结构域错误折叠快速溶解度测定方法

期刊:Genetics in Medicine
影响因子:6.2
doi:10.1038/s41436-020-0842-1
Anderson, Corey L; Routes, Tim C; Eckhardt, Lee L; Delisle, Brian P; January, Craig T; Kamp, Timothy J
发表日期：2020
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Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the KCNH2-Encoded Kv11.1 Channel

KCNH2编码的Kv11.1通道中假定的与婴儿猝死综合征相关的变异的功能失效

期刊:Circulation-Arrhythmia and Electrophysiology
影响因子:9.8
doi:10.1161/CIRCEP.117.005859
Smith, Jennifer L; Tester, David J; Hall, Allison R; Burgess, Don E; Hsu, Chun-Chun; Elayi, Samy Claude; Anderson, Corey L; January, Craig T; Luo, Jonathan Z; Hartzel, Dustin N; Mirshahi, Uyenlinh L; Murray, Michael F; Mirshahi, Tooraj; Ackerman, Michael J; Delisle, Brian P
KCNH2
发表日期：2018
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Molecular pathogenesis of long QT syndrome type 2

长QT间期综合征2型的分子发病机制

期刊:Journal of Arrhythmia
影响因子:1.7
doi:10.1016/j.joa.2015.11.009
Smith, Jennifer L; Anderson, Corey L; Burgess, Don E; Elayi, Claude S; January, Craig T; Delisle, Brian P
发表日期：2016
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