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

Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults

全外显子组测序在成人遗传性心血管疾病临床诊断和治疗中的应用

期刊:Circulation-Cardiovascular Genetics
影响因子:
doi:10.1161/CIRCGENETICS.116.001573
Seidelmann, Sara B; Smith, Emily; Subrahmanyan, Lakshman; Dykas, Daniel; Abou Ziki, Maen D; Azari, Bani; Hannah-Shmouni, Fady; Jiang, Yuexin; Akar, Joseph G; Marieb, Mark; Jacoby, Daniel; Bale, Allen E; Lifton, Richard P; Mani, Arya
心血管
心血管疾病
发表日期：2017
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Psychosocial and cardiac outcomes of yoga for ICD patients: a randomized clinical control trial

瑜伽对ICD患者的心理社会和心脏结局的影响：一项随机临床对照试验

期刊:Pace-Pacing and Clinical Electrophysiology
影响因子:1.3
doi:10.1111/pace.12252
Toise, Stefanie C F; Sears, Samuel F; Schoenfeld, Mark H; Blitzer, Mark L; Marieb, Mark A; Drury, John H; Slade, Martin D; Donohue, Thomas J
发表日期：2014
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P02.35. Methodology in integrative medicine research: challenges and solutions from a randomized clinical control trial using adapted yoga

P02.35. 整合医学研究方法：一项采用改良瑜伽的随机临床对照试验所面临的挑战和解决方案

期刊:
影响因子:
doi:10.4172/1948-5956.s2-001
Janelsins, Michelle C; Mustian, Karen M; Peppone, Luke J; Sprod, Lisa K; Shayne, Michelle; Mohile, Supriya; Chandwani, Kavita; Gewandter, Jennifer S; Morrow, Gary R; Kielczynska, B; Kligler, B; Toise, S; Sears, S; Schoenfeld, M; Blitzer, M; Marieb, M; Drury, J; Slade, M; Donohue, T
发表日期：2012
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

心脏 L 型钙通道突变与遗传性 J 波综合征和心源性猝死相关

期刊:Heart Rhythm
影响因子:5.6
doi:10.1016/j.hrthm.2010.08.026
Elena Burashnikov, Ryan Pfeiffer, Héctor Barajas-Martinez, Eva Delpón, Dan Hu, Mayurika Desai, Martin Borggrefe, Michel Häissaguerre, Ronald Kanter, Guido D Pollevick, Alejandra Guerchicoff, Ruben Laiño, Mark Marieb, Koonlawee Nademanee, Gi-Byoung Nam, Roberto Robles, Rainer Schimpf, Dwight D Staple
心血管
发表日期：2010
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Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome

CACNB2b基因突变导致L型钙电流加速失活，这是布鲁加达综合征的病理基础。

期刊:Journal of Molecular and Cellular Cardiology
影响因子:4.7
doi:10.1016/j.yjmcc.2009.01.014
Cordeiro, Jonathan M; Marieb, Mark; Pfeiffer, Ryan; Calloe, Kirstine; Burashnikov, Elena; Antzelevitch, Charles
发表日期：2009
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