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

Leadless Pacemaker Implantation in the Presence of the Bioprosthetic Tricuspid Valve: Case Presentation and Literature Review

生物瓣膜三尖瓣置换术后无导线起搏器植入：病例报告及文献综述

期刊:Clinical Case Reports
影响因子:0.6
doi:10.1002/ccr3.70077
Mohammadi, Mahsa; Iranian, MohammadReza; Saedi, Sedigheh; Toloueitabar, Yaser; Fazelifar, Amirfarjam; Haghjoo, Majid
发表日期：2025
文献求助 收藏

Long-term outcomes of ventricular tachycardia ablation in ischemic and non-ischemic cardiomyopathy patients: Data from a single center ablation registry

缺血性和非缺血性心肌病患者室性心动过速消融术的长期疗效：来自单中心消融登记研究的数据

期刊:Indian Pacing and Electrophysiology Journal
影响因子:
doi:10.1016/j.ipej.2025.07.002
Khosravi, Reza; Kamali, Farzad; Simiyari, Saba; Ghaffarinejad, Zahra; Arbabi, Mahta; Bavil, Mozhgan Hadavi; Entezari, Amin; Haghjoo, Majid; Fazelifar, Amir Farjam; Madadi, Shabnam; Emkanjoo, Zahra
心血管
心肌病
发表日期：2025
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Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

探索 TTN 变异作为心肌病发病机制的遗传学见解以及心肌病分子机制的潜在新线索

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-56154-7
Jolfayi, Amir Ghaffari; Kohansal, Erfan; Ghasemi, Serwa; Naderi, Niloofar; Hesami, Mahshid; MozafaryBazargany, MohammadHossein; Moghadam, Maryam Hosseini; Fazelifar, Amir Farjam; Maleki, Majid; Kalayinia, Samira
心血管
心肌病
发表日期：2024
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Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features

伊朗一个家族中，FLNC和JUP变异体的组合导致心律失常性心肌病，并表现出不同的临床特征。

期刊:BMC Cardiovascular Disorders
影响因子:2.3
doi:10.1186/s12872-024-04126-0
Mehdizadeh, Kasra; Soveizi, Mahdieh; Askarinejad, Amir; Elahifar, Amin; Masoumi, Tannaz; Fazelifar, Amir Farjam; Asadian, Sanaz; Maleki, Majid; Kalayinia, Samira
心血管
心肌病
发表日期：2024
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Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencing

利用全外显子组测序检测到与长QT综合征2相关的KCNH2基因中的一种新型致病变异

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-024-01900-z
Kohansal, Erfan; Naderi, Niloofar; Fazelifar, Amir Farjam; Maleki, Majid; Kalayinia, Samira
KCNH2
发表日期：2024
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Role of non-coding variants in cardiovascular disease

非编码变异在心血管疾病中的作用

期刊:Journal of Cellular and Molecular Medicine
影响因子:4.2
doi:10.1111/jcmm.17762
Heshmatzad, Katayoun; Naderi, Niloofar; Maleki, Majid; Abbasi, Shiva; Ghasemi, Serwa; Ashrafi, Nooshin; Fazelifar, Amir Farjam; Mahdavi, Mohammad; Kalayinia, Samira
心血管疾病
心血管
发表日期：2023
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Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole-exome sequencing

通过全外显子组测序鉴定出伊朗长 QT 综合征 2 型家族中 KCNH2 的新型致病变异

期刊:Journal of Arrhythmia
影响因子:2.2
doi:10.1002/joa3.12857
Amir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, Alireza Biglari, Majid Maleki, Samira Kalayinia
KCNH2
发表日期：2023
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Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

伊朗长QT间期家族中一种新型KCNQ1移码突变的鉴定及文献综述

期刊:Iranian Biomedical Journal
影响因子:1.1
doi:10.29252/.23.3.228
Amirian, Azam; Zafari, Zahra; Karimipoor, Morteza; Kordafshari, Alireza; Dalili, Mohammad; Saber, Siamak; Farjam Fazelifar, Amir; Zeinali, Sirous
发表日期：2019
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Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome

KCNQ1 基因中的新型移码突变导致 Jervell 和 Lange-Nielsen 综合征

期刊:Iranian Journal of Basic Medical Sciences
影响因子:2.7
doi:10.22038/IJBMS.2017.23207.5908
Amirian, Azam; Dalili, Seyed Mohammad; Zafari, Zahra; Saber, Siamak; Karimipoor, Morteza; Akbari, Vahid; Fazelifar, Amir Farjam; Zeinali, Sirous
发表日期：2018
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Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families

在两个伊朗家族中检测到与杰维尔综合征和兰格-尼尔森综合征相关的新的KCNQ1移码突变

期刊:Journal of Arrhythmia
影响因子:1.7
doi:10.1002/joa3.12042
Amirian, Azam; Zafari, Zahra; Dalili, Mohammad; Saber, Siamak; Karimipoor, Morteza; Dabbagh Bagheri, Samira; Fazelifar, Amir Farjam; Zeinali, Sirous
发表日期：2018
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