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Genetic Testing for Early-Onset Atrial Fibrillation-Is It Time to Personalize Care?

作者信息

McNally Elizabeth M, Khan Sadiya S

机构信息

Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Bluhm Cardiovascular Institute, Northwestern University Feinberg School of Medicine, Chicago, Illinois.

出版信息

JAMA Cardiol. 2022 Jul 1;7(7):669-671. doi: 10.1001/jamacardio.2022.0909.

DOI:10.1001/jamacardio.2022.0909
PMID:35544088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10032337/
Abstract
摘要

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JAMA Cardiol. 2022 Jul 1;7(7):733-741. doi: 10.1001/jamacardio.2022.0810.
2
Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality.致心肌病的致病性 DNA 变异与心血管疾病结局和全因死亡率的相关性研究。
JAMA Cardiol. 2022 Jul 1;7(7):723-732. doi: 10.1001/jamacardio.2022.0901.
3
Correspondence on "ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)" by Miller et al.米勒等人就“美国医学遗传学与基因组学学会(ACMG)关于临床外显子组和基因组测序中次要发现报告的ACMG SF v3.0清单:政策声明”的通信
Genet Med. 2022 Mar;24(3):744-746. doi: 10.1016/j.gim.2021.10.020. Epub 2021 Nov 30.
4
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes.早发性心房颤动与心肌病和心律失常基因罕见变异的患病率。
JAMA Cardiol. 2021 Dec 1;6(12):1371-1379. doi: 10.1001/jamacardio.2021.3370.
5
Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals.少数民族个体中罕见遗传变异与早发性心房颤动的关联。
JAMA Cardiol. 2021 Jul 1;6(7):811-819. doi: 10.1001/jamacardio.2021.0994.
6
Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond.2020 年心房颤动的遗传学:GWAS、基因组测序、多基因风险及其他。
Circ Res. 2020 Jun 19;127(1):21-33. doi: 10.1161/CIRCRESAHA.120.316575. Epub 2020 Jun 18.
7
Diversity and inclusion for the All of Us research program: A scoping review.《全民研究计划的多样性和包容性:范围综述》。
PLoS One. 2020 Jul 1;15(7):e0234962. doi: 10.1371/journal.pone.0234962. eCollection 2020.
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Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank.单基因和多基因对心房颤动风险的贡献:来自国家生物库的结果。
Circ Res. 2020 Jan 17;126(2):200-209. doi: 10.1161/CIRCRESAHA.119.315686. Epub 2019 Nov 6.
9
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.基于基因组优先的策略评估与截断性肌联蛋白变异相关的心脏病。
Circulation. 2019 Jul 2;140(1):42-54. doi: 10.1161/CIRCULATIONAHA.119.039573. Epub 2019 Jun 20.
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Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.肌联蛋白功能丧失变异与早发性心房颤动的关联。
JAMA. 2018 Dec 11;320(22):2354-2364. doi: 10.1001/jama.2018.18179.