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中南大学 [5]

中国医学科学院北京... [3]

西安交通大学 [2]

兰州大学 [1]

深圳先进技术研究院 [1]

水生生物研究所 [1]

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	Identification of LBX2 as a novel causal gene of atrial septal defect 期刊论文 INTERNATIONAL JOURNAL OF CARDIOLOGY, 2018, 卷号: 265, 期号: 1, 页码: 188-194 作者: Wang, Jing; Luo, Jing; Chenc, Qiuhong; Wang, Xi; He, Jiangyan 收藏 \| 浏览/下载：52/0 \| 提交时间：2019/07/03 Atrial septal defect LBX2 Neural crest cells Whole exome sequencing
	A novel totally biodegradable device for effective atrial septal defect closure: A 2-year study in sheep 期刊论文 2018, 卷号: 31, 期号: 6, 页码: 841-848 作者: Lu, Wenxin; Ouyang, Wenbin; Wang, Shouzheng; Liu, Yao; Zhang, Fengwen 收藏 \| 浏览/下载：4/0 \| 提交时间：2020/01/03 atrial septal defect (ASD) biodegradable device closure congenital heart disease echocardiographic guidance
	Mismatch in size of occluding devices for atrial septal defect (ASD) impairs endothelialization of the occluder surface in a canine ASD model 期刊论文 INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 卷号: 10, 页码: 385-393 作者: Cheng, Ge-Sheng; Zhang, Yu-Shun; Zhang, Ting-Ting; Wan, Chen; He, Xu-Mei 收藏 \| 浏览/下载：3/0 \| 提交时间：2019/11/26 occluder Atrial septal defect endothelialization
	Quantitative Assessment of Intra-Cardiac Dissipative Energy Loss Derived from Vector Flow Mapping in Patients with Atrial Septal Defect 期刊论文 JOURNAL OF MEDICAL IMAGING AND HEALTH INFORMATICS, 2017, 卷号: 7, 期号: 6, 页码: 1219-1225 作者: Javed, Saeed; Li Gui-Shuang; Lin MingJie; Wang Xujing; Ferdous, Misbahul 收藏 \| 浏览/下载：5/0 \| 提交时间：2019/12/11 Atrial Septal Defect (ASD) Vector Flow Mapping (VFM) Energy Loss (EL) Echocardiography Atrial Septal Occluder (ASO)
	CT angiography for diagnosis and subcategorization of unroofed coronary sinus syndrome 期刊论文 2017, 卷号: 9, 期号: 10, 页码: 3946-3955 作者: Zhi, Ai-Hua; Dai, Ru-Ping; Ma, Wei-Guo; Zhang, Pei; Lv, Bin 收藏 \| 浏览/下载：6/0 \| 提交时间：2020/01/04 Unroofed coronary sinus syndrome (URCS) CT angiography (CTA) atrial septal defect (ASD) congenital heart defect left superior vena cava (LSVC)
	A novel mutation of GATA4 (K300T) associated with familial atrial septal defect 期刊论文 Gene, 2015, 卷号: 575, 期号: 2, 页码: 473-477 作者: Chen, Jia; Qi, Bingyang; Zhao, Juan; Liu, Wei; Duan, Ranhui* 收藏 \| 浏览/下载：9/0 \| 提交时间：2019/12/03 CHD congenital heart diseases ToF tetralogy of Fallot ASD atrial septal defect VSD ventricular septal defect AVSD atrioventricular septal defect DCM dilated cardiomyopathy HGMD human gene mutation database dbSNP database of Single Nucleotide Polymorphisms EVSD Exome Variant Server Database NLS nuclear localization signal SNP Single nucleotide polymorphism GATK Genome Analysis Toolkit PolyPhen-2 Polymorphism Phenotyping v2 SIFT Sorting Intolerant From Tolerant TAD transcription activation domain N-Znf N-terminal zinc finger C-Znf C-terminal zinc finger Ventricular septal defect Incomplete penetrance Whole exome sequencing Post-translational modification Methylation
	Safety and feasibility of transseptal puncture for atrial fibrillation ablation in patients with atrial septal defect closure devices 期刊论文 Heart Rhythm, 2014, 卷号: 11, 期号: 2, 页码: 330-335 作者: Li, Xuping; Wissner, Erik; Kamioka, Masashi; Makimoto, Hisaki; Rausch, Peter 收藏 \| 浏览/下载：9/0 \| 提交时间：2019/12/03 AF ASD Atrial fibrillation Atrial septal defect closure device Catheter ablation ICE LA PCI PV PVI TSP Transseptal puncture atrial septal defect atrial fi brillation intracardiac echocardiography left atrium/atrial percutaneous coronary intervention pulmonary vein pulmonary vein isolation transseptal puncture
	A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect 期刊论文 Journal of Zhejiang University. Science B, Biomedicine & Biotechnology, 2014, 卷号: 15, 期号: 9, 页码: 830-837 作者: Liu Jijia; Fan Liangliang; Chen Jinlan; Tan Zhiping; Yang Yifeng 收藏 \| 浏览/下载：5/0 \| 提交时间：2019/12/03 Congenital heart disease (CHD) Atrial septal defect (ASD) Whole-exome sequencing CHD-related gene filter TBX20
	Oversized atrial septal defect (ASD) occluder and incomplete endothelialization 会议论文作者: Zhang Tingting; Wan Chen; Cheng Ge-Sheng; He Xu-Mei; Du Ya-Juan 收藏 \| 浏览/下载：5/0 \| 提交时间：2019/12/02
	A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis 期刊论文 Gene, 2014, 卷号: 534, 期号: 2, 页码: 320-323 作者: Xiang, Rong; Fan, Liang-Liang; Huang, Hao; Cao, Bei-Bei; Li, Xiang-Ping 收藏 \| 浏览/下载：2/0 \| 提交时间：2019/12/03 CHD congenital heart defects PS pulmonary valve stenosis polyphen2 polymorphism phenotyping SIFT Sorting Intolerant From Tolerant dbSNP Single Nucleotide Polymorphism Database ASD atrial septal defect VSD ventricular septal defect TOF tetralogy of Fallot HRV hypoplastic right ventricle TAPVR total anomalous pulmonary venous retour NLS nuclear localization signals SNP single nucleotide polymorphism PCR polymerase chain reaction Congenital heart disease Atrial septal defect ASD GATA4 Transcription factor

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