标题
Spontaneous Coronary Artery Dissection
作者
关键词
-
出版物
Circulation-Genomic and Precision Medicine
Volume 13, Issue 6, Pages -
出版商
Ovid Technologies (Wolters Kluwer Health)
发表日期
2020-10-31
DOI
10.1161/circgen.120.003030
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mantis-ml: Disease-Agnostic Gene Prioritization from High-Throughput Genomic Screens by Stochastic Semi-supervised Learning
- (2020) Dimitrios Vitsios et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Enrichment of Rare Variants in Loeys–Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia
- (2020) Aline Verstraeten et al. CIRCULATION
- Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
- (2019) David Adlam et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Spontaneous Coronary Artery Dissection
- (2019) Robert Jackson et al. JACC-Cardiovascular Imaging
- Exome-Based Rare-Variant Analyses in CKD
- (2019) Sophia Cameron-Christie et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Association of TSR1 Variants and Spontaneous Coronary Artery Dissection
- (2019) Yang Sun et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection
- (2019) Tamiel N. Turley et al. Circulation-Genomic and Precision Medicine
- Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association
- (2018) Sharonne N. Hayes et al. CIRCULATION
- European Society of Cardiology, acute cardiovascular care association, SCAD study group: a position paper on spontaneous coronary artery dissection
- (2018) David Adlam et al. EUROPEAN HEART JOURNAL
- LOXMutations Predispose to Thoracic Aortic Aneurysms and DissectionsNovelty and Significance
- (2016) Dong-chuan Guo et al. CIRCULATION RESEARCH
- Spontaneous coronary artery dissection and its association with heritable connective tissue disorders
- (2016) Stanislav Henkin et al. HEART
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
- (2015) E. T. Cirulli et al. SCIENCE
- Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome
- (2015) Philipp von Hundelshausen et al. THROMBOSIS AND HAEMOSTASIS
- Elevated expression of mechanosensory polycystins in human carotid atherosclerotic plaques: association with p53 activation and disease severity
- (2015) Aimilia Varela et al. Scientific Reports
- Familial Spontaneous Coronary Artery Dissection
- (2015) Kashish Goel et al. JAMA Internal Medicine
- Recurrent Gain-of-Function Mutation in PRKG1 Causes Thoracic Aortic Aneurysms and Acute Aortic Dissections
- (2013) Dong-chuan Guo et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Hes1 and Hes5 regulate vascular remodeling and arterial specification of endothelial cells in brain vascular development
- (2013) Masashi Kitagawa et al. MECHANISMS OF DEVELOPMENT
- The Genotype-Tissue Expression (GTEx) project
- (2013) John Lonsdale et al. NATURE GENETICS
- DLL1-mediated Notch activation regulates endothelial identity in mouse fetal arteries
- (2009) I. Sorensen et al. BLOOD
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation