Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Authors
Keywords
-
Journal
GENETICS IN MEDICINE
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2021-01-26
DOI
10.1038/s41436-020-01049-x
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy
- (2020) Francesco Mazzarotto et al. CIRCULATION
- A structural variation reference for medical and population genetics
- (2020) Ryan L. Collins et al. NATURE
- Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death
- (2020) Emma S. Singer et al. GENETICS IN MEDICINE
- A systematic review and meta-analysis of the prevalence of left ventricular non-compaction in adults
- (2019) Samantha B Ross et al. EUROPEAN HEART JOURNAL
- Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy
- (2019) Jaap I. van Waning et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy
- (2018) Jaap I. van Waning et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity
- (2018) Pascale Richard et al. CLINICAL GENETICS
- Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
- (2016) Roddy Walsh et al. GENETICS IN MEDICINE
- Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
- (2015) Angharad M. Roberts et al. Science Translational Medicine
- Precursors of Hypertensive Heart Phenotype Develop in Healthy Adults
- (2015) Antonio de Marvao et al. JACC-Cardiovascular Imaging
- Reversible De Novo Left Ventricular Trabeculations in Pregnant Women
- (2014) Sabiha Gati et al. CIRCULATION
- Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
- (2013) Anne-Karin Arndt et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Increased left ventricular trabeculation in highly trained athletes: do we need more stringent criteria for the diagnosis of left ventricular non-compaction in athletes?
- (2013) Sabiha Gati et al. HEART
- Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy
- (2013) Guillermo Luxán et al. NATURE MEDICINE
- Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical Phenotype
- (2011) Susanne Probst et al. Circulation-Cardiovascular Genetics
- The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction Cardiomyopathy
- (2010) Yvonne M. Hoedemaekers et al. Circulation-Cardiovascular Genetics
- Mutations in Sarcomere Protein Genes in Left Ventricular Noncompaction
- (2008) Sabine Klaassen et al. CIRCULATION
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started