Dilated Cardiomyopathy
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Last Posted: Mar 19, 2024
- Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients.
Oana Raluca Voinescu et al. Int J Mol Sci 2024 25(5) - "Inherited cardiovascular disease mindset" can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.
Rebeca Lorca et al. Int J Cardiol 2024 131825 - Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening.
Rebeca Lorca et al. J Clin Med 2024 13(1) - Genetic contributions to risk of adverse pregnancy outcomes.
Zachary H Hughes et al. Curr Cardiovasc Risk Rep 2024 17(11) 185-193 - QALYs and rare diseases: exploring the responsiveness of SF-6D, EQ-5D-5L and AQoL-8D following genomic testing for childhood and adult-onset rare genetic conditions in Australia.
Tianxin Pan et al. Health Qual Life Outcomes 2023 21(1) 132 - Real-world utilization of guideline-directed genetic testing in inherited cardiovascular diseases.
Mauro Longoni et al. Front Cardiovasc Med 2023 101272433 - Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.
Yuri Kim et al. Circ Genom Precis Med 2023 e004062 - Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study.
Mark Hofmeyer et al. Circulation 2023 - Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.
Mark Jansen et al. JACC Heart Fail 2023 - Yield of family screening in dilated cardiomyopathy within low-income setting: Tanzanian experience.
L S Fundikira et al. Cardiovasc J Afr 2023 341-6 - Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
Elizabeth Jordan et al. JAMA 2023 8 (5) 432-441 - Age and Sex Differences in the Genetics of Cardiomyopathy.
Oyediran Akinrinade et al. J Cardiovasc Transl Res 2023 - The next step toward personalized recommendations for genetic cardiomyopathies
SLVM Stroeks et al, EJHG, June 6, 2023 - Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy.
Sophie L V M Stroeks et al. Eur J Hum Genet 2023 5 - A systematic literature review of economic evaluations and cost-of-illness studies of inherited cardiomyopathies.
Isabell Wiethoff et al. Neth Heart J 2023 - Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.
Daniel D Kinnamon et al. Circulation 2023 - Prevalence and Clinical Consequences of Multiple Pathogenic Variants in Dilated Cardiomyopathy
SLVM Stroeks et al, Circ Genomics & Prec Med, March 27, 2023 - Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients.
María Salgado et al. Journal of clinical medicine 2023 12(3) - DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort.
Francesca Di Lorenzo et al. International journal of molecular sciences 2023 24(3) - Prognosis of Myocarditis Developing After mRNA COVID-19 Vaccination Compared With Viral Myocarditis.
Lai Francisco Tsz Tsun et al. Journal of the American College of Cardiology 2022 80(24) 2255-2265 - An intervention strategy to improve genetic testing for dilated cardiomyopathy in a heart failure clinic.
Mohananey Akanksha et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022 - The Use of Cell-free DNA in Clinical Practice: Work in Progress
M Clyne et al, CDC Blog Post, December 14, 2022 - ECG-based techniques to enhance clinical practice in cardiac genetic disease management.
Boonstra Machteld et al. Journal of electrocardiology 2022 7655-60 - Equitable and Informed Consent in Genetic Studies.
Navar Ann Marie et al. JAMA cardiology 2022 11 - Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy.
Ni Hanyu et al. JAMA cardiology 2022 11 - Mechanical Circulatory Support Devices Among Patients With Familial Dilated Cardiomyopathy: Insights From the INTERMACS.
Shetty Naman S et al. Circulation 2022 146(19) 1486-1488 - Family Screening in Dilated Cardiomyopathy: Prevalence, Incidence, and Potential for Limiting Follow-Up.
Vissing Christoffer R et al. JACC. Heart failure 2022 10(11) 792-803 - The addition of genetic testing and cardiovascular magnetic resonance to routine clinical data for stratification of etiology in dilated cardiomyopathy.
Amin Ravi J et al. Frontiers in cardiovascular medicine 2022 91017119 - Clinical Implication of Genetic Testing in Dilated Cardiomyopathy.
Lee Ju-Hee et al. International journal of heart failure 2022 4(1) 1-11 - Genetic Basis of Childhood Cardiomyopathy.
Bagnall Richard D et al. Circulation. Genomic and precision medicine 2022 e003686 - A descriptive investigation of clinical practice models used by cardiovascular genetic counselors in North America.
Rickman Allison F et al. Journal of genetic counseling 2022 - Genetic Architecture of Acute Myocarditis and the Overlap with Inherited Cardiomyopathy.
Lota Amrit S et al. Circulation 2022 - Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification.
van der Meulen Marijke H et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN120002981 - Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service.
Trachoo Objoon et al. PloS one 2022 17(9) e0267770 - Artificial Intelligence Applied to Cardiomyopathies: Is It Time for Clinical Application?
Kim Kyung-Hee et al. Current cardiology reports 2022 - Machine learning to predict left ventricular reverse remodeling by guideline-directed medical therapy by utilizing texture feature of extracellular volume fraction in patients with non-ischemic dilated cardiomyopathy.
Suyama Shun et al. Heart and vessels 2022 - Loss-of-Function FLNC Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population.
Carruth Eric D et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003645 - Incidence rates of dilated cardiomyopathy in adult first-degree relatives versus matched controls.
Andersson Charlotte et al. International journal of cardiology. Heart & vasculature 2022 41101065 - Molecular genetics in 4 408 cardiomyopathy probands and 3 008 relatives in Norway: 17 years of genetic testing in a national laboratory.
Stava Tonje Talsnes et al. European journal of preventive cardiology 2022 - Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional Data.
Tayal Upasana et al. Journal of the American College of Cardiology 2022 79(22) 2219-2232 - Arrhythmias as Presentation of Genetic Cardiomyopathy.
Lukas Laws J et al. Circulation research 2022 130(11) 1698-1722 - Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy.
Burke Wylie et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003541 - Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent "Lone AF" Patients: Results and Insights.
Pessente Gabrielle D'Arezzo et al. Frontiers in cardiovascular medicine 2022 9823717 - TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study
BH Trachtenberg et al, Genetics in Medicine, April 18, 2022 - Targeting the sarcomere in inherited cardiomyopathies
SJ Lehman, et al, Nat Rev Cardiology, March 18, 2022 - Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study.
Shen Cheng et al. Annals of translational medicine 2022 10(3) 129 - Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies.
Walsh Roddy et al. Nature reviews. Cardiology 2021 9 (3) 151-167 - Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
Huggins Gordon S et al. JAMA 2022 327(5) 454-463 - Association of Titin Variations With Late-Onset Dilated Cardiomyopathy
A Cannata et al, JAMA Cardiology, February 9, 2022 - Prevalence of Inherited Cardiac Conditions in Pediatric First-Degree Relatives of Patients with Idiopathic Ventricular Fibrillation.
Brunet-Garcia Laia et al. Pediatric cardiology 2022 - Identifying Dilated Cardiomyopathy Through Family-Based Screening
KG Aragam, JAMA, February 1, 2022 - Artificial intelligence study on left ventricular function among normal individuals, hypertrophic cardiomyopathy and dilated cardiomyopathy patients using 1.5T cardiac cine MR images obtained by SSFP sequence.
Guo Jiajun et al. The British journal of radiology 2022 20201060 - Rate of Heart Failure Following Atrial Fibrillation According to Presence of Family History of Dilated Cardiomyopathy or Heart Failure: A Nationwide Study.
Ebbesen Magnus N et al. Journal of the American Heart Association 2021 e021286 - Filamin C variant-associated Cardiomyopathy: A Pooled Analysis of Individual Patient Data to Evaluate the Clinical Profile and Risk of Sudden Cardiac Death.
Celeghin Rudy et al. Heart rhythm 2021 - mTOR-Activating Mutations in RRAGD are Causative for Kidney Tubulopathy and Cardiomyopathy.
Schlingmann Karl-Peter et al. Journal of the American Society of Nephrology : JASN 2021 - Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utility.
Cheema Huma et al. NPJ genomic medicine 2021 5(1) 44 - Estimating the Population Benefits of Blood Pressure Lowering: A Wide-Angled Mendelian Randomization Study in UK Biobank.
Higgins Hannah et al. Journal of the American Heart Association 2021 e021098 - Clinical impact of re-evaluating genes and variants implicated in dilated cardiomyopathy.
Stroeks Sophie L V M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 - Development and evaluation of decision aids to guide families' predictive testing choices for children at risk for arrhythmia or cardiomyopathy.
Christian Susan et al. The Canadian journal of cardiology 2021 - Phenotype and progression among patients with dilated cardiomyopathy and RBM20 mutations.
Robles-Mezcua Ainhoa et al. European journal of medical genetics 2021 64(9) 104278
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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