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Genomics & Health Impact Scan Database|Search|PHGKB

Last data update: Jun 25, 2022. (Total: 47911 Documents since 2012)
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Query Trace: Cardiomyopathy[original query]>>Original Studies[Product Type]
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
The value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathy.
de Brouwer Remco et al. Heart rhythm 2022
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
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy.
Kurzlechner Leonie M et al. Journal of personalized medicine 2022 12(5)
The Genetic Architecture of Hypertrophic Cardiomyopathy in Hungary: Analysis of 242 Patients with a Panel of 98 Genes.
Sepp Róbert et al. Diagnostics (Basel, Switzerland) 2022 12(5)
Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.
Biddinger Kiran J et al. JAMA cardiology 2022
Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy.
Burke Wylie et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003541
Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes.
Yoneda Zachary T et al. JAMA cardiology 2022
Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality.
Patel Aniruddh P et al. JAMA cardiology 2022
Experiences of athletes with arrhythmogenic cardiac conditions in returning to play.
Shapero Kayle et al. Heart rhythm O2 2022 3(2) 133-140
Establishment of a Dedicated Inherited Cardiomyopathy Clinic: From Challenges to Improved Patients' Outcome.
Smith Emily et al. Journal of the American Heart Association 2022 e024501
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
Muscle LIM Protein Force-Sensing Mediates Sarcomeric Biomechanical Signaling in Human Familial Hypertrophic Cardiomyopathy.
Riaz Muhammad et al. Circulation 2022
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy.
Roudijk Robert W et al. JACC. Clinical electrophysiology 2022 8(3) 306-318
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
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy
R LeSurf et al, NPJ Genomic Medicine, March 14, 2022
It Is Not Carved in Stone-The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies.
Westphal Dominik Sebastian et al. Journal of cardiovascular development and disease 2022 9(2)
Gender Related Differences in the Clinical Presentation of Hypertrophic Cardiomyopathy-An Analysis from the SILICOFCM Database.
Preveden Andrej et al. Medicina (Kaunas, Lithuania) 2022 58(2)
Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.
Martínez-Barrios Estefanía et al. Journal of personalized medicine 2022 12(2)
High-Throughput Precision Phenotyping of Left Ventricular Hypertrophy With Cardiovascular Deep Learning.
Duffy Grant et al. JAMA cardiology 2022
Real life experience with the wearable cardioverter-defibrillator in an international multicenter Registry.
El-Battrawy Ibrahim et al. Scientific reports 2022 12(1) 3203
Causative Variants for Inherited Cardiac Conditions in a Southeast Asian Population Cohort.
Tomar Swati et al. Circulation. Genomic and precision medicine 2022 CIRCGEN121003536
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
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy
GS Huggins et al, 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
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