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Public Health Genomics and Precision Health Knowledge Base (v7.8)
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Last data update: Jul 03, 2022
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Cardiomyopathy[original query]>>Evidence Synthesis [Product Type]
Arrhythmogenic Right Ventricular Cardiomyopathy Prevalence and Arrhythmic Outcomes in At-Risk Family Members: A Systematic Review and Meta-Analysis.
Sharma Apurva et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003530
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A Decade of Progress in Gene Targeted Therapeutic Strategies in Duchenne Muscular Dystrophy: A Systematic Review.
Chung Liang Lam et al. Frontiers in bioengineering and biotechnology 2022 10833833
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Diagnostic validity and clinical utility of genetic testing for hypertrophic cardiomyopathy: a systematic review and meta-analysis.
Christian Susan et al. Open heart 2022 9(1)
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Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome.
Mehboob Riffat et al. Frontiers in pediatrics 2021 9742225
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Cascade health service use in family members following genetic testing in children: a scoping literature review.
Cernat Alexandra et al. European journal of human genetics : EJHG 2021
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Estimating the health benefits of timely diagnosis and treatment of transthyretin amyloid cardiomyopathy.
Rozenbaum Mark H et al. Journal of comparative effectiveness research 2021
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An Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Jordan Elizabeth et al. Circulation 2021
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An Integrated Review of Hypertrophic Cardiomyopathy in Black Populations: Underrecognized and Understudied.
Arabadjian Milla et al. The Journal of cardiovascular nursing 36(2) 104-115
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Angiotensinogen M235T polymorphism and susceptibility to hypertrophic cardiomyopathy in Asian population: A meta analysis.
Zhen Zhen et al. Journal of the renin-angiotensin-aldosterone system : JRAAS 21(4) 1470320320978100
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Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review.
Fraser Hannah et al. Orphanet journal of rare diseases 2019 Nov 14(1) 258
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CLINGEN Actionability Report for Dilated cardiomyopathy - DMD, LMNA, TNNT2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Fabry Disease - GLA
ClinGen Actionability Working Group
CLINGEN Actionability Report for Glycogen Storage Disease 2 - GAA
ClinGen Actionability Working Group
CLINGEN Actionability Report for Familial Hypertrophic Cardiomyopathy - ACTC1, CSRP3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hemochromatosis, Type 1-HFE
ClinGen Actionability Working Group
CLINGEN Actionability Report for Catecholaminergic Polymorphic Ventricular Tachycardia - RYR2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Very Long Chain Actyl-CoA Dehydrogenase Deficiency (ACADVLD) - ACADVL
ClinGen Actionability Working Group
CLINGEN Actionability Report for Emery-Dreifuss Muscular Dystrophy (AD, XL) - LMNA, EMD, FHL1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary transthyretin-related amyloidosis - TTR
ClinGen Actionability Working Group
CLINGEN Actionability Report for Myofibrillar Myopathy -DES, BAG3, FLNC
ClinGen Actionability Working Group
CLINGEN Actionability Report for Glycogen Storage Disease V - PYGM
ClinGen Actionability Working Group
CLINGEN Actionability Report for Arrhythmogenic Right Ventricular Dysplasia - PKP2, DSP, DSC2, TMEM43, DSG2
ClinGen Actionability Working Group
A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy.
Catchpool Max et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jun
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Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.
Ingles Jodie et al. Circulation. Genomic and precision medicine 2019 Jan
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Cost Efficacy of ?-Galactosidase A Enzyme Screening for Fabry Disease.
Newman Darrell B et al. Mayo Clinic proceedings 2019 Jan 94(1) 84-88
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Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review.
Naik Rakhi P, et al. Annals of internal medicine 2018 11 0. (9) 619-627
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Using Decision Analysis to Support Newborn Screening Policy Decisions: A Case Study for Pompe Disease.
Prosser Lisa A et al. MDM policy & practice 3(1)
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Next Generation DNA Sequencing: A Review of the Cost Effectiveness and Guidelines
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Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC).
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Clinical utility gene card for: dilated cardiomyopathy (CMD).
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Oct 1, 2021
Page last updated:
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