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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 23, 2024
. (Total: 63653 Documents since 2012)
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The outcome of genetic and non-genetic pediatric cardiomyopathies.
Ali AlAlakhfash et al. Egypt Heart J 2024 76(1) 43
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Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance.
Jane Murphy et al. Ir J Med Sci 2024
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Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients.
Oana Raluca Voinescu et al. Int J Mol Sci 2024 25(5)
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Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry.
Juan Pablo Kaski et al. Eur Heart J 2024
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Genetic Testing in Hypertrophic Cardiomyopathy.
Catherine G Ireland et al. Am J Cardiol 2024 212SS4-S13
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"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
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The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Megan J Puckelwartz et al. Genome Med 2024 16(1) 13
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Genetic contributions to risk of adverse pregnancy outcomes.
Zachary H Hughes et al. Curr Cardiovasc Risk Rep 2024 17(11) 185-193
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Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening.
Rebeca Lorca et al. J Clin Med 2024 13(1)
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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
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Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies.
Emanuele Monda et al. Circ Genom Precis Med 2023 e004252
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Diagnostic Yield of Exome Sequencing in Pediatric Cardiomyopathy.
Julia Keisling et al. J Pediatr 2023 113808
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Real-world utilization of guideline-directed genetic testing in inherited cardiovascular diseases.
Mauro Longoni et al. Front Cardiovasc Med 2023 101272433
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Stigma manifestations in cardiomyopathy care impact outcomes for black patients: a qualitative study.
Morgan Wolfgang et al. BMC Cardiovasc Disord 2023 23(1) 553
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Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives.
Søren K Nielsen et al. J Am Coll Cardiol 2023 82(18) 1751-1761
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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Jodell E Linder et al. Am J Hum Genet 2023
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Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review.
Linda Koshy et al. Indian J Med Res 2023 158(2) 119-135
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How and Why to Organize Family-Based Screening Clinics for Hypertrophic Cardiomyopathy.
Bryana J Rivers et al. Can J Cardiol 2023
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Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.
Yuri Kim et al. Circ Genom Precis Med 2023 e004062
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Burden of untreated transthyretin amyloid cardiomyopathy on patients and their caregivers by disease severity: results from a multicenter, non-interventional, real-world study.
Lucia Ponti et al. Front Cardiovasc Med 2023 101238843
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Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study.
Mark Hofmeyer et al. Circulation 2023
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Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.
Katherine A Martinez et al. J Am Coll Cardiol 2023 82(8) 661-670
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Atrial Abnormalities in Brugada Syndrome: Evaluation With ECG Imaging.
Antonio Bisignani et al. JACC Clin Electrophysiol 2023
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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study.
Mark Jansen et al. JACC Heart Fail 2023
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A Practical Guide to Genetic Testing in Inherited Heart Disease.
Emily E Brown et al. Card Electrophysiol Clin 2023 15(3) 241-247
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Yield of family screening in dilated cardiomyopathy within low-income setting: Tanzanian experience.
L S Fundikira et al. Cardiovasc J Afr 2023 341-6
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Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
Elizabeth Jordan et al. JAMA 2023 330(5) 432-441
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Age and Sex Differences in the Genetics of Cardiomyopathy.
Oyediran Akinrinade et al. J Cardiovasc Transl Res 2023
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Transthyretin Cardiac Amyloidosis: Underrecognized in the Underrepresented.
Douglas J Leedy et al. J Am Heart Assoc 2023 e030802
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Clinical Penetrance of the Transthyretin V122I Variant in Older Black Patients With Heart Failure: The SCAN-MP (Screening for Cardiac Amyloidosis With Nuclear Imaging in Minority Populations) Study.
Avni Madhani et al. J Am Heart Assoc 2023 e028973
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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