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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 23, 2024
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Records 1 - 27 (of 27 Records)
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Cascade screening[original query]>>Evidence Synthesis [Product Type]
Strategies to improve implementation of cascade testing in hereditary cancer syndromes: a systematic review
J Chiang et al, NPJ Genomic Medicine, April 5, 2024
Cost-Effectiveness of Screening Strategies for Familial Hypercholesterolaemia: An Updated Systematic Review.
Clara Marquina et al. Pharmacoeconomics 2024
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A systematic review of cost-effectiveness analysis of different screening strategies for familial hypercholesterolemia.
Rui Meng et al. J Clin Lipidol 2023
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Cost-effectiveness and Return on Investment of a Nationwide Case-Finding Program for Familial Hypercholesterolemia in Children in the Netherlands.
Zanfina Ademi et al. JAMA Pediatr 2023
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Genetic Testing for Familial Hypercholesterolemia: Health Technology Assessment.
et al. Ontario health technology assessment series 2022 22(3) 1-155
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The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy-A systematic review and meta-analysis.
Cirino Allison L et al. Journal of genetic counseling 2022
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Accounting for Intergenerational Cascade Testing in Economic Evaluations of Clinical Genomics: A Scoping Review.
Zischke Jason et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2022 25(6) 944-953
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Swiss cost-effectiveness analysis of universal screening for Lynch syndrome of patients with colorectal cancer followed by cascade genetic testing of relatives.
Salikhanov Islam et al. Journal of medical genetics 2021
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Familial hypercholesterolemia (FH) registry worldwide: A systematic review.
Amerizadeh Atefeh et al. Current problems in cardiology 2021 100999
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Cascade health service use in family members following genetic testing in children: a scoping literature review
A Cernat et al, EJHG, August 26, 2021
Cost-effectiveness analysis of screening for first-degree relatives of patients with bicuspid aortic valve.
Tessler Idit et al. European heart journal. Quality of care & clinical outcomes 2021
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Interventions Facilitating Family Communication of Genetic Testing Results and Cascade Screening in Hereditary Breast/Ovarian Cancer or Lynch Syndrome: A Systematic Review and Meta-Analysis.
Baroutsou Vasiliki et al. Cancers 2021 13(4)
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Cost-Effectiveness of Targeted Genetic Testing for Breast and Ovarian Cancer: A Systematic Review.
Koldehoff Andreas et al. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2021 Feb 24(2) 303-312
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Barriers and facilitators for cascade testing in genetic conditions: a systematic review
S Srinivasan et al, EJHG, September 18, 2020
Health economic evaluation of screening and treating children with familial hypercholesterolemia early in life: Many happy returns on investment?
Ademi Zanfina et al. Atherosclerosis 2020 May 3041-8
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CLINGEN Actionability Report for Acute Intermittent Porphyria - HMBS
ClinGen Actionability Working Group
CLINGEN Actionability Report for Homozygous Familial Hypercholesterolemia - LDLR, APOB, PCSK9
ClinGen Actionability Working Group
Integration of child-parent screening and cascade testing for familial hypercholesterolaemia.
Wald David S et al. Journal of medical screening 2018 Oct 969141318796856
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How Can We Reach At-Risk Relatives? Efforts to Enhance Communication and Cascade Testing Uptake: a Mini-Review
R Schwiter et al. Curr Genet Med Rep, Apr 2018
Family Communication About Genetic Risk of Hereditary Cardiomyopathies and Arrhythmias: an Integrative Review.
Shah Lisa L et al. Journal of genetic counseling 2018 Feb
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The cost-effectiveness of screening strategies for familial hypercholesterolaemia in Poland.
Pelczarska Aleksandra et al. Atherosclerosis 2018 Jan 270132-138
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The Cost-effectiveness of Genetic Screening for Familial Hypercholesterolemia: a Systematic Review.
Rosso A et al. Annali di igiene : medicina preventiva e di comunita 29(5) 464-480
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The panorama of familial hypercholesterolemia in Latin America: a systematic review.
Mehta Roopa et al. Journal of lipid research 2016 Oct
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Fourfold increased detection of Lynch syndrome by raising age limit for tumour genetic testing from 50 to 70 years is cost-effective.
Sie A S et al. Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2014 Oct 25(10) 2001-7
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Communicating risk with relatives in a familial hypercholesterolemia cascade screening program: a summary of the evidence.
Allison Melanie et al. The Journal of cardiovascular nursing 30(4) E1-E12
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Cascade screening based on genetic testing is cost-effective: evidence for the implementation of models of care for familial hypercholesterolemia.
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Criteria for Diagnosis of Familial Hypercholesterolemia: A Comprehensive Analysis of the Different Guidelines, Appraising their Suitability in the Omani Arab Population.
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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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