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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)
Heart, Lung, Blood and Sleep Disorders
Last data update: Apr 23, 2024
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all[original query]>>Guidelines Related[Product Type]
A focused update to the 2019 NLA scientific statement on use of lipoprotein(a) in clinical practice.
Marlys L Koschinsky et al. J Clin Lipidol 2024
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Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
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International Atherosclerosis Society Roadmap for Familial Hypercholesterolaemia.
Gerald F Watts et al. Glob Heart 2024 19(1) 12
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Screening for Lipid Disorders in Children and Adolescents: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2023 330(3) 253-260
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EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.
Jesse B Hayesmoore et al. Eur J Hum Genet 2023
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Lipid Disorders in Children and Adolescents: Screening
USPSTF recommendation, July 18, 2023
EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias
JB Hayesmoore et al. EJHG July 13, 2023
The Lancet Haematology Commission on sickle cell disease: key recommendations
The Lancet Haematology Commission on sickle cell disease: Lancet Hematology, July 2023
International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia.
Gerald F Watts et al. Nat Rev Cardiol 2023
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Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG)
JL Deignan et al, Genetics in Medicine, June 13, 2023
Significant haemoglobinopathies: A guideline for screening and diagnosis: A British Society for Haematology Guideline: A British Society for Haematology Guideline.
Barbara J Bain et al. Br J Haematol 2023 201(6) 1047-1065
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2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance.
Marina Cuchel et al. Eur Heart J 2023
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Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care.
Mikyla L Janzen et al. CJC Open 2023 5(4) 268-284
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2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death.
Katja Zeppenfeld et al. Eur Heart J 2022 43(40) 3997-4126
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Spotlight on the 2022 ESC guideline management of ventricular arrhythmias and prevention of sudden cardiac death: 10 novel key aspects.
Hilke Könemann et al. Europace 2023
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Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association.
Andrew P Landstrom et al. Circulation. Genomic and precision medicine 2023 e000092
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Bempedoic acid in the management of lipid disorders and cardiovascular risk. 2023 position paper of the international lipid expert panel (ILEP).
Maciej Banach et al. Progress in cardiovascular diseases 2023
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Guidelines for the Diagnosis and Treatment of Adult Familial Hypercholesterolemia 2022.
Mariko Harada-Shiba et al. Journal of atherosclerosis and thrombosis 2023
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Current German Guidelines on Diagnosis and Treatment of Secondary Hemochromatosis in Patients with Congenital Anemias.
Cario Holger et al. Klinische Padiatrie 2022 234(6) 368-373
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Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.
Bourke John et al. Open heart 2022 9(2)
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Delphi Panel Consensus Recommendations for Screening and Managing Childhood Cancer Survivors at Risk for Cardiomyopathy.
Aziz-Bose Rahela et al. JACC. CardioOncology 2022 4(3) 354-367
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Guidelines for Cystic Fibrosis Carrier Screening in the Prenatal/Preconception Period.
Hopkins Maeve K et al. Obstetrical & gynecological survey 2022 77(10) 606-610
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Screening, diagnosis and follow-up of Brugada syndrome in children: a Dutch expert consensus statement.
Peltenburg P J et al. Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2022
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2022 Consensus Statement on the Management of Familial Hypercholesterolemia in Korea.
Lee Chan Joo et al. Journal of lipid and atherosclerosis 2022 11(3) 213-228
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PAEDIATRIC FAMILIAL HYPERCHOLESTEROLAEMIA SCREENING IN EUROPE - PUBLIC POLICY BACKGROUND AND RECOMMENDATIONS.
Gidding Samuel S et al. European journal of preventive cardiology 2022
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Lipoprotein(a) in atherosclerotic cardiovascular disease and aortic stenosis: a European Atherosclerosis Society consensus statement.
Kronenberg Florian et al. European heart journal 2022
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Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.
O'Sullivan Jack W et al. Circulation 2022 101161CIR0000000000001077
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Molecular genetic testing in athletes: Why and when a position statement from the Italian society of sports cardiology.
Castelletti Silvia et al. International journal of cardiology 2022
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PCSK9 inhibitors and ezetimibe for the reduction of cardiovascular events: a clinical practice guideline with risk-stratified recommendations.
Hao Qiukui et al. BMJ (Clinical research ed.) 2022 377e069066
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2021 ISHNE/HRS/EHRA/APHRS Collaborative Statement on mHealth in Arrhythmia Management: Digital Medical Tools for Heart Rhythm Professionals: From the International Society for Holter and Noninvasive Electrocardiology/Heart Rhythm Society/European Heart Rhythm Association/Asia Pacific Heart Rhythm Society.
Varma Niraj et al. Cardiovascular digital health journal 2022 2(1) 4-54
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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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