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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 19, 2024
. (Total: 63627 Documents since 2012)
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Efficacy of Inclisiran in patients having familial hypercholesterolemia: heterozygous compared to homozygous trait, a systematic review and meta analysis.
Rahul Rai et al. Crit Pathw Cardiol 2024
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Association of Clinical Characteristics With Familial Hypercholesterolaemia Variants in a Lipid Clinic Setting: A Case-Control Study.
Bobby V Li et al. J Lipid Atheroscler 2024 13(1) 29-40
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Measuring Costs of Cardiovascular Disease Prevention for Patients with Familial Hypercholesterolemia in Administrative Claims Data.
Lauren E Passero et al. High Blood Press Cardiovasc Prev 2024
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A retrospective study of people with familial hypercholesterolaemia in a Belgian lipid clinic.
V Ide et al. Acta Cardiol 2023 1-10
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Long-term safety and effectiveness of alirocumab and evolocumab in familial hypercholesterolemia (FH) in Belgium.
Marc Snel et al. Acta Cardiol 2023 1-8
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Genetic testing for familial hypercholesterolemia in Quebec, Canada: a single-centre retrospective cohort study.
Amanda Guerin et al. CMAJ Open 2023 11(4) E754-E764
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Is Lipoprotein(a) Clinically Actionable with Today's Evidence? The Answer is Yes.
Gary S Ma et al. Curr Cardiol Rep 2023
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Familial Hyperlipidemia Caused by Apolipoprotein B Mutation in the Pediatric Amish Population: A Mini Review.
Corey Snyder et al. Interv Cardiol (Lond) 2023 15(Suppl 17) 433-437
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Genetic Characteristics of Latvian Patients with Familial Hypercholesterolemia: The First Analysis from Genome-Wide Sequencing.
Gustavs Latkovskis et al. J Clin Med 2023 12(15)
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Proteomics and Lipidomics to unveil the contribution of PCSK9 beyond cholesterol lowering: a narrative review.
Erica Gianazza et al. Front Cardiovasc Med 2023 101191303
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LDLR gene's promoter region hypermethylation in patients with familial hypercholesterolemia.
R A Zorzo et al. Sci Rep 2023 13(1) 9241
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Identification of pathogenic variants in the Brazilian cohort with Familial Hypercholesterolemia using exon-targeted gene sequencing.
Jéssica Bassani Borges et al. Gene 2023 147501
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Genetic Testing Enables the Diagnosis of Familial Hypercholesterolemia Underdiagnosed by Clinical Criteria: Analysis of Japanese Early-Onset Coronary Artery Disease Patients.
Hiroshi Miyama et al. Cardiol Res Pract 2023 20232236422
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Reducing Premature Coronary Artery Disease in Malaysia by Early Identification of Familial Hypercholesterolaemia using FAMCAT Primary Care Screening Tool: A Mixed-Methods Evaluation Study Protocol.
Anis Safura Ramli et al. JMIR Res Protoc 2023
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LDL cholesterol targets rarely achieved in familial hypercholesterolemia patients: A sex and gender-specific analysis.
M M Schreuder et al. Atherosclerosis
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Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.
Ozan Dikilitas et al. Circ Genom Precis Med 2023 16(2) e003816
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Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program.
Xin Wang et al. J Hum Genet
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PCSK9 inhibition in atherosclerotic cardiovascular disease.
Dimitrios Delialis et al. Curr Pharm Des 2023
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Novel and future lipid-modulating therapies for the prevention of cardiovascular disease.
Julia Brandts et al. Nat Rev Cardiol 2023
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How Genetic Variants in Children with Familial Hypercholesterolemia Not Only Guide Detection, but Also Treatment.
Sibbeliene E van den Bosch et al. Genes 2023 14(3)
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Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors.
Nor Azian Abdul Murad et al. Genes 2023 14(3)
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Monoclonal Antibodies, Gene Silencing and Gene Editing (CRISPR) Therapies for the Treatment of Hyperlipidemia-The Future Is Here.
Melody Hermel et al. Pharmaceutics 2023 15(2)
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Genetic Heterogeneity of Familial Hypercholesterolemia: Repercussions for Molecular Diagnosis.
Maria Donata Di Taranto et al. International journal of molecular sciences 2023 24(4)
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Management and clinical outcomes of patients with homozygous familial hypercholesteremia in Saudi Arabia.
Naji Kholaif et al. Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace 2023
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Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia.
Andrea Aparicio et al. Journal of clinical medicine 2023 12(3)
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Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients.
María Salgado et al. Journal of clinical medicine 2023 12(3)
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Gene editing for dyslipidemias: New tools to "cut" lipids.
Sylvia Stankov et al. Atherosclerosis 2023
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Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.
Jacqueline S Dron et al. JAMA cardiology 2023
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Targeted sequencing of a gene panel in patients with Familial Hypercholesterolemia from Southern Poland.
Toton-Zuranska Justyna et al. Polish archives of internal medicine 2023
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Safety and Effectiveness of Alirocumab, a Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitor, in Patients With Familial or Non-Familial Hypercholesterolemia - A Post-Marketing Survey (J-POSSIBLE).
Kiyosue Arihiro et al. Circulation journal : official journal of the Japanese Circulation Society 2023
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 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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