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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 25, 2024
. (Total: 63675 Documents since 2012)
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Lipoprotein(a): An important piece of the ASCVD risk factor puzzle across diverse populations.
Nicole Ciffone et al. Am Heart J Plus 2024 38100350
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Sex Differences in Diagnosis, Treatment, and Cardiovascular Outcomes in Homozygous Familial Hypercholesterolemia.
Janneke W C M Mulder et al. JAMA Cardiol 2024
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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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Modern approaches to the management of homozygous familial hypercholesterolemia in the Middle East and North Africa.
Abdullah Al-Ashwal et al. J Clin Lipidol 2023
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Influence of pharmacogenetics on the diversity of response to statins associated with adverse drug reactions.
Jaime I Sainz de Medrano Sainz et al. Adv Lab Med 2023 4(4) 341-352
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Misperceptions and management of LDL-cholesterol in secondary prevention of patients with familial hypercholesterolemia in cardiology practice: Real-life evidence from the EPHESUS registry.
Meral Kayikcioglu et al. J Clin Lipidol 2023 17(6) 732-742
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Patient-Level Exposure to Actionable Pharmacogenomic Medications in a Nationally Representative Insurance Claims Database.
Monica L Bianchini et al. J Pers Med 2023 13(11)
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Premature atherosclerosis: An analysis over 39 years in the Netherlands. Implications for young individuals in high-risk families.
Juliette Crooijmans et al. Atherosclerosis 2023 117267
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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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Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric Group.
Cristina Pederiva et al. Nutrients 2023 15(15)
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Real-world pharmacogenetics of statin intolerance: effects of SLCO1B1, ABCG2, and CYP2C9 variants.
K Ivar Lönnberg et al. Pharmacogenet Genomics 2023
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Determinants of lipid-lowering medication prescribing in a multi-ethnic adult population diagnosed with familial hypercholesterolaemia in South London.
Aya Ayoub et al. Br J Gen Pract 2023 73(suppl 1)
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Screening for Lipid Disorders in Children and Adolescents: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.
Janelle M Guirguis-Blake et al. JAMA 2023 330(3) 261-274
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Mapping of familial hypercholesterolemia and dyslipidemias basic management infrastructure in Pakistan: a cross-sectional study.
Fouzia Sadiq et al. Lancet Reg Health Southeast Asia 2023 12100163
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Gaps in the Care of Subjects with Familial Hypercholesterolemia: Insights from the Thai Familial Hypercholesterolemia Registry.
Poranee Ganokroj et al. J Atheroscler Thromb 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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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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Risk Factors for Early Onset Sporadic Colorectal Cancer in Male Veterans.
Thomas F Imperiale et al. Cancer Prev Res (Phila)
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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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Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis.
Noel Peretti et al. The Journal of pediatrics 2022
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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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Predictive Value of SLCO1B1 c.521T>C Polymorphism on Observed Changes in the Treatment of 1136 Statin-Users.
Marleen E Jansen et al. Genes 2023 14(2)
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Association of clinical and genetic risk factors with management of dyslipidaemia: analysis of repeated cross-sectional studies in the general population of Lausanne, Switzerland.
Valeriya Chekanova et al. BMJ open 2023 13(2) e065409
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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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Adherence to statin treatment in patients with familial hypercholesterolemia: A dynamic prediction model.
Arjen J Cupido et al. Journal of clinical lipidology 2023
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Burden of cardiovascular disease in a large contemporary cohort of patients with heterozygous familial hypercholesterolemia.
Ferrières Jean et al. Atherosclerosis plus 2023 5017-24
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Attainment of Low-Density Lipoprotein Cholesterol Targets and Prescribing Pattern of Lipid-Lowering Medications among Patients with Familial Hypercholesterolemia Attending Specialist Clinics.
Chua Yung-An et al. Journal of atherosclerosis and thrombosis 2022
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Familial Hypercholesterolemia and Its Current Diagnostics and Treatment Possibilities: A Literature Analysis.
Zubieliene Kristina et al. Medicina (Kaunas, Lithuania) 2022 58(11)
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Screening and Management of Dyslipidemia in Children and Adolescents.
Schefelker Juliette M et al. Journal of clinical medicine 2022 11(21)
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Pharmacogenomics in Stroke and Cardiovascular Disease: State of the Art.
Ross Stephanie et al. Stroke 2022
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 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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