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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 18, 2024
. (Total: 63623 Documents since 2012)
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Statins [original query]>>Original Studies[Product Type]
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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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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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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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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Assessing statins use in a real-world primary care digital strategy: a cross-sectional analysis of a population-wide digital health approach
MJM Carrion et al, Lancet Regional Health, June 22, 2023
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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Natural language processing to identify reasons for sex disparity in statin prescriptions.
Celeste Witting et al. Am J Prev Cardiol 2023 14100496
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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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A novel machine learning-based screening identifies statins as inhibitors of the calcium pump SERCA.
Carlos Cruz-Cortés et al. The Journal of biological chemistry 2023 104681
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Identifying Reasons for Statin Nonuse in Patients With Diabetes Using Deep Learning of Electronic Health Records.
Ashish Sarraju et al. Journal of the American Heart Association 2023 e028120
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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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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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Artificial intelligence-enabled screening strategy for drug repurposing in monoclonal gammopathy of undetermined significance.
Alexander J Ryu et al. Blood cancer journal 2023 13(1) 28
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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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Major Adverse Cardiovascular Events in Coronary Type 2 Diabetic Patients: Identification of Associated Factors Using Electronic Health Records and Natural Language Processing.
González-Juanatey Carlos et al. Journal of clinical medicine 2022 11(20)
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Pharmacogenomics implementation in cardiovascular disease in a highly diverse population: initial findings and lessons learned from a pilot study in United Arab Emirates.
Al-Mahayri Zeina N et al. Human genomics 2022 16(1) 42
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Prevalence and Treatment of Familial Hypercholesterolemia and Severe Hypercholesterolemia in Older Adults in Ontario, Canada.
Akioyamen Leo E et al. CJC open 2022 4(9) 739-747
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Cost impact of undertaking detection and management of familial hypercholesterolaemia in Australian general practice.
Li Ian W et al. Australian journal of general practice 2022 51(8) 604-609
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Cost-Effectiveness of Polygenic Risk Scores to Guide Statin Therapy for Cardiovascular Disease Prevention.
Kiflen Michel et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003423
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Using deep learning-based natural language processing to identify reasons for statin nonuse in patients with atherosclerotic cardiovascular disease.
Sarraju Ashish et al. Communications medicine 2022 288
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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