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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Apr 25, 2024
. (Total: 226468Documents)
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Syndrome and meta-analysis and CYP2C19[original query]
Impact of CYP2C19 variant genotypes on clinical efficacy of antiplatelet treatment with clopidogrel: systematic review and meta-analysis.
BMJ (Clinical research ed.) 2011 343 d4588.
Bauer Tim, Bouman Heleen J, van Werkum Jochem W, Ford Neville F, ten Berg Jurriën M, Taubert Di
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Risk of major adverse cardiovascular events of CYP2C19 loss-of-function genotype guided prasugrel/ticagrelor vs clopidogrel therapy for acute coronary syndrome patients undergoing percutaneous coronary intervention: a meta-analysis.
Platelets 2020 7 32 (5): 591-600.
Biswas Mohitosh, Kali Most Sumaiya Khatun, Biswas Tapash Kumar, Ibrahim Baharud
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The efficacy and safety of CYP2C19 genotype-guided antiplatelet therapy compared with conventional antiplatelet therapy in patients with acute coronary syndrome or undergoing percutaneous coronary intervention: A meta-analysis of randomized controlled trials.
Platelets 2020 6 31 (8): 971-980.
Lyu Si-Qi, Yang Yan-Min, Zhu Jun, Wang Juan, Wu Shuang, Zhang Han, Shao Xing-Hui, Ren Jia-Me
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Effects of the CYP2C19 LoF allele on major adverse cardiovascular events associated with clopidogrel in acute coronary syndrome patients undergoing percutaneous coronary intervention: a meta-analysis.
Pharmacogenomics 2022 1 23 (3): 207-220.
Biswas Mohitosh, Sukasem Chonlaphat, Khatun Kali Most Sumaiya, Ibrahim Baharud
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Effect of Genotype-Guided Oral P2Y12 Inhibitor Selection After Percutaneous Coronary Intervention: A Systematic Review and Meta-Analysis of Randomized Clinical Trials.
Cardiovascular revascularization medicine : including molecular interventions 2022 1 41 115-121.
Malik Aaqib H, Gupta Rahul, Chakraborty Sandipan, Mahajan Pranav, Bandyopadhyay Dhrubajyoti, Yandrapalli Srikanth, Zaid Syed, Sreenivasan Jayakumar, Chaturvedi Abhishek, Mehta Sanjay S, Vyas Apurva V, Patel Nainesh C, Combs William G, Ahmad Has
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 22, 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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