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Laura J. Train

Mayo Clinic

9

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223

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VALIDATION AND PERFORMANCE OF POINT-OF-CARE RAPID CYP2C19 GENOTYPING IN THE TAILOR-PCI MULTICENTER INTERNATIONAL RANDOMIZED CLINICAL TRIAL

2021 Journal of the American College of Cardiology
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Comparison of αLEPRA and αLELY Co-Inheritance with a SPTA1 Whole Gene Deletion, a Family Study

2019 Blood
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Genetic variation in statin intolerance and a possible protective role for UGT1A1.

2018 Pharmacogenomics
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Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade

2016 The Journal of Molecular Diagnostics
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Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis

2014 Journal of Clinical Apheresis
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Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing

2010 American Journal of Cardiology
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Relation of ADRB1, CYP2D6, and UGT1A1 Polymorphisms With Dose of, and Response to, Carvedilol or Metoprolol Therapy in Patients With Chronic Heart Failure

2010 American Journal of Cardiology
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LDLR promoter variant and exon 14 mutation on the same chromosome are associated with an unusually severe FH phenotype and treatment resistance.

2009 European Journal of Human Genetics
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