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Laura J. Train

Preemptive Pharmacogenomic Testing for Precision Medicine
2016 · Yuan Ji, Jennifer M. Skierka, et al. · Journal of Molecular Diagnostics · 198
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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 · Linnea M. Baudhuin, Wayne L. Miller, et al. · The American Journal of Cardiology · 62
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 · David J. Tester, Amber J. Benton, et al. · The American Journal of Cardiology · 58
Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death
2017 · Linnea M. Baudhuin, Charles Leduc, et al. · Circulation Cardiovascular Genetics · 26
LDLR promoter variant and exon 14 mutation on the same chromosome are associated with an unusually severe FH phenotype and treatment resistance
2008 · Christine LH Snozek, Susan A Lagerstedt, et al. · European Journal of Human Genetics · 21
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Point of care CYP2C19 genotyping after percutaneous coronary intervention
2022 · Linnea M. Baudhuin, Laura J. Train, et al. · The Pharmacogenomics Journal · 15
Atrial arrhythmia in adults with sickle cell anemia: a missing link toward understanding and preventing strokes
2024 · Thomas d’Humières, Zineb Sadraoui, et al. · Blood Advances · 13
Genetic Variation in Statin Intolerance and a Possible Protective Role for UGT1A1
2017 · Maria Alice V Willrich, Erin J Kaleta, et al. · Pharmacogenomics · 11
Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis
2014 · Leslie J. Donato, Amy K. Saenger, et al. · Journal of Clinical Apheresis · 4
Confirmation of Insertion, Deletion, and Deletion-Insertion Variants Detected by Next-Generation Sequencing
2023 · Lauren A Choate, Alaa Koleilat, et al. · Clinical Chemistry · 3
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Validation and Performance of Point-of-care Rapid Cyp2c19 Genotyping in the Tailor-pci Multicenter International Randomized Clinical Trial
2021 · Linnea Baudhuin, Laura Train, et al. · Journal of the American College of Cardiology · 1
eP407: Aberrant KCNQ1 splicing as an emerging mechanism underlying the pathogenesis of familial Beckwith-Wiedemann syndrome with reduced penetrance
2022 · Laura Thompson, Emily Thoreson, et al. · Genetics in Medicine
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Comparison of αLEPRA and αLELY Co-Inheritance with a SPTA1 Whole Gene Deletion, a Family Study
2019 · Molly S. Hein, Lea Coon, et al. · Blood
Works count: 13
Citation count: 412
H-index: 8
I10-index: 8
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