Triin Lauri - Search Results

Year	Number of Results
2008	1
2009	1
2010	2
2014	1
2016	1
2017	2
2018	1
2022	1
2023	1
2024	0

1

Point of care CYP2C19 genotyping after percutaneous coronary intervention.

Baudhuin LM, Train LJ, Goodman SG, Lane GE, Lennon RJ, Mathew V, Murthy V, Nazif TM, So DYF, Sweeney JP, Wu AHB, Rihal CS, Farkouh ME, Pereira NL. Baudhuin LM, et al. Among authors: train lj. Pharmacogenomics J. 2022 Dec;22(5-6):303-307. doi: 10.1038/s41397-022-00278-4. Epub 2022 Apr 21. Pharmacogenomics J. 2022. PMID: 35449399 Free PMC article. Review.

2

Confirmation of Insertion, Deletion, and Deletion-Insertion Variants Detected by Next-Generation Sequencing.

Choate LA, Koleilat A, Harris K, Vidal-Folch N, Guenzel A, Newman J, Peterson BJ, Peterson SE, Rice CS, Train LJ, Hasadsri L, Marcou CA, Moyer AM, Baudhuin LM. Choate LA, et al. Among authors: train lj. Clin Chem. 2023 Oct 3;69(10):1155-1162. doi: 10.1093/clinchem/hvad110. Clin Chem. 2023. PMID: 37566393

3

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

V Willrich MA, Kaleta EJ, Bryant SC, Spears GM, Train LJ, Peterson SE, Lennon VA, Kopecky SL, Baudhuin LM. V Willrich MA, et al. Among authors: train lj. Pharmacogenomics. 2018 Jan;19(2):83-94. doi: 10.2217/pgs-2017-0146. Epub 2017 Dec 6. Pharmacogenomics. 2018. PMID: 29210320

4

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.

Ji Y, Skierka JM, Blommel JH, Moore BE, VanCuyk DL, Bruflat JK, Peterson LM, Veldhuizen TL, Fadra N, Peterson SE, Lagerstedt SA, Train LJ, Baudhuin LM, Klee EW, Ferber MJ, Bielinski SJ, Caraballo PJ, Weinshilboum RM, Black JL 3rd. Ji Y, et al. Among authors: train lj. J Mol Diagn. 2016 May;18(3):438-445. doi: 10.1016/j.jmoldx.2016.01.003. Epub 2016 Mar 3. J Mol Diagn. 2016. PMID: 26947514 Free PMC article.

5

Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis.

Donato LJ, Saenger AK, Train LJ, Kotzer KE, Lagerstedt SA, Hornseth JM, Basu A, Winters JL, Baudhuin LM. Donato LJ, et al. Among authors: train lj. J Clin Apher. 2014 Oct;29(5):256-65. doi: 10.1002/jca.21317. Epub 2014 Jan 13. J Clin Apher. 2014. PMID: 24420163

6

Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood Spots.

Baudhuin LM, Leduc C, Train LJ, Avula R, Kluge ML, Kotzer KE, Lin PT, Ackerman MJ, Maleszewski JJ. Baudhuin LM, et al. Among authors: train lj. Circ Cardiovasc Genet. 2017 Dec;10(6):e001844. doi: 10.1161/CIRCGENETICS.117.001844. Circ Cardiovasc Genet. 2017. PMID: 29237689

7

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.

Tester DJ, Benton AJ, Train L, Deal B, Baudhuin LM, Ackerman MJ. Tester DJ, et al. Among authors: train l. Am J Cardiol. 2010 Oct 15;106(8):1124-8. doi: 10.1016/j.amjcard.2010.06.022. Am J Cardiol. 2010. PMID: 20920651 Free PMC article.

8

Relation of ADRB1, CYP2D6, and UGT1A1 polymorphisms with dose of, and response to, carvedilol or metoprolol therapy in patients with chronic heart failure.

Baudhuin LM, Miller WL, Train L, Bryant S, Hartman KA, Phelps M, Larock M, Jaffe AS. Baudhuin LM, et al. Among authors: train l. Am J Cardiol. 2010 Aug 1;106(3):402-8. doi: 10.1016/j.amjcard.2010.03.041. Am J Cardiol. 2010. PMID: 20643254

9

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

Snozek CL, Lagerstedt SA, Khoo TK, Rubenfire M, Isley WL, Train LJ, Baudhuin LM. Snozek CL, et al. Among authors: train lj. Eur J Hum Genet. 2009 Jan;17(1):85-90. doi: 10.1038/ejhg.2008.138. Epub 2008 Jul 23. Eur J Hum Genet. 2009. PMID: 18648394 Free PMC article.

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