Van Driest SL - Search Results

1

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy.

Van Driest SL, Ellsworth EG, Ommen SR, Tajik AJ, Gersh BJ, Ackerman MJ. Van Driest SL, et al. Circulation. 2003 Jul 29;108(4):445-51. doi: 10.1161/01.CIR.0000080896.52003.DF. Epub 2003 Jul 14. Circulation. 2003. PMID: 12860912

2

Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection.

Schuler BA, Bastarache L, Wang J, He J, Van Driest SL, Denny JC. Schuler BA, et al. Among authors: van driest sl. PLoS One. 2023 Aug 31;18(8):e0286469. doi: 10.1371/journal.pone.0286469. eCollection 2023. PLoS One. 2023. PMID: 37651384 Free PMC article.

3

Developing and evaluating pediatric phecodes (Peds-Phecodes) for high-throughput phenotyping using electronic health records.

Grabowska ME, Van Driest SL, Robinson JR, Patrick AE, Guardo C, Gangireddy S, Ong HH, Feng Q, Carroll R, Kannankeril PJ, Wei WQ. Grabowska ME, et al. Among authors: van driest sl. J Am Med Inform Assoc. 2024 Jan 18;31(2):386-395. doi: 10.1093/jamia/ocad233. J Am Med Inform Assoc. 2024. PMID: 38041473 Free PMC article.

4

Pediatric considerations for pharmacogenetic selective serotonin reuptake inhibitors clinical decision support.

Liu M, Rossow KM, Maxwell-Horn AC, Saucier LA, Van Driest SL. Liu M, et al. Among authors: van driest sl. Pharmacotherapy. 2023 Jul;43(7):691-704. doi: 10.1002/phar.2751. Epub 2022 Dec 28. Pharmacotherapy. 2023. PMID: 36524442 Review.

5

Tutorial: Using Community Engagement Studios to Enhance Pharmacogenetic Study Design for Maximizing Enrollment of Diverse Children and Pregnant People.

Jasper EA, Holley SE, Jones SH, Liu M, Israel T, Van Driest SL, Velez Edwards DR. Jasper EA, et al. Among authors: van driest sl. Clin Pharmacol Ther. 2023 Mar;113(3):607-614. doi: 10.1002/cpt.2792. Epub 2022 Nov 24. Clin Pharmacol Ther. 2023. PMID: 36366911 Free PMC article.

6

Pediatric CYP2D6 metabolizer status and post-tonsillectomy nausea and vomiting after ondansetron.

Black K, Brenn BR, Gaedigk A, Wanderer JP, Van Driest SL. Black K, et al. Among authors: van driest sl. Clin Transl Sci. 2023 Feb;16(2):269-278. doi: 10.1111/cts.13447. Epub 2022 Nov 25. Clin Transl Sci. 2023. PMID: 36350309 Free PMC article.

7

Variant-based heritability assessment of dexmedetomidine and fentanyl clearance in pediatric patients.

Shannon ML, Muhammad A, James NT, Williams ML, Breeyear J, Edwards T, Mosley JD, Choi L, Kannankeril P, Van Driest S. Shannon ML, et al. Clin Transl Sci. 2023 Sep;16(9):1628-1638. doi: 10.1111/cts.13574. Epub 2023 Jun 26. Clin Transl Sci. 2023. PMID: 37353859 Free PMC article.

8

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective.

Ackerman MJ, VanDriest SL, Ommen SR, Will ML, Nishimura RA, Tajik AJ, Gersh BJ. Ackerman MJ, et al. J Am Coll Cardiol. 2002 Jun 19;39(12):2042-8. doi: 10.1016/s0735-1097(02)01900-9. J Am Coll Cardiol. 2002. PMID: 12084606 Free article.

9

A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood.

Van Driest SL, Will ML, Atkins DL, Ackerman MJ. Van Driest SL, et al. Am J Cardiol. 2002 Nov 15;90(10):1123-7. doi: 10.1016/s0002-9149(02)02780-7. Am J Cardiol. 2002. PMID: 12423715

10

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy.

Van Driest SL, Ackerman MJ, Ommen SR, Shakur R, Will ML, Nishimura RA, Tajik AJ, Gersh BJ. Van Driest SL, et al. Circulation. 2002 Dec 10;106(24):3085-90. doi: 10.1161/01.cir.0000042675.59901.14. Circulation. 2002. PMID: 12473556

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