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Sara Van Driest
Sara Van Driest
Vanderbilt University Medical Center
Verified email at vanderbilt.edu
Title
Cited by
Cited by
Year
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
SL Van Driest, VC Vasile, SR Ommen, ML Will, AJ Tajik, BJ Gersh, ...
Journal of the American College of Cardiology 44 (9), 1903-1910, 2004
5062004
Return of genomic results to research participants: the floor, the ceiling, and the choices in between
GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ...
The American Journal of Human Genetics 94 (6), 818-826, 2014
4202014
Clinically actionable genotypes among 10,000 patients with preemptive pharmacogenomic testing
SL Van Driest, Y Shi, EA Bowton, JS Schildcrout, JF Peterson, J Pulley, ...
Clinical Pharmacology & Therapeutics 95 (4), 423-431, 2014
3322014
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6, OPRM1, and COMT Genotypes and Select Opioid Therapy
KR Crews, AA Monte, R Huddart, KE Caudle, ED Kharasch, A Gaedigk, ...
Clinical Pharmacology & Therapeutics 110 (4), 888-896, 2021
2692021
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
SL Van Driest, EG Ellsworth, SR Ommen, AJ Tajik, BJ Gersh, ...
Circulation 108 (4), 445-451, 2003
2692003
Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations
J Binder, SR Ommen, BJ Gersh, SL Van Driest, AJ Tajik, RA Nishimura, ...
Mayo Clinic Proceedings 81 (4), 459-467, 2006
2632006
Prevalence and severity of “benign” mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy
SL Van Driest, MJ Ackerman, SR Ommen, R Shakur, ML Will, ...
Circulation 106 (24), 3085-3090, 2002
2482002
Yield of genetic testing in hypertrophic cardiomyopathy
SL Van Driest, SR Ommen, AJ Tajik, BJ Gersh, MJ Ackerman
Mayo Clinic Proceedings 80 (6), 739-744, 2005
2402005
Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
SL Van Driest, MA Jaeger, SR Ommen, ML Will, BJ Gersh, AJ Tajik, ...
Journal of the American College of Cardiology 44 (3), 602-610, 2004
2302004
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing
JJ Lima, CD Thomas, J Barbarino, Z Desta, SL Van Driest, N El Rouby, ...
Clinical Pharmacology & Therapeutics 109 (6), 1417-1423, 2021
2082021
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns
L Bastarache, JJ Hughey, S Hebbring, J Marlo, W Zhao, WT Ho, ...
Science 359 (6381), 1233-1239, 2018
1922018
Sarcomeric genotyping in hypertrophic cardiomyopathy
SL Van Driest, SR Ommen, AJ Tajik, BJ Gersh, MJ Ackerman
Mayo Clinic Proceedings 80 (4), 463-469, 2005
1922005
Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records
SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ...
Jama 315 (1), 47-57, 2016
1892016
Biobanks and electronic medical records: enabling cost-effective research
E Bowton, JR Field, S Wang, JS Schildcrout, SL Van Driest, JT Delaney, ...
Science translational medicine 6 (234), 234cm3-234cm3, 2014
1342014
Acute kidney injury incidence in noncritically ill hospitalized children, adolescents, and young adults: a retrospective observational study
TL McGregor, DP Jones, L Wang, I Danciu, BC Bridges, GM Fleming, ...
American Journal of Kidney Diseases 67 (3), 384-390, 2016
1292016
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin–angiotensin–aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy
MJ Perkins, SL Van Driest, EG Ellsworth, ML Will, BJ Gersh, SR Ommen, ...
European heart journal 26 (22), 2457-2462, 2005
1282005
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia
SE Karol, W Yang, SL Van Driest, TY Chang, S Kaste, E Bowton, ...
Blood, The Journal of the American Society of Hematology 126 (15), 1770-1776, 2015
1122015
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
922019
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome
P Weeke, JD Mosley, D Hanna, JT Delaney, C Shaffer, QS Wells, ...
Journal of the American College of Cardiology 63 (14), 1430-1437, 2014
912014
Benefit of preemptive pharmacogenetic information on clinical outcome
DM Roden, SL Van Driest, JD Mosley, QS Wells, JR Robinson, JC Denny, ...
Clinical Pharmacology & Therapeutics 103 (5), 787-794, 2018
892018
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