Clinically Actionable Genotypes Among 10,000 Patients With Preemptive Pharmacogenomic Testing by Van Driest, SL, Shi, Y, Bowton, EA, Schildcrout, JS, Peterson, JF, Pulley, J, Denny, JC, Roden, DM

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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy by Van Driest, Sara L., Vasile, Vlad C., Ommen, Steve R., Will, Melissa L., Tajik, A.Jamil, Gersh, Bernard J., Ackerman, Michael J.

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Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy by Van Driest, Sara L, Ellsworth, Erik G, Ommen, Steve R, Tajik, A Jamil, Gersh, Bernard J, Ackerman, Michael J

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Comprehensive Analysis of the Beta-Myosin Heavy Chain Gene in 389 Unrelated Patients With Hypertrophic Cardiomyopathy by Van Driest, Sara L., Jaeger, Michele A., Ommen, Steve R., Will, Melissa L., Gersh, Bernard J., Tajik, A. Jamil, Ackerman, Michael J.

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Serious Adverse Events Associated with Off-Label Use of Azithromycin or Fentanyl in Children in Intensive Care Units: A Retrospective Chart Review by Oshikoya, Kazeem A., Wharton, Gerold T., Avant, Debbie, Van Driest, Sara L., Fenn, Norman E., Lardieri, Allison, Doe, Edwin, Sood, Beena G., Taketomo, Carol, Lieu, Phuong, Yen, Lilly, McMahon, Ann W.

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Prevalence and severity of benign mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy by VAN DRIEST, Sara L, ACKERMAN, Michael J, OMMEN, Steve R, SHAKUR, Rameen, WILL, Melissa L, NISHIMURA, Rick A, TAJIK, A. Jamil, GERSH, Bernard J

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Gene-specific modifying effects of pro-LVH polymorphisms involving the renin–angiotensin–aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy by Perkins, Meghan J., Van Driest, Sara L., Ellsworth, Erik G., Will, Melissa L., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.

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From malignant mutations to malignant domains: the continuing search for prognostic significance in the mutant genes causing hypertrophic cardiomyopathy by Van Driest, S L, Maron, B J, Ackerman, M J

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Are Longitudinal, Natural History Studies the Next Step in Genotype-Phenotype Translational Genomics in Hypertrophic Cardiomyopathy? by Ackerman, Michael J., Van Driest, Sara L., Bos, Martijn

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Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy by Van Driest, Sara L., Gakh, Oleksandr, Ommen, Steve R., Isaya, Grazia, Ackerman, Michael J.

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A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood by Van Driest, Sara L, Will, Melissa L, Atkins, Dianne L, Ackerman, Michael J

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Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective by Ackerman, Michael J, VanDriest, Sara L, Ommen, Steve R, Will, Melissa L, Nishimura, Rick A, Tajik, A Jamil, Gersh, Bernard J

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