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Author Details

Stuart A Scott
Stanford University
2000
130
48
PMIDPaper TitleJournal TitlePublished Year
36372942Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.Clin Pharmacol Ther2023
36657977An efficient genotyper and star-allele caller for pharmacogenomics.Genome Res2023
35177334Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG).Genet Med2022
35931342Characterization of Reference Materials for TPMT and NUDT15: A GeT-RM Collaborative Project.J Mol Diagn2022
36057977Long-read HiFi sequencing of NUDT15: Phased full-gene haplotyping and pharmacogenomic allele discovery.Hum Mutat2022
36116036Human Mutation special issue on innovations in genomic diagnostics.Hum Mutat2022
35916546Attitudes on pharmacogenomic results as secondary findings among medical geneticists.Pharmacogenet Genomics2022
35244702Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.JAMA Netw Open2022
35034351Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update.Clin Pharmacol Ther2022
32931151Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection.Clin Transl Sci2021
33882174Pharmacogenomic education among genetic counseling training programs in North America.J Genet Couns2021
33801919Pharmacogenomic Determinants of Interindividual Drug Response Variability: From Discovery to Implementation.Genes (Basel)2021
34384553Novel Pharmacogenomic Locus Implicated in Angiotensin-Converting Enzyme Inhibitor-Induced Angioedema.J Am Coll Cardiol2021
34776967Machine Learning for Prediction of Stable Warfarin Dose in US Latinos and Latin Americans.Front Pharmacol2021
34185914Understanding the Role of Pharmacometrics-Based Clinical Decision Support Systems in Pediatric Patient Management: A Case Study Using Lyv Software.J Clin Pharmacol2021
34071920Multi-Institutional Implementation of Clinical Decision Support for <i>APOL1, NAT2,</i> and <i>YEATS4</i> Genotyping in Antihypertensive Management.J Pers Med2021
34118403Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy.J Mol Diagn2021
34117072Deletion of <i>ERF</i> and <i>CIC</i> causes abnormal skull morphology and global developmental delay.Cold Spring Harb Mol Case Stud2021
34109627PharmVar GeneFocus: CYP2C9.Clin Pharmacol Ther2021
32860733Multi-site Investigation of Genetic Determinants of Warfarin Dose Variability in Latinos.Clin Transl Sci2021
32770672Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2C19 and Proton Pump Inhibitor Dosing.Clin Pharmacol Ther2021
32602114PharmVar GeneFocus: CYP2C19.Clin Pharmacol Ther2021
32134193Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.Am J Med Genet A2020
31647186Standardizing CYP2D6 Genotype to Phenotype Translation: Consensus Recommendations from the Clinical Pharmacogenetics Implementation Consortium and Dutch Pharmacogenetics Working Group.Clin Transl Sci2020
31869433Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.Clin Pharmacol Ther2020
31751680VarCover: Allele Min-Set Cover Software.J Mol Diagn2020
31664715A Call for Clear and Consistent Communications Regarding the Role of Pharmacogenetics in Antidepressant Pharmacotherapy.Clin Pharmacol Ther2020
31983733Knowledge and attitudes on pharmacogenetics among pediatricians.J Hum Genet2020
33198140Phased Haplotype Resolution of the <i>SLC6A4</i> Promoter Using Long-Read Single Molecule Real-Time (SMRT) Sequencing.Genes (Basel)2020
33114567Digital Health Applications for Pharmacogenetic Clinical Trials.Genes (Basel)2020
32764090Implementing a pharmacogenetic-driven algorithm to guide dual antiplatelet therapy (DAPT) in Caribbean Hispanics: protocol for a non-randomised clinical trial.BMJ Open2020
32592592Clinical Pharmacogenetic Testing and the Posttest Counseling Conundrum.Clin Pharmacol Ther2020
32308829Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.AMIA Annu Symp Proc2020
32380173Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists.J Mol Diagn2020
30406943Essential Characteristics of Pharmacogenomics Study Publications.Clin Pharmacol Ther2019
31401124Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles: A GeT-RM Collaborative Project.J Mol Diagn2019
31218851Prenatal cytogenomic identification and molecular refinement of compound heterozygous STRC deletion breakpoints.Mol Genet Genomic Med2019
30885185Familial inheritance of the 3q29 microdeletion syndrome: case report and review.BMC Med Genomics2019
30730286Integrated CYP2D6 interrogation for multiethnic copy number and tandem allele detection.Pharmacogenomics2019
31162629Interpreting and Implementing Clinical Pharmacogenetic Tests: Perspectives From Service Providers.Clin Pharmacol Ther2019
31075510Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists.J Mol Diagn2019
30515762Pharmacogene Variation Consortium Gene Introduction: NUDT15.Clin Pharmacol Ther2019
30506689Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals.Clin Pharmacol Ther2019
29280137Multisite Investigation of Strategies for the Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy.Clin Pharmacol Ther2018
29892015Multi-ethnic genome-wide association study for atrial fibrillation.Nat Genet2018
29922082Pharmacogenetic association study on clopidogrel response in Puerto Rican Hispanics with cardiovascular disease: a novel characterization of a Caribbean population.Pharmgenomics Pers Med2018
29474986Recommendations for Clinical CYP2C19 Genotyping Allele Selection: A Report of the Association for Molecular Pathology.J Mol Diagn2018
29408797Effect of cilostazol on platelet reactivity among patients with peripheral artery disease on clopidogrel therapy.Drug Metab Pers Ther2018
29790428Multi-ethnic SULT1A1 copy number profiling with multiplex ligation-dependent probe amplification.Pharmacogenomics2018
29367880Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a <i>Bardet-Biedl Syndrome 9</i> (<i>BBS9</i>) deletion.NPJ Genom Med2018
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Collaborators

Teri E Klein
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Victoria M Pratt
Indiana University School of Medicine
Co-authored papers 14
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
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Aniwaa Owusu Obeng
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Co-authored papers 14
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Vanderbilt University School of Medicine
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Josh F Peterson
Vanderbilt University Medical Center
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Teri A Manolio
National Human Genome Research Institute
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Marc S Williams
University of Washington Medical Center
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Laura J Rasmussen-Torvik
Northwestern University, Center for Genetic Medicine
Co-authored papers 5
Noura S Abul-Husn
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 5
Paola Nicoletti
Icahn School of Medicine at Mount Sinai
Co-authored papers 5
Mary V Relling
Departments of Pharmaceutical Sciences.
Co-authored papers 5
Michiaki Kubo
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Alan R Shuldiner
University of Maryland School of Medicine
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Kimberly F Doheny
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Release 1.2