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Author Details

Catherine Hajek
SD Sanford School of Medicine, University of South Dakota
2016
19
6
PMIDPaper TitleJournal TitlePublished Year
37232094<i>SLCO1B1</i> gene-based clinical decision support reduces statin-associated muscle symptoms risk with simvastatin.Pharmacogenomics2023
37546893Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.medRxiv2023
37458095Attitudes about pharmacogenomic testing vary by healthcare specialty.Pharmacogenomics2023
34906462Improved provider preparedness through an 8-part genetics and genomic education program.Genet Med2022
35685436Pharmacogenetic Review: Germline Genetic Variants Possessing Increased Cancer Risk With Clinically Actionable Therapeutic Relationships.Front Genet2022
36422106Workforce Considerations When Building a Precision Medicine Program.J Pers Med2022
36893027Cytochrome P450 2D6 Genotyping for Post-Operative Opioids.S D Med2022
35952728Association of polygenic risk scores with incident atherosclerotic cardiovascular disease events among individuals with coronary artery calcium score of zero: The multi-ethnic study of atherosclerosis.Prog Cardiovasc Dis2022
35287663Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets.BMC Med Genomics2022
35034348SLCO1B1*5 Allele Is Associated With Atorvastatin Discontinuation and Adverse Muscle Symptoms in the Context of Routine Care.Clin Pharmacol Ther2022
34113000Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance.Genet Med2021
33776625Expanding the Phenotype of <i>TUBB2A</i>-Related Tubulinopathy: Three Cases of a Novel, Heterozygous <i>TUBB2A</i> Pathogenic Variant p.Gly98Arg.Mol Syndromol2021
34154743CYP2C19 genotype-directed P<sub>2</sub>Y<sub>12</sub> inhibitor antiplatelet therapy normalizes risk for major adverse cardiovascular events after percutaneous coronary intervention.Indian Heart J2021
30476213Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.Nucleic Acids Res2019
31453774Implementation of wide-scale pharmacogenetic testing in primary care.Pharmacogenomics2019
30354305Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women.Circ Genom Precis Med2018
29928177Interstitial Chromosome 3p13p14 Deletions: An Update and Review.Mol Syndromol2018
28817866Genomic Medicine in Primary Care.S D Med2017
27194973Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.Mol Syndromol2016
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Collaborators

Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 5
Harvard Medical School, Harvard Pilgrim Health Care Institute
Co-authored papers 5
Co-authored papers 3
University of South Dakota Sanford School of Medicine
Co-authored papers 3
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The Genome Institute, Washington University in St. Louis
Co-authored papers 2
University of British Columbia
Co-authored papers 2
Boston University School of Public Health
Co-authored papers 2
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National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers 1
Co-authored papers 1
Instituto Politecnico Nacional
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
Co-authored papers 1
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 1
Curtin University
Co-authored papers 1
Institut de Genetique Medicale d'Alsace, Hopitaux Universitaires de Strasbourg
Co-authored papers 1
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 1
Columbia University
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Baylor College of Medicine
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William Harvey Research Institute, Queen Mary University of London
Co-authored papers 1
Vrije Universiteit Brussel
Co-authored papers 1
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