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Author Details
Full Name
Catherine Hajek
Affiliation
SD Sanford School of Medicine, University of South Dakota
ORCID
Career Start Year
2016
Papers
19
H Index
6
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37232094
<i>SLCO1B1</i> gene-based clinical decision support reduces statin-associated muscle symptoms risk with simvastatin.
Pharmacogenomics
2023
37546893
Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.
medRxiv
2023
37458095
Attitudes about pharmacogenomic testing vary by healthcare specialty.
Pharmacogenomics
2023
34906462
Improved provider preparedness through an 8-part genetics and genomic education program.
Genet Med
2022
35685436
Pharmacogenetic Review: Germline Genetic Variants Possessing Increased Cancer Risk With Clinically Actionable Therapeutic Relationships.
Front Genet
2022
36422106
Workforce Considerations When Building a Precision Medicine Program.
J Pers Med
2022
36893027
Cytochrome P450 2D6 Genotyping for Post-Operative Opioids.
S D Med
2022
35952728
Association 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 Dis
2022
35287663
Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets.
BMC Med Genomics
2022
35034348
SLCO1B1*5 Allele Is Associated With Atorvastatin Discontinuation and Adverse Muscle Symptoms in the Context of Routine Care.
Clin Pharmacol Ther
2022
34113000
Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance.
Genet Med
2021
33776625
Expanding the Phenotype of <i>TUBB2A</i>-Related Tubulinopathy: Three Cases of a Novel, Heterozygous <i>TUBB2A</i> Pathogenic Variant p.Gly98Arg.
Mol Syndromol
2021
34154743
CYP2C19 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 J
2021
30476213
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.
Nucleic Acids Res
2019
31453774
Implementation of wide-scale pharmacogenetic testing in primary care.
Pharmacogenomics
2019
30354305
Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women.
Circ Genom Precis Med
2018
29928177
Interstitial Chromosome 3p13p14 Deletions: An Update and Review.
Mol Syndromol
2018
28817866
Genomic Medicine in Primary Care.
S D Med
2017
27194973
Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.
Mol Syndromol
2016
1 - 19 of 19
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Co-authored papers
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Co-authored papers
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Co-authored papers
3
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Co-authored papers
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The Genome Institute, Washington University in St. Louis
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Cornelius F Boerkoel
University of British Columbia
Co-authored papers
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Boston University School of Public Health
Co-authored papers
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2
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2
Bruce M Psaty
Co-authored papers
2
Amy D Klion
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Co-authored papers
1
Paul S de Vries
Co-authored papers
1
Francisco Castellanos
Instituto Politecnico Nacional
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1
Melissa A Haendel
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1
Josée Dupuis
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Scott M Damrauer
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