Katrina E. Kotzer

Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events

Linnea M. Baudhuin, Katrina E. Kotzer, Susan A. Lagerstedt · Genetics in Medicine · 2014 · 106 citations

Aortic Events, Mendelian Disorder, Genetic Disorder +7

Implementation of preemptive DNA sequence–based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study

Liewei Wang, Steven E. Scherer, Suzette J. Bielinski et al. · Genetics in Medicine · 2022 · 65 citations · Full text

Dna Sequencing, Sequencing, Mayo-baylor Right 10K +9

UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia

Jennifer M. Skierka, Katrina E. Kotzer, Susan A. Lagerstedt et al. · The Journal of Pediatrics · 2013 · 47 citations

Genetic Testing, Ugt1a1 Genetic Analysis, Unconjugated Hyperbilirubinemia +10

Looking Back and Moving Forward: An Historical Perspective from Laboratory Genetic Counselors

Lindsay H. Zetzsche, Katrina E. Kotzer, Karen E. Wain · Journal of Genetic Counseling · 2013 · 29 citations

Targeted Genotyping in Clinical Pharmacogenomics

Jaime L. Lopes, Kimberley Harris, Mary Beth Karow et al. · Journal of Molecular Diagnostics · 2022 · 29 citations · Full text

Medicine, Genetics, Pharmacogenomics +4