Report of Confirmation of the rs7853758 and rs885004 Haplotype in SLC28A3

Bằng Stansberry, Wesley M., Swart, Marelize, Medeiros, Elizabeth B., Skaar, Todd C., Pratt, Victoria M.
Xuất bản năm Genet Test Mol Biomarkers (2018)

PharmVar and the Landscape of Pharmacogenetic Resources

Bằng Gaedigk, Andrea, Whirl-Carrillo, Michelle, Pratt, Victoria M., Miller, Neil A, Klein, Teri E
Xuất bản năm Clin Pharmacol Ther (2019)

Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data

Bằng Numanagić, Ibrahim, Malikić, Salem, Pratt, Victoria M., Skaar, Todd C., Flockhart, David A., Sahinalp, S. Cenk
Xuất bản năm Bioinformatics (2015)

FDA's Draft Guidance on Laboratory-Developed Tests Increases Clinical and Economic Risk to Adoption of Pharmacogenetic Testing

Bằng Levy, Kenneth D., Pratt, Victoria M., Skaar, Todd C., Vance, Gail H., Flockhart, David A.
Xuất bản năm J Clin Pharmacol (2015)

Expanding Evidence Leads to New Pharmacogenomics Payer Coverage

Bằng Empey, Philip E., Pratt, Victoria M., Hoffman, James M., Caudle, Kelly E., Klein, Teri E.
Xuất bản năm Genet Med (2021)

Standardization can accelerate the adoption of pharmacogenomics: current status and the path forward

Bằng Caudle, Kelly E, Keeling, Nicholas J, Klein, Teri E, Whirl-Carrillo, Michelle, Pratt, Victoria M, Hoffman, James M
Xuất bản năm Pharmacogenomics (2018)

Development of a Web-Based Query Tool for Quality Assurance of Clinical Molecular Genetic Test Results

Bằng McGinniss, Matthew J., Chen, Rebecca, Pratt, Victoria M., Buller, Arlene, Quan, Franklin, Strom, Charles M., Sun, Weimin, Crossley, Beryl
Được phát hành 2007

Identification of Novel CYP2D7-2D6 Hybrids: Non-Functional and Functional Variants

Bằng Gaedigk, Andrea, Jaime, Lazara Karelia Montane, Bertino, Joseph S., Bérard, Anick, Pratt, Victoria M., Bradfordand, L. DiAnne, Leeder, J. Steven
Được phát hành 2010

Report of New Haplotype for ABCC2 Gene: rs17222723 and rs8187718 in cis

Bằng Pratt, Victoria M., Beyer, Brittany N., Koller, Daniel L., Skaar, Todd C., Flockhart, David A., Levy, Kenneth D., Vance, Gail H.
Xuất bản năm J Mol Diagn (2015)

Influence of Uridine Diphosphate Glucuronosyltransferase Family 1 Member A1 and Solute Carrier Organic Anion Transporter Family 1 Member B1 Polymorphisms and Efavirenz on Bilirubin...

Bằng Collins, Kimberly S., Metzger, Ingrid F., Gufford, Brandon T., Lu, Jessica B., Medeiros, Elizabeth B., Pratt, Victoria M., Skaar, Todd C., Desta, Zeruesenay
Xuất bản năm Drug Metab Dispos (2020)

Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology

Bằng Swart, Marelize, Stansberry, Wesley M., Pratt, Victoria M., Medeiros, Elizabeth B., Kiel, Patrick J., Shen, Fei, Schneider, Bryan P., Skaar, Todd C.
Xuất bản năm J Mol Diagn (2019)

Identification of Cystic Fibrosis Variants by Polymerase Chain Reaction/Oligonucleotide Ligation Assay

Bằng Schwartz, Karen M., Pike-Buchanan, Lisa L., Muralidharan, Kasinathan, Redman, Joy B., Wilson, Jean Amos, Jarvis, Michael, Cura, M. Grace, Pratt, Victoria M.
Được phát hành 2009

Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes

Bằng Numanagić, Ibrahim, Malikić, Salem, Ford, Michael, Qin, Xiang, Toji, Lorraine, Radovich, Milan, Skaar, Todd C., Pratt, Victoria M., Berger, Bonnie, Scherer, Steve, Sahinalp, S. Cenk
Xuất bản năm Nat Commun (2018)

Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric Patients

Bằng Hargreaves, Katherine A., Pratt, Victoria M., Medeiros, Elizabeth B., Lynnes, Ty C., Granfield, Caitlin A., Skaar, Todd C., Iwata‐Otsubo, Aiko, Tillman, Emma M.
Xuất bản năm Clin Transl Sci (2021)

Pharmacogenetic testing in the Veterans Health Administration: Policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee

Bằng Vassy, Jason L., Stone, Annjanette, Callaghan, John T., Mendes, Margaret, Meyer, Laurence J., Pratt, Victoria M., Przygodzki, Ronald M., Scheuner, Maren T., Wang-Rodriguez, Jessica, Schichman, Steven A.
Xuất bản năm Genet Med (2018)

Recommendations for Clinical CYP2C9 Genotyping Allele Selection: A Joint Recommendation of the Association for Molecular Pathology and College of American Pathologists

Bằng Pratt, Victoria M., Cavallari, Larisa H., Del Tredici, Andria L., Hachad, Houda, Ji, Yuan, Moyer, Ann M., Scott, Stuart A., Whirl-Carrillo, Michelle, Weck, Karen E.
Xuất bản năm J Mol Diagn (2019)

Severe Capecitabine Toxicity Associated With a Rare DPYD Variant Identified Through Whole-Genome Sequencing

Bằng Ly, Reynold C., Schmidt, Remington E., Kiel, Patrick J., Pratt, Victoria M., Schneider, Bryan P., Radovich, Milan, Offer, Steven M., Diasio, Robert B., Skaar, Todd C.
Xuất bản năm JCO Precis Oncol (2020)

CpG Methylation Analysis—Current Status of Clinical Assays and Potential Applications in Molecular Diagnostics: A Report of the Association for Molecular Pathology

Bằng Sepulveda, Antonia R., Jones, Dan, Ogino, Shuji, Samowitz, Wade, Gulley, Margaret L., Edwards, Robin, Levenson, Victor, Pratt, Victoria M., Yang, Bin, Nafa, Khedoudja, Yan, Liying, Vitazka, Patrick
Được phát hành 2009

Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy

Bằng Collins, Kimberly S., Pratt, Victoria M., Stansberry, Wesley M., Medeiros, Elizabeth B., Kannegolla, Karthik, Swart, Marelize, Skaar, Todd C., Chapman, Arlene B., Decker, Brian S., Moorthi, Ranjani N., Eadon, Michael T.
Xuất bản năm Pharmacogenet Genomics (2019)

Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles: A GeT-RM Collaborative Project

Bằng Gaedigk, Andrea, Turner, Amy, Everts, Robin E., Scott, Stuart A., Aggarwal, Praful, Broeckel, Ulrich, McMillin, Gwendolyn A., Melis, Roberta, Boone, Erin C., Pratt, Victoria M., Kalman, Lisa V.
Xuất bản năm J Mol Diagn (2019)