The IGNITE Pharmacogenetics Working Group: An Opportunity for Building Evidence with Pharmacogenetic Implementation in a Real‐World Setting
Cavallari, LH, Beitelshees, AL, Blake, KV, Dressler, LG, Duarte, JD, Elsey, A, Eichmeyer, JN, Empey, PE, Franciosi, JP, Hicks, JK, Holmes, AM, Jeng, LJB, Lee, CR, Lima, JJ, Limdi, NA, Modlin, J, Obeng, AO, Petry, N, Pratt, VM, Skaar, TC, Tuteja, S, Voora, D, Wagner, M, Weitzel, KW, Wilke, RA, Peterson, JF, Johnson, JA
Published in Clinical and translational science (01.05.2017)
Published in Clinical and translational science (01.05.2017)
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Journal Article
PharmVar GeneFocus: CYP3A5
Rodriguez-Antona, Cristina, Savieo, Jessica L, Lauschke, Volker M, Sangkuhl, Katrin, Drögemöller, Britt I, Wang, Danxin, van Schaik, Ron H N, Gilep, Andrei A, Peter, Arul P, Boone, Erin C, Ramey, Bronwyn E, Klein, Teri E, Whirl-Carrillo, Michelle, Pratt, Victoria M, Gaedigk, Andrea
Published in Clinical pharmacology and therapeutics (01.12.2022)
Published in Clinical pharmacology and therapeutics (01.12.2022)
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Journal Article
Implementation of a pharmacogenomics consult service to support the INGENIOUS trial
Eadon, M T, Desta, Z, Levy, K D, Decker, B S, Pierson, R C, Pratt, V M, Callaghan, J T, Rosenman, M B, Carpenter, J S, Holmes, A M, McDonald, C A, Benson, E A, Patil, A S, Vuppalanchi, R, Gufford, B T, Dave, N, Robarge, J D, Hyder, M A, Haas, D M, Kreutz, R P, Dexter, P R, Skaar, T C, Flockhart, D A
Published in Clinical pharmacology and therapeutics (01.07.2016)
Published in Clinical pharmacology and therapeutics (01.07.2016)
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Journal Article
Development of Genomic Reference Materials for Cystic Fibrosis Genetic Testing
Pratt, Victoria M, Caggana, Michele, Bridges, Christina, Buller, Arlene M, DiAntonio, Lisa, Highsmith, W. Edward, Holtegaard, Leonard M, Muralidharan, Kasinathan, Rohlfs, Elizabeth M, Tarleton, Jack, Toji, Lorraine, Barker, Shannon D, Kalman, Lisa V
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
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Journal Article
Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study
Monaghan, K.G., Highsmith, W.E., Amos, J., Pratt, V.M., Roa, B., Friez, M., Pike-Buchanan, L.L., Buyse, I.M., Redman, J.B., Strom, C.M., Young, A.L., Sun, W.
Published in Genetics in medicine (01.09.2004)
Published in Genetics in medicine (01.09.2004)
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Journal Article
Duplication 6q21q23 in two unrelated patients
Pratt, V M, Roberson, J R, Weiss, L, Van Dyke, D L
Published in American journal of medical genetics (02.11.1998)
Published in American journal of medical genetics (02.11.1998)
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Journal Article
Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results
Brown, Nicholas M., Pratt, Victoria M., Buller, Arlene, Pike-Buchanan, Lisa, Redman, Joy B., Sun, Weimin, Chen, Rebecca, Crossley, Beryl, McGinniss, Matthew J., Quan, Franklin, Strom, Charles M.
Published in Genetics in medicine (01.04.2005)
Published in Genetics in medicine (01.04.2005)
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Journal Article
DNA Studies of Limb-Girdle Muscular Dystrophy Type 2A in the Amish Exclude a Modifying Mitochondrial Gene and Show No Evidence for a Modifying Nuclear Gene
Pratt, V.M., Jackson, C.E., Wallace, D.C., Gurley, D.S., Feit, A., Feldman, G.L.
Published in American journal of human genetics (01.07.1997)
Published in American journal of human genetics (01.07.1997)
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Journal Article
Genetically Characterized Positive Control Cell Lines Derived from Residual Clinical Blood Samples
Bernacki, Susan H, Beck, Jeanne C, Stankovic, Ana K, Williams, Laurina O, Amos, Jean, Snow-Bailey, Karen, Farkas, Daniel H, Friez, Michael J, Hantash, Feras M, Matteson, Karla J, Monaghan, Kristin G, Muralidharan, Kasinathan, Pratt, Victoria M, Prior, Thomas W, Richie, Kristy L, Levin, Barbara C, Rohlfs, Elizabeth M, Schaefer, Frederick V, Shrimpton, Antony E, Spector, Elaine B, Stolle, Catherine A, Strom, Charles M, Thibodeau, Stephen N, Cole, Eugene C, Goodman, Barbara K, Stenzel, Timothy T
Published in Clinical chemistry (Baltimore, Md.) (01.11.2005)
Published in Clinical chemistry (Baltimore, Md.) (01.11.2005)
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Journal Article
Additional Copies of the Proteolipid Protein Gene Causing Pelizaeus-Merzbacher Disease Arise by Separate Integration into the X Chromosome
Hodes, M.E., Woodward, Karen, Spinner, Nancy B., Emanuel, Beverly S., Enrico-Simon, Agnes, Kamholz, John, Stambolian, Dwight, Zackai, Elaine H., Pratt, Victoria M., Thomas, I.T., Crandall, Kerry, Dlouhy, Stephen R., Malcolm, Sue
Published in American journal of human genetics (01.07.2000)
Published in American journal of human genetics (01.07.2000)
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Journal Article
Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations
Bernacki, Susan H, Farkas, Daniel H, Shi, Wenmei, Chan, Vivian, Liu, Yenbou, Beck, Jeanne C, Bailey, Karen Snow, Pratt, Victoria M, Monaghan, Kristin G, Matteson, Karla J, Schaefer, Frederick V, Friez, Michael, Shrimpton, Antony E, Stenzel, Timothy T
Published in Archives of pathology & laboratory medicine (1976) (01.12.2003)
Published in Archives of pathology & laboratory medicine (1976) (01.12.2003)
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Journal Article
Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred
PRATT, V. M, KIEFER, J. R, LÄHDETIE, J, SCHLEUTKER, J, HODES, M. E, DLOUHY, S. R
Published in American journal of human genetics (01.06.1993)
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Published in American journal of human genetics (01.06.1993)
Journal Article
AhaII polymorphism in human X-linked proteolipid protein gene (PLP)
Trofatter, J A, Pratt, V M, Dlouhy, S R, Hodes, M E
Published in Nucleic acids research (11.11.1991)
Published in Nucleic acids research (11.11.1991)
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