Search Results - Greyson P Twist

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  1. 1
    The Evolution of PharmVar

    The Evolution of PharmVar by Andrea Gaedigk, Katrin Sangkuhl, Michelle Whirl‐Carrillo, Greyson P Twist, Teri E. Klein, Neil Miller

    Published 2018
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  2. 2
    Developmental Expression of CYP2B6: A Comprehensive Analysis of mRNA Expression, Protein Content and Bupropion Hydroxylase Activity and the Impact of Genetic Variation

    Developmental Expression of CYP2B6: A Comprehensive Analysis of mRNA Expression, Protein Content and Bupropion Hydroxylase Activity and the Impact of Genetic Variation by Robin E. Pearce, Roger Gaedigk, Greyson P Twist, Hongying Dai, Amanda K. Riffel, J. Steven Leeder, Andrea Gaedigk

    Published 2015
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  3. 3
    Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences

    Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences by Greyson P Twist, Andrea Gaedigk, Neil Miller, Emily Farrow, Laurel K. Willig, Darrell L. Dinwiddie, Josh E Petrikin, Sarah Soden, Suzanne Herd, Margaret Gibson, Julie A. Cakici, Amanda K. Riffel, J. Steven Leeder, Deendayal Dinakarpandian, Stephen F. Kingsmore

    Published 2016
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  4. 4
    A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases

    A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases by Neil Miller, Emily Farrow, Margaret Gibson, Laurel K. Willig, Greyson P Twist, Byunggil Yoo, T. C. Marrs, Shane Corder, Lisa Ann Krivohlavek, Adam Walter, Josh E Petrikin, Carol Saunders, Isabelle Thiffault, Sarah Soden, Laurie D. Smith, Darrell L. Dinwiddie, Suzanne Herd, Julie A. Cakici, Severine Catreux, Mike Ruehle, Stephen F. Kingsmore

    Published 2015
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  5. 5
    Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings

    Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings by Laurel K. Willig, Josh E Petrikin, Laurie D. Smith, Carol Saunders, Isabelle Thiffault, Neil Miller, Sarah Soden, Julie A. Cakici, Suzanne Herd, Greyson P Twist, Aaron Noll, Mitchell Creed, Patria Alba, Shannon L. Carpenter, Mark A. Clements, Ryan T. Fischer, J. Allyson Hays, Howard W. Kilbride, Ryan McDonough, Jamie L. Rosterman, Sarah L. Tsai, Lee Zellmer, Emily Farrow, Stephen F. Kingsmore

    Published 2015
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  6. 6
    Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders

    Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders by Sarah Soden, Carol Saunders, Laurel K. Willig, Emily Farrow, Laurie D. Smith, Josh E Petrikin, Jean-Baptiste LePichon, Neil Miller, Isabelle Thiffault, Darrell L. Dinwiddie, Greyson P Twist, Aaron Noll, Bryce A. Heese, Lee Zellmer, Andrea M. Atherton, Ahmed Abdelmoity, Nicole P. Safina, Sarah S. Nyp, Britton Zuccarelli, Ingrid A. Larson, Ann Modrcin, Suzanne Herd, Mitchell Creed, Zhaohui Ye, Xuan Yuan, Robert A. Brodsky, Stephen F. Kingsmore

    Published 2014
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