Hasil Pencarian - Meagan Cochran

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  1. 1
    P522: Personalized prescriptions: Potential clinical impact of pharmacogenetic screening

    P522: Personalized prescriptions: Potential clinical impact of pharmacogenetic screening oleh Jada Pugh, Madison Thomas, Meagan Cochran, Kelly East

    Diterbitkan 2024-01-01
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  2. 2
    P149: Seeing double: A case series of patients with multiple genetic diagnoses in a small genomics clinic

    P149: Seeing double: A case series of patients with multiple genetic diagnoses in a small genomics clinic oleh Tanner Coleman, Meagan Cochran, Jada Pugh, Melissa Kelly, Anna Hurst

    Diterbitkan 2023-01-01
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  3. 3
    P332: Two independent molecular diagnoses of Loeys-Dietz syndrome in a sibship and their children: A case report

    P332: Two independent molecular diagnoses of Loeys-Dietz syndrome in a sibship and their children: A case report oleh Tanner Coleman, Jada Pugh, Emily Gordon, Stephanie Felker, Anna Hurst, Nadiya Sosonkina, Meagan Cochran, Sara Cooper

    Diterbitkan 2024-01-01
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  4. 4
    A study of elective genome sequencing and pharmacogenetic testing in an unselected population

    A study of elective genome sequencing and pharmacogenetic testing in an unselected population oleh Meagan Cochran, Kelly East, Veronica Greve, Melissa Kelly, Whitley Kelley, Troy Moore, Richard M. Myers, Katherine Odom, Molly C. Schroeder, David Bick

    Diterbitkan 2021-09-01
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  5. 5
    O23: Comparison of polygenic risk score in patients with early-onset vs late-onset dementia and the contribution of rare genetic variation*

    O23: Comparison of polygenic risk score in patients with early-onset vs late-onset dementia and the contribution of rare genetic variation* oleh Carter Wright, Sara Cooper, Nicholas Cochran, Meagan Cochran, Belle Moyers, Erik Roberson, James Lawlor, Richard Myers, Jared Taylor, Veronika Solomon, David Geldmacher, Marissa Natelson Love

    Diterbitkan 2023-01-01
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