Genome Assembly Improvement and Mapping Convergently Evolved Skeletal Traits in Sticklebacks with Genotyping-by-Sequencing

por Glazer, Andrew M., Killingbeck, Emily E., Mitros, Therese, Rokhsar, Daniel S., Miller, Craig T.
Publicado 2015

Exploring the Genetic Basis of Variation in Gene Predictions with a Synthetic Association Study

por Levin, Tera C., Glazer, Andrew M., Pachter, Lior, Brem, Rachel B., Eisen, Michael B.
Publicado 2010

Parallel developmental genetic features underlie stickleback gill raker evolution

por Glazer, Andrew M, Cleves, Phillip A, Erickson, Priscilla A, Lam, Angela Y, Miller, Craig T
Publicado 2014

Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel Na(V)1.5

por Gulsevin, Alican, Glazer, Andrew M., Shields, Tiffany, Kroncke, Brett M., Roden, Dan M., Meiler, Jens
Publicado 2022

A Bayesian method to estimate variant-induced disease penetrance

por Kroncke, Brett M., Smith, Derek K., Zuo, Yi, Glazer, Andrew M., Roden, Dan M., Blume, Jeffrey D.
Publicado 2020

ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants

por O’Neill, Matthew J., Yang, Tao, Laudeman, Julie, Calandranis, Maria, Solus, Joseph, Roden, Dan M., Glazer, Andrew M.
Publicado 2023

Incessant atrial and ventricular tachycardias associated with an SCN5A mutation

por Papagiannis, John, Yang, Tao, Glazer, Andrew M., Tisma-Dupanovic, Svjetlana, Avramidis, Dimosthenis, Kannankeril, Prince J., Viskin, Sami, Walsh, Edward P., Roden, Dan M.
Publicado 2021

Comparison of HLA allelic imputation programs

por Karnes, Jason H., Shaffer, Christian M., Bastarache, Lisa, Gaudieri, Silvana, Glazer, Andrew M., Steiner, Heidi E., Mosley, Jonathan D., Mallal, Simon, Denny, Joshua C., Phillips, Elizabeth J., Roden, Dan M.
Publicado 2017

High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology

por Muhammad, Ayesha, Calandranis, Maria E., Li, Bian, Yang, Tao, Blackwell, Daniel J., Harvey, M. Lorena, Smith, Jeremy E., Chew, Ashli E., Capra, John A., Matreyek, Kenneth A., Fowler, Douglas M., Roden, Dan M., Glazer, Andrew M.
Publicado 2023

Minimum information and guidelines for reporting a Multiplexed Assay of Variant Effect

por Claussnitzer, Melina, Parikh, Victoria N., Wagner, Alex H., Arbesfeld, Jeremy A., Bult, Carol J., Firth, Helen V., Muffley, Lara A., Nguyen Ba, Alex N., Riehle, Kevin, Roth, Frederick P., Tabet, Daniel, Bolognesi, Benedetta, Glazer, Andrew M., Rubin, Alan F.
Publicado 2023

Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes

por Yoneda, Zachary T., Anderson, Katherine C., Quintana, Joseph A., O’Neill, Matthew J., Sims, Richard A., Glazer, Andrew M., Shaffer, Christian M., Crawford, Diane M., Stricker, Thomas, Ye, Fei, Wells, Quinn, Stevenson, Lynne W., Michaud, Gregory F., Darbar, Dawood, Lubitz, Steven A., Ellinor, Patrick T., Roden, Dan M., Shoemaker, M. Benjamin
Publicado 2021

KCNQ1 and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine

por Streeten, Elizabeth A., See, Vincent Y., Jeng, Linda B.J., Maloney, Kristin A., Lynch, Megan, Glazer, Andrew M., Yang, Tao, Roden, Dan, Pollin, Toni I., Daue, Melanie, Ryan, Kathleen A., Van Hout, Cristopher, Gosalia, Nehal, Gonzaga-Jauregui, Claudia, Economides, Aris, Perry, James A., O’Connell, Jeffrey, Beitelshees, Amber, Palmer, Kathleen, Mitchell, Braxton D., Shuldiner, Alan R
Publicado 2020

Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes

por Yoneda, Zachary T., Anderson, Katherine C., Ye, Fei, Quintana, Joseph A., O’Neill, Matthew J., Sims, Richard A., Sun, Lili, Glazer, Andrew M., Davogustto, Giovanni, El-Harasis, Majd, Laws, James L., Saldivar, Brittany N., Crawford, Diane M., Stricker, Thomas, Wells, Quinn, Darbar, Dawood, Michaud, Gregory F., Stevenson, Lynne W., Lubitz, Steven A., Ellinor, Patrick T., Roden, Dan M., Shoemaker, M. Benjamin
Publicado 2022