Items where Author is "Glazer, Andrew M."

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Number of items: 4.

O’Neill, Matthew J. and Ng, Chai-Ann and Aizawa, Takanori and Sala, Luca and Bains, Sahej and Winbo, Annika and Ullah, Rizwan and Shen, Qianyi and Tan, Chek-Ying and Kozek, Krystian and Vanags, Loren R. and Mitchell, Devyn W. and Shen, Alex and Wada, Yuko and Kashiwa, Asami and Crotti, Lia and Dagradi, Federica and Musu, Giulia and Spazzolini, Carla and Neves, Raquel and Bos, J. Martijn and Giudicessi, John R. and Bledsoe, Xavier and Gamazon, Eric R. and Lancaster, Megan C. and Glazer, Andrew M. and Knollmann, Bjorn C. and Roden, Dan M. and Weile, Jochen and Roth, Frederick and Salem, Joe-Elie and Earle, Nikki and Stiles, Rachael and Agee, Taylor and Johnson, Christopher N. and Horie, Minoru and Skinner, Jonathan R. and Ackerman, Michael J. and Schwartz, Peter J. and Ohno, Seiko and Vandenberg, Jamie I. and Kroncke, Brett M. (2024) Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk Stratification. Circulation, 150 (23). pp.1869-1881. ISSN 0009-7322

Ma, Joanne G. and O’Neill, Matthew J. and Richardson, Ebony and Thomson, Kate L. and Ingles, Jodie and Muhammad, Ayesha and Solus, Joseph F. and Davogustto, Giovanni and Anderson, Katherine C. and Shoemaker, M. Benjamin and Stergachis, Andrew B. and Floyd, Brendan J. and Dunn, Kyla and Parikh, Victoria N. and Chubb, Henry and Perrin, Mark J. and Roden, Dan M. and Vandenberg, Jamie I. and Ng, Chai-Ann and Glazer, Andrew M. (2024) Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants. Circulation: Genomic and Precision Medicine, 17 (4). ISSN 2574-8300

O’Neill, Matthew J. and Chen, Suet Nee and Rumping, Lynne and Johnson, Renee and van Slegtenhorst, Marjon and Glazer, Andrew M. and Yang, Tao and Solus, Joseph F. and Laudeman, Julie and Mitchell, Devyn W. and Vanags, Loren R. and Kroncke, Brett M. and Anderson, Katherine and Gao, Shanshan and Verdonschot, Job A.J. and Brunner, Han and Hellebrekers, Debby and Taylor, Matthew R.G. and Roden, Dan M. and Wessels, Marja W. and Lekanne Dit Deprez, Ronald H. and Fatkin, Diane and Mestroni, Luisa and Shoemaker, M. Benjamin (2023) Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant. Heart Rhythm, 20 (8). pp.1158-1166. ISSN 15475271

Kozek, Krystian A. and Glazer, Andrew M. and Ng, Chai-Ann and Blackwell, Daniel and Egly, Christian L. and Vanags, Loren R. and Blair, Marcia and Mitchell, Devyn and Matreyek, Kenneth A. and Fowler, Douglas M. and Knollmann, Bjorn C. and Vandenberg, Jamie I. and Roden, Dan M. and Kroncke, Brett M. (2020) High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel KV11.1. Heart Rhythm. ISSN 15475271

This list was generated on Sun Aug 3 16:46:05 2025 UTC.