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Andrew Glazer - Publications

Affiliations: 
Biomedical Informatics Vanderbilt University School of Medicine, Nashville, TN, United States 
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Wada Y, Wang L, Hall LD, Yang T, Short LL, Solus JF, Glazer AM, Roden DM. The electrophysiologic effects of KCNQ1 extend beyond expression of IKs: evidence from genetic and pharmacologic block. Cardiovascular Research. PMID 38442735 DOI: 10.1093/cvr/cvae042  0.427
2024 Glazer AM, Yang T, Li B, Page D, Fouda M, Wada Y, Lancaster MC, O'Neill MJ, Muhammad A, Gao X, Ackerman MJ, Sanatani S, Ruben PC, Roden DM. Multifocal Ectopic Purkinje Premature Contractions due to neutralization of an negative charge: structural insights into the gating pore hypothesis. Biorxiv : the Preprint Server For Biology. PMID 38405820 DOI: 10.1101/2024.02.13.580021  0.382
2024 O'Neill MJ, Ng CA, Aizawa T, Sala L, Bains S, Denjoy I, Winbo A, Ullah R, Shen Q, Tan CY, Kozek K, Vanags LR, Mitchell DW, Shen A, Wada Y, ... ... Glazer AM, et al. Prognostic Value of Multiplexed Assays of Variant Effect and Automated Patch-clamping for -LQTS Risk Stratification. Medrxiv : the Preprint Server For Health Sciences. PMID 38370760 DOI: 10.1101/2024.02.01.24301443  0.496
2023 Ma JG, O'Neill MJ, Richardson E, Thomson KL, Ingles J, Muhammad A, Solus JF, Davogustto G, Anderson KC, Benjamin Shoemaker M, Stergachis AB, Floyd BJ, Dunn K, Parikh VN, Chubb H, ... ... Glazer AM, et al. Multi-site validation of a functional assay to adjudicate Brugada Syndrome-associated variants. Medrxiv : the Preprint Server For Health Sciences. PMID 38196587 DOI: 10.1101/2023.12.19.23299592  0.509
2023 O'Neill MJ, Yang T, Laudeman J, Calandranis M, Solus J, Roden DM, Glazer AM. ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants. Medrxiv : the Preprint Server For Health Sciences. PMID 37732247 DOI: 10.1101/2023.09.04.23295019  0.437
2023 O'Neill MJ, Chen SN, Rumping L, Johnson R, van Slegtenhorst M, Glazer AM, Yang T, Solus JF, Laudeman J, Mitchell DW, Vanags LR, Kroncke BM, Anderson K, Gao S, Verdonschot JAJ, et al. Multicenter Clinical and Functional Evidence Reclassifies a Recurrent Non-canonical Filamin C Splice-altering Variant. Heart Rhythm. PMID 37164047 DOI: 10.1016/j.hrthm.2023.05.006  0.455
2023 Muhammad A, Calandranis ME, Li B, Yang T, Blackwell DJ, Harvey ML, Smith JE, Chew AE, Capra JA, Matreyek KA, Fowler DM, Roden DM, Glazer AM. High-throughput functional mapping of variants in an arrhythmia gene, , reveals novel biology. Biorxiv : the Preprint Server For Biology. PMID 37162834 DOI: 10.1101/2023.04.28.538612  0.506
2023 Floyd BJ, Weile J, Kannankeril PJ, Glazer AM, Reuter CM, MacRae CA, Ashley EA, Roden DM, Roth FP, Parikh VN. Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and Precision Medicine. PMID 36716194 DOI: 10.1161/CIRCGEN.122.003792  0.392
2022 Bersell KR, Yang T, Mosley JD, Glazer AM, Hale AT, Kryshtal DO, Kim K, Steimle JD, Brown JD, Salem JE, Campbell CC, Hong CC, Wells QS, Johnson AN, Short L, et al. Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Circulation. PMID 36524479 DOI: 10.1161/CIRCULATIONAHA.122.062193  0.447
2022 Glazer AM. Genetics of congenital arrhythmia syndromes: the challenge of variant interpretation. Current Opinion in Genetics & Development. 77: 102004. PMID 36368182 DOI: 10.1016/j.gde.2022.102004  0.406
2022 O'Neill MJ, Wada Y, Hall LD, Mitchell DW, Glazer A, Roden DM. Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian Channelopathies. Circulation. Genomic and Precision Medicine. 101161CIRCGEN1220037. PMID 36197721 DOI: 10.1161/CIRCGEN.122.003782  0.494
2022 Yoneda ZT, Anderson KC, Ye F, Quintana JA, O'Neill MJ, Sims RA, Sun L, Glazer AM, Davogustto G, El-Harasis M, Laws JL, Saldivar BN, Crawford DM, Stricker T, Wells Q, et al. Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes. Jama Cardiology. PMID 35544069 DOI: 10.1001/jamacardio.2022.0810  0.447
2022 O'Neill MJ, Muhammad A, Li B, Wada Y, Hall L, Solus JF, Short L, Roden DM, Glazer AM. Dominant negative effects of SCN5A missense variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35305865 DOI: 10.1016/j.gim.2022.02.010  0.489
2022 Gulsevin A, Glazer AM, Shields T, Kroncke BM, Roden DM, Meiler J. Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel Na1.5. International Journal of Molecular Sciences. 23. PMID 35216338 DOI: 10.3390/ijms23042225  0.322
2022 Wada Y, Yang T, Shaffer CM, Daniel LL, Glazer AM, Davogustto GE, Lowery BD, Farber-Eger E, Wells QS, Roden DM. Common Ancestry-specific Ion Channel Variants Predispose to Drug-induced Arrhythmias. Circulation. PMID 34994586 DOI: 10.1161/CIRCULATIONAHA.121.054883  0.449
2021 Papagiannis J, Yang T, Glazer AM, Tisma-Dupanovic S, Avramidis D, Kannankeril PJ, Viskin S, Walsh EP, Roden DM. Incessant atrial and ventricular tachycardias associated with an mutation. Heartrhythm Case Reports. 7: 806-811. PMID 34987964 DOI: 10.1016/j.hrcr.2021.08.013  0.394
2021 Glazer AM, Davogustto GE, Shaffer CM, Vanoye CG, Desai RR, Farber-Eger E, Dikilitas O, Shang N, Pacheco JA, Yang T, Muhammad A, Mosley JD, Van Driest SL, Wells QS, Shaffer LL, et al. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. Circulation. PMID 34930020 DOI: 10.1161/CIRCULATIONAHA.121.055562  0.714
2021 Yoneda ZT, Anderson KC, Quintana JA, O'Neill MJ, Sims RA, Glazer AM, Shaffer CM, Crawford DM, Stricker T, Ye F, Wells Q, Stevenson LW, Michaud GF, Darbar D, Lubitz SA, et al. Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes. Jama Cardiology. PMID 34495297 DOI: 10.1001/jamacardio.2021.3370  0.431
2021 Kozek K, Wada Y, Sala L, Denjoy I, Egly C, O'Neill MJ, Aiba T, Shimizu W, Makita N, Ishikawa T, Crotti L, Spazzolini C, Kotta MC, Dagradi F, Castelletti S, ... ... Glazer AM, et al. Estimating the Post-Test Probability of Long QT Syndrome Diagnosis for Rare Variants. Circulation. Genomic and Precision Medicine. PMID 34309407 DOI: 10.1161/CIRCGEN.120.003289  0.571
2020 Streeten EA, See VY, Jeng LBJ, Maloney KA, Lynch M, Glazer AM, Yang T, Roden DM, Pollin TI, Daue M, Ryan KA, Van Hout C, Gosalia N, Gonzaga-Jauregui C, Economides A, et al. and Long QT Syndrome in 1/45 Amish: The Road from Identification to Implementation of Culturally Appropriate Precision Medicine. Circulation. Genomic and Precision Medicine. PMID 33141630 DOI: 10.1161/CIRCGEN.120.003133  0.461
2020 Kroncke BM, Smith DK, Zuo Y, Glazer AM, Roden DM, Blume JD. A Bayesian method to estimate variant-induced disease penetrance. Plos Genetics. 16: e1008862. PMID 32569262 DOI: 10.1371/Journal.Pgen.1008862  0.554
2020 Glazer AM, Wada Y, Li B, Muhammad A, Kalash OR, O'Neill MJ, Shields T, Hall L, Short L, Blair MA, Kroncke BM, Capra JA, Roden DM. High-Throughput Reclassification of SCN5A Variants. American Journal of Human Genetics. PMID 32533946 DOI: 10.1016/J.Ajhg.2020.05.015  0.529
2020 Kozek KA, Glazer AM, Ng CA, Blackwell D, Egly CL, Vanags LR, Blair M, Mitchell D, Matreyek KA, Fowler DM, Knollmann BC, Vandenberg JI, Roden DM, Kroncke BM. High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel K11.1. Heart Rhythm. PMID 32522694 DOI: 10.1016/J.Hrthm.2020.05.041  0.447
2020 Glazer AM, Kroncke BM, Matreyek KA, Yang T, Wada Y, Shields T, Salem JE, Fowler DM, Roden DM. Deep Mutational Scan of an Voltage Sensor. Circulation. Genomic and Precision Medicine. PMID 31928070 DOI: 10.1161/CIRCGEN.119.002786  0.466
2020 Davogustto GE, Glazer A, Shaffer CM, Farber-Eger E, Dikilitas O, Ning S, Pacheco J, Mosley J, Van Driest S, Wells Q, Rinke LL, Kalash O, Wada Y, Bland S, Yoneda ZT, et al. Abstract 14663: High Rate of Arrhythmia Diagnoses Following Return of Pathogenic/likely Pathogenic Variants in an Unselected Population Circulation. 142. DOI: 10.1161/CIRC.142.SUPPL_3.14663  0.475
2019 Salem JE, Yang T, Moslehi JJ, Waintraub X, Gandjbakhch E, Bachelot A, Hidden-Lucet F, Hulot JS, Knollmann BC, Lebrun-Vignes B, Funck-Brentano C, Glazer AM, Roden DM. Androgenic Effects on Ventricular Repolarization: A Translational Study From the International Pharmacovigilance Database to iPSC-Cardiomyocytes. Circulation. PMID 31378084 DOI: 10.1161/CIRCULATIONAHA.119.040162  0.353
2019 Chavali NV, Kryshtal DO, Parikh SS, Wang L, Glazer AM, Blackwell DJ, Kroncke BM, Shoemaker MB, Knollmann BC. The patient-independent human iPSC model - a new tool for rapid determination of genetic variant pathogenicity in long QT syndrome. Heart Rhythm. PMID 31004778 DOI: 10.1016/J.Hrthm.2019.04.031  0.374
2019 Salem JE, Shoemaker MB, Bastarache L, Shaffer CM, Glazer AM, Kroncke B, Wells QS, Shi M, Straub P, Jarvik GP, Larson EB, Velez Edwards DR, Edwards TL, Davis LK, Hakonarson H, et al. Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysis. Jama Cardiology. PMID 30673079 DOI: 10.1001/Jamacardio.2018.4615  0.54
2019 Salem JE, Yang T, Moslehi JJ, Waintraub X, Gandjbakhch E, Bachelot A, Hidden-Lucet F, Hulot JS, Knollmann BC, Lebrun-Vignes B, Funck-Brentano C, Glazer AM, Roden DM. P6590Androgenic effects on ventricular repolarization: a translational study from pharmacovigilance databases to iPSC-cardiomyocytes European Heart Journal. 40. DOI: 10.1093/eurheartj/ehz746.1178  0.379
2018 Kroncke BM, Glazer AM, Smith DK, Blume JD, Roden DM. (Na1.5) Variant Functional Perturbation and Clinical Presentation: Variants of a Certain Significance. Circulation. Genomic and Precision Medicine. 11: e002095. PMID 29728395 DOI: 10.1161/CIRCGEN.118.002095  0.529
2018 Grouthier V, Lebrun-Vignes B, Glazer AM, Touraine P, Funck-Brentano C, Pariente A, Courtillot C, Bachelot A, Roden DM, Moslehi JJ, Salem JE. Increased long QT and torsade de pointes reporting on tamoxifen compared with aromatase inhibitors. Heart (British Cardiac Society). PMID 29720397 DOI: 10.1136/heartjnl-2017-312934  0.307
2018 Roden DM, Glazer AM, Kroncke B. Arrhythmia genetics: Not dark and lite, but fifty shades of grey. Heart Rhythm. PMID 29709575 DOI: 10.1016/J.Hrthm.2018.04.031  0.438
2018 Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, ... ... Glazer A, et al. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science (New York, N.Y.). 359: 1233-1239. PMID 29590070 DOI: 10.1126/Science.Aal4043  0.633
2018 Parikh S, Chavali N, Glazer A, Shaffer C, Blair M, Roden D, Knollmann B. High-Throughput Investigation of Contractile and Electrophysiological Properties of Optically Stimulated hiPSC-CM Monolayers Biophysical Journal. 114. DOI: 10.1016/J.Bpj.2017.11.2122  0.358
2017 Wells QS, Veatch OJ, Fessel JP, Joon AY, Levinson RT, Mosley JD, Held EP, Lindsay CS, Shaffer CM, Weeke PE, Glazer AM, Bersell KR, Van Driest SL, Karnes JH, Blair MA, et al. Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults. Pharmacogenetics and Genomics. PMID 28542097 DOI: 10.1097/Fpc.0000000000000284  0.566
2017 Karnes JH, Bastarache L, Shaffer CM, Gaudieri S, Xu Y, Glazer AM, Mosley JD, Zhao S, Raychaudhuri S, Mallal S, Ye Z, Mayer JG, Brilliant MH, Hebbring SJ, Roden DM, et al. Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants. Science Translational Medicine. 9. PMID 28490672 DOI: 10.1126/Scitranslmed.Aai8708  0.611
2017 Karnes JH, Shaffer CM, Bastarache L, Gaudieri S, Glazer AM, Steiner HE, Mosley JD, Mallal S, Denny JC, Phillips EJ, Roden DM. Comparison of HLA allelic imputation programs. Plos One. 12: e0172444. PMID 28207879 DOI: 10.1371/Journal.Pone.0172444  0.518
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