Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort von Chalazan, Brandon, Mol, Denise, Sridhar, Arvind, Alzahrani, Zain, Darbar, Sara D, Ornelas-Loredo, Aylin, Farooqui, Abdullah, Argos, Maria, Daviglus, Martha L, Konda, Sreenivas, Rehman, Jalees, Darbar, Dawood

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A new paradigm for predicting risk of Torsades de Pointes during drug development: Commentary on: "Improved prediction of drug-induced Torsades de Pointes through simulations of dy... von McCauley, MD, Darbar, D

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Association Between Family History and Early-Onset Atrial Fibrillation Across Racial and Ethnic Groups von Alzahrani, Zain, Ornelas-Loredo, Aylin, Darbar, Sara D, Farooqui, Abdullah, Mol, Denise, Chalazan, Brandon, Villagrana, N Elizabeth, McCauley, Mark, Lazar, Sorin, Wissner, Erik, Bhan, Adarsh, Konda, Sreenivas, Darbar, Dawood

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12 Validation of a Clinical Decision Aid for 30-Day Adverse Events in Emergency Department Patients With Atrial Fibrillation von Barrett, T.W, Self, W.H, Jenkins, C.A, Darbar, D

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Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation von Delaney, Jessica T, Muhammad, Raafia, Shi, Yaping, Schildcrout, Jonathan S, Blair, Marcia, Short, Laura, Roden, Dan M, Darbar, Dawood

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ST ELEVATION AS AN ECG ENDOPHENOTYPE FOR ATRIAL FIBRILLATION PATIENTS HARBORING RARE SODIUM CHANNEL SUBUNIT GENE VARIANTS von Ochieng', F.O, Kolek, M.J, Abraham, R.L, Kucera, G.A, Stubblefield, T, Blair, M.A, Shoemaker, B.M, Short, L.L, Roden, D.M, Darbar, D

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MICE THAT OVEREXPRESS A FRAMESHIFT MUTATION IN HUMAN NATRIURETIC PEPTIDE PRECURSOR A GENE EXHIBIT INCREASED ATRIAL FIBRILLATION BURDEN BUT NO ATRIAL STRUCTURAL REMODELING von Savio Galimberti, E, Kannankeril, P, Kor, K, Kupershmidt, S, Ansani, S, Blair, M, Darbar, D

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SCN10A Rare Variants Associated with Atrial Fibrillation and Slow Ventricular Rates Reveal Increased Late Sodium Current von Savio Galimberti, E, Vanoye, C.G, Yang, T, Atack, T.C, Muhammad, R, Roden, D.M, Darbar, D

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On the relationship among QT interval, atrial fibrillation, and torsade de pointes von Roden, Dan M, Kannankeril, Prince, Darbar, Dawood

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A Common β-Adrenergic Receptor Polymorphism Modulates Response to Rate Control in Atrial Fibrillation von Parvez, B, Chopra, N, Rowan, S, Vaglio, J, Muhammad, R, Roden, D, Darbar, D

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Sequencing candidate genes in African American and Hispanic/ Latino probands with early-onset Atrial Fibrillation von Chalazan, B, Mol, D, Sridhar, A, Ornelas-Loredo, A, Darbar, F, Qiao, V, Alzahrani, Z, Chen, Y, Ellinor, P, Darbar, D

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P4622Comorbid malignancy as an independent predictor of in-hospital mortality in patients with atrial fibrillation von Voudris, K., Darbar, D., Chalazan, B., Vidovich, M.

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Myosin light chain dephosphorylation by ppp1r12c promotes atrial hypocontractility in atrial fibrillation von Gonzalez-Gonzalez, F J, Perike, S, Abu-Taha, I, Damen, F W, Lizama, K, Aboonabi, A, Aguilar-Sanchez, Y, Ong, S G, Darbar, D, Goergen, C J, Wolska, B, Dobrev, D, Wehrens, X H T, Mccauley, M

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Electrophysiologic Characterization of Calcium Handling in Human Induced Pluripotent Stem Cell-Derived Atrial Cardiomyocytes von Argenziano, Mariana, Lambers, Erin, Hong, Liang, Sridhar, Arvind, Zhang, Meihong, Chalazan, Brandon, Menon, Ambili, Savio-Galimberti, Eleonora, Wu, Joseph C., Rehman, Jalees, Darbar, Dawood

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1: A Clinical Prediction Model to Estimate Risk for 30-Day Adverse Events in Emergency Department Patients With Symptomatic Atrial Fibrillation von Barrett, T.W, Martin, A.R, Storrow, A.B, Jenkins, C.A, Russ, S, Darbar, D

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A KCNJ8 mutation associated with early repolarization and atrial fibrillation von Delaney, Jessica T, Muhammad, Raafia, Blair, Marcia A, Kor, Kaylen, Fish, Frank A, Roden, Dan M, Darbar, Dawood

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Voltage-gated sodium channels: biophysics, pharmacology, and related channelopathies von Savio-Galimberti, Eleonora, Gollob, Michael H, Darbar, Dawood

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Detection of left ventricular dysfunction after acute myocardial infarction: comparison of clinical, echocardiographic, and neurohormonal methods von Choy, A M, Darbar, D, Lang, C C, Pringle, T H, McNeill, G P, Kennedy, N S, Struthers, A D

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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation von Kääb, Stefan, Darbar, Dawood, van Noord, Charlotte, Dupuis, Josée, Pfeufer, Arne, Newton-Cheh, Christopher, Schnabel, Renate, Makino, Seiko, Sinner, Moritz F., Kannankeril, Prince J., Beckmann, Britt M., Choudry, Subbarao, Donahue, Brian S., Heeringa, Jan, Perz, Siegfried, Lunetta, Kathryn L., Larson, Martin G., Levy, Daniel, MacRae, Calum A., Ruskin, Jeremy N., Wacker, Annette, Schömig, Albert, Wichmann, H.-Erich, Steinbeck, Gerhard, Meitinger, Thomas, Uitterlinden, André G., Witteman, Jacqueline C.M., Roden, Dan M., Benjamin, Emelia J., Ellinor, Patrick T.

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Familial atrial fibrillation is a genetically heterogeneous disorder von Darbar, Dawood, Herron, Kathleen J, Ballew, Jeffrey D, Jahangir, Arshad, Gersh, Bernard J, Shen, Win-K, Hammill, Stephen C, Packer, Douglas L, Olson, Timothy M

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