Impact of Genetics on the Clinical Management of Channelopathies von Schwartz, Peter J., MD, Ackerman, Michael J., MD, PhD, George, Alfred L., MD, Wilde, Arthur A.M., MD, PhD

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Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update von Phillips, Elizabeth J., Sukasem, Chonlaphat, Whirl‐Carrillo, Michelle, Müller, Daniel J., Dunnenberger, Henry M., Chantratita, Wasun, Goldspiel, Barry, Chen, Yuan‐Tsong, Carleton, Bruce C., George, Alfred L., Mushiroda, Taisei, Klein, Teri, Gammal, Roseann S., Pirmohamed, Munir

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Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice von Mistry, Akshitkumar M, Thompson, Christopher H, Miller, Alison R, Vanoye, Carlos G, George,, Alfred L, Kearney, Jennifer A

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In Memoriam Arthur J. Atkinson, Jr. (1938–2024) von Lertora, Juan J. L., Huang, Shiew‐Mei, George, Alfred L.

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Molecular and genetic basis of sudden cardiac death von George, Jr, Alfred L

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Modifier genes for sudden cardiac death von Schwartz, Peter J, Crotti, Lia, George, Alfred L

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Novel mouse model of alternating hemiplegia of childhood exhibits prominent motor and seizure phenotypes von Hawkins, Nicole A., DeKeyser, Jean-Marc, Kearney, Jennifer A., George, Alfred L.

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Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity von Chai, Sam, Wan, Xiaoping, Ramirez-Navarro, Angelina, Tesar, Paul J, Kaufman, Elizabeth S, Ficker, Eckhard, George, Jr, Alfred L, Deschênes, Isabelle

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RNA-based translation activators for targeted gene upregulation von Cao, Yang, Liu, Huachun, Lu, Shannon S., Jones, Krysten A., Govind, Anitha P., Jeyifous, Okunola, Simmons, Christine Q., Tabatabaei, Negar, Green, William N., Holder, Jimmy. L., Tahmasebi, Soroush, George, Alfred L., Dickinson, Bryan C.

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De novo KCNB1 mutations in epileptic encephalopathy von Torkamani, Ali, Bersell, Kevin, Jorge, Benjamin S., Bjork Jr, Robert L., Friedman, Jennifer R., Bloss, Cinnamon S., Cohen, Julie, Gupta, Siddharth, Naidu, Sakkubai, Vanoye, Carlos G., George Jr, Alfred L., Kearney, Jennifer A.

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Susceptibility to innate immune activation in genetically mediated myocarditis von Selgrade, Daniel F, Fullenkamp, Dominic E, Chychula, Ivana A, Li, Binjie, Dellefave-Castillo, Lisa, Dubash, Adi D, Ohiri, Joyce, Monroe, Tanner O, Blancard, Malorie, Tomar, Garima, Holgren, Cory, Burridge, Paul W, George, Jr, Alfred L, Demonbreun, Alexis R, Puckelwartz, Megan J, George, Sharon A, Efimov, Igor R, Green, Kathleen J, McNally, Elizabeth M

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome von ARNESTAD, Marianne, CROTTI, Lia, SCHWARTZ, Peter J, ROGNUM, Torleiv O, INSOLIA, Roberto, PEDRAZZINI, Matteo, FERRANDI, Chiara, VEGE, Ashild, WANG, Dao W, RHODES, Troy E, GEORGE, Alfred L

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Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes von Rocchetti, Marcella, Sala, Luca, Dreizehnter, Lisa, Crotti, Lia, Sinnecker, Daniel, Mura, Manuela, Pane, Luna Simona, Altomare, Claudia, Torre, Eleonora, Mostacciuolo, Gaspare, Severi, Stefano, Porta, Alberto, De Ferrari, Gaetano M, George, Jr, Alfred L, Schwartz, Peter J, Gnecchi, Massimiliano, Moretti, Alessandra, Zaza, Antonio

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Predicting the functional impact of KCNQ1 variants with artificial neural networks von Phul, Saksham, Kuenze, Georg, Vanoye, Carlos G, Sanders, Charles R, George, Jr, Alfred L, Meiler, Jens

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Autonomic Control of Heart Rate and QT Interval Variability Influences Arrhythmic Risk in Long QT Syndrome Type 1 von Porta, Alberto, MS, PhD, Girardengo, Giulia, MD, Bari, Vlasta, MS, George, Alfred L., MD, Brink, Paul A., MD, PhD, Goosen, Althea, RN, Crotti, Lia, MD, PhD, Schwartz, Peter J., MD

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Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant von Kang, Seok Kyu, Hawkins, Nicole A., Thompson, Christopher H., Baker, Erin M., Echevarria-Cooper, Dennis M., Barse, Levi, Thenstedt, Tyler, Dixon, Conor J., Speakes, Nathan, George, Alfred L., Kearney, Jennifer A.

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Late Sodium Current Promotes Ventricular Arrhythmia in Epilepsy-Related Sudden Death von George, Alfred L.

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Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub von Forrest, Marc P., Dos Santos, Marc, Piguel, Nicolas H., Wang, Yi-Zhi, Hawkins, Nicole A., Bagchi, Vikram A., Dionisio, Leonardo E., Yoon, Sehyoun, Simkin, Dina, Martin-de-Saavedra, Maria Dolores, Gao, Ruoqi, Horan, Katherine E., George, Alfred L., LeDoux, Mark S., Kearney, Jennifer A., Savas, Jeffrey N., Penzes, Peter

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NOS1AP Is a Genetic Modifier of the Long-QT Syndrome von CROTTI, Lia, MONTI, Maria Cristina, INSOLIA, Roberto, PELJTO, Anna, GOOSEN, Althea, BRINK, Paul A, GREENBERG, David A, SCHWARTZ, Peter J, GEORGE, Alfred L

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The Need for Speed; Investigating Channelopathy-Associated Epilepsy Using High Throughput Electrophysiological Approaches von George, Alfred L., Kiskinis, Evangelos

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