Clinical Pharmacogenetics Implementation Consortium Guidelines for HLA-B Genotype and Carbamazepine Dosing von Leckband, S G, Kelsoe, J R, Dunnenberger, H M, George Jr, A L, Tran, E, Berger, R, Müller, D J, Whirl-Carrillo, M, Caudle, K E, Pirmohamed, M

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Rationale and design for an investigation to optimize selective serotonin reuptake inhibitor treatment for pregnant women with depression von Avram, MJ, Stika, CS, Rasmussen-Torvik, LJ, Ciolino, JD, Pinheiro, E, George Jr, AL, Wisner, KL

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Maternal obesity and increased nutrient intake before and during gestation in the ewe results in altered growth, adiposity, and glucose tolerance in adult offspring von Long, N.M, George, L.A, Uthlaut, A.B, Smith, D.T, Nijland, M.J, Nathanielsz, P.W, Ford, S.P

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Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome von Plaster, Nikki M., Tawil, Rabi, Tristani-Firouzi, Martin, Canún, Sonia, Bendahhou, Saı̈d, Tsunoda, Akiko, Donaldson, Matthew R., Iannaccone, Susan T., Brunt, Ewout, Barohn, Richard, Clark, John, Deymeer, Feza, George, Alfred L., Fish, Frank A., Hahn, Angelika, Nitu, Alexandru, Ozdemir, Coskun, Serdaroglu, Piraye, Subramony, S.H., Wolfe, Gil, Fu, Ying-Hui, Ptáček, Louis J.

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Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation von ABOU-KHALIL, B, GE, Q, DESAI, R, RYTHER, R, BAZYK, A, BAILEY, R, HAINES, J. L, SUTCLIFFE, J. S, GEORGE, A. L

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Molecular mechanism for an inherited cardiac arrhythmia von Bennett, Paul B., Yazawa, Kazuto, Makita, Naomasa, George, Alfred L.

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Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines von Chhibber, A, French, C E, Yee, S W, Gamazon, E R, Theusch, E, Qin, X, Webb, A, Papp, A C, Wang, A, Simmons, C Q, Konkashbaev, A, Chaudhry, A S, Mitchel, K, Stryke, D, Ferrin, T E, Weiss, S T, Kroetz, D L, Sadee, W, Nickerson, D A, Krauss, R M, George, A L, Schuetz, E G, Medina, M W, Cox, N J, Scherer, S E, Giacomini, K M, Brenner, S E

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Enhanced Na+ Channel Intermediate Inactivation in Brugada Syndrome von Wang, Dao W, Makita, Naomasa, Kitabatake, Akira, Balser, Jeffrey R, George, Alfred L

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Molecular Basis of Charge Movement in Voltage-Gated Sodium Channels von Yang, Naibo, George, Alfred L, Horn, Richard

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Statins and fenofibrate affect skeletal muscle chloride conductance in rats by differently impairing ClC‐1 channel regulation and expression von Pierno, S, Camerino, GM, Cippone, V, Rolland, J‐F, Desaphy, J‐F, De Luca, A, Liantonio, A, Bianco, G, Kunic, JD, George Jr, AL, Conte Camerino, D

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Cloning and Characterization of KCC3 and KCC4, New Members of the Cation-Chloride Cotransporter Gene Family von Mount, D B, Mercado, A, Song, L, Xu, J, George, Jr, A L, Delpire, E, Gamba, G

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Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes von Ramirez, A H, Shaffer, C M, Delaney, J T, Sexton, D P, Levy, S E, Rieder, M J, Nickerson, D A, George, A L, Roden, D M

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Molecular Cloning of a Human, Hemicholinium-3-Sensitive Choline Transporter von Apparsundaram, Subbu, Ferguson, Shawn M., George, Alfred L., Blakely, Randy D.

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Primary Structure and Functional Expression of the Human Cardiac Tetrodotoxin-Insensitive Voltage-Dependent Sodium Channel von Gellens, Mary E., George, Alfred L., Chen, Liqiong, Chahine, Mohamed, Horn, Richard, Barchi, Robert L., Kallen, Roland G.

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Drug Transporter and Metabolizing Enzyme Gene Variants and Nonnucleoside Reverse-Transcriptase Inhibitor Hepatotoxicity von Ritchie, Marylyn D., Haas, David W., Motsinger, Alison A., Donahue, John P., Erdem, Huso, Raffanti, Stephen, Rebeiro, Peter, George, Alfred L., Kim, Richard B., Haines, Jonathan L., Sterling, Timothy R.

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GDF15 linked to maternal risk of nausea and vomiting during pregnancy von Fejzo, M., Rocha, N., Cimino, I., Lockhart, S. M., Petry, C. J., Kay, R. G., Burling, K., Barker, P., George, A. L., Yasara, N., Premawardhena, A., Gong, S., Cook, E., Rimmington, D., Rainbow, K., Withers, D. J., Cortessis, V., Mullin, P. M., MacGibbon, K. W., Jin, E., Kam, A., Campbell, A., Polasek, O., Tzoneva, G., Gribble, F. M., Yeo, G. S. H., Lam, B. Y. H., Saudek, V., Hughes, I. A., Ong, K. K., Perry, J. R. B., Sutton Cole, A., Baumgarten, M., Welsh, P., Sattar, N., Smith, G. C. S., Charnock-Jones, D. S., Coll, A. P., Meek, C. L., Mettananda, S., Hayward, C., Mancuso, N., O’Rahilly, S.

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Molecular determinants of state‐dependent block of voltage‐gated sodium channels by pilsicainide von Desaphy, J‐F, Dipalma, A, Costanza, T, Bruno, C, Lentini, G, Franchini, C, George, AL, Conte Camerino, D

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Pore-forming segments in voltage-gated chloride channels von Fahlke, Christoph, Yu, Henry T., Beck, Carol L., Rhodes, Thomas H., George, Alfred L.

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A Common Polymorphism Associated with Antibiotic-Induced Cardiac Arrhythmia von Sesti, Federico, Abbott, Geoffrey W., Wei, Jian, Murray, Katherine T., Saksena, Sanjeev, Schwartz, Peter J., Priori, Silvia G., Roden, Dan M., George, Alfred L., Steve A. N. Goldstein

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Sodium Channel Mutations in Paramyotonia Congenita Exhibit Similar Biophysical Phenotypes In vitro von Yang, Naibo, Ji, Sen, Zhou, Ming, Ptacek, Louis J., Barchi, Robert L., Horn, Richard, George, Alfred L.

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