Bezzina CR, Shimizu W, Yang P, Koopmann T, Tanck MWT, Miyamoto Y, Kamakura S, Roden DM, Wilde AAM: Common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction.  Circulation 2006;113:338-344.

Knollmann BC, Chopra N, Hlaing T, Akin B, Yang T, Ettensohn K, Knollmann BEC, Horton KD, Weissman NJ, Holinstat IA, Zhang W, Roden DM, Jones LR, Franzini-Armstrong C, Pfeifer K: Casq2 Deletion Causes Sarcoplasmic Reticulum Volume Increase, Premature Ca2+ Release, And Catecholaminergic Polymorphic Ventricular Tachycardia. J Clin Invest 2006;116:2510–2520

Liu K, Hipkens S, Yang T, Abraham R, Zhang W, Chopra N, Knollmann B, Magnuson MA, Roden DM: Recombinase-Mediated Cassette Exchange to rapidly and efficiently generate mice with human cardiac sodium channels. Genesis 2006;44:556-64.

Roden DM, Altman RB, Benowitz NL, Flockhart DA, Giacomini KM, Johnson JA, Krauss RM, McLeod HL, Ratain MJ, Relling MV, Ring H, Shuldiner AR, Weinshilboum RM, Weiss ST, for the Pharmacogenetics Research Network: Pharmacogenomics: challenges and opportunities. Ann Int Med 2006;149:749-757.

Mohler PJ, Le Scouarnec S, Denjoy I, Lowe JS, Guicheney P, Caron L, Driskell IM, Schott J-J, Norris K, Kim RB, Escande D, Roden DM: Defining the Cellular Phenotype of "Ankyrin-B Syndrome" Variants: Human ANK2 Variants Associated With Clinical Phenotypes Display a Spectrum of Activities in Cardiomyocytes. Circulation 2007;115:432-441.

Chopra SS, Watanabe H, Zhong TP, Roden DM: Molecular cloning and analysis of zebrafish voltage-gated sodium channel beta subunit genes: Implications for the evolution of electrical signaling in vertebrates. BMC Evolutionary Biology, BMC Evolutionary Biology 2007, 7:113.

McCray R, Ritchie MD, Roden DM, Darbar D: Persistent Atrial Fibrillation is Associated with Reduced Risk of Torsades de Pointes in Patients with Drug-Induced Long QT Syndrome. Accepted for publication, J Am Coll Cardiol

Yang P, Bezzina CR, Koopman T, Kupershmidt S, Kim RB, Wilde AA, Roden DM: Identification and functional characterization of DNA variants in the promoter of the human cardiac sodium channel gene SCN5A. Eur J Hum Genetics, accepted for publication

Roden DM, Kannankeril PJ, Darbar D: On the relationship among QT interval, atrial fibrillation, and torsade de pointes. Europace 2007; 9(Supplement 4):iv1-iv3.

Tian C, Vanoye CG, Kang C, Welch RC, Kim HJ, George AL Jr, Sanders CR: Preparation, Functional Characterization, and NMR Studies of Human KCNE1, a Voltage-Gated Potassium Channel Accessory Subunit Associated with Deafness and Long QT Syndrome(,). Biochemistry. 2007 Oct 16;46(41):11459-72. Epub 2007 Sep 25.

Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Schwartz PJ, George AL Jr.: Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation. 2007 Jan 23;115(3):368-76. Epub 2007 Jan 8.