Dan Roden
Faculty Member
Last active: 2/8/2016

  1. Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction. Bezzina CR, Pazoki R, Bardai A, Marsman RF, de Jong JSSG, Blom MT, Scicluna BP, Jukema JW, Bindraban NR, Lichtner P, Pfeufer A, Bishopric NH, Roden DM, Meitinger T, Chugh SS, Myerburg RJ, Jouven X, Kääb S, Dekker LRC, Tan HL, Tanck MWT, Wilde AAM (2010) Nat Genet 42(8): 688-691
    › Primary publication · 20622880 (PubMed) · PMC3966292 (PubMed Central)
  2. Drug-induced long QT syndrome. Kannankeril P, Roden DM, Darbar D (2010) Pharmacol Rev 62(4): 760-81
    › Primary publication · 21079043 (PubMed) · PMC2993258 (PubMed Central)
  3. Common variants in KCNN3 are associated with lone atrial fibrillation. Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, de Bakker PI, Mueller M, Lubitz SA, Fox E, Darbar D, Smith NL, Smith JD, Schnabel RB, Soliman EZ, Rice KM, Van Wagoner DR, Beckmann BM, van Noord C, Wang K, Ehret GB, Rotter JI, Hazen SL, Steinbeck G, Smith AV, Launer LJ, Harris TB, Makino S, Nelis M, Milan DJ, Perz S, Esko T, Köttgen A, Moebus S, Newton-Cheh C, Li M, Möhlenkamp S, Wang TJ, Kao WH, Vasan RS, Nöthen MM, MacRae CA, Stricker BH, Hofman A, Uitterlinden AG, Levy D, Boerwinkle E, Metspalu A, Topol EJ, Chakravarti A, Gudnason V, Psaty BM, Roden DM, Meitinger T, Wichmann HE, Witteman JC, Barnard J, Arking DE, Benjamin EJ, Heckbert SR, Kääb S (2010) Nat Genet 42(3): 240-4
    › Primary publication · 20173747 (PubMed) · PMC2871387 (PubMed Central)
  4. Brugada syndrome: lots of questions, some answers. Roden DM (2010) Heart Rhythm 7(1): 47-9
    › Primary publication · 20129284 (PubMed)
  5. Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation. Abraham RL, Yang T, Blair M, Roden DM, Darbar D (2010) J Mol Cell Cardiol 48(1): 181-90
    › Primary publication · 19646991 (PubMed) · PMC2813326 (PubMed Central)
  6. Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records. Dumitrescu L, Ritchie MD, Brown-Gentry K, Pulley JM, Basford M, Denny JC, Oksenberg JR, Roden DM, Haines JL, Crawford DC (2010) Genet Med 12(10): 648-50
    › Primary publication · 20733501 (PubMed) · PMC2952033 (PubMed Central)
  7. An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records. Schildcrout JS, Basford MA, Pulley JM, Masys DR, Roden DM, Wang D, Chute CG, Kullo IJ, Carrell D, Peissig P, Kho A, Denny JC (2010) J Biomed Inform 43(6): 914-23
    › Primary publication · 20688191 (PubMed) · PMC2991387 (PubMed Central)
  8. Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery. Body SC, Collard CD, Shernan SK, Fox AA, Liu KY, Ritchie MD, Perry TE, Muehlschlegel JD, Aranki S, Donahue BS, Pretorius M, Estrada JC, Ellinor PT, Newton-Cheh C, Seidman CE, Seidman JG, Herman DS, Lichtner P, Meitinger T, Pfeufer A, Kääb S, Brown NJ, Roden DM, Darbar D (2009) Circ Cardiovasc Genet 2(5): 499-506
    › Primary publication · 20031626 (PubMed) · PMC2801871 (PubMed Central)
  9. The organic cation transporter, OCTN1, expressed in the human heart, potentiates antagonism of the HERG potassium channel. McBride BF, Yang T, Liu K, Urban TJ, Giacomini KM, Kim RB, Roden DM (2009) J Cardiovasc Pharmacol 54(1): 63-71
    › Primary publication · 19528813 (PubMed) · PMC3745652 (PubMed Central)
  10. Relative contribution of CYP2C9 and VKORC1 genotypes and early INR response to the prediction of warfarin sensitivity during initiation of therapy. Li C, Schwarz UI, Ritchie MD, Roden DM, Stein CM, Kurnik D (2009) Blood 113(17): 3925-30
    › Primary publication · 19074728 (PubMed) · PMC2673121 (PubMed Central)