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

  1. Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic. Yang T, Atack TC, Stroud DM, Zhang W, Hall L, Roden DM (2012) Circ Res 111(3): 322-32
    › Primary publication · 22723299 (PubMed) · PMC3412150 (PubMed Central)
  2. A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. Kääb S, Crawford DC, Sinner MF, Behr ER, Kannankeril PJ, Wilde AA, Bezzina CR, Schulze-Bahr E, Guicheney P, Bishopric NH, Myerburg RJ, Schott JJ, Pfeufer A, Beckmann BM, Martens E, Zhang T, Stallmeyer B, Zumhagen S, Denjoy I, Bardai A, Van Gelder IC, Jamshidi Y, Dalageorgou C, Marshall V, Jeffery S, Shakir S, Camm AJ, Steinbeck G, Perz S, Lichtner P, Meitinger T, Peters A, Wichmann HE, Ingram C, Bradford Y, Carter S, Norris K, Ritchie MD, George AL, Roden DM (2012) Circ Cardiovasc Genet 5(1): 91-9
    › Primary publication · 22100668 (PubMed) · PMC3288202 (PubMed Central)
  3. A KCNJ8 mutation associated with early repolarization and atrial fibrillation. Delaney JT, Muhammad R, Blair MA, Kor K, Fish FA, Roden DM, Darbar D (2012) Europace 14(10): 1428-32
    › Primary publication · 22562657 (PubMed) · PMC3458578 (PubMed Central)
  4. A connexin40 mutation associated with a malignant variant of progressive familial heart block type I. Makita N, Seki A, Sumitomo N, Chkourko H, Fukuhara S, Watanabe H, Shimizu W, Bezzina CR, Hasdemir C, Mugishima H, Makiyama T, Baruteau A, Baron E, Horie M, Hagiwara N, Wilde AA, Probst V, Le Marec H, Roden DM, Mochizuki N, Schott JJ, Delmar M (2012) Circ Arrhythm Electrophysiol 5(1): 163-72
    › Primary publication · 22247482 (PubMed) · PMC4274644 (PubMed Central)
  5. A common β1-adrenergic receptor polymorphism predicts favorable response to rate-control therapy in atrial fibrillation. Parvez B, Chopra N, Rowan S, Vaglio JC, Muhammad R, Roden DM, Darbar D (2012) J Am Coll Cardiol 59(1): 49-56
    › Primary publication · 22192668 (PubMed) · PMC3245828 (PubMed Central)
  6. Visual integration of results from a large DNA biobank (BioVU) using synthesis-view. Pendergrass S, Dudek SM, Roden DM, Crawford DC, Ritchie MD (2011) Pac Symp Biocomput : 265-75
    › Primary publication · 21121054 (PubMed) · PMC3065108 (PubMed Central)
  7. Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. Denny JC, Crawford DC, Ritchie MD, Bielinski SJ, Basford MA, Bradford Y, Chai HS, Bastarache L, Zuvich R, Peissig P, Carrell D, Ramirez AH, Pathak J, Wilke RA, Rasmussen L, Wang X, Pacheco JA, Kho AN, Hayes MG, Weston N, Matsumoto M, Kopp PA, Newton KM, Jarvik GP, Li R, Manolio TA, Kullo IJ, Chute CG, Chisholm RL, Larson EB, McCarty CA, Masys DR, Roden DM, de Andrade M (2011) Am J Hum Genet 89(4): 529-42
    › Primary publication · 21981779 (PubMed) · PMC3188836 (PubMed Central)
  8. The phenotype standardization project: improving pharmacogenetic studies of serious adverse drug reactions. Pirmohamed M, Aithal GP, Behr E, Daly A, Roden D (2011) Clin Pharmacol Ther 89(6): 784-5
    › Primary publication · 21593754 (PubMed)
  9. The emerging role of electronic medical records in pharmacogenomics. Wilke RA, Xu H, Denny JC, Roden DM, Krauss RM, McCarty CA, Davis RL, Skaar T, Lamba J, Savova G (2011) Clin Pharmacol Ther 89(3): 379-86
    › Primary publication · 21248726 (PubMed) · PMC3204342 (PubMed Central)
  10. The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. McCarty CA, Chisholm RL, Chute CG, Kullo IJ, Jarvik GP, Larson EB, Li R, Masys DR, Ritchie MD, Roden DM, Struewing JP, Wolf WA, eMERGE Team (2011) BMC Med Genomics : 13
    › Primary publication · 21269473 (PubMed) · PMC3038887 (PubMed Central)