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The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
Hateley S, Lopez-Izquierdo A, Jou CJ, Cho S, Schraiber JG, Song S, Maguire CT, Torres N, Riedel M, Bowles NE, Arrington CB, Kennedy BJ, Etheridge SP, Lai S, Pribble C, Meyers L, Lundahl D, Byrnes J, Granka JM, Kauffman CA, Lemmon G, Boyden S, Scott Watkins W, Karren MA, Knight S, Brent Muhlestein J, Carlquist JF, Anderson JL, Chahine KG, Shah KU, Ball CA, Benjamin IJ, Yandell M, Tristani-Firouzi M. Hateley S, et al. Among authors: jou cj. Nat Commun. 2021 Nov 8;12(1):6442. doi: 10.1038/s41467-021-26741-7. Nat Commun. 2021. PMID: 34750360 Free PMC article.
A near-infrared fluorescent voltage-sensitive dye allows for moderate-throughput electrophysiological analyses of human induced pluripotent stem cell-derived cardiomyocytes.
Lopez-Izquierdo A, Warren M, Riedel M, Cho S, Lai S, Lux RL, Spitzer KW, Benjamin IJ, Tristani-Firouzi M, Jou CJ. Lopez-Izquierdo A, et al. Among authors: jou cj. Am J Physiol Heart Circ Physiol. 2014 Nov 1;307(9):H1370-7. doi: 10.1152/ajpheart.00344.2014. Epub 2014 Aug 29. Am J Physiol Heart Circ Physiol. 2014. PMID: 25172899 Free PMC article.
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
Bowles NE, Jou CJ, Arrington CB, Kennedy BJ, Earl A, Matsunami N, Meyers LL, Etheridge SP, Saarel EV, Bleyl SB, Yost HJ, Yandell M, Leppert MF, Tristani-Firouzi M, Gruber PJ; Baylor Hopkins Centers for Mendelian Genomics. Bowles NE, et al. Among authors: jou cj. Am J Med Genet A. 2015 Dec;167A(12):2975-84. doi: 10.1002/ajmg.a.37297. Epub 2015 Aug 18. Am J Med Genet A. 2015. PMID: 26284702 Free PMC article.
Efficient Precision Genome Editing in iPSCs via Genetic Co-targeting with Selection.
Mitzelfelt KA, McDermott-Roe C, Grzybowski MN, Marquez M, Kuo CT, Riedel M, Lai S, Choi MJ, Kolander KD, Helbling D, Dimmock DP, Battle MA, Jou CJ, Tristani-Firouzi M, Verbsky JW, Benjamin IJ, Geurts AM. Mitzelfelt KA, et al. Among authors: jou cj. Stem Cell Reports. 2017 Mar 14;8(3):491-499. doi: 10.1016/j.stemcr.2017.01.021. Epub 2017 Feb 24. Stem Cell Reports. 2017. PMID: 28238794 Free PMC article.
A Functional Assay for Sick Sinus Syndrome Genetic Variants.
Jou CJ, Arrington CB, Barnett S, Shen J, Cho S, Sheng X, McCullagh PC, Bowles NE, Pribble CM, Saarel EV, Pilcher TA, Etheridge SP, Tristani-Firouzi M. Jou CJ, et al. Cell Physiol Biochem. 2017;42(5):2021-2029. doi: 10.1159/000479897. Epub 2017 Aug 11. Cell Physiol Biochem. 2017. PMID: 28803248 Free article.
Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.
Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N. Ishikawa T, et al. Among authors: jou cj. Circ Arrhythm Electrophysiol. 2015 Apr;8(2):400-8. doi: 10.1161/CIRCEP.114.002534. Epub 2015 Feb 25. Circ Arrhythm Electrophysiol. 2015. PMID: 25717017 Free article.
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