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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: etheridge sp. Nat Commun. 2021 Nov 8;12(1):6442. doi: 10.1038/s41467-021-26741-7. Nat Commun. 2021. PMID: 34750360 Free PMC article.
Congenital long QT syndrome in children identified by family screening.
Petko C, Bradley DJ, Tristani-Firouzi M, Cohen MI, Sanatani S, Saarel EV, Albaro CA, Etheridge SP. Petko C, et al. Among authors: etheridge sp. Am J Cardiol. 2008 Jun 15;101(12):1756-8. doi: 10.1016/j.amjcard.2008.02.068. Epub 2008 Apr 9. Am J Cardiol. 2008. PMID: 18549854
Resuscitated sudden cardiac death in Andersen-Tawil syndrome.
Airey KJ, Etheridge SP, Tawil R, Tristani-Firouzi M. Airey KJ, et al. Among authors: etheridge sp. Heart Rhythm. 2009 Dec;6(12):1814-7. doi: 10.1016/j.hrthm.2009.08.032. Epub 2009 Aug 29. Heart Rhythm. 2009. PMID: 19959136 Free PMC article. No abstract available.
Kir 2.1 channelopathies: the Andersen-Tawil syndrome.
Tristani-Firouzi M, Etheridge SP. Tristani-Firouzi M, et al. Among authors: etheridge sp. Pflugers Arch. 2010 Jul;460(2):289-94. doi: 10.1007/s00424-010-0820-6. Epub 2010 Mar 21. Pflugers Arch. 2010. PMID: 20306271 Review.
Somatic mosaicism contributes to phenotypic variation in Timothy syndrome.
Etheridge SP, Bowles NE, Arrington CB, Pilcher T, Rope A, Wilde AA, Alders M, Saarel EV, Tavernier R, Timothy KW, Tristani-Firouzi M. Etheridge SP, et al. Am J Med Genet A. 2011 Oct;155A(10):2578-83. doi: 10.1002/ajmg.a.34223. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910241
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: etheridge sp. 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.
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. Among authors: etheridge sp. Cell Physiol Biochem. 2017;42(5):2021-2029. doi: 10.1159/000479897. Epub 2017 Aug 11. Cell Physiol Biochem. 2017. PMID: 28803248 Free article.
143 results