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Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk.
Mann SA, Otway R, Guo G, Soka M, Karlsdotter L, Trivedi G, Ohanian M, Zodgekar P, Smith RA, Wouters MA, Subbiah R, Walker B, Kuchar D, Sanders P, Griffiths L, Vandenberg JI, Fatkin D. Mann SA, et al. Among authors: wouters ma. J Am Coll Cardiol. 2012 Mar 13;59(11):1017-25. doi: 10.1016/j.jacc.2011.11.039. J Am Coll Cardiol. 2012. PMID: 22402074 Free article.
Gentrepid V2.0: a web server for candidate disease gene prediction.
Ballouz S, Liu JY, George RA, Bains N, Liu A, Oti M, Gaeta B, Fatkin D, Wouters MA. Ballouz S, et al. Among authors: wouters ma. BMC Bioinformatics. 2013 Aug 16;14:249. doi: 10.1186/1471-2105-14-249. BMC Bioinformatics. 2013. PMID: 23947436 Free PMC article.
General mutation databases: analysis and review.
George RA, Smith TD, Callaghan S, Hardman L, Pierides C, Horaitis O, Wouters MA, Cotton RG. George RA, et al. Among authors: wouters ma. J Med Genet. 2008 Feb;45(2):65-70. doi: 10.1136/jmg.2007.052639. Epub 2007 Sep 24. J Med Genet. 2008. PMID: 17893115 Free article. Review.
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets.
Bouveret R, Waardenberg AJ, Schonrock N, Ramialison M, Doan T, de Jong D, Bondue A, Kaur G, Mohamed S, Fonoudi H, Chen CM, Wouters MA, Bhattacharya S, Plachta N, Dunwoodie SL, Chapman G, Blanpain C, Harvey RP. Bouveret R, et al. Among authors: wouters ma. Elife. 2015 Jul 6;4:e06942. doi: 10.7554/eLife.06942. Elife. 2015. PMID: 26146939 Free PMC article.
41 results