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Cui H, Bansal V, Schulz K, Malecova B, Dall'Agnese A, Latella L, Gatto S, Chen W, Grunert M, Dorn C, Puri PL, and Sperling SR. Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation. 2017. Plos One.
Grunert M, Dorn C, Cui H, Dunkel I, Schulz K, Schoenhals S, Sun W, Berger F, Chen W, Sperling SR. DNA methylation alterations associated with gene expression changes depict congenital heart disease: Tetralogy of Fallot and ventricular septal defects. 2016. Cardiovascular Research.
Ben Jehuda R, Eisen B, Shemer Y, Mekies L.N, Szantai A, Reiter I, Cui H, Guan K, Haron-Khun S, Freimark D, Sperling S.R, Gherghiceanu M, Arad M, Binah O. CRISPR correction of the PRKAG2 gene mutation in the patient's iPSC-derived cardiomyocytes eliminates the electrophysiological and structural abnormalities. 2017. Heart Rhythm.