Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease
Developmental Cell2020Vol. 56(3), pp. 292–309.e9
Citations Over TimeTop 10% of 2020 papers
Irfan S. Kathiriya, Kavitha S. Rao, Giovanni Iacono, W. Patrick Devine, Andrew P. Blair, Swetansu K. Hota, Michael H. Lai, Bayardo I. Garay, Reuben Thomas, Henry Gong, Lauren K. Wasson, Piyush Goyal, Tatyana Sukonnik, Kevin Hu, Güneş Akgün, Laure D. Bernard, Brynn N. Akerberg, Fei Gu, Kai Li, Matthew L Speir, Maximilian Haeussler, William T. Pu, Joshua M. Stuart, Christine E. Seidman, J G Seidman, Holger Heyn, Benoit G. Bruneau
Related Papers
- → NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autism(2017)115 cited
- → BOP, a regulator of right ventricular heart development, is a direct transcriptional target of MEF2C in the developing heart(2005)123 cited
- → MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review(2016)59 cited
- → 5q14.3 neurocutaneous syndrome: A novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C(2011)32 cited
- → An Nkx-Dependent Enhancer Regulates cGATA-6 Gene Expression during Early Stages of Heart Development(2000)55 cited