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Science (New York, N.Y.)|August 29, 2015
HEART DISEASE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathyJohn T Hinson, Anant Chopra, Navid Nafissi, et al.Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.Circulation Research|February 9, 2021
Mechanisms of Congenital Heart Disease Caused by NAA15 HaploinsufficiencyTarsha Ward, Warren Tai, Sarah Morton, et al.Circulation. Genomic and Precision Medicine|August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart DiseaseMarko T Boskovski, Jason Homsy, Meena Nathan, et al.Nature Genetics|July 1, 2020
Genomic analyses implicate noncoding de novo variants in congenital heart diseaseFelix Richter, Sarah U Morton, Seong Won Kim, et al.Science (New York, N.Y.)|January 20, 2016
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJason Homsy, Samir Zaidi, Yufeng Shen, et al.Nature Genetics|October 10, 2017
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsSheng Chih Jin, Jason Homsy, Samir Zaidi, et al.Pageof 2