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American Journal of Medical Genetics. Part A|November 2, 2011
Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heartGiorgia Esposito, Tanya L Butler, Gillian M Blue, et al.
American Heart Journal|June 19, 2018
Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart diseaseGillian M Blue, Eddie Ip, Karen Walker, et al.
Journal of the American College of Cardiology|December 16, 2014
Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart diseaseGillian M Blue, Edwin P Kirk, Eleni Giannoulatou, et al.
Genetic Testing and Molecular Biomarkers|September 30, 2010
GATA4 mutations in 357 unrelated patients with congenital heart malformationTanya L Butler, Giorgia Esposito, Gillian M Blue, et al.
Stem Cells Translational Medicine|October 30, 2015
A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem CellsHananeh Fonoudi, Hassan Ansari, Saeed Abbasalizadeh, et al.
Circulation. Genomic and Precision Medicine|March 21, 2018
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome DataJustin O Szot, Hartmut Cuny, Gillian M Blue, et al.
Nature Communications|January 22, 2026
Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract developmentSophie Wiszniak, Dimuthu Alankarage, Iman Lohraseb, et al.
Genome Medicine|October 14, 2024
A validated heart-specific model for splice-disrupting variants in childhood heart diseaseRobert Lesurf, Jeroen Breckpot, Jade Bouwmeester, et al.
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