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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.American Heart Journal|October 20, 2021
Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genesGillian M Blue, Mauk Mekel, Debjani Das, et al.Plos One|June 16, 2011
Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4Mahdi Moradi Marjaneh, Edwin P Kirk, Maximilian G Posch, 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.Pageof 4