Search results (78)
« Back to PublicationsMaternal anaemia and congenital heart disease in offspring: a case-control study using linked electronic health records in the United Kingdom
Nair M. et al, (2025), BJOG: An International Journal of Obstetrics and Gynaecology
Noncoding regulation of epicardial gene expression and epithelial-to-mesenchymal transition during heart development
Vieira JN. et al, (2024), CIRCULATION RESEARCH, 135
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2
Broadway-Stringer S. et al, (2023), Cells
Better communication between experts is needed to solve the environmental origins of birth defects.
Sparrow DB., (2022), Bioessays, 44
Analysis of Placental Arteriovenous Formation Reveals New Insights Into Embryos With Congenital Heart Defects
KALISCH-SMITH J. et al, (2022), Frontiers in Genetics
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors.
Alankarage D. et al, (2022), Differentiation, 128, 1 - 12
Small change, big impact: A Z-disc missense genetic variant causes dramatic morphological changes in the embryonic heart
Jiang H. et al, (2022), JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 173, S44 - S44
The onset of circulation triggers a metabolic switch required for endothelial to hematopoietic transition.
Azzoni E. et al, (2021), Cell Rep, 37
Maternal iron deficiency perturbs embryonic cardiovascular development in mice.
Kalisch-Smith JI. et al, (2021), Nature communications, 12
Maternal iron deficiency perturbs embryonic cardiovascular development in mice
SPARROW D. et al, (2021), Nature Communications
Functional analysis of a gene-edited mouse to gain insights into the disease mechanisms of a titin missense variant
JIANG H. et al, (2021), Basic Research in Cardiology
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
Martin E. et al, (2020), Human Molecular Genetics