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- W197228064 abstract "Congenital heart disease (CHD) is the most common birth defect and the leading cause of infant morbidity in the Western world. CHD represents a heterogeneous multifactorial disorder caused by a complex interplay of numerous genetic and environmental risk factors. Despite remarkable progress in understanding the genetic basis and molecular mechanism of cardiovascular malformations, the etiology for the majority of CHDs remain poorly understood. The highly complex circuitries of signaling pathways and transcription factors and regulators orchestrate cardiovascular development, and defects in any component of this regulatory network can lead to CHD. Contemporary genomic and transcriptomic technologies, such as single-nucleotide arrays, next-generation sequencing, expression profiling, and genome-wide association studies, highly accelerate the identification of molecular causes of CHD. Significantly, these novel technologies allow researchers to analyze not only syndromic but also the most common sporadic cases of CHD. This chapter discusses new insights into the molecular mechanisms underlying the development of CHD and overview current technologies employed for evaluation of molecular determinants of CHD." @default.
- W197228064 created "2016-06-24" @default.
- W197228064 creator A5022739391 @default.
- W197228064 date "2014-01-01" @default.
- W197228064 modified "2023-09-24" @default.
- W197228064 title "Molecular Determinants of Congenital Heart Disease" @default.
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