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Insights into the genetic architecture of congenital heart disease from animal modeling
by
Zhu, Wenjuan
, Lo, Cecilia W
in
Aetiology
/ Animal diseases
/ Birth defects
/ Cardiovascular disease
/ Cardiovascular diseases
/ Congenital defects
/ Congenital diseases
/ Consortia
/ Defects
/ Etiology
/ Gene expression
/ Genes
/ Genetic counseling
/ Genetic testing
/ Genomics
/ Heart
/ Heart diseases
/ MicroRNAs
/ Mortality
/ Mutation
/ Parturition
/ Pathogenesis
/ Pediatrics
/ Precision medicine
/ Prenatal diagnosis
2023
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Insights into the genetic architecture of congenital heart disease from animal modeling
by
Zhu, Wenjuan
, Lo, Cecilia W
in
Aetiology
/ Animal diseases
/ Birth defects
/ Cardiovascular disease
/ Cardiovascular diseases
/ Congenital defects
/ Congenital diseases
/ Consortia
/ Defects
/ Etiology
/ Gene expression
/ Genes
/ Genetic counseling
/ Genetic testing
/ Genomics
/ Heart
/ Heart diseases
/ MicroRNAs
/ Mortality
/ Mutation
/ Parturition
/ Pathogenesis
/ Pediatrics
/ Precision medicine
/ Prenatal diagnosis
2023
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Do you wish to request the book?
Insights into the genetic architecture of congenital heart disease from animal modeling
by
Zhu, Wenjuan
, Lo, Cecilia W
in
Aetiology
/ Animal diseases
/ Birth defects
/ Cardiovascular disease
/ Cardiovascular diseases
/ Congenital defects
/ Congenital diseases
/ Consortia
/ Defects
/ Etiology
/ Gene expression
/ Genes
/ Genetic counseling
/ Genetic testing
/ Genomics
/ Heart
/ Heart diseases
/ MicroRNAs
/ Mortality
/ Mutation
/ Parturition
/ Pathogenesis
/ Pediatrics
/ Precision medicine
/ Prenatal diagnosis
2023
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Insights into the genetic architecture of congenital heart disease from animal modeling
Journal Article
Insights into the genetic architecture of congenital heart disease from animal modeling
2023
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Overview
Congenital heart disease (CHD) is observed in up to 1% of live births and is one of the leading causes of mortality from birth defects. While hundreds of genes have been implicated in the genetic etiology of CHD, their role in CHD pathogenesis is still poorly understood. This is largely a reflection of the sporadic nature of CHD, as well as its variable expressivity and incomplete penetrance. We reviewed the monogenic causes and evidence for oligogenic etiology of CHD, as well as the role of de novo mutations, common variants, and genetic modifiers. For further mechanistic insight, we leveraged single-cell data across species to investigate the cellular expression characteristics of genes implicated in CHD in developing human and mouse embryonic hearts. Understanding the genetic etiology of CHD may enable the application of precision medicine and prenatal diagnosis, thereby facilitating early intervention to improve outcomes for patients with CHD.
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