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Publications by Sabrina G. Ellesøe

Systems Genetics Analysis Identify Calcium Signalling Defects as Novel Cause of Congenital Heart Disease

English

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What Is New in Genetics of Congenital Heart Defects?

Frontiers in Pediatrics

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Vulnerability of the Developing Heart to Oxygen Deprivation as a Cause of Congenital Heart Defects

Journal of the American Heart Association

Cardiovascular Medicine

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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American Journal of Human Genetics

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Genetics and Genetic Testing in Congenital Heart Disease

Clinics in Perinatology

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Extracardiac Defects in Children With Congenital Heart Disease.

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Of Mice and Men: Molecular Genetics of Congenital Heart Disease

Cellular and Molecular Life Sciences

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Somatic NKX2-5 Mutations as a Novel Mechanism of Disease in Complex Congenital Heart Disease

Journal of Medical Genetics

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Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics

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Advancing Prenatal Detection of Congenital Heart Disease: A Novel Screening Protocol Improves Early Diagnosis of Complex Congenital Heart Disease

Journal of Ultrasound in Medicine

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English