Last Posted: Oct 19, 2019
- Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease
E Fotieu et al, Circulation Genomics and Precision Medicine, October 2019 - Implementing Artificial Intelligence and Digital Health in Resource-Limited Settings? Top 10 Lessons We Learned in Congenital Heart Defects and Cardiology.
Thomford Nicholas Ekow et al. Omics : a journal of integrative biology 2019 Oct - Pregnancy outcomes of reciprocal translocation carriers with two or more unfavorable pregnancy histories: before and after preimplantation genetic testing.
Huang Caiyi et al. Journal of assisted reproduction and genetics 2019 Sep - Congenital Heart Disease: Prenatal Diagnosis and Genetic Associations.
Hopkins Maeve K et al. Obstetrical & gynecological survey 2019 Aug 74(8) 497-503 - Biomarkers improve prediction of 30-day unplanned readmission or mortality after paediatric congenital heart surgery.
Brown Jeremiah R et al. Cardiology in the young 2019 Jul 1-6 - Fetal diagnosis of Mowat-Wilson syndrome by whole exome sequencing.
Evans Carey-Anne et al. American journal of medical genetics. Part A 2019 Jul - A familys medical mystery sheds light on the surprising ways disease-causing genes can be inherited
A Joseph, Stat News, July 8, 2019 - Genetic counselling and testing in congenital heart defects and hereditary thoracic aortic disease: Complex but essential.
Breckpot Jeroen et al. European journal of preventive cardiology 2019 Jun 2047487319860296 - Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics.
De Backer Julie et al. European journal of preventive cardiology 2019 Jun 2047487319854552 - Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health.
Sgardioli Ilária Cristina et al. Orphanet journal of rare diseases 2019 Jun 14(1) 123
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