Heart Disorders
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Last Posted: Jul 28, 2023
- Ocular, cardiovascular, and genetic characteristics and their associations in children with Marfan syndrome and related fibrillinopathies.
Dongwei Guo, et al. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2023 0 - 22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders.
Maiara A Floriani et al. Molecular syndromology 2023 14(1) 1-10 - Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes.
Balistreri Carmela Rita, et al. Genes 2020 11 (12) - Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses.
Scheiper Stefanie et al. Forensic science international 2018 Oct 29370-76 - Exome sequencing-based molecular autopsy of formalin-fixed paraffin-embedded tissue after sudden death.
Bagnall Richard D, et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 0 0. (10) 1127-1133 - Variants in the NOTCH1 gene in patients with aortic coarctation.
Freylikhman Olga, et al. Congenital heart disease 0 0 (5) 391-6 - Electrocardiogram
From NHLBI health topic site - Apolipoprotein E genotyping method by real time PCR, a fast and cost-effective alternative to the TaqMan and FRET assays.
Calero O, et al. Journal of neuroscience methods 2009 7
About HLBS-PopOmics
HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Site Citation:
Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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