Sudden Infant Death Syndrome
Last Posted: Feb 10, 2022
- Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome.
Neubauer Jacqueline et al. Pediatric research 2022
- Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome.
Mehboob Riffat et al. Frontiers in pediatrics 2021 9742225
- Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.
Köffer Jasmin et al. International journal of legal medicine 2020 Aug
- A Review of Long QT Syndrome: Everything a Hospitalist Should Know.
Sharma Nandita et al. Hospital pediatrics 2020 Mar
- What Causes SIDS? Thousands of infants die unexpectedly each year, and experts are working to figure out why.
C Arnold, New York Times, June 2019
- Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
CP Muller et al, EJHG, May 2019
- Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester David J et al. The Journal of pediatrics 2018 Sep
- Management of survivors of cardiac arrest - the importance of genetic investigation.
Schwartz Peter J et al. Nature reviews. Cardiology 2016 13(9) 560-6
- Noncardiac genetic predisposition in sudden infant death syndrome.
Gray Belinda et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Aug
- CLINGEN Actionability Report for Brugada Syndrome - SCN5A
ClinGen Actionability Working Group
- Diagnostic potential of stored dried blood spots for inborn errors of metabolism: a metabolic autopsy of medium-chain acyl-CoA dehydrogenase deficiency.
Kaku Noriyuki et al. Journal of clinical pathology 2018 May
- Gene therapy helps patients avoid blood transfusion, study says
CNN, Apr 19, 2018
- Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.
Tester David J et al. Journal of the American College of Cardiology 2018 Mar 71(11) 1217-1227
- Sudden Infant Death Syndrome and Genetics: Don't Throw Out the Infant With the Dirty Water.
Schwartz Peter J et al. Journal of the American College of Cardiology 2018 Mar 71(11) 1228-1230
- Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes.
Asatryan Babken et al. Cardiology in review 2018 Mar
- Sudden infant death syndrome and inherited cardiac conditions.
Baruteau Alban-Elouen et al. Nature reviews. Cardiology 2017 Sep
- Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence.
Ioakeimidis Nikolaos S et al. Journal of biological research (Thessalonike, Greece) 2017 Dec 246
- Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.
Neubauer Jacqueline, et al. European journal of human genetics : EJHG 2017 0 0. (4) 404-409
- Sudden Infant Death Syndrome (SIDS)
- The role of mutations in the SCN5A gene in cardiomyopathies.
Zaklyazminskaya Elena et al. Biochimica et biophysica acta 2016 Jul 1863(7 Pt B) 1799-805
Reproductive and Child Health PHGKB 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 reproductive and child Health...more
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Birth Defects
- Carrier Testing
- Cerebral Palsy
- Congenital heart defects
- Pregnancy loss
- Developmental Disabilities
- Gestational Diabetes
- Hearing loss
- Neural tube defects
- Infant Mortality
- Learning disability
- Newborn Screening
- Prenatal Testing
- Sudden Infant Death Syndrome
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