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CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v8.8)
PHGKB
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Public Health Genomics Branch
Genomics and Precision Health Update
Genomics (A-Z)
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Last data update: Dec 01, 2023
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Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark.
Charlotte Glinge et al. JAMA network open 2023 6(1) e2252724
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Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome.
Neubauer Jacqueline et al. Pediatric research 2022
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Comprehensive Analysis of Genes Associated With Sudden Infant Death Syndrome.
Mehboob Riffat et al. Frontiers in pediatrics 2021 9742225
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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
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A Review of Long QT Syndrome: Everything a Hospitalist Should Know.
Sharma Nandita et al. Hospital pediatrics 2020 Mar
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CLINGEN Actionability Report for Brugada Syndrome - SCN5A
ClinGen Actionability Working Group
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.
Paludan-Müller Christian, et al. European journal of human genetics : EJHG 2019 5 0.
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Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester David J et al. The Journal of pediatrics 2018 Sep
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Management of survivors of cardiac arrest - the importance of genetic investigation.
Schwartz Peter J et al. Nature reviews. Cardiology 2016 13(9) 560-6
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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
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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
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Gene therapy helps patients avoid blood transfusion, study says
CNN, Apr 19, 2018
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
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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
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Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes.
Asatryan Babken et al. Cardiology in review 2018 Mar
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Sudden infant death syndrome and inherited cardiac conditions.
Baruteau Alban-Elouen et al. Nature reviews. Cardiology 2017 Sep
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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
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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
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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
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Sudden infant death syndrome and the genetics of inflammation.
Ferrante Linda et al. Front Immunol 2015 63
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Page last reviewed:
Oct 1, 2023
Page last updated:
Dec 01, 2023
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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