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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Reproductive and Child Health
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Sudden Infant Death Syndrome [original query]>>Original Studies[Product Type]
Multiomic Analysis of Neuroinflammation and Occult Infection in Sudden Infant Death Syndrome.
Prashanth S Ramachandran et al. JAMA Neurol 2024
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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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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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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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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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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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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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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 2024
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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