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Public Health Genomics and Precision Health Knowledge Base (v8.9)
PHGKB
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Public Health Genomics Branch
Genomics and Precision Health Update
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Last data update: Dec 08, 2023
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Records 1 - 18 (of 18 Records)
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Infant Mortality[original query]>>Reviews/Commentaries[Product Type]
Newborn sequencing is only part of the solution for better child health.
Luca Brunelli et al. Lancet Reg Health Am 2023 25100581
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Genomic newborn screening for rare diseases.
Zornitza Stark et al. Nat Rev Genet 2023
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New ASH initiatives to improve patient care of the long-overlooked Sickle Cell Disease.
Venée N Tubman et al. Blood 2023
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Implications of Genomic Newborn Screening for Infant Mortality.
Monica H Wojcik et al. International journal of neonatal screening 2023 9(1)
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Implications of Genomic Newborn Screening for Infant Mortality
MH Wojick et al, IJNS, March 2023
Perinatal health predictors using artificial intelligence: A review.
Ramakrishnan Rema et al. Women's health (London, England) 2021 1717455065211046132
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Inequities in newborn screening: Race and the role of medicaid ☆ .
Sohn Heeju et al. SSM - population health 2019 Dec 9100496
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The promise and pitfalls of precision medicine to resolve black-white racial disparities in preterm birth.
Burris Heather H et al. Pediatric research 2019 Aug
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Medical genetics and genomic medicine in Japan.
Suzuki Hisato et al. American journal of medical genetics. Part C, Seminars in medical genetics 2019 May
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Status of Newborn Screening and Inborn Errors of Metabolism in India.
Kapoor Seema et al. Indian journal of pediatrics 2018 Dec 85(12) 1110-1117
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Newborn screening in the developing countries.
Therrell Bradford L et al. Current opinion in pediatrics 2018 Aug
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Opening the window: The case for carrier and perinatal screening for spinal muscular atrophy.
Burns Joseph K et al. Neuromuscular disorders : NMD 2016 Sep 26(9) 551-9
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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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Genetic tests for low- and middle-income countries: a literature review.
Maltese P E et al. Genetics and molecular research : GMR 2017 Feb 16(1)
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Emerging Field of Cardiomics: High-Throughput Investigations into Transcriptional Regulation of Cardiovascular Development and Disease.
Slagle Christopher E et al. Trends in genetics : TIG 2016 Oct
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Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England.
Salway Sarah et al. Journal of community genetics 2016 Jun
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Changing Trends in Carrier Screening for Genetic Disease in the United States.
Nazareth Shivani B et al. Prenat. Diagn. 2015 Jul 3.
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Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm.
Larrandaburu Mariela et al. J Community Genet 2015 May 29.
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Page last reviewed:
Oct 1, 2023
Page last updated:
Dec 08, 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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