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Precision Health Database


Precision Health Database|Search|PHGKB

Reproductive and Child Health

Last data update: Dec 08, 2023. (Total: 62301 Documents since 2012)
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Records 1 - 18 (of 18 Records)

Query Trace: 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
Genomic newborn screening for rare diseases.
Zornitza Stark et al. Nat Rev Genet 2023
New ASH initiatives to improve patient care of the long-overlooked Sickle Cell Disease.
Venée N Tubman et al. Blood 2023
Implications of Genomic Newborn Screening for Infant Mortality.
Monica H Wojcik et al. International journal of neonatal screening 2023 9(1)
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
Inequities in newborn screening: Race and the role of medicaid ☆ .
Sohn Heeju et al. SSM - population health 2019 Dec 9100496
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
Medical genetics and genomic medicine in Japan.
Suzuki Hisato et al. American journal of medical genetics. Part C, Seminars in medical genetics 2019 May
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
Newborn screening in the developing countries.
Therrell Bradford L et al. Current opinion in pediatrics 2018 Aug
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
Sudden infant death syndrome and inherited cardiac conditions.
Baruteau Alban-Elouen et al. Nature reviews. Cardiology 2017 Sep
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)
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
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
Changing Trends in Carrier Screening for Genetic Disease in the United States.
Nazareth Shivani B et al. Prenat. Diagn. 2015 Jul 3.
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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