 Neonatal Screening
"Neonatal Screening" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The identification of selected parameters in newborn infants by various tests, examinations, or other procedures. Screening may be performed by clinical or laboratory measures. A screening test is designed to sort out healthy neonates (INFANT, NEWBORN) from those not well, but the screening test is not intended as a diagnostic device, rather instead as epidemiologic.
| Descriptor ID |
D015997
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| MeSH Number(s) |
E01.370.225.910 E01.370.500.580 E05.200.910 E05.318.308.980.438.580.580 N02.421.726.233.443.816 N05.715.360.300.800.438.500.575 N06.850.520.308.980.438.580.580 N06.850.780.500.580
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| Concept/Terms |
Neonatal Screening- Neonatal Screening
- Neonatal Screenings
- Screening, Neonatal
- Screenings, Neonatal
- Infant, Newborn, Screening
- Newborn Infant Screening
- Newborn Infant Screenings
- Screening, Newborn Infant
- Screenings, Newborn Infant
- Newborn Screening
- Newborn Screenings
- Screening, Newborn
- Screenings, Newborn
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Below are MeSH descriptors whose meaning is more general than "Neonatal Screening".
Below are MeSH descriptors whose meaning is more specific than "Neonatal Screening".
This graph shows the total number of publications written about "Neonatal Screening" by people in this website by year, and whether "Neonatal Screening" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 | | 1999 | 1 | 1 | 2 | | 2000 | 1 | 0 | 1 | | 2003 | 1 | 3 | 4 | | 2004 | 3 | 2 | 5 | | 2005 | 0 | 1 | 1 | | 2006 | 3 | 0 | 3 | | 2007 | 0 | 1 | 1 | | 2008 | 2 | 0 | 2 | | 2009 | 0 | 2 | 2 | | 2010 | 3 | 1 | 4 | | 2011 | 1 | 0 | 1 | | 2012 | 2 | 2 | 4 | | 2013 | 3 | 1 | 4 | | 2014 | 4 | 0 | 4 | | 2015 | 4 | 1 | 5 | | 2016 | 6 | 2 | 8 | | 2017 | 6 | 2 | 8 | | 2018 | 3 | 1 | 4 | | 2019 | 2 | 3 | 5 | | 2020 | 4 | 3 | 7 | | 2021 | 2 | 4 | 6 | | 2022 | 1 | 4 | 5 | | 2023 | 0 | 4 | 4 | | 2024 | 5 | 2 | 7 | | 2025 | 1 | 2 | 3 |
To return to the timeline, click here.
Below are the most recent publications written about "Neonatal Screening" by people in Profiles.
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Gold C, Bourque SL, Wagner K, Wymore EM, Seidel Halmo L. Advances, Nuances, and Future Directions in Neonatal Toxicology Testing. Neoreviews. 2025 Apr 01; 26(4):e233-e246.
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Heath A, von Alvensleben I, Spielvogel JA, Freudenthal P, Trapp J, Noya I, G?lvez M, Mendiz?bal F, Gonzales M, Apaza C, Sanga L, Mc Cann E, Julian CG. Prolonged postnatal adaptation and enhanced prevalence of congenital heart diseases due to altitude may contribute to newborn mortality in Bolivia. Exp Physiol. 2025 Aug; 110(8):1060-1070.
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Nokoff NJ, Buchanan C, Barker JM. Clinical Manifestations and Treatment Challenges in Infants and Children With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. J Clin Endocrinol Metab. 2025 Jan 21; 110(Supplement_1):S13-S24.
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Pauly K, Woontner M, Abdenur JE, Chaudhari BP, Gosselin R, Kripps KA, Thomas JA, Wempe MF, Gospe SM, Coughlin CR. Feasibility of newborn screening for pyridoxine-dependent epilepsy. Mol Genet Metab. 2025 Jan; 144(1):109002.
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Kingsmore SF, Wright M, Smith LD, Liang Y, Mowrey WR, Protopsaltis L, Bainbridge M, Baker M, Batalov S, Blincow E, Cao B, Caylor S, Chambers C, Ellsworth K, Feigenbaum A, Frise E, Guidugli L, Hall KP, Hansen C, Kiel M, Van Der Kraan L, Krilow C, Kwon H, Madhavrao L, Lefebvre S, Leipzig J, Mardach R, Moore B, Oh D, Olsen L, Ontiveros E, Owen MJ, Reimers R, Scharer G, Schleit J, Shelnutt S, Mehtalia SS, Oriol A, Sanford E, Schwartz S, Wigby K, Willis MJ, Yandell M, Kunard CM, Defay T. Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection. Am J Hum Genet. 2024 Dec 05; 111(12):2618-2642.
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Oltman SP, Rogers EE, Baer RJ, Amsalu R, Bandoli G, Chambers CD, Cho H, Dagle JM, Karvonen KL, Kingsmore SF, McKenzie-Sampson S, Momany A, Ontiveros E, Protopsaltis LD, Rand L, Kobayashi ES, Steurer MA, Ryckman KK, Jelliffe-Pawlowski LL. Early Newborn Metabolic Patterning and Sudden Infant Death Syndrome. JAMA Pediatr. 2024 Nov 01; 178(11):1183-1191.
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Gold NB, Omorodion JO, Del Rosario MC, Rivera-Cruz G, Hsu CY, Ziniel SI, Holm IA. Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns. J Genet Couns. 2025 Apr; 34(2):e1994.
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Mall MA, Burgel PR, Castellani C, Davies JC, Salathe M, Taylor-Cousar JL. Cystic fibrosis. Nat Rev Dis Primers. 2024 Aug 08; 10(1):53.
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Orb QT, Pesch M, Allen CM, Wilkes A, Ahmad I, Alfonso K, Antonio SM, Mithal LB, Brinkmeier JV, Carvalho D, Chan D, Cheng AG, Chi D, Cohen M, Discolo CM, Duran C, Germiller J, Gibson L, Grunstein E, Harrison G, Lee K, Hawley K, Kohlhoff S, Melvin A, MacArthur C, Nassar M, Neff L, Pecha P, Salvatore C, Schoem S, Virgin F, Saunders J, Schleiss M, Smith RJH, Sood S, Park AH. Congenital Cytomegalovirus Testing Outcomes From the ValEAR Trial. Otolaryngol Head Neck Surg. 2024 May; 170(5):1430-1441.
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Armstrong N, Apkon S, Berggren KN, Braun C, Ciafaloni E, Connolly A, Kennedy A, Kuntz N, Mathews K, McGuire M, Parad R, Scavina M, Scharf RJ, Waldrop M. The Early Care (0-3 Years) In Duchenne Muscular Dystrophy Meeting Report. J Neuromuscul Dis. 2024; 11(2):525-533.
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