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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Nov 04, 2024
. (Total: 6390 publications)
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Year
Journal
Records 1-7 (of 7 Records)
Query Trace:
Cuthbert C[original query]
Can incorporating molecular testing improve the accuracy of newborn screening for congenital adrenal hyperplasia?
Sarafoglou K , Gaviglio A , Wolf C , Lorentz CP , Lteif A , Kyllo J , Radloff G ,
Detwiler Z
,
Cuthbert CD
,
Hodges JS ,
Grosse SD
,
Greene CN
,
Cordovado S .
J Clin Endocrinol Metab 2024
CDC Grand Rounds: Newborn screening and improved outcomes.
Howell RR , Terry S , Tait VF ,
Olney R
,
Hinton CF
,
Grosse S
,
Eichwald J
,
Cuthbert C
,
Popovic T
,
Glidewell J
.
MMWR Morb Mortal Wkly Rep 2012 61 (21) 390-3
Progress in expanding newborn screening in the United States
Grosse SD
,
Cuthbert C
,
Gaffney M
,
Gaviglio A
,
Hinton CF
,
Kellar-Guenther Y , Kemper AR , McKasson S , Ojodu J ,
Riley C
,
Singh S , Sontag MK ,
Shapira SK
.
Am J Hum Genet 2023 110 (6) 1015-1016
Infants with Congenital Disorders Identified Through Newborn Screening - United States, 2015-2017.
Sontag MK , Yusuf C ,
Grosse SD
,
Edelman S , Miller JI , McKasson S , Kellar-Guenther Y ,
Gaffney M
,
Hinton CF
,
Cuthbert C
,
Singh S , Ojodu J ,
Shapira SK
.
MMWR Morb Mortal Wkly Rep 2020 69 (36) 1265-1268
Assessing the Performance of Dried-Blood-Spot DNA Extraction Methods in Next Generation Sequencing.
Hendrix MM
,
Cuthbert CD
,
Cordovado SK
.
Int J Neonatal Screen 2020 6 (2) 1-15
Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs.
De Jesus VR
,
Adam BW
,
Mandel D
,
Cuthbert CD
,
Matern D .
Mol Genet Metab 2014 113 67-75
Determination of total homocysteine, methylmalonic acid, and 2-methylcitric acid in dried blood spots by tandem mass spectrometry
Turgeon CT , Magera MJ ,
Cuthbert CD
,
Loken PR , Gavrilov DK , Tortorelli S , Raymond KM , Oglesbee D , Rinaldo P , Matern D .
Clin Chem 2010 56 (11) 1686-95
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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