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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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Public Health Genomics Branch
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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: Apr 18, 2025
. (Total: 6649 publications)
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Records 1-8 (of 8 Records)
Query Trace:
De Jesus VR[original query]
Non-derivatized Assay for the Simultaneous Detection of Amino Acids, Acylcarnitines, Succinylacetone, Creatine, and Guanidinoacetic Acid in Dried Blood Spots by Tandem Mass Spectrometry.
Asef CK
,
Khaksarfard KM
,
De Jesús VR
.
Int J Neonatal Screen 2016 2 (4)
The clinical laboratory is an integral component to health care delivery : An expanded representation of the total testing process
Lubin IM
,
Astles JR
,
Bunn JD
,
Cornish NE
,
Lazaro G
,
Marshall AA
,
Stang HL
,
De Jesús VR
.
Am J Clin Pathol 2023 160 (2) 124-129
Associations between Biomarkers of Exposure and Lung Cancer Risk among Exclusive Cigarette Smokers in the Golestan Cohort Study.
Rostron BL , Wang J , Etemadi A , Thakur S , Chang JT ,
Bhandari D
,
Botelho JC
,
De Jesús VR
,
Feng J
,
Gail MH , Inoue-Choi M , Malekzadeh R , Pourshams A , Poustchi H , Roshandel G , Shiels MS , Wang Q , Wang Y , Xia B , Boffetta P , Brennan P , Abnet CC , Calafat AM , Wang L , Blount BC , Freedman ND , Chang CM .
Int J Environ Res Public Health 2021 18 (14)
Galactose-1-phosphate uridyltransferase dried blood spot quality control materials for newborn screening tests
Adam BW
,
Flores SR
,
Hou Y , Allen TW ,
De Jesus VR
.
Clin Biochem 2014 48 (6) 437-42
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
Improved analysis of C26:0-lysophosphatidylcholine in dried-blood spots via negative ion mode HPLC-ESI-MS/MS for X-linked adrenoleukodystrophy newborn screening.
Haynes CA
,
De Jesus VR
.
Clin Chim Acta 2012 413 1217-21
Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria.
Mechtler TP , Stary S , Metz TF ,
De Jesus VR
,
Greber-Platzer S , Pollak A , Herkner KR , Streubel B , Kasper DC .
Lancet 2012 379 (9813) 335-41
Improving and assuring newborn screening laboratory quality worldwide: 30-year experience at the Centers for Disease Control and Prevention
De Jesus VR
,
Mei JV
,
Bell CJ
,
Hannon WH
.
Semin Perinatol 2010 34 (2) 125-33
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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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