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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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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: Oct 07, 2024
. (Total: 6342 publications)
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Year
Journal
Records 1-10 (of 10 Records)
Query Trace:
Koontz D[original query]
Folate-related gene variants in Irish families affected by neural tube defects.
Fisk Green R
,
Byrne J ,
Crider KS
,
Gallagher M
,
Koontz D
,
Berry RJ
.
Front Genet 2013 4 223
Evaluation of rapid and sensitive DNA extraction methods for detection of cytomegalovirus in dried blood spots.
Koontz D
,
Dollard S
,
Cordovado S
.
J Virol Methods 2019 265 117-120
MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots.
Kobrynski LJ ,
Yazdanpanah GK
,
Koontz D
,
Lee FK
,
Vogt RF
.
Clin Chem 2015 62 (1) 287-92
Evaluation of DNA extraction methods for the detection of Cytomegalovirus in dried blood spots.
Koontz D
,
Baecher K
,
Amin M
,
Nikolova S
,
Gallagher M
,
Dollard S
.
J Clin Virol 2015 66 95-9
A pyrosequencing-based assay for the rapid detection of the 22q11.2 deletion in DNA from buccal and dried blood spot samples.
Koontz D
,
Baecher K
,
Kobrynski L ,
Nikolova S
,
Gallagher M
.
J Mol Diagn 2014 16 (5) 533-540
Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Jenkins MM
,
Reefhuis J
,
Gallagher ML
,
Mulle JG , Hoffmann TJ ,
Koontz DA
,
Sturchio C ,
Rasmussen SA
,
Witte JS ,
Richter P
,
Honein MA
.
Am J Med Genet A 2014 164A (6) 1454-63
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.
Jiang B , Ryan KA , Hamedani A , Cheng Y , Sparks MJ ,
Koontz D
,
Bean CJ
,
Gallagher M
,
Hooper WC
,
McArdle PF , O'Connell JR , Stine OC , Wozniak MA , Stern BJ , Mitchell BD , Kittner SJ , Cole JW .
Stroke 2014 45 (4) 961-7
Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects.
Gallagher ML
,
Sturchio C
,
Smith A ,
Koontz D
,
Jenkins MM
,
Honein MA
,
Rasmussen SA
.
Birth Defects Res A Clin Mol Teratol 2011 91 (7) 642-8
Rapid detection of the CYP2A6*12 hybrid allele by Pyrosequencing technology
Koontz DA
,
Huckins JJ , Spencer A ,
Gallagher ML
.
BMC Med Genet 2009 10 80
Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank.
Yang Quan-He, Botto Lorenzo D, Gallagher Margaret, Friedman J M, Sanders Christopher L, Koontz Deborah, Nikolova Stanimila, Erickson J David, Steinberg Karen. The American journal of clinical nutrition 2008 88(1) 232-46 .
The American journal of clinical nutrition 2008 88(1) 232-46
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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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