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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: Sep 30, 2024
. (Total: 6327 publications)
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Records 1-6 (of 6 Records)
Query Trace:
Berry RJ[original query]
Genomic DNA methylation changes in response to folic acid supplementation in a population-based intervention study among women of reproductive age.
Crider KS
,
Quinlivan EP ,
Berry RJ
,
Hao L , Li Z , Maneval D , Yang TP ,
Rasmussen SA
,
Yang Q
,
Zhu JH ,
Hu DJ
,
Bailey LB .
PLoS One 2011 6 (12) e28144
Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's role.
Crider KS
,
Yang TP ,
Berry RJ
,
Bailey LB .
Adv Nutr 2012 3 (1) 21-38
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
Maternal Periconceptional Folic Acid Supplementation and DNA Methylation Patterns in Adolescent Offspring.
Crider KS , Wang A , Ling H , Potischman N , Bailey RL , Lichen Y ,
Pfeiffer CM
,
Killian JK , Rose C , Sampson J , Zhu L , Berry RJ , Linet M , Yu W , Su LJ .
J Nutr 2023 152 (12) 2669-2676
Assessing the association between the methylenetetrahydrofolate reductase (MTHFR) 677C>T polymorphism and blood folate concentrations: a systematic review and meta-analysis of trials and observational studies.
Tsang BL ,
Devine OJ
,
Cordero AM
,
Marchetta CM ,
Mulinare J
,
Mersereau P
,
Guo J
,
Qi YP ,
Berry RJ
,
Rosenthal J
,
Crider KS
,
Hamner HC
.
Am J Clin Nutr 2015 101 (6) 1286-94
MTHFR 677C->T genotype is associated with folate and homocysteine concentrations in a large, population-based, double-blind trial of folic acid supplementation.
Crider KS
,
Zhu JH , Hao L ,
Yang QH
,
Yang TP ,
Gindler J
,
Maneval DR , Quinlivan EP , Li Z , Bailey LB ,
Berry RJ
.
Am J Clin Nutr 2011 93 (6) 1365-72
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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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