Similar articles for PMID: 18247058

Year	Number of Results
1996	1
1998	1
1999	3
2000	3
2001	4
2002	5
2003	4
2004	7
2005	4
2006	3
2007	6
2008	7
2009	5
2010	6
2011	4
2012	5
2013	4
2014	4
2015	8
2016	1
2017	3
2018	3
2019	1
2020	4
2021	3
2022	2
2023	1
2024	0

1

An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women.

Stanisławska-Sachadyn A, Brown KS, Mitchell LE, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. Stanisławska-Sachadyn A, et al. Hum Genet. 2008 Apr;123(3):289-95. doi: 10.1007/s00439-008-0475-y. Epub 2008 Feb 5. Hum Genet. 2008. PMID: 18247058

2

A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate.

Kalmbach RD, Choumenkovitch SF, Troen AP, Jacques PF, D'Agostino R, Selhub J. Kalmbach RD, et al. J Nutr. 2008 Dec;138(12):2323-7. doi: 10.3945/jn.108.096404. J Nutr. 2008. PMID: 19022952 Free PMC article.

3

The Dihydrofolate Reductase 19 bp Polymorphism Is Not Associated with Biomarkers of Folate Status in Healthy Young Adults, Irrespective of Folic Acid Intake.

Ozaki M, Molloy AM, Mills JL, Fan R, Wang Y, Gibney ER, Shane B, Brody LC, Parle-McDermott A. Ozaki M, et al. J Nutr. 2015 Oct;145(10):2207-11. doi: 10.3945/jn.115.216101. Epub 2015 Aug 12. J Nutr. 2015. PMID: 26269242 Free PMC article.

4

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations.

Kealey C, Brown KS, Woodside JV, Young I, Murray L, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Whitehead AS. Kealey C, et al. Hum Genet. 2005 Apr;116(5):347-53. doi: 10.1007/s00439-004-1243-2. Epub 2005 Jan 29. Hum Genet. 2005. PMID: 15682292

5

Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels.

Gellekink H, Blom HJ, van der Linden IJ, den Heijer M. Gellekink H, et al. Eur J Hum Genet. 2007 Jan;15(1):103-9. doi: 10.1038/sj.ejhg.5201713. Epub 2006 Sep 13. Eur J Hum Genet. 2007. PMID: 16969375

6

Dihydrofolate reductase 19-bp deletion polymorphism modifies the association of folate status with memory in a cross-sectional multi-ethnic study of adults.

Philip D, Buch A, Moorthy D, Scott TM, Parnell LD, Lai CQ, Ordovás JM, Selhub J, Rosenberg IH, Tucker KL, Troen AM. Philip D, et al. Am J Clin Nutr. 2015 Nov;102(5):1279-88. doi: 10.3945/ajcn.115.111054. Epub 2015 Sep 9. Am J Clin Nutr. 2015. PMID: 26354538 Free PMC article.

7

19-base pair deletion polymorphism of the dihydrofolate reductase (DHFR) gene: maternal risk of Down syndrome and folate metabolism.

Mendes CC, Biselli JM, Zampieri BL, Goloni-Bertollo EM, Eberlin MN, Haddad R, Riccio MF, Vannucchi H, Carvalho VM, Pavarino-Bertelli EC. Mendes CC, et al. Sao Paulo Med J. 2010 Jul;128(4):215-8. doi: 10.1590/s1516-31802010000400008. Sao Paulo Med J. 2010. PMID: 21120433 Free PMC article.

8

DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome.

Mendes CC, Raimundo AM, Oliveira LD, Zampieri BL, Marucci GH, Biselli JM, Goloni-Bertollo EM, Eberlin MN, Haddad R, Riccio MF, Vannucchi H, Carvalho VM, Pavarino ÉC. Mendes CC, et al. Genet Test Mol Biomarkers. 2013 Apr;17(4):274-7. doi: 10.1089/gtmb.2012.0293. Epub 2013 Feb 19. Genet Test Mol Biomarkers. 2013. PMID: 23421317 Free PMC article.

9

High concentrations of folate and unmetabolized folic acid in a cohort of pregnant Canadian women and umbilical cord blood.

Plumptre L, Masih SP, Ly A, Aufreiter S, Sohn KJ, Croxford R, Lausman AY, Berger H, O'Connor DL, Kim YI. Plumptre L, et al. Am J Clin Nutr. 2015 Oct;102(4):848-57. doi: 10.3945/ajcn.115.110783. Epub 2015 Aug 12. Am J Clin Nutr. 2015. PMID: 26269367 Free article.

10

Association of FOLH1, DHFR, and MTHFR gene polymorphisms with susceptibility of Neural Tube Defects: A case control study from Eastern India.

Paul S, Sadhukhan S, Munian D, Bankura B, Das M. Paul S, et al. Birth Defects Res. 2018 Aug 15;110(14):1129-1138. doi: 10.1002/bdr2.1365. Epub 2018 Aug 18. Birth Defects Res. 2018. PMID: 30120883

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

94 results

Results by year