Scott JM - Search Results

1

MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae.

Parle-McDermott A, Mills JL, Kirke PN, Cox C, Signore CC, Kirke S, Molloy AM, O'Leary VB, Pangilinan FJ, O'Herlihy C, Brody LC, Scott JM. Parle-McDermott A, et al. Among authors: scott jm. Am J Med Genet A. 2005 Feb 1;132A(4):365-8. doi: 10.1002/ajmg.a.30354. Am J Med Genet A. 2005. PMID: 15633187

2

MTRR and MTHFR polymorphism: link to Down syndrome?

O'Leary VB, Parle-McDermott A, Molloy AM, Kirke PN, Johnson Z, Conley M, Scott JM, Mills JL. O'Leary VB, et al. Among authors: scott jm. Am J Med Genet. 2002 Jan 15;107(2):151-5. doi: 10.1002/ajmg.10121. Am J Med Genet. 2002. PMID: 11807890

3

Maternal and fetal plasma homocysteine concentrations at birth: the influence of folate, vitamin B12, and the 5,10-methylenetetrahydrofolate reductase 677C-->T variant.

Molloy AM, Mills JL, McPartlin J, Kirke PN, Scott JM, Daly S. Molloy AM, et al. Among authors: scott jm. Am J Obstet Gynecol. 2002 Mar;186(3):499-503. doi: 10.1067/mob.2002.121105. Am J Obstet Gynecol. 2002. PMID: 11904614

4

Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.

Parle-McDermott A, Mills JL, Kirke PN, O'Leary VB, Swanson DA, Pangilinan F, Conley M, Molloy AM, Cox C, Scott JM, Brody LC. Parle-McDermott A, et al. Among authors: scott jm. J Hum Genet. 2003;48(4):190-3. doi: 10.1007/s10038-003-0008-4. Epub 2003 Mar 5. J Hum Genet. 2003. PMID: 12730722

5

Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study.

Kirke PN, Mills JL, Molloy AM, Brody LC, O'Leary VB, Daly L, Murray S, Conley M, Mayne PD, Smith O, Scott JM. Kirke PN, et al. Among authors: scott jm. BMJ. 2004 Jun 26;328(7455):1535-6. doi: 10.1136/bmj.38036.646030.EE. Epub 2004 May 21. BMJ. 2004. PMID: 15155469 Free PMC article. No abstract available.

6

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.

O'Leary VB, Mills JL, Pangilinan F, Kirke PN, Cox C, Conley M, Weiler A, Peng K, Shane B, Scott JM, Parle-McDermott A, Molloy AM, Brody LC; Members of the Birth Defects Research Group. O'Leary VB, et al. Among authors: scott jm. Mol Genet Metab. 2005 Jul;85(3):220-7. doi: 10.1016/j.ymgme.2005.02.003. Epub 2005 Mar 17. Mol Genet Metab. 2005. PMID: 15979034

7

A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss.

Parle-McDermott A, Pangilinan F, Mills JL, Signore CC, Molloy AM, Cotter A, Conley M, Cox C, Kirke PN, Scott JM, Brody LC. Parle-McDermott A, et al. Among authors: scott jm. Mol Hum Reprod. 2005 Jul;11(7):477-80. doi: 10.1093/molehr/gah204. Mol Hum Reprod. 2005. PMID: 16123074

8

Screening for new MTHFR polymorphisms and NTD risk.

O'Leary VB, Mills JL, Parle-McDermott A, Pangilinan F, Molloy AM, Cox C, Weiler A, Conley M, Kirke PN, Scott JM, Brody LC; Birth Defects Research Group. O'Leary VB, et al. Among authors: scott jm. Am J Med Genet A. 2005 Oct 1;138A(2):99-106. doi: 10.1002/ajmg.a.30846. Am J Med Genet A. 2005. PMID: 16145688

9

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.

Parle-McDermott A, Kirke PN, Mills JL, Molloy AM, Cox C, O'Leary VB, Pangilinan F, Conley M, Cleary L, Brody LC, Scott JM. Parle-McDermott A, et al. Among authors: scott jm. Eur J Hum Genet. 2006 Jun;14(6):768-72. doi: 10.1038/sj.ejhg.5201603. Eur J Hum Genet. 2006. PMID: 16552426

10

The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels.

Parle-McDermott A, Mills JL, Molloy AM, Carroll N, Kirke PN, Cox C, Conley MR, Pangilinan FJ, Brody LC, Scott JM. Parle-McDermott A, et al. Among authors: scott jm. Mol Genet Metab. 2006 Jul;88(3):290-4. doi: 10.1016/j.ymgme.2006.02.011. Epub 2006 Apr 18. Mol Genet Metab. 2006. PMID: 16621645

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