Brody LC - Search Results

1

The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.

Shane B, Pangilinan F, Mills JL, Fan R, Gong T, Cropp CD, Kim Y, Ueland PM, Bailey-Wilson JE, Wilson AF, Brody LC, Molloy AM. Shane B, et al. Among authors: brody lc. Am J Clin Nutr. 2018 Dec 1;108(6):1334-1341. doi: 10.1093/ajcn/nqy209. Am J Clin Nutr. 2018. PMID: 30339177 Free PMC article.

2

Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects.

Brody LC, Baker PJ, Chines PS, Musick A, Molloy AM, Swanson DA, Kirke PN, Ghosh S, Scott JM, Mills JL. Brody LC, et al. Mol Genet Metab. 1999 Aug;67(4):324-33. doi: 10.1006/mgme.1999.2881. Mol Genet Metab. 1999. PMID: 10444343

3

Targeted disruption of the methionine synthase gene in mice.

Swanson DA, Liu ML, Baker PJ, Garrett L, Stitzel M, Wu J, Harris M, Banerjee R, Shane B, Brody LC. Swanson DA, et al. Among authors: brody lc. Mol Cell Biol. 2001 Feb;21(4):1058-65. doi: 10.1128/MCB.21.4.1058-1065.2001. Mol Cell Biol. 2001. PMID: 11158293 Free PMC article.

4

A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.

Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, Molloy AM, O'Leary VB, Parle-McDermott A, Scott JM, Swanson DA. Brody LC, et al. Am J Hum Genet. 2002 Nov;71(5):1207-15. doi: 10.1086/344213. Epub 2002 Oct 16. Am J Hum Genet. 2002. PMID: 12384833 Free PMC article.

5

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: brody lc. 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

6

Analysis of the human folate receptor beta gene for an association with neural tube defects.

O'Leary VB, Mills JL, Kirke PN, Parle-McDermott A, Swanson DA, Weiler A, Pangilinan F, Conley M, Molloy AM, Lynch M, Cox C, Scott JM, Brody LC. O'Leary VB, et al. Among authors: brody lc. Mol Genet Metab. 2003 Jun;79(2):129-33. doi: 10.1016/s1096-7192(03)00075-1. Mol Genet Metab. 2003. PMID: 12809644

7

Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects.

Parle-McDermott A, McManus EJ, Mills JL, O'Leary VB, Pangilinan F, Cox C, Weiler A, Molloy AM, Conley M, Watson D, Scott JM, Brody LC, Kirke PN; Birth Defects Research Group. Parle-McDermott A, et al. Among authors: brody lc. Mol Genet Metab. 2003 Dec;80(4):463-8. doi: 10.1016/j.ymgme.2003.09.009. Mol Genet Metab. 2003. PMID: 14654360

8

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: brody lc. 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.

9

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: brody lc. 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

10

Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.

Swanson DA, Pangilinan F, Mills JL, Kirke PN, Conley M, Weiler A, Frey T, Parle-McDermott A, O'Leary VB, Seltzer RR, Moynihan KA, Molloy AM, Burke H, Scott JM, Brody LC. Swanson DA, et al. Among authors: brody lc. Birth Defects Res A Clin Mol Teratol. 2005 Apr;73(4):239-44. doi: 10.1002/bdra.20122. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15782407

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