Molloy AM - Search Results

1

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: molloy am. Am J Med Genet. 2002 Jan 15;107(2):151-5. doi: 10.1002/ajmg.10121. Am J Med Genet. 2002. PMID: 11807890

2

Effects of the disruption of transmethylation in the central nervous system: an animal model.

Scott JM, Molloy AM, Kennedy DG, Kennedy S, Weir DG. Scott JM, et al. Among authors: molloy am. Acta Neurol Scand Suppl. 1994;154:27-31. doi: 10.1111/j.1600-0404.1994.tb05406.x. Acta Neurol Scand Suppl. 1994. PMID: 7941962

3

Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects.

Kirke PN, Molloy AM, Daly LE, Burke H, Weir DG, Scott JM. Kirke PN, et al. Among authors: molloy am. Q J Med. 1993 Nov;86(11):703-8. Q J Med. 1993. PMID: 8265769

4

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, Weir DG, Shields DC, Scott JM. Whitehead AS, et al. Among authors: molloy am. QJM. 1995 Nov;88(11):763-6. QJM. 1995. PMID: 8542260

5

Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations.

Molloy AM, Daly S, Mills JL, Kirke PN, Whitehead AS, Ramsbottom D, Conley MR, Weir DG, Scott JM. Molloy AM, et al. Lancet. 1997 May 31;349(9065):1591-3. doi: 10.1016/S0140-6736(96)12049-3. Lancet. 1997. PMID: 9174561

6

Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method.

Molloy AM, Scott JM. Molloy AM, et al. Methods Enzymol. 1997;281:43-53. doi: 10.1016/s0076-6879(97)81007-5. Methods Enzymol. 1997. PMID: 9250965 No abstract available.

7

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.

Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM. Molloy AM, et al. Am J Med Genet. 1998 Jun 30;78(2):155-9. Am J Med Genet. 1998. PMID: 9674907

8

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS. Shields DC, et al. Among authors: molloy am. Am J Hum Genet. 1999 Apr;64(4):1045-55. doi: 10.1086/302310. Am J Hum Genet. 1999. PMID: 10090889 Free PMC article.

9

Gene-gene interactions and neural tube defects.

Whitehead AS, Molloy AM, Ramsbottom D, Weir DG, Kirke PN, Mills JL, Gallagher PM, Scott JM. Whitehead AS, et al. Among authors: molloy am. Clin Genet. 1999 Feb;55(2):133-4. doi: 10.1034/j.1399-0004.1999.550213.x. Clin Genet. 1999. PMID: 10189094 No abstract available.

10

Methylenetetrahydrofolate reductase thermolabile variant and oral clefts.

Mills JL, Kirke PN, Molloy AM, Burke H, Conley MR, Lee YJ, Mayne PD, Weir DG, Scott JM. Mills JL, et al. Among authors: molloy am. Am J Med Genet. 1999 Sep 3;86(1):71-4. Am J Med Genet. 1999. PMID: 10440833

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