Swanson DA - Search Results

1

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: swanson da. 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

2

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. Among authors: swanson da. 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.

3

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: swanson da. Mol Genet Metab. 2003 Jun;79(2):129-33. doi: 10.1016/s1096-7192(03)00075-1. Mol Genet Metab. 2003. PMID: 12809644

4

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. 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

5

Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.

Pangilinan F, Geiler K, Dolle J, Troendle J, Swanson DA, Molloy AM, Sutton M, Conley M, Kirke PN, Scott JM, Mills JL, Brody LC. Pangilinan F, et al. Among authors: swanson da. Am J Med Genet A. 2008 Oct 15;146A(20):2617-25. doi: 10.1002/ajmg.a.32504. Am J Med Genet A. 2008. PMID: 18798306 Free PMC article.

6

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. Among authors: swanson da. Mol Genet Metab. 1999 Aug;67(4):324-33. doi: 10.1006/mgme.1999.2881. Mol Genet Metab. 1999. PMID: 10444343

7

Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiae.

Dougherty KM, Swanson DA, Brody LC, Valle D. Dougherty KM, et al. Among authors: swanson da. Hum Mol Genet. 1993 Nov;2(11):1835-40. doi: 10.1093/hmg/2.11.1835. Hum Mol Genet. 1993. PMID: 8281144

8

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. 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.

9

Identification and characterization of the human ortholog of rat STXBP1, a protein implicated in vesicle trafficking and neurotransmitter release.

Swanson DA, Steel JM, Valle D. Swanson DA, et al. Genomics. 1998 Mar 15;48(3):373-6. doi: 10.1006/geno.1997.5202. Genomics. 1998. PMID: 9545644 Free article.

10

Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors.

Swanson DA, Chang JT, Campochiaro PA, Zack DJ, Valle D. Swanson DA, et al. Invest Ophthalmol Vis Sci. 1998 Oct;39(11):2085-94. Invest Ophthalmol Vis Sci. 1998. PMID: 9761287

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