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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.
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.
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
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
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
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
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.
A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders.
Swanson DA, Freund CL, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Hum Mol Genet. 1996 Apr;5(4):533-8. doi: 10.1093/hmg/5.4.533. Hum Mol Genet. 1996. PMID: 8845848
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
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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