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Items: 1 to 20 of 24

1.

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.

Pangilinan F, Molloy AM, Mills JL, Troendle JF, Parle-McDermott A, Kay DM, Browne ML, McGrath EC, Abaan HO, Sutton M, Kirke PN, Caggana M, Shane B, Scott JM, Brody LC.

BMC Med Genet. 2014 Oct 8;15:102. doi: 10.1186/s12881-014-0102-9.

2.

Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects.

Mills JL, Fan R, Brody LC, Liu A, Ueland PM, Wang Y, Kirke PN, Shane B, Molloy AM.

Am J Clin Nutr. 2014 Oct;100(4):1069-74. doi: 10.3945/ajcn.113.079319.

3.

Is low iron status a risk factor for neural tube defects?

Molloy AM, Einri CN, Jain D, Laird E, Fan R, Wang Y, Scott JM, Shane B, Brody LC, Kirke PN, Mills JL.

Birth Defects Res A Clin Mol Teratol. 2014 Feb;100(2):100-6. doi: 10.1002/bdra.23223.

4.

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.

Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, Mirel DB, Kim Y, Cropp CD, Molloy AM, Kirke PN, Bailey-Wilson JE, Wilson AF, Mills JL, Scott JM, Brody LC, Li JZ, Ginsburg D.

Proc Natl Acad Sci U S A. 2013 Jan 8;110(2):588-93. doi: 10.1073/pnas.1219885110.

5.

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.

Pangilinan F, Molloy AM, Mills JL, Troendle JF, Parle-McDermott A, Signore C, O'Leary VB, Chines P, Seay JM, Geiler-Samerotte K, Mitchell A, VanderMeer JE, Krebs KM, Sanchez A, Cornman-Homonoff J, Stone N, Conley M, Kirke PN, Shane B, Scott JM, Brody LC.

BMC Med Genet. 2012 Aug 2;13:62.

6.

Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genes.

Stone N, Pangilinan F, Molloy AM, Shane B, Scott JM, Ueland PM, Mills JL, Kirke PN, Sethupathy P, Brody LC.

PLoS One. 2011;6(7):e21851. doi: 10.1371/journal.pone.0021851.

7.

Do high blood folate concentrations exacerbate metabolic abnormalities in people with low vitamin B-12 status?

Mills JL, Carter TC, Scott JM, Troendle JF, Gibney ER, Shane B, Kirke PN, Ueland PM, Brody LC, Molloy AM.

Am J Clin Nutr. 2011 Aug;94(2):495-500. doi: 10.3945/ajcn.111.014621.

8.

Maternal folate, vitamin B12 and homocysteine levels in pregnancies affected by congenital malformations other than neural tube defects.

Sutton M, Mills JL, Molloy AM, Troendle JF, Brody LC, Conley M, Mc Donnell R, Scott JM, Kirke PN.

Birth Defects Res A Clin Mol Teratol. 2011 Jul;91(7):610-5. doi: 10.1002/bdra.20817. No abstract available.

9.

Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

Carter TC, Pangilinan F, Troendle JF, Molloy AM, VanderMeer J, Mitchell A, Kirke PN, Conley MR, Shane B, Scott JM, Brody LC, Mills JL.

Am J Med Genet A. 2011 Jan;155A(1):14-21. doi: 10.1002/ajmg.a.33755.

10.

Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.

Pangilinan F, Mitchell A, VanderMeer J, Molloy AM, Troendle J, Conley M, Kirke PN, Sutton M, Sequeira JM, Quadros EV, Scott JM, Mills JL, Brody LC.

J Med Genet. 2010 Oct;47(10):677-85. doi: 10.1136/jmg.2009.073775. Erratum in: J Med Genet. 2012 Dec;49(12):784.

11.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.

Beaty TH, Murray JC, Marazita ML, Munger RG, Ruczinski I, Hetmanski JB, Liang KY, Wu T, Murray T, Fallin MD, Redett RA, Raymond G, Schwender H, Jin SC, Cooper ME, Dunnwald M, Mansilla MA, Leslie E, Bullard S, Lidral AC, Moreno LM, Menezes R, Vieira AR, Petrin A, Wilcox AJ, Lie RT, Jabs EW, Wu-Chou YH, Chen PK, Wang H, Ye X, Huang S, Yeow V, Chong SS, Jee SH, Shi B, Christensen K, Melbye M, Doheny KF, Pugh EW, Ling H, Castilla EE, Czeizel AE, Ma L, Field LL, Brody L, Pangilinan F, Mills JL, Molloy AM, Kirke PN, Scott JM, Arcos-Burgos M, Scott AF.

Nat Genet. 2010 Jun;42(6):525-9. doi: 10.1038/ng.580. Erratum in: Nat Genet. 2010 Aug;42(8):727. Scott, James M [corrected to Scott, John M].

12.

Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.

Carter TC, Molloy AM, Pangilinan F, Troendle JF, Kirke PN, Conley MR, Orr DJ, Earley M, McKiernan E, Lynn EC, Doyle A, Scott JM, Brody LC, Mills JL.

Birth Defects Res A Clin Mol Teratol. 2010 Feb;88(2):84-93. doi: 10.1002/bdra.20639.

13.

A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency.

Parle-McDermott A, Pangilinan F, O'Brien KK, Mills JL, Magee AM, Troendle J, Sutton M, Scott JM, Kirke PN, Molloy AM, Brody LC.

Hum Mutat. 2009 Dec;30(12):1650-6. doi: 10.1002/humu.21109.

14.

Lack of association between folate-receptor autoantibodies and neural-tube defects.

Molloy AM, Quadros EV, Sequeira JM, Troendle JF, Scott JM, Kirke PN, Mills JL.

N Engl J Med. 2009 Jul 9;361(2):152-60. doi: 10.1056/NEJMoa0803783.

15.

Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification.

Molloy AM, Kirke PN, Troendle JF, Burke H, Sutton M, Brody LC, Scott JM, Mills JL.

Pediatrics. 2009 Mar;123(3):917-23. doi: 10.1542/peds.2008-1173.

16.

Uncoupling protein 2 polymorphisms as risk factors for NTDs.

Mitchell A, Pangilinan F, Van der Meer J, Molloy AM, Troendle J, Conley M, Kirke PN, Scott JM, Brody LC, Mills JL.

Birth Defects Res A Clin Mol Teratol. 2009 Feb;85(2):156-60. doi: 10.1002/bdra.20520.

17.

Analysis of the MTHFD1 promoter and risk of neural tube defects.

Carroll N, Pangilinan F, Molloy AM, Troendle J, Mills JL, Kirke PN, Brody LC, Scott JM, Parle-McDermott A.

Hum Genet. 2009 Apr;125(3):247-56. doi: 10.1007/s00439-008-0616-3.

18.

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.

Am J Med Genet A. 2008 Oct 15;146A(20):2617-25. doi: 10.1002/ajmg.a.32504.

19.

Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.

Mills JL, Molloy AM, Parle-McDermott A, Troendle JF, Brody LC, Conley MR, Cox C, Pangilinan F, Orr DJ, Earley M, McKiernan E, Lynn EC, Doyle A, Scott JM, Kirke PN.

Birth Defects Res A Clin Mol Teratol. 2008 Sep;82(9):636-43. doi: 10.1002/bdra.20491.

20.

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.

BMJ. 2004 Jun 26;328(7455):1535-6. No abstract available.

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