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Items: 1 to 20 of 114

1.

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.

PMID:
19137581
2.

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.

PMID:
22856873
3.

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.

PMID:
20577008
4.

Screening for new MTHFR polymorphisms and NTD risk.

O'Leary VB, Mills JL, Parle-McDermott A, Pangilinan F, Molloy AM, Cox C, Weiler A, Conley M, Kirke PN, Scott JM, Brody LC; Birth Defects Research Group..

Am J Med Genet A. 2005 Oct 1;138A(2):99-106.

PMID:
16145688
5.

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V.

Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7.

PMID:
11813127
6.

Thymidylate synthase repeat polymorphisms and risk of neural tube defects in a population from the northern United Kingdom.

Wilding CS, Relton CL, Sutton MJ, Jonas PA, Lynch SA, Tawn EJ, Burn J.

Birth Defects Res A Clin Mol Teratol. 2004 Jul;70(7):483-5.

PMID:
15259039
7.

Uncoupling protein-2 polymorphisms in type 2 diabetes, obesity, and insulin secretion.

Wang H, Chu WS, Lu T, Hasstedt SJ, Kern PA, Elbein SC.

Am J Physiol Endocrinol Metab. 2004 Jan;286(1):E1-7.

PMID:
12915397
8.

Association between a 45-bp 3'untranslated insertion/deletion polymorphism in exon 8 of UCP2 gene and neural tube defects in a high-risk area of China.

Wang J, Liu C, Zhao H, Wang F, Guo J, Xie H, Lu X, Bao Y, Pei L, Niu B, Zhong R, Zheng X, Zhang T.

Reprod Sci. 2011 Jun;18(6):556-60. doi: 10.1177/1933719110393026.

PMID:
21266666
9.

Uncoupling protein 2 -866G/A and uncoupling protein 3 -55C/T polymorphisms in young South African Indian coronary artery disease patients.

Phulukdaree A, Moodley D, Khan S, Chuturgoon AA.

Gene. 2013 Jul 25;524(2):79-83. doi: 10.1016/j.gene.2013.04.048. Review.

PMID:
23639961
10.

UCP2 A55V variant is associated with obesity and related phenotypes in an aboriginal community in Taiwan.

Wang TN, Huang MC, Lin HL, Hsiang CH, Ko AM, Chang WT, Ko YC.

Int J Obes (Lond). 2007 Nov;31(11):1746-52.

PMID:
17502873
11.

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria.

Houcher B, Bourouba R, Djabi F, Yilmaz E, Eğin Y, Akar N.

Pediatr Neurosurg. 2009;45(6):472-7. doi: 10.1159/000283086.

PMID:
20160465
12.

Mitochondrial uncoupling protein 2 (UCP2) gene polymorphisms are associated with childhood obesity and related metabolic disorders.

Oguzkan-Balci S, Col-Araz N, Nacak M, Araz M, Sabanci H, Balat A, Pehlivan S.

J Pediatr Endocrinol Metab. 2013;26(3-4):277-83. doi: 10.1515/jpem-2012-0267.

PMID:
23314523
13.

Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts.

VanderMeer JE, Carter TC, Pangilinan F, Mitchell A, Kurnat-Thoma E, Kirke PN, Troendle JF, Molloy AM, Munger RG, Feldkamp ML, Mansilla MA, Mills JL, Murray JC, Brody LC.

Am J Med Genet A. 2016 Apr;170A(4):1007-16. doi: 10.1002/ajmg.a.37539.

PMID:
26789141
14.

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.

PMID:
21204206
15.

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.

Birth Defects Res A Clin Mol Teratol. 2005 Apr;73(4):239-44.

PMID:
15782407
16.

Genetic association of adipokine and UCP2 polymorphism with recurrent miscarriage among non-obese women.

Verma PK, Prakash S, Parveen F, Faridi RM, Agrawal S.

Reprod Biomed Online. 2012 Nov;25(5):527-35. doi: 10.1016/j.rbmo.2012.07.006. Erratum in: Reprod Biomed Online. 2013 Apr;26(4):407.

PMID:
22995745
17.

Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.

Volcik KA, Shaw GM, Zhu H, Lammer EJ, Finnell RH.

Birth Defects Res A Clin Mol Teratol. 2003 Mar;67(3):158-61.

PMID:
12797456
18.

Reduced folate carrier polymorphism (80A-->G) and neural tube defects.

De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V.

Eur J Hum Genet. 2003 Mar;11(3):245-52.

PMID:
12673279
19.

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V.

J Hum Genet. 2002;47(6):319-24.

PMID:
12111380
20.

Reduced folate carrier polymorphisms and neural tube defect risk.

O'leary VB, Pangilinan F, Cox C, Parle-McDermott A, Conley M, Molloy AM, Kirke PN, Mills JL, Brody LC, Scott JM; Members of the Birth Defects Research Group..

Mol Genet Metab. 2006 Apr;87(4):364-9.

PMID:
16343969

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