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Items: 1 to 20 of 27

1.

Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study.

Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Sconberg JL, Schmidt LC, Volk HE, Tassone F.

Early Hum Dev. 2015 Aug;91(8):483-9. doi: 10.1016/j.earlhumdev.2015.05.008. Epub 2015 Jun 11.

2.

Genetic variation affects congenital heart defect susceptibility in offspring exposed to maternal tobacco use.

Tang X, Hobbs CA, Cleves MA, Erickson SW, MacLeod SL, Malik S; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2015 Oct;103(10):834-42. doi: 10.1002/bdra.23370. Epub 2015 Jun 2.

PMID:
26033827
3.

Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation.

Tang X, Cleves MA, Nick TG, Li M, MacLeod SL, Erickson SW, Li J, Shaw GM, Mosley BS, Hobbs CA; National Birth Defects Prevention Study.

Am J Med Genet A. 2015 Jun;167(6):1231-42. doi: 10.1002/ajmg.a.36867. Epub 2015 Apr 2.

4.

Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects.

Tang X, Nick TG, Cleves MA, Erickson SW, Li M, Li J, MacLeod SL, Hobbs CA.

PLoS One. 2014 Oct 2;9(9):e108903. doi: 10.1371/journal.pone.0108903. eCollection 2014.

5.

Detecting disease variants in case-parent trio studies using the bioconductor software package trio.

Schwender H, Li Q, Neumann C, Taub MA, Younkin SG, Berger P, Scharpf RB, Beaty TH, Ruczinski I.

Genet Epidemiol. 2014 Sep;38(6):516-22. doi: 10.1002/gepi.21836. Epub 2014 Jul 21.

6.

Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways.

Hobbs CA, Cleves MA, Macleod SL, Erickson SW, Tang X, Li J, Li M, Nick T, Malik S; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2014 Feb;100(2):116-26. doi: 10.1002/bdra.23225. Epub 2014 Feb 18.

7.

A multi-locus likelihood method for assessing parent-of-origin effects using case-control mother-child pairs.

Lin D, Weinberg CR, Feng R, Hochner H, Chen J.

Genet Epidemiol. 2013 Feb;37(2):152-62. doi: 10.1002/gepi.21700. Epub 2012 Nov 26.

8.

PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling.

Howey R, Cordell HJ.

BMC Bioinformatics. 2012 Jun 27;13:149. doi: 10.1186/1471-2105-13-149.

9.

X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia.

Jugessur A, Skare Ø, Lie RT, Wilcox AJ, Christensen K, Christiansen L, Nguyen TT, Murray JC, Gjessing HK.

PLoS One. 2012;7(6):e39240. doi: 10.1371/journal.pone.0039240. Epub 2012 Jun 19.

10.

Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study.

Schmidt RJ, Tancredi DJ, Ozonoff S, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tassone F, Hertz-Picciotto I.

Am J Clin Nutr. 2012 Jul;96(1):80-9. doi: 10.3945/ajcn.110.004416. Epub 2012 May 30.

11.

Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exome.

Fardo DW, Druen AR, Liu J, Mirea L, Infante-Rivard C, Breheny P.

BMC Proc. 2011 Nov 29;5 Suppl 9:S28. doi: 10.1186/1753-6561-5-S9-S28.

12.

Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads.

Myking S, Myhre R, Gjessing HK, Morken NH, Sengpiel V, Williams SM, Ryckman KK, Magnus P, Jacobsson B.

BMC Med Genet. 2011 Dec 30;12:174. doi: 10.1186/1471-2350-12-174.

13.

Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism.

Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tancredi DJ, Tassone F, Hertz-Picciotto I.

Epidemiology. 2011 Jul;22(4):476-85. doi: 10.1097/EDE.0b013e31821d0e30.

14.

Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring.

Ainsworth HF, Unwin J, Jamison DL, Cordell HJ.

Genet Epidemiol. 2011 Jan;35(1):19-45. doi: 10.1002/gepi.20547.

15.

Caffeine, selected metabolic gene variants, and risk for neural tube defects.

Schmidt RJ, Romitti PA, Burns TL, Murray JC, Browne ML, Druschel CM, Olney RS; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):560-9. doi: 10.1002/bdra.20681.

16.

Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.

Healy J, Bourgey M, Richer C, Sinnett D, Roy-Gagnon MH.

J Biomed Biotechnol. 2010;2010:369534. doi: 10.1155/2010/369534. Epub 2010 Jun 9.

17.

Association of combined maternal-fetal TNF-alpha gene G308A genotypes with preterm delivery: a gene-gene interaction study.

Liang M, Wang X, Li J, Yang F, Fang Z, Wang L, Hu Y, Chen D.

J Biomed Biotechnol. 2010;2010:396184. doi: 10.1155/2010/396184. Epub 2010 Mar 9.

18.

Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms.

Sull JW, Liang KY, Hetmanski JB, Wu T, Fallin MD, Ingersoll RG, Park JW, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Park BY, Jee SH, Jabs EW, Redett R, Scott AF, Beaty TH.

Hum Genet. 2009 Sep;126(3):385-94. doi: 10.1007/s00439-009-0680-3. Epub 2009 May 15.

19.

Differential parental transmission of markers in BCL3 among Korean cleft case-parent trios.

Park BY, Sull JW, Park JY, Jee SH, Beaty TH.

J Prev Med Public Health. 2009 Jan;42(1):1-4. doi: 10.3961/jpmph.2009.42.1.1.

20.

Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations.

Sull JW, Liang KY, Hetmanski JB, Fallin MD, Ingersoll RG, Park J, Wu-Chou YH, Chen PK, Chong SS, Cheah F, Yeow V, Park BY, Jee SH, Jabs EW, Redett R, Scott AF, Beaty TH.

Eur J Hum Genet. 2009 Jun;17(6):831-9. doi: 10.1038/ejhg.2008.250. Epub 2009 Jan 14.

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