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Results: 1 to 20 of 89

1.

Genome-wide association study of maternal and inherited loci for conotruncal heart defects.

Agopian AJ, Mitchell LE, Glessner J, Bhalla AD, Sewda A, Hakonarson H, Goldmuntz E.

PLoS One. 2014 May 6;9(5):e96057. doi: 10.1371/journal.pone.0096057. eCollection 2014.

PMID:
24800985
[PubMed - in process]
Free PMC Article
2.

Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.

Mitchell LE, Agopian AJ, Bhalla A, Glessner JT, Kim CE, Swartz MD, Hakonarson H, Goldmuntz E.

Hum Mol Genet. 2015 Jan 1;24(1):265-73. doi: 10.1093/hmg/ddu420. Epub 2014 Aug 18.

PMID:
25138779
[PubMed - in process]
3.

Evaluation of heterogeneity in the association between congenital heart defects and variants of folate metabolism genes: conotruncal and left-sided cardiac defects.

Long J, Lupo PJ, Goldmuntz E, Mitchell LE.

Birth Defects Res A Clin Mol Teratol. 2011 Oct;91(10):879-84. doi: 10.1002/bdra.22849. Epub 2011 Aug 24.

PMID:
21987465
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
24535845
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
25275547
[PubMed - in process]
Free PMC Article
6.

MI-GWAS: a SAS platform for the analysis of inherited and maternal genetic effects in genome-wide association studies using log-linear models.

Agopian AJ, Mitchell LE.

BMC Bioinformatics. 2011 Apr 22;12:117. doi: 10.1186/1471-2105-12-117.

PMID:
21513519
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.

Noth I, Zhang Y, Ma SF, Flores C, Barber M, Huang Y, Broderick SM, Wade MS, Hysi P, Scuirba J, Richards TJ, Juan-Guardela BM, Vij R, Han MK, Martinez FJ, Kossen K, Seiwert SD, Christie JD, Nicolae D, Kaminski N, Garcia JG.

Lancet Respir Med. 2013 Jun;1(4):309-17. doi: 10.1016/S2213-2600(13)70045-6. Epub 2013 Apr 17.

PMID:
24429156
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Variants of folate metabolism genes and risk of left-sided cardiac defects.

Mitchell LE, Long J, Garbarini J, Paluru P, Goldmuntz E.

Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):48-53. doi: 10.1002/bdra.20622.

PMID:
19777601
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects.

Lupo PJ, Goldmuntz E, Mitchell LE.

J Biomed Biotechnol. 2010;2010:630940. doi: 10.1155/2010/630940. Epub 2010 Jan 12.

PMID:
20111745
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The keeshond defect in cardiac conotruncal development is oligogenic.

Werner P, Raducha MG, Prociuk U, Ostrander EA, Spielman RS, Kirkness EF, Patterson DF, Henthorn PS.

Hum Genet. 2005 Apr;116(5):368-77. Epub 2005 Feb 12.

PMID:
15711798
[PubMed - indexed for MEDLINE]
11.

Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.

Li M, Erickson SW, Hobbs CA, Li J, Tang X, Nick TG, Macleod SL, Cleves MA; National Birth Defect Prevention Study.

Genet Epidemiol. 2014 Apr;38(3):198-208. doi: 10.1002/gepi.21793. Epub 2014 Mar 2.

PMID:
24585533
[PubMed - indexed for MEDLINE]
12.

Comparative mapping of the DiGeorge region in the dog and exclusion of linkage to inherited canine conotruncal heart defects.

Werner P, Raducha MG, Prociuk U, Budarf M, Henthorn PS, Patterson DF.

J Hered. 1999 Jul-Aug;90(4):494-8.

PMID:
10485139
[PubMed - indexed for MEDLINE]
Free Article
13.

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K.

BMC Med Genet. 2011 Dec 21;12:169. doi: 10.1186/1471-2350-12-169.

PMID:
22185286
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Shaw GM, Iovannisci DM, Yang W, Finnell RH, Carmichael SL, Cheng S, Lammer EJ.

Am J Med Genet A. 2005 Sep 15;138(1):21-6.

PMID:
16100725
[PubMed - indexed for MEDLINE]
15.

Variants of folate metabolism genes and the risk of conotruncal cardiac defects.

Goldmuntz E, Woyciechowski S, Renstrom D, Lupo PJ, Mitchell LE.

Circ Cardiovasc Genet. 2008 Dec;1(2):126-32. doi: 10.1161/CIRCGENETICS.108.796342. Epub 2008 Dec 9.

PMID:
20031554
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.

Tin A, Woodward OM, Kao WH, Liu CT, Lu X, Nalls MA, Shriner D, Semmo M, Akylbekova EL, Wyatt SB, Hwang SJ, Yang Q, Zonderman AB, Adeyemo AA, Palmer C, Meng Y, Reilly M, Shlipak MG, Siscovick D, Evans MK, Rotimi CN, Flessner MF, Köttgen M, Cupples LA, Fox CS, Köttgen A; CARe and CHARGE Consortia.

Hum Mol Genet. 2011 Oct 15;20(20):4056-68. doi: 10.1093/hmg/ddr307. Epub 2011 Jul 18.

PMID:
21768215
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

Kim J, Stirling KJ, Cooper ME, Ascoli M, Momany AM, McDonald EL, Ryckman KK, Rhea L, Schaa KL, Cosentino V, Gadow E, Saleme C, Shi M, Hallman M, Plunkett J, Teramo KA, Muglia LJ, Feenstra B, Geller F, Boyd HA, Melbye M, Marazita ML, Dagle JM, Murray JC.

BMC Med Genet. 2013 Jul 26;14:77. doi: 10.1186/1471-2350-14-77.

PMID:
23889750
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J.

Hum Mol Genet. 2012 Apr 15;21(8):1897-906. doi: 10.1093/hmg/ddr607. Epub 2011 Dec 30.

PMID:
22210626
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.

Carty CL, Spencer KL, Setiawan VW, Fernandez-Rhodes L, Malinowski J, Buyske S, Young A, Jorgensen NW, Cheng I, Carlson CS, Brown-Gentry K, Goodloe R, Park A, Parikh NI, Henderson B, Le Marchand L, Wactawski-Wende J, Fornage M, Matise TC, Hindorff LA, Arnold AM, Haiman CA, Franceschini N, Peters U, Crawford DC.

Hum Reprod. 2013 Jun;28(6):1695-706. doi: 10.1093/humrep/det071. Epub 2013 Mar 18.

PMID:
23508249
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Genome-wide association study identifies multiple loci associated with bladder cancer risk.

Figueroa JD, Ye Y, Siddiq A, Garcia-Closas M, Chatterjee N, Prokunina-Olsson L, Cortessis VK, Kooperberg C, Cussenot O, Benhamou S, Prescott J, Porru S, Dinney CP, Malats N, Baris D, Purdue M, Jacobs EJ, Albanes D, Wang Z, Deng X, Chung CC, Tang W, Bas Bueno-de-Mesquita H, Trichopoulos D, Ljungberg B, Clavel-Chapelon F, Weiderpass E, Krogh V, Dorronsoro M, Travis R, Tjønneland A, Brenan P, Chang-Claude J, Riboli E, Conti D, Gago-Dominguez M, Stern MC, Pike MC, Van Den Berg D, Yuan JM, Hohensee C, Rodabough R, Cancel-Tassin G, Roupret M, Comperat E, Chen C, De Vivo I, Giovannucci E, Hunter DJ, Kraft P, Lindstrom S, Carta A, Pavanello S, Arici C, Mastrangelo G, Kamat AM, Lerner SP, Barton Grossman H, Lin J, Gu J, Pu X, Hutchinson A, Burdette L, Wheeler W, Kogevinas M, Tardón A, Serra C, Carrato A, García-Closas R, Lloreta J, Schwenn M, Karagas MR, Johnson A, Schned A, Armenti KR, Hosain GM, Andriole G Jr, Grubb R 3rd, Black A, Ryan Diver W, Gapstur SM, Weinstein SJ, Virtamo J, Haiman CA, Landi MT, Caporaso N, Fraumeni JF Jr, Vineis P, Wu X, Silverman DT, Chanock S, Rothman N.

Hum Mol Genet. 2014 Mar 1;23(5):1387-98. doi: 10.1093/hmg/ddt519. Epub 2013 Oct 24.

PMID:
24163127
[PubMed - indexed for MEDLINE]

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