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Results: 1 to 20 of 89

1.

Missing genetic risk in neural tube defects: can exome sequencing yield an insight?

Krupp DR, Soldano KL, Garrett ME, Cope H, Ashley-Koch AE, Gregory SG.

Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):642-6. doi: 10.1002/bdra.23276. Epub 2014 Jul 21.

PMID:
25044326
[PubMed - in process]
Free PMC Article
2.

Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics.

Markunas CA, Lock E, Soldano K, Cope H, Ding CK, Enterline DS, Grant G, Fuchs H, Ashley-Koch AE, Gregory SG.

BMC Med Genomics. 2014 Jun 25;7:39. doi: 10.1186/1755-8794-7-39.

PMID:
24962150
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG; FECD Genetics Consortium.

Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4577-84. doi: 10.1167/iovs.13-13517.

PMID:
24917144
[PubMed - indexed for MEDLINE]
4.

Induction or augmentation of labor and autism--reply.

Miranda ML, Anthopolos R, Gregory SG.

JAMA Pediatr. 2014 Feb;168(2):191-2. doi: 10.1001/jamapediatrics.2013.4792. No abstract available.

PMID:
24492875
[PubMed - indexed for MEDLINE]
5.

Genetic predisposition of behavioral response.

Gregory SG.

Proc Natl Acad Sci U S A. 2014 Feb 4;111(5):1672-3. doi: 10.1073/pnas.1323421111. Epub 2014 Jan 21. No abstract available.

PMID:
24449895
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Association of autism with induced or augmented childbirth.

Miranda ML, Anthopolos R, Gregory SG.

Am J Obstet Gynecol. 2014 May;210(5):492-3. doi: 10.1016/j.ajog.2013.12.038. Epub 2013 Dec 28. No abstract available.

PMID:
24380745
[PubMed - indexed for MEDLINE]
7.

Urinary fumonisin B1 and estimated fumonisin intake in women from high- and low-exposure communities in Guatemala.

Torres O, Matute J, Gelineau-van Waes J, Maddox JR, Gregory SG, Ashley-Koch AE, Showker JL, Zitomer NC, Voss KA, Riley RT.

Mol Nutr Food Res. 2014 May;58(5):973-83. doi: 10.1002/mnfr.201300481. Epub 2013 Dec 23.

PMID:
24375966
[PubMed - indexed for MEDLINE]
8.

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.

Markunas CA, Enterline DS, Dunlap K, Soldano K, Cope H, Stajich J, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE.

Ann Hum Genet. 2014 Jan;78(1):1-12. doi: 10.1111/ahg.12041. Epub 2013 Oct 6.

PMID:
24359474
[PubMed - indexed for MEDLINE]
9.

Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.

Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG.

Mol Vis. 2013 Dec 12;19:2508-16. eCollection 2013.

PMID:
24348007
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.

Soldano KL, Garrett ME, Cope HL, Rusnak JM, Ellis NJ, Dunlap KL, Speer MC, Gregory SG, Ashley-Koch AE.

Birth Defects Res B Dev Reprod Toxicol. 2013 Oct;98(5):365-73. doi: 10.1002/bdrb.21079. Epub 2013 Dec 9.

PMID:
24323870
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Interactions between social/ behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China.

Zeng Y, Cheng L, Zhao L, Tan Q, Feng Q, Chen H, Shen K, Li J, Zhang F, Cao H, Gregory SG, Yang Z, Gu J, Tao W, Tian XL, Hauser ER.

BMC Geriatr. 2013 Sep 9;13:91. doi: 10.1186/1471-2318-13-91.

PMID:
24016068
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Association of autism with induced or augmented childbirth in North Carolina Birth Record (1990-1998) and Education Research (1997-2007) databases.

Gregory SG, Anthopolos R, Osgood CE, Grotegut CA, Miranda ML.

JAMA Pediatr. 2013 Oct;167(10):959-66. doi: 10.1001/jamapediatrics.2013.2904.

PMID:
23938610
[PubMed - indexed for MEDLINE]
13.

Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.

Nolan D, Kraus WE, Hauser E, Li YJ, Thompson DK, Johnson J, Chen HC, Nelson S, Haynes C, Gregory SG, Kraus VB, Shah SH.

PLoS One. 2013 Aug 2;8(8):e71779. doi: 10.1371/journal.pone.0071779. Print 2013.

PMID:
23936524
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.

Connelly JJ, Cherepanova OA, Doss JF, Karaoli T, Lillard TS, Markunas CA, Nelson S, Wang T, Ellis PD, Langford CF, Haynes C, Seo DM, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, Hauser ER, Gregory SG.

Hum Mol Genet. 2013 Dec 20;22(25):5107-20. doi: 10.1093/hmg/ddt365. Epub 2013 Aug 2.

PMID:
23912340
[PubMed - indexed for MEDLINE]
15.

Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.

Ward-Caviness C, Haynes C, Blach C, Dowdy E, Gregory SG, Shah SH, Horne BD, Kraus WE, Hauser ER.

Hum Genet. 2013 Dec;132(12):1371-82. doi: 10.1007/s00439-013-1339-7. Epub 2013 Aug 2.

PMID:
23907653
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

Markunas CA, Soldano K, Dunlap K, Cope H, Asiimwe E, Stajich J, Enterline D, Grant G, Fuchs H, Gregory SG, Ashley-Koch AE.

PLoS One. 2013 Apr 19;8(4):e61521. doi: 10.1371/journal.pone.0061521. Print 2013.

PMID:
23620759
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Cleavage and polyadenylation specificity factor 1 (CPSF1) regulates alternative splicing of interleukin 7 receptor (IL7R) exon 6.

Evsyukova I, Bradrick SS, Gregory SG, Garcia-Blanco MA.

RNA. 2013 Jan;19(1):103-15. doi: 10.1261/rna.035410.112. Epub 2012 Nov 14.

PMID:
23151878
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

The kinetics of urinary fumonisin B1 excretion in humans consuming maize-based diets.

Riley RT, Torres O, Showker JL, Zitomer NC, Matute J, Voss KA, Gelineau-van Waes J, Maddox JR, Gregory SG, Ashley-Koch AE.

Mol Nutr Food Res. 2012 Sep;56(9):1445-55. doi: 10.1002/mnfr.201200166. Epub 2012 Jul 20.

PMID:
22815244
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).

Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2012 Sep;94(9):683-92. doi: 10.1002/bdra.23040. Epub 2012 Jul 18.

PMID:
22806986
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

Markunas CA, Tubbs RS, Moftakhar R, Ashley-Koch AE, Gregory SG, Oakes WJ, Speer MC, Iskandar BJ.

J Neurosurg Pediatr. 2012 Apr;9(4):372-8. doi: 10.3171/2011.12.PEDS11113.

PMID:
22462700
[PubMed - indexed for MEDLINE]
Free PMC Article
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