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Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis.

Kraus WE, Muoio DM, Stevens R, Craig D, Bain JR, Grass E, Haynes C, Kwee L, Qin X, Slentz DH, Krupp D, Muehlbauer M, Hauser ER, Gregory SG, Newgard CB, Shah SH.

PLoS Genet. 2015 Nov 5;11(11):e1005553. doi: 10.1371/journal.pgen.1005553. eCollection 2015 Nov.


Interaction Between the FOXO1A-209 Genotype and Tea Drinking Is Significantly Associated with Reduced Mortality at Advanced Ages.

Zeng Y, Chen H, Ni T, Ruan R, Nie C, Liu X, Feng L, Zhang F, Lu J, Li J, Li Y, Tao W, Gregory SG, Gottschalk W, Lutz MW, Land KC, Yashin A, Tan Q, Yang Z, Bolund L, Ming Q, Yang H, Min J, Willcox DC, Willcox BJ, Gu J, Hauser E, Tian XL, Vaupel JW.

Rejuvenation Res. 2016 Feb 10. [Epub ahead of print]


Epigenetic profiling identifies novel genes for ascending aortic aneurysm formation with bicuspid aortic valves.

Shah AA, Gregory SG, Krupp D, Feng S, Dorogi A, Haynes C, Grass E, Lin SS, Hauser ER, Kraus WE, Shah SH, Hughes GC.

Heart Surg Forum. 2015 Aug 30;18(4):E134-9. doi: 10.1532/hsf.1247.


Evidence for fumonisin inhibition of ceramide synthase in humans consuming maize-based foods and living in high exposure communities in Guatemala.

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

Mol Nutr Food Res. 2015 Nov;59(11):2209-24. doi: 10.1002/mnfr.201500499. Epub 2015 Sep 3.


Using circulating tumor cells to inform on prostate cancer biology and clinical utility.

Li J, Gregory SG, Garcia-Blanco MA, Armstrong AJ.

Crit Rev Clin Lab Sci. 2015;52(4):191-210. doi: 10.3109/10408363.2015.1023430. Epub 2015 Jun 16.


Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.

Shah AA, Haynes C, Craig DM, Sebek J, Grass E, Abramson K, Hauser E, Gregory SG, Kraus WE, Smith PK, Shah SH.

Heart Surg Forum. 2015 Feb 27;18(1):E1-5. doi: 10.1532/hsf.1214.


A blood spot method for detecting fumonisin-induced changes in putative sphingolipid biomarkers in LM/Bc mice and humans.

Riley RT, Showker JL, Lee CM, Zipperer CE, Mitchell TR, Voss KA, Zitomer NC, Torres O, Matute J, Gregory SG, Ashley-Koch AE, Maddox JR, Gardner N, Gelineau-Van Waes JB.

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2015;32(6):934-49. doi: 10.1080/19440049.2015.1027746. Epub 2015 Apr 10.


Association of Roadway Proximity with Fasting Plasma Glucose and Metabolic Risk Factors for Cardiovascular Disease in a Cross-Sectional Study of Cardiac Catheterization Patients.

Ward-Caviness CK, Kraus WE, Blach C, Haynes CS, Dowdy E, Miranda ML, Devlin RB, Diaz-Sanchez D, Cascio WE, Mukerjee S, Stallings C, Smith LA, Gregory SG, Shah SH, Hauser ER, Neas LM.

Environ Health Perspect. 2015 Oct;123(10):1007-14. doi: 10.1289/ehp.1306980. Epub 2015 Mar 24.


Comparison of GC-MS and GC×GC-MS in the analysis of human serum samples for biomarker discovery.

Winnike JH, Wei X, Knagge KJ, Colman SD, Gregory SG, Zhang X.

J Proteome Res. 2015 Apr 3;14(4):1810-7. doi: 10.1021/pr5011923. Epub 2015 Mar 16.


Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.

Lock EF, Soldano KL, Garrett ME, Cope H, Markunas CA, Fuchs H, Grant G, Dunson DB, Gregory SG, Ashley-Koch AE.

BMC Genomics. 2015 Jan 22;16:11. doi: 10.1186/s12864-014-1211-8.


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.


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.


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.


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.


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.


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.


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.


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.


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.


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.

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