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Items: 1 to 20 of 201

1.

Fatty acids linked to cardiovascular mortality are associated with risk factors.

Ebbesson SO, Voruganti VS, Higgins PB, Fabsitz RR, Ebbesson LO, Laston S, Harris WS, Kennish J, Umans BD, Wang H, Devereux RB, Okin PM, Weissman NJ, MacCluer JW, Umans JG, Howard BV.

Int J Circumpolar Health. 2015 Aug 12;74:28055. doi: 10.3402/ijch.v74.28055. eCollection 2015.

2.

Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.

Laston SL, Voruganti VS, Haack K, Shah VO, Bobelu A, Bobelu J, Ghahate D, Harford AM, Paine SS, Tentori F, Cole SA, MacCluer JW, Comuzzie AG, Zager PG.

Front Genet. 2015 Jan 30;6:6. doi: 10.3389/fgene.2015.00006. eCollection 2015.

3.

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees.

Bickeböller H, Bailey JN, Beyene J, Cantor RM, Cordell HJ, Culverhouse RC, Engelman CD, Fardo DW, Ghosh S, König IR, Lorenzo Bermejo J, Melton PE, Santorico SA, Satten GA, Sun L, Tintle NL, Ziegler A, MacCluer JW, Almasy L.

BMC Proc. 2014 Jun 17;8(Suppl 1):S1. doi: 10.1186/1753-6561-8-S1-S1. eCollection 2014.

4.

Both rare and common variants in PCSK9 influence plasma low-density lipoprotein cholesterol level in American Indians.

Tsai CW, North KE, Tin A, Haack K, Franceschini N, Saroja Voruganti V, Laston S, Zhang Y, Best LG, MacCluer JW, Beaty TH, Navas-Acien A, Kao WH, Howard BV.

J Clin Endocrinol Metab. 2015 Feb;100(2):E345-9. doi: 10.1210/jc.2014-3340. Epub 2014 Nov 20.

5.

Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans.

Voruganti VS, Kent JW Jr, Debnath S, Cole SA, Haack K, Göring HH, Carless MA, Curran JE, Johnson MP, Almasy L, Dyer TD, Maccluer JW, Moses EK, Abboud HE, Mahaney MC, Blangero J, Comuzzie AG.

Front Genet. 2013 Dec 16;4:279. doi: 10.3389/fgene.2013.00279. eCollection 2013.

6.

Generalization of associations of kidney-related genetic loci to American Indians.

Franceschini N, Haack K, Almasy L, Laston S, Lee ET, Best LG, Fabsitz RR, MacCluer JW, Howard BV, Umans JG, Cole SA.

Clin J Am Soc Nephrol. 2014 Jan;9(1):150-8. doi: 10.2215/CJN.02300213. Epub 2013 Dec 5.

7.

Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians.

Voruganti VS, Franceschini N, Haack K, Laston S, MacCluer JW, Umans JG, Comuzzie AG, North KE, Cole SA.

Eur J Hum Genet. 2014 Jul;22(7):938-43. doi: 10.1038/ejhg.2013.264. Epub 2013 Dec 4.

8.

QTL mapping of leukocyte telomere length in American Indians: the Strong Heart Family Study.

Zhu Y, Voruganti VS, Lin J, Matsuguchi T, Blackburn E, Best LG, Lee ET, MacCluer JW, Cole SA, Zhao J.

Aging (Albany NY). 2013 Sep;5(9):704-16.

9.

SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study.

Gribble MO, Voruganti VS, Cropp CD, Francesconi KA, Goessler W, Umans JG, Silbergeld EK, Laston SL, Haack K, Kao WH, Fallin MD, Maccluer JW, Cole SA, Navas-Acien A.

Toxicol Sci. 2013 Nov;136(1):19-25. doi: 10.1093/toxsci/kft181. Epub 2013 Aug 22.

10.

Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family study.

Bella JN, Cole SA, Laston S, Almasy L, Comuzzie A, Lee ET, Best LG, Fabsitz RR, Howard BV, Maccluer JW, Roman MJ, Devereux RB, Göring HH.

Int J Cardiol. 2013 Oct 9;168(4):3902-8. doi: 10.1016/j.ijcard.2013.06.048. Epub 2013 Jul 18.

11.

Epidemiology and genetic determinants of progressive deterioration of glycaemia in American Indians: the Strong Heart Family Study.

Franceschini N, Haack K, Göring HH, Voruganti VS, Laston S, Almasy L, Lee ET, Best LG, Fabsitz RR, North KE, Maccluer JW, Meigs JB, Pankow JS, Cole SA.

Diabetologia. 2013 Oct;56(10):2194-202. doi: 10.1007/s00125-013-2988-8. Epub 2013 Jul 14.

12.

Statistical genetic analysis of serological measures of common, chronic infections in Alaska Native participants in the GOCADAN study.

Rubicz R, Zhu J, Laston S, Cole SA, Voruganti VS, Ebbesson SO, Howard BV, Maccluer JW, Davidson M, Umans JG, Comuzzie AG, Göring HH.

Genet Epidemiol. 2013 Nov;37(7):751-7. doi: 10.1002/gepi.21745. Epub 2013 Jun 24.

13.

Localization of a major susceptibility locus influencing preterm birth.

Chittoor G, Farook VS, Puppala S, Fowler SP, Schneider J, Dyer TD, Cole SA, Lynch JL, Curran JE, Almasy L, Maccluer JW, Comuzzie AG, Hale DE, Ramamurthy RS, Dudley DJ, Moses EK, Arya R, Lehman DM, Jenkinson CP, Bradshaw BS, Defronzo RA, Blangero J, Duggirala R.

Mol Hum Reprod. 2013 Oct;19(10):687-96. doi: 10.1093/molehr/gat036. Epub 2013 May 20.

14.

Genetic architecture of carotid artery intima-media thickness in Mexican Americans.

Melton PE, Carless MA, Curran JE, Dyer TD, Göring HH, Kent JW Jr, Drigalenko E, Johnson MP, Maccluer JW, Moses EK, Comuzzie AG, Mahaney MC, O'Leary DH, Blangero J, Almasy L.

Circ Cardiovasc Genet. 2013 Apr;6(2):211-21. doi: 10.1161/CIRCGENETICS.113.000079. Epub 2013 Mar 13.

15.

Heritability and preliminary genome-wide linkage analysis of arsenic metabolites in urine.

Tellez-Plaza M, Gribble MO, Voruganti VS, Francesconi KA, Goessler W, Umans JG, Silbergeld EK, Guallar E, Franceschini N, North KE, Kao WH, MacCluer JW, Cole SA, Navas-Acien A.

Environ Health Perspect. 2013 Mar;121(3):345-51. doi: 10.1289/ehp.1205305. Epub 2013 Jan 15.

16.

Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos.

Voruganti VS, Higgins PB, Ebbesson SO, Kennish J, Göring HH, Haack K, Laston S, Drigalenko E, Wenger CR, Harris WS, Fabsitz RR, Devereux RB, Maccluer JW, Curran JE, Carless MA, Johnson MP, Moses EK, Blangero J, Umans JG, Howard BV, Cole SA, Comuzzie AG.

Front Genet. 2012 Jun 11;3:86. doi: 10.3389/fgene.2012.00086. eCollection 2012.

17.

Novel associations of nonstructural Loci with paraoxonase activity.

Quillen EE, Rainwater DL, Dyer TD, Carless MA, Curran JE, Johnson MP, Göring HH, Cole SA, Rutherford S, Maccluer JW, Moses EK, Blangero J, Almasy L, Mahaney MC.

J Lipids. 2012;2012:189681. doi: 10.1155/2012/189681. Epub 2012 Apr 17.

18.

The association of genetic variants of type 2 diabetes with kidney function.

Franceschini N, Shara NM, Wang H, Voruganti VS, Laston S, Haack K, Lee ET, Best LG, Maccluer JW, Cochran BJ, Dyer TD, Howard BV, Cole SA, North KE, Umans JG.

Kidney Int. 2012 Jul;82(2):220-5. doi: 10.1038/ki.2012.107. Epub 2012 Apr 18.

19.

Heart rate is associated with markers of fatty acid desaturation: the GOCADAN study.

Ebbesson SO, Lopez-Alvarenga JC, Okin PM, Devereux RB, Tejero ME, Harris WS, Ebbesson LO, MacCluer JW, Wenger C, Laston S, Fabsitz RR, Kennish J, Howard WJ, Howard BV, Umans J, Comuzzie AG.

Int J Circumpolar Health. 2012 Mar 19;71:17343. doi: 10.3402/ijch.v71i0.17343.

20.

Identifying rare variants from exome scans: the GAW17 experience.

Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J Jr, Laird N, Pankratz N, Paterson A, Pugh E, Suarez B, Sun Y, Thomas A, Tintle N, Zhu X, Ziegler A, Maccluer JW, Almasy L.

BMC Proc. 2011 Nov 29;5 Suppl 9:S1. doi: 10.1186/1753-6561-5-S9-S1.

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