PubMed

Extent and distribution of linkage disequilibrium in the Old Order Amish.

Van Hout CV, Levin AM, Rampersaud E, Shen H, O'Connell JR, Mitchell BD, Shuldiner AR, Douglas JA.

Genet Epidemiol. 2009 Aug 20. [Epub ahead of print]PMID: 19697356 [PubMed - as supplied by publisher]Related articles

Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish.

Michos ED, Streeten EA, Ryan KA, Rampersaud E, Peyser PA, Bielak LF, Shuldiner AR, Mitchell BD, Post W.

Calcif Tissue Int. 2009 Mar;84(3):195-202. Epub 2009 Jan 16.PMID: 19148561 [PubMed - indexed for MEDLINE]Related articles

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

Wang Y, O'Connell JR, McArdle PF, Wade JB, Dorff SE, Shah SJ, Shi X, Pan L, Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC, Welling PA, Chakravarti A, Weder AB, Cooper RS, Mitchell BD, Shuldiner AR, Chang YP.

Proc Natl Acad Sci U S A. 2009 Jan 6;106(1):226-31. Epub 2008 Dec 29.PMID: 19114657 [PubMed - indexed for MEDLINE]Related articlesFree article

Radiation exposure in the acute and short-term management of urolithiasis at 2 academic centers.

Ferrandino MN, Bagrodia A, Pierre SA, Scales CD Jr, Rampersaud E, Pearle MS, Preminger GM.

J Urol. 2009 Feb;181(2):668-72; discussion 673. Epub 2008 Dec 18.PMID: 19100573 [PubMed - indexed for MEDLINE]Related articles

Investigating parent of origin effects in studies of type 2 diabetes and obesity.

Rampersaud E, Mitchell BD, Naj AC, Pollin TI.

Curr Diabetes Rev. 2008 Nov;4(4):329-39. Review.PMID: 18991601 [PubMed - indexed for MEDLINE]Related articles

The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults.

Rampersaud E, Bielak LF, Parsa A, Shen H, Post W, Ryan KA, Donnelly P, Rumberger JA, Sheedy PF 2nd, Peyser PA, Shuldiner AR, Mitchell BD.

Am J Epidemiol. 2008 Nov 1;168(9):1016-23. Epub 2008 Sep 19.PMID: 18805900 [PubMed - indexed for MEDLINE]Related articlesFree article

Physical activity and the association of common FTO gene variants with body mass index and obesity.

Rampersaud E, Mitchell BD, Pollin TI, Fu M, Shen H, O'Connell JR, Ducharme JL, Hines S, Sack P, Naglieri R, Shuldiner AR, Snitker S.

Arch Intern Med. 2008 Sep 8;168(16):1791-7. Erratum in: Arch Intern Med. 2009 Mar 9;169(5):453. PMID: 18779467 [PubMed - indexed for MEDLINE]Related articlesFree article

TCF7L2 variants associate with CKD progression and renal function in population-based cohorts.

Köttgen A, Hwang SJ, Rampersaud E, Coresh J, North KE, Pankow JS, Meigs JB, Florez JC, Parsa A, Levy D, Boerwinkle E, Shuldiner AR, Fox CS, Kao WH.

J Am Soc Nephrol. 2008 Oct;19(10):1989-99. Epub 2008 Jul 23.PMID: 18650481 [PubMed - indexed for MEDLINE]Related articlesFree article

Percent tumor involvement and risk of biochemical progression after radical prostatectomy.

Rampersaud EN, Sun L, Moul JW, Madden J, Freedland SJ.

J Urol. 2008 Aug;180(2):571-6; discussion 576. Epub 2008 Jun 12.PMID: 18554662 [PubMed - indexed for MEDLINE]Related articles

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study.

Mitchell BD, McArdle PF, Shen H, Rampersaud E, Pollin TI, Bielak LF, Jaquish C, Douglas JA, Roy-Gagnon MH, Sack P, Naglieri R, Hines S, Horenstein RB, Chang YP, Post W, Ryan KA, Brereton NH, Pakyz RE, Sorkin J, Damcott CM, O'Connell JR, Mangano C, Corretti M, Vogel R, Herzog W, Weir MR, Peyser PA, Shuldiner AR.

Am Heart J. 2008 May;155(5):823-8. Epub 2008 Mar 5.PMID: 18440328 [PubMed - indexed for MEDLINE]Related articlesFree article

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations.

Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YP, Ott SH, Zhang L, Zhao Y, Mitchell BD, O'Connell J, Shuldiner AR.

Diabetes. 2007 Dec;56(12):3053-62. Epub 2007 Sep 10.PMID: 17846126 [PubMed - indexed for MEDLINE]Related articlesFree article

Prostate-specific antigen (PSA) and PSA velocity for prostate cancer detection in men aged <50 years.

Sun L, Moul JW, Hotaling JM, Rampersaud E, Dahm P, Robertson C, Fitzsimons N, Albala D, Polascik TJ.

BJU Int. 2007 Apr;99(4):753-7. Epub 2007 Jan 19.PMID: 17244286 [PubMed - indexed for MEDLINE]Related articles

Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available.

Rampersaud E, Morris RW, Weinberg CR, Speer MC, Martin ER.

Genet Epidemiol. 2007 Jan;31(1):18-30.PMID: 17096358 [PubMed - indexed for MEDLINE]Related articlesFree article

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.

Stamm DS, Rampersaud E, Slifer SH, Mehltretter L, Siegel DG, Xie J, Hu-Lince D, Craig DW, Stephan DA, George TM, Gilbert JR, Speer MC; NTD Collaborative Group.

Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):499-505.PMID: 16933213 [PubMed - indexed for MEDLINE]Related articles

Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs.

Rampersaud E, Scott WK, Hauser ER, Speer MC.

J Med Genet. 2005 Dec;42(12):e68.PMID: 16326825 [PubMed - indexed for MEDLINE]Related articlesFree article

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.

Rampersaud E, Bassuk AG, Enterline DS, George TM, Siegel DG, Melvin EC, Aben J, Allen J, Aylsworth A, Brei T, Bodurtha J, Buran C, Floyd LE, Hammock P, Iskandar B, Ito J, Kessler JA, Lasarsky N, Mack P, Mackey J, McLone D, Meeropol E, Mehltretter L, Mitchell LE, Oakes WJ, Nye JS, Powell C, Sawin K, Stevenson R, Walker M, West SG, Worley G, Gilbert JR, Speer MC.

J Med Genet. 2005 Dec;42(12):940-6. Epub 2005 Apr 14.PMID: 15831595 [PubMed - indexed for MEDLINE]Related articlesFree article

A man with saphenous vein graft aneurysms after bypass surgery.

Williams ML, Rampersaud E, Wolfe WG.

Ann Thorac Surg. 2004 May;77(5):1815-7.PMID: 15111195 [PubMed - indexed for MEDLINE]Related articles

Targeted beta-adrenergic receptor kinase (betaARK1) inhibition by gene transfer in failing human hearts.

Williams ML, Hata JA, Schroder J, Rampersaud E, Petrofski J, Jakoi A, Milano CA, Koch WJ.

Circulation. 2004 Apr 6;109(13):1590-3. Epub 2004 Mar 29.PMID: 15051637 [PubMed - indexed for MEDLINE]Related articlesFree article

Adjusting for covariates on a slippery slope: linkage analysis of change over time.

Rampersaud E, Allen A, Li YJ, Shao Y, Bass M, Haynes C, Ashley-Koch A, Martin ER, Schmidt S, Hauser ER.

BMC Genet. 2003 Dec 31;4 Suppl 1:S50.PMID: 14975118 [PubMed - indexed for MEDLINE]Related articlesFree article

No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives.

Rampersaud E, Brusato C, Melvin EC, Speer MC, Metcalf K; NTD Collaborative Group.

Genet Med. 2004 Jan-Feb;6(1):69-70. No abstract available. PMID: 14726815 [PubMed - indexed for MEDLINE]Related articles

Effects of covariates: a summary of Group 5 contributions.

Hauser ER, Hsu FC, Daley D, Olson JM, Rampersaud E, Lin JP, Paterson AD, Poisson LM, Chase GA, Dahmen G, Ziegler A.

Genet Epidemiol. 2003;25 Suppl 1:S43-9.PMID: 14635168 [PubMed - indexed for MEDLINE]Related articles

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects.

Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC; NTD Collaborative Group.

Clin Genet. 2003 Mar;63(3):210-4.PMID: 12694231 [PubMed - indexed for MEDLINE]Related articles

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families.

Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS; NTD Collaborative Group. Neural Tube Defects.

Am J Med Genet. 2002 Jul 1;110(3):215-8.PMID: 12116228 [PubMed - indexed for MEDLINE]Related articles

Complete genomic screen in Parkinson disease: evidence for multiple genes.

Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D, Mastaglia F, Laing NG, Stajich JM, Slotterbeck B, Booze MW, Ribble RC, Rampersaud E, West SG, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Vance JM, Pericak-Vance MA.

JAMA. 2001 Nov 14;286(18):2239-44.PMID: 11710888 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy.

Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC.

J Clin Neuromuscul Dis. 2001 Sep;3(1):1-7.PMID: 19078645 [PubMed - as supplied by publisher]Related articles

A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.

Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM.

Am J Hum Genet. 2001 Feb;68(2):491-4. Epub 2001 Jan 16.PMID: 11170897 [PubMed - indexed for MEDLINE]Related articlesFree article