Rampersaud E - Search Results

1

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. Stamm DS, et al. Among authors: rampersaud e. Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):499-505. doi: 10.1002/bdra.20272. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16933213 Free PMC article.

2

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. Speer MC, et al. Among authors: rampersaud e. Am J Med Genet. 2002 Jul 1;110(3):215-8. doi: 10.1002/ajmg.10436. Am J Med Genet. 2002. PMID: 12116228

3

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. Rampersaud E, et al. J Med Genet. 2005 Dec;42(12):940-6. doi: 10.1136/jmg.2005.031658. Epub 2005 Apr 14. J Med Genet. 2005. PMID: 15831595 Free PMC article.

4

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

Rampersaud E, Scott WK, Hauser ER, Speer MC. Rampersaud E, et al. J Med Genet. 2005 Dec;42(12):e68. doi: 10.1136/jmg.2005.032029. J Med Genet. 2005. PMID: 16326825 Free PMC article.

5

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. Rampersaud E, et al. Clin Genet. 2003 Mar;63(3):210-4. doi: 10.1034/j.1399-0004.2003.00043.x. Clin Genet. 2003. PMID: 12694231

6

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. Rampersaud E, et al. Genet Epidemiol. 2007 Jan;31(1):18-30. doi: 10.1002/gepi.20189. Genet Epidemiol. 2007. PMID: 17096358 Free PMC article.

7

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. Tim RW, et al. Among authors: rampersaud e. J Clin Neuromuscul Dis. 2001 Sep;3(1):1-7. doi: 10.1097/00131402-200109000-00001. J Clin Neuromuscul Dis. 2001. PMID: 19078645

8

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. Rampersaud E, et al. Genet Med. 2004 Jan-Feb;6(1):69-70. doi: 10.1097/01.gim.0000106162.27561.68. Genet Med. 2004. PMID: 14726815 No abstract available.

9

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. Allingham RR, et al. Among authors: rampersaud e. Am J Hum Genet. 2001 Feb;68(2):491-4. doi: 10.1086/318194. Epub 2001 Jan 16. Am J Hum Genet. 2001. PMID: 11170897 Free PMC article.

10

Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort.

Damas OM, Gomez L, Quintero MA, Rampersaud E, Slifer S, Beecham GW, Kerman DH, Deshpande AR, Sussman DA, Abreu MT, McCauley JL. Damas OM, et al. Among authors: rampersaud e. Clin Transl Gastroenterol. 2017 Apr 13;8(4):e87. doi: 10.1038/ctg.2017.13. Clin Transl Gastroenterol. 2017. PMID: 28406493 Free PMC article.

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