Marcy C. Speer

Duke University, Durham, NC 
Genetics, Statistics, Bioinformatics Biology
"Marcy Speer"


Sign in to add trainee
Evadnie Rampersaud grad student 2005 Duke
Abee L. Boyles grad student 2006 Duke
Kristen L. Deak grad student 2006 Duke
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Rampersaud E, Morris RW, Weinberg CR, et al. (2007) 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. Genetic Epidemiology. 31: 18-30
Stamm DS, Rampersaud E, Slifer SH, et al. (2006) 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. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 499-505
Rampersaud E, Scott WK, Hauser ER, et al. (2005) Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs. Journal of Medical Genetics. 42: e68
Deak KL, Dickerson ME, Linney E, et al. (2005) Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 868-75
Deak KL, Boyles AL, Etchevers HC, et al. (2005) SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Human Genetics. 117: 133-42
Rampersaud E, Bassuk AG, Enterline DS, et al. (2005) Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. Journal of Medical Genetics. 42: 940-6
Sebold CD, Melvin EC, Siegel D, et al. (2005) Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele Genetics in Medicine. 7: 64-67
Benz LP, Swift FE, Graham FL, et al. (2004) TERC is not a major gene in human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 531-3
Rampersaud E, Brusato C, Melvin EC, et al. (2004) No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 6: 69-70
Rampersaud E, Melvin EC, Siegel D, et al. (2003) Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clinical Genetics. 63: 210-4
See more...