Marcy C. Speer

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

Children

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Evadnie Rampersaud grad student 2005 Duke
Abee L. Boyles grad student 2006 Duke
Kristen L. Deak grad student 2006 Duke
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Publications

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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
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