Marcy C. Speer - Publications

Duke University, Durham, NC 
Genetics, Statistics, Bioinformatics Biology

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2007 Rampersaud E, Morris RW, Weinberg CR, Speer MC, Martin ER. 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. PMID 17096358 DOI: 10.1002/gepi.20189  0.52
2006 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. 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. PMID 16933213 DOI: 10.1002/bdra.20272  0.52
2005 Rampersaud E, Scott WK, Hauser ER, Speer MC. Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs. Journal of Medical Genetics. 42: e68. PMID 16326825 DOI: 10.1136/jmg.2005.032029  0.52
2005 Deak KL, Dickerson ME, Linney E, Enterline DS, George TM, Melvin EC, Graham FL, Siegel DG, Hammock P, Mehltretter L, Bassuk AG, Kessler JA, Gilbert JR, Speer MC. 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. PMID 16237707 DOI: 10.1002/bdra.20183  0.52
2005 Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, ... Speer MC, et al. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Human Genetics. 117: 133-42. PMID 15883837 DOI: 10.1007/s00439-005-1299-7  0.52
2005 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, ... ... Speer MC, et al. Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. Journal of Medical Genetics. 42: 940-6. PMID 15831595 DOI: 10.1136/jmg.2005.031658  0.52
2005 Sebold CD, Melvin EC, Siegel D, Mehltretter L, Enterline DS, Nye JS, Kessler J, Bassuk A, Speer MC, George TM. Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele Genetics in Medicine. 7: 64-67. PMID 15654231 DOI: 10.1097/01.GIM.0000151158.09278.2B  0.52
2004 Benz LP, Swift FE, Graham FL, Enterline DS, Melvin EC, Hammock P, Gilbert JR, Speer MC, Bassuk AG, Kessler JA, George TM. TERC is not a major gene in human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 531-3. PMID 15329831 DOI: 10.1002/bdra.20057  0.52
2004 Rampersaud E, Brusato C, Melvin EC, Speer MC, Metcalf K. 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. PMID 14726815 DOI: 10.1097/01.GIM.0000106162.27561.68  0.52
2003 Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC. Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clinical Genetics. 63: 210-4. PMID 12694231 DOI: 10.1034/j.1399-0004.2003.00043.x  0.52
2002 Bauer KA, George TM, Enterline DS, Stottmann RW, Melvin EC, Siegel D, Samal S, Hauser MA, Klingensmith J, Nye JS, Speer MC. A novel mutation in the gene encoding noggin is not causative in human neural tube defects. Journal of Neurogenetics. 16: 65-71. PMID 12420790  0.52
2002 Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS. T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. American Journal of Medical Genetics. 110: 215-8. PMID 12116228 DOI: 10.1002/ajmg.10436  0.52
2001 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. Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy. Journal of Clinical Neuromuscular Disease. 3: 1-7. PMID 19078645  0.52
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