Marcy C. Speer
Affiliations: | Duke University, Durham, NC |
Area:
Genetics, Statistics, Bioinformatics BiologyGoogle:
"Marcy Speer"Children
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 |
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Publications
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| Xu P, Thomas S, Dellinger A, et al. (2016) Transcriptome analysis of genes involved in neural tube closure during human embryonic development using Long-SAGE F1000research. 5 |
| Soldano KL, Garrett ME, Cope HL, et al. (2013) Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype. Birth Defects Research. Part B, Developmental and Reproductive Toxicology. 98: 365-73 |
| Krupp DR, Xu PT, Thomas S, et al. (2012) Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 683-92 |
| Zhang X, Nicholls PJ, Laje G, et al. (2011) A functional alternative splicing mutation in human tryptophan hydroxylase-2. Molecular Psychiatry. 16: 1169-76 |
| Gelineau-van Waes J, Voss KA, Stevens VL, et al. (2009) Chapter 5 Maternal Fumonisin Exposure as a Risk Factor for Neural Tube Defects Advances in Food and Nutrition Research. 56: 145-181 |
| Deak KL, Siegel DG, George TM, et al. (2008) Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 662-9 |
| Stamm DS, Powell CM, Stajich JM, et al. (2008) Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1. Neurology. 71: 1764-9 |
| Stamm DS, Aylsworth AS, Stajich JM, et al. (2008) Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia. American Journal of Medical Genetics. Part A. 146: 1832-41 |
| Stamm DS, Siegel DG, Mehltretter L, et al. (2008) Refinement of 2q and 7p loci in a large multiplex NTD family. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 441-52 |
| Züchner S, Roberts ST, Speer MC, et al. (2007) Update on psychiatric genetics. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 332-40 |