Children
Sign in to add trainee| Mollie A. Minear | grad student | 2012 | Duke |
| Christina A. Markunas | grad student | 2013 | Duke |
| Deidre Krupp | grad student | 2014 | Duke |
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Publications
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| Siecinski SK, Giamberardino SN, Spanos M, et al. (2023) Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder. Autism Research : Official Journal of the International Society For Autism Research |
| Kousa YA, Zhu H, Fakhouri WD, et al. (2019) The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Human Molecular Genetics |
| Towers AJ, Tremblay MW, Chung L, et al. (2018) Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders. Jci Insight. 3 |
| Armstrong AJ, Gupta S, Healy P, et al. (2018) Genomic and phenotypic evidence for prostate cancer osteomimicry in circulating tumor cells from men with metastatic castration resistant prostate cancer (mCRPC) treated with radium-223. Journal of Clinical Oncology. 36: 160-160 |
| Afshari NA, Igo RP, Morris NJ, et al. (2017) Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898 |
| Zeng Y, Nie C, Min J, et al. (2016) Novel loci and pathways significantly associated with longevity. Scientific Reports. 6: 21243 |
| Kraus WE, Muoio DM, Stevens R, et al. (2015) Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Plos Genetics. 11: e1005553 |
| Shah AA, Gregory SG, Krupp D, et al. (2015) Epigenetic Profiling Identifies Novel Genes for Ascending Aortic Aneurysm Formation with Bicuspid Aortic Valves. The Heart Surgery Forum. 18: E134-9 |
| Lock EF, Soldano KL, Garrett ME, et al. (2015) Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. Bmc Genomics. 16: 11 |
| Krupp DR, Soldano KL, Garrett ME, et al. (2014) Missing genetic risk in neural tube defects: can exome sequencing yield an insight? Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 642-6 |