Courtney Hanna
Affiliations: | 2013 | Medical Genetics | University of British Columbia, Vancouver, Vancouver, BC, Canada |
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| Del Gobbo GF, Price EM, Hanna CW, et al. (2018) No evidence for association of677C>T and 1298A>C variants with placental DNA methylation. Clinical Epigenetics. 10: 34 |
| Barha CK, Salvante KG, Hanna CW, et al. (2017) Child mortality, hypothalamic-pituitary-adrenal axis activity and cellular aging in mothers. Plos One. 12: e0177869 |
| Hanna CW, Peñaherrera MS, Saadeh H, et al. (2016) Pervasive polymorphic imprinted methylation in the human placenta. Genome Research |
| Barha CK, Hanna CW, Salvante KG, et al. (2016) Number of Children and Telomere Length in Women: A Prospective, Longitudinal Evaluation. Plos One. 11: e0146424 |
| Del Gobbo G, Price EM, Hanna C, et al. (2016) Placental MTHFR 677C>T genotypes in pregnancy pathologies Placenta. 45: 112 |
| Wen J, Hanna CW, Martell S, et al. (2015) Functional consequences of copy number variants in miscarriage. Molecular Cytogenetics. 8: 6 |
| Bagheri H, Wen J, Hanna CW, et al. (2015) MG-123 Genomics of early pregnancy loss Journal of Medical Genetics. 52: A6.1-A6 |
| Hanna C, Penaherrera M, Saadeh H, et al. (2015) Transient and placenta-specific imprinting in human development Placenta. 36: A39 |
| Hanna CW, McFadden DE, Robinson WP. (2013) DNA methylation profiling of placental villi from karyotypically normal miscarriage and recurrent miscarriage. The American Journal of Pathology. 182: 2276-84 |
| Manokhina I, Hanna CW, Stephenson MD, et al. (2013) Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage. Molecular Human Reproduction. 19: 539-44 |