Mollie A. Minear, Ph.D.
Affiliations: | 2012 | Genetics and Genomics | Duke University, Durham, NC |
Area:
Genetics, OphthalmologyGoogle:
"Mollie Minear"Parents
Sign in to add mentor| Simon Gregory | grad student | 2012 | Duke | |
| (Elucidating the Genetic Basis of Fuchs Endothelial Corneal Dystrophy.) | ||||
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Publications
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| Taliun D, Harris DN, Kessler MD, et al. (2021) Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299 |
| 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 |
| Minear MA, Alessi S, Allyse M, et al. (2015) Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues. Annual Review of Genomics and Human Genetics. 16: 369-98 |
| Katsanis SH, Minear MA, Vorderstrasse A, et al. (2015) Perspectives on genetic and genomic technologies in an academic medical center: the duke experience. Journal of Personalized Medicine. 5: 67-82 |
| Allyse M, Minear MA, Berson E, et al. (2015) Non-invasive prenatal testing: a review of international implementation and challenges. International Journal of Women's Health. 7: 113-26 |
| Li YJ, Minear MA, Qin X, et al. (2014) Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 55: 4577-84 |
| Chandrasekharan S, Minear MA, Hung A, et al. (2014) Noninvasive prenatal testing goes global. Science Translational Medicine. 6: 231fs15 |
| Minear MA, Li YJ, Rimmler J, et al. (2013) Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular Vision. 19: 2508-16 |
| Li YJ, Minear MA, Rimmler J, et al. (2011) Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Plos One. 6: e18044 |
| Minear MA, Crosslin DR, Sutton BS, et al. (2011) Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease. Human Genetics. 129: 641-54 |