Amy Cristine Lossie
Affiliations: | Beautiful You MRKH Foundation |
Area:
Genetics, rare diseases, development, substance use disorders, epigeneticsGoogle:
"Amy Lossie"Parents
Sign in to add mentorSally Camper | research assistant | 1991-1994 | University of Michigan Medical School Ann Arbor (Neurotree) |
Daniel J. Driscoll | grad student | 1995-2001 | University of Florida College of Medicine |
Monica J. Justice | post-doc | 2001-2006 | Baylor College of Medicine (Cell Biology Tree) |
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Publications
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Williams LS, Demir Eksi D, Shen Y, et al. (2017) Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families. Fertility and Sterility |
Lo CL, Lossie AC, Liang T, et al. (2016) High Resolution Genomic Scans Reveal Genetic Architecture Controlling Alcohol Preference in Bidirectionally Selected Rat Model. Plos Genetics. 12: e1006178 |
Chowdhury B, Seetharam A, Wang Z, et al. (2016) A Study of Alterations in DNA Epigenetic Modifications (5mC and 5hmC) and Gene Expression Influenced by Simulated Microgravity in Human Lymphoblastoid Cells. Plos One. 11: e0147514 |
Lossie AC, Lo CL, Baumgarner KM, et al. (2012) ENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation development. Bmc Genetics. 13: 106 |
Jiang Z, Lossie AC, Applegate TJ. (2011) Evolution of trefoil factor(s): genetic and spatio-temporal expression of trefoil factor 2 in the chicken (Gallus gallus domesticus). Plos One. 6: e22691 |
Lossie AC, Meehan TP, Castillo A, et al. (2005) 18th international mouse genome conference. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 471-5 |
Lossie AC, Nakamura H, Thomas SE, et al. (2005) Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation. Genetics. 169: 285-99 |
Boyar FZ, Whitney MM, Lossie AC, et al. (2001) A family with a grand-maternally derived interstitial duplication of proximal 15q. Clinical Genetics. 60: 421-30 |
Lossie AC, Whitney MM, Amidon D, et al. (2001) Distinct phenotypes distinguish the molecular classes of Angelman syndrome. Journal of Medical Genetics. 38: 834-45 |
Williams CA, Lossie A, Driscoll D, et al. (2001) Angelman syndrome: mimicking conditions and phenotypes. American Journal of Medical Genetics. 101: 59-64 |