Lucy Osborne
Affiliations: | Molecular and Medical Genetics | University of Toronto, Toronto, ON, Canada |
Area:
Genetics, Human DevelopmentWebsite:
http://www.moleculargenetics.utoronto.ca/faculty/2014/9/30/lucy-osborneGoogle:
"Lucy Osborne"Parents
Sign in to add mentor| Lap-Chee Tsui | post-doc | 1993-1998 | University of Toronto (Cell Biology Tree) |
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Publications
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| Strong E, Mervis CB, Tam E, et al. (2023) DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number. Npj Genomic Medicine. 8: 25 |
| Kozel BA, Barak B, Kim CA, et al. (2021) Williams syndrome. Nature Reviews. Disease Primers. 7: 42 |
| Osborne LR, Mervis CB. (2021) 7q11.23 deletion and duplication. Current Opinion in Genetics & Development. 68: 41-48 |
| Deurloo MHS, Turlova E, Chen WL, et al. (2018) Transcription Factor 2I Regulates Neuronal Development via TRPC3 in 7q11.23 Disorder Models. Molecular Neurobiology |
| Kelsey L, Flenniken AM, Qu D, et al. (2013) ENU-induced mutation in the DNA-binding domain of KLF3 reveals important roles for KLF3 in cardiovascular development and function in mice. Plos Genetics. 9: e1003612 |
| Beunders G, Voorhoeve E, Golzio C, et al. (2013) Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. American Journal of Human Genetics. 92: 210-20 |
| Mervis CB, Dida J, Lam E, et al. (2012) Duplication of GTF2I results in separation anxiety in mice and humans. American Journal of Human Genetics. 90: 1064-70 |
| Osborne LR. (2010) Animal models of Williams syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 154: 209-19 |
| Marshall CR, Young EJ, Pani AM, et al. (2008) Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11. American Journal of Human Genetics. 83: 106-11 |
| Tam E, Young EJ, Morris CA, et al. (2008) The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms. American Journal of Medical Genetics. Part A. 146: 1797-806 |