Osborne, Lucy R.

A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome

Osborne, L. R., Li, M., Pober, B., Chitayat, D., Bodurtha, J., Mandel, A., Costa, T., Grebe, T., Cox, S., Tsui, L.-C., et al. (2001) · Nature Genetics

Williams Syndrome ResearchGenomic variations and chromosomal abnormalities

Cited by 344

Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity

Ellegood, J., Anagnostou, E., Babineau, B. A., Crawley, J. N., Lin, L., Genestine, M., DiCicco-Bloom, E., Lai, J. K. Y., Foster, J. A., Peñagarikano, O., et al. (2015) · Molecular Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 288

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

Flenniken, A. M., Osborne, L. R., Anderson, N., Ciliberti, N., Fleming, C., Gittens, J. E. I., Gong, X.-Q., Kelsey, L. B., Lounsbury, C., Moreno, L., et al. (2005) · Development

Connexins and lens biologydental development and anomalies

Cited by 231

Symmetrical dose-dependent dna-methylation profiles in children with deletion or duplication of 7q11.23

Strong, E., Butcher, D. T., Singhania, R., Mervis, C. B., Morris, C. A., De Carvalho, D., Weksberg, R., & Osborne, L. R. (2015) · The American Journal of Human Genetics

Williams Syndrome ResearchEpigenetics and DNA Methylation

Cited by 71

Enhanced prefrontal serotonin 5-HT1A currents in a mouse model of Williams-Beuren syndrome with low innate anxiety

Proulx, É., Young, E. J., Osborne, L. R., & Lambe, E. K. (2010) · Journal of Neurodevelopmental Disorders

Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders

Cited by 35