Baxter, Laura L.

Discovery and genetic localization of down syndrome cerebellar phenotypes using the Ts65Dn mouse

Baxter, L. L. (2000) · Human Molecular Genetics

Down syndrome and intellectual disability researchGenetics and Neurodevelopmental Disorders

Cited by 275

down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

Olson, L. E., Roper, R. J., Baxter, L. L., Carlson, E. J., Epstein, C. J., & Reeves, R. H. (2004) · Developmental Dynamics

Down syndrome and intellectual disability researchGenetics and Neurodevelopmental Disorders

Cited by 165

A curated gene list for expanding the horizons of pigmentation biology

Baxter, L. L., Watkins‐Chow, D. E., Pavan, W. J., & Loftus, S. K. (2019) · Pigment Cell & Melanoma Research

melanin and skin pigmentationBioinformatics and Genomic Networks

Cited by 136

A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy

Matera, I., Watkins-Chow, D. E., Loftus, S. K., Hou, L., Incao, A., Silver, D. L., Rivas, C., Elliott, E. C., Baxter, L. L., & Pavan, W. J. (2008) · Human Molecular Genetics

melanin and skin pigmentationHedgehog Signaling Pathway Studies

Cited by 60

A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus

Loftus, S. K., Lundh, L., Watkins‐Chow, D. E., Baxter, L. L., Pairo‐Castineira, E., Program, N. C. S., Jackson, I. J., Oetting, W. S., Pavan, W. J., & Adams, D. R. (2021) · Human Mutation

melanin and skin pigmentationGenomics and Rare Diseases

Cited by 12