Sarah J. Hernandez

Integrated transcriptome analysis of Huntington’s disease iPSC-derived and mouse astrocytes implicates dysregulated synaptogenesis, actin, and astrocyte maturation

L. Thompson, V. Swarup, Ryan G. Lim, 2022, bioRxiv.

Childbearing vs. clinical trial participation: is it one or the other?

Lindsay A Hohsfield, Sarah J. Hernandez, Lindsay A. Hohsfield, 2021, Journal of translational medicine.

Single-nuclei transcriptome analysis of Huntington disease iPSC and mouse astrocytes implicates maturation and functional deficits

L. Thompson, V. Swarup, Ryan G. Lim, 2022, iScience.

Cellular Models: HD Patient-Derived Pluripotent Stem Cells.

L. Thompson, V. Mattis, Virginia B. Mattis, 2018, Methods in molecular biology.

IKKβ slows Huntington’s disease progression in R6/1 mice

D. Housman, L. Thompson, Ryan G. Lim, 2019, Proceedings of the National Academy of Sciences.

Aberrant Development Corrected in Adult-Onset Huntington's Disease iPSC-Derived Neuronal Cultures via WNT Signaling Modulation

Maxwell P. Gold, E. Fraenkel, L. Thompson, 2020, Stem cell reports.

An altered extracellular matrix–integrin interface contributes to Huntington’s disease-associated CNS dysfunction in glial and vascular cells

Mark A. Dane, Laura M. Heiser, Katherine L. Thompson-Peer, 2022, Human molecular genetics.

Longitudinal Biochemical Assay Analysis of Mutant Huntingtin Exon 1 Protein in R6/2 Mice.

L. Thompson, J. Overman, J. Steffan, 2018, Journal of Huntington's disease.