Lisa M Anderson

Memory: salvage and invention

Lisa M Anderson, 1996 .

HACE1 is essential for astrocyte mitochondrial function and influences Huntington disease phenotypes in vivo

Lisa M Anderson, D. Ehrnhoefer, M. Hayden, 2018, Human molecular genetics.

Reevaluation of the South Asian MYBPC3Δ25bp Intronic Deletion in Hypertrophic Cardiomyopathy

Lisa M Anderson, M. Farrall, C. Autore, 2020, Circulation. Genomic and precision medicine.

Huntingtin suppression restores cognitive function in a mouse model of Huntington’s disease

Lisa M Anderson, L. Raymond, M. Hayden, 2018, Science Translational Medicine.

DAPK1 Promotes Extrasynaptic GluN2B Phosphorylation and Striatal Spine Instability in the YAC128 Mouse Model of Huntington Disease

Lisa M Anderson, L. Raymond, M. Hayden, 2020, Frontiers in Cellular Neuroscience.

An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypes.

Lisa M Anderson, L. Raymond, M. Hayden, 2016, Human molecular genetics.

Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease

Lisa M Anderson, M. Hayden, E. Petretto, 2019, Proceedings of the National Academy of Sciences.

Cerebrospinal fluid mutant huntingtin is a biomarker for huntingtin lowering in the striatum of Huntington disease mice

Lisa M Anderson, M. Hayden, N. Caron, 2022, Neurobiology of Disease.