Louisa Dal Cengio

Stanford Medicine — United States

Neuroscience · Life Sciences

7h-index455citations14works0.02yr avg
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Research Topics

Genetic Neurodegenerative Diseases(10), Mitochondrial Function and Pathology(6), Muscle Physiology and Disorders(5), Neurological disorders and treatments(3), Circadian rhythm and melatonin(2)

Publications14 total

Environmental factors contribute to cancer therapy toxicity
2025
0085 Extended Amygdala Neural Circuits Linking Hormonal Influences on Body Temperature to Sleep and Circadian Rhythms
SLEEP·2025Open Access
Corrigendum to “Reducing huntingtin by immunotherapy delays disease progression in a mouse model of Huntington disease” [Neurobiology of Disease, 2024 Jan:190:106376]
Neurobiology of Disease·2024Open Access
Reducing huntingtin by immunotherapy delays disease progression in a mouse model of Huntington disease
Neurobiology of Disease·2023· 4 citedOpen Access
BMAL1 loss in oligodendroglia contributes to abnormal myelination and sleep
Neuron·2023· 39 citedOpen Access
BMAL1 loss in oligodendroglial lineage cells dysregulates myelination and sleep
2022Open Access
DAPK1 Promotes Extrasynaptic GluN2B Phosphorylation and Striatal Spine Instability in the YAC128 Mouse Model of Huntington Disease
Frontiers in Cellular Neuroscience·2020· 27 citedOpen Access
Potent and sustained huntingtin lowering via AAV5 encoding miRNA preserves striatal volume and cognitive function in a humanized mouse model of Huntington disease
Nucleic Acids Research·2019· 73 citedOpen Access
Huntingtin suppression restores cognitive function in a mouse model of Huntington’s disease
Science Translational Medicine·2018· 122 cited
I09 Antibodies inhibit cell to cell transmission of mutant HTT
2018
Altering cortical input unmasks synaptic phenotypes in the YAC128 cortico-striatal co-culture model of Huntington disease
BMC Biology·2018· 18 citedOpen Access
Additional file 1: of Altering cortical input unmasks synaptic phenotypes in the YAC128 cortico-striatal co-culture model of Huntington disease
Figshare·2018Open Access
A novel humanized mouse model of Huntington disease for preclinical development of therapeutics targeting mutant huntingtin alleles
Human Molecular Genetics·2017· 36 citedOpen Access
An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypes
Human Molecular Genetics·2016· 136 citedOpen Access

Frequent Co-authors

Michael R. Hayden(10), Amber L. Southwell(7), Yuanyun Xie(7), Lynn A. Raymond(5), Erika B. Villanueva(4), Lisa M. Anderson(4), Daphne Cheung(4), Erin M. Gibson(4), Nicholas S. Caron(3), Lindsey Catherine Mehl(3), Mandi E. Schmidt(3), Stefan Bartl(3), Abid Oueslati(3), Michela Parth(3), Nina Salhat(3), Alberto Siddu(3), Oskar W. Smrzka(3), Francesca Cicchetti(3), Chris Kay(2), Matthew P. Parsons(2)