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Neurology. Genetics|October 5, 2018
Protein network analysis reveals selectively vulnerable regions and biological processes in FTDLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Plos Medicine|March 29, 2017
Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control studyNatasha Z R Steele, Jessie S Carr, Luke W Bonham, et al.
Science Advances|November 5, 2021
TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagyCarolina Alquezar, Kathleen M Schoch, Ethan G Geier, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 13, 2019
Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr)Laura Ramirez Aguilar, Juliana Acosta-Uribe, Margarita M Giraldo, et al.
Scientific Reports|July 28, 2019
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasiaLuke W Bonham, Natasha Z R Steele, Celeste M Karch, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory allelesJ Nicholas Cochran, Emily C McKinley, Meagan Cochran, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|October 2, 2023
Early-onset Alzheimer's disease explained by polygenic risk of late-onset disease?William G Mantyh, J Nicholas Cochran, Jared W Taylor, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 29, 2022
Radiogenomics of <i>C9orf72</i> Expansion Carriers Reveals Global Transposable Element Derepression and Enables Prediction of Thalamic Atrophy and Clinical ImpairmentLuke W Bonham, Ethan G Geier, Daniel W Sirkis, et al.
Translational Psychiatry|April 12, 2018
CXCR4 involvement in neurodegenerative diseasesLuke W Bonham, Celeste M Karch, Chun C Fan, et al.
Acta Neuropathologica|November 2, 2018
Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementiaEthan G Geier, Mathieu Bourdenx, Nadia J Storm, et al.
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