A. J. Thomas

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

Creating the Pick’s disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick’s disease

Derek H. Oakley, A. Singleton, D. Vitale, 2023, medRxiv.

Molecular changes in the absence of severe pathology in the pulvinar in dementia with Lewy bodies

I. McKeith, A. Khundakar, P. Hanson, 2018, Movement disorders : official journal of the Movement Disorder Society.

Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

Ryan L. Collins, Sonja W. Scholz, Toshiko Tanaka, 2023, Cell genomics.

Predicting cognitive decline using neuropsychiatric symptoms in prodromal Lewy body dementia: A longitudinal study.

J. O'Brien, John-Paul Taylor, D. Burn, 2023, Parkinsonism & related disorders.

Age-related hearing loss and dementia-related neuropathology: An analysis of the United Kingdom brains for dementia research cohort.

J. Attems, L. Walker, Calum A. Hamilton, 2023, Brain Pathology.

Distribution of Amyloid β42 in Relation to the Cerebral Microvasculature in an Elderly Cohort with Alzheimer's Disease

I. Ferrier, C. Morris, R. Kalaria, 2000 .

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Analysis of primary visual cortex in dementia with Lewy bodies indicates GABAergic involvement associated with recurrent complex visual hallucinations

I. McKeith, A. Khundakar, P. Hanson, 2016, Acta Neuropathologica Communications.