Author

Christopher M. Morris

Alzheimer's SocietyORCID 0000-0002-3749-0993Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 3 Research Focus:gene regulatory network inference· 2 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Alan J. ThomasiD· 2 shared Dena G. HernandeziD· 2 shared John HardyiD· 2 shared Mike A. NallsiD· 2 shared A. James BarkovichiD· 1 shared Adaikalavan RamasamyiD· 1 shared Adrian DanekiD· 1 shared Agustı́n RuiziD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersNeuroscience

Alan J. ThomasORCID

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3 papers

Recent·Most cited

Dopaminergic Changes in the Subgenual Cingulate Cortex in Dementia with Lewy Bodies Associates with Presence of Depression

Lina Gliaudelytė, Steven Rushton, Rolando Berlinguer Palmini, Alan J. Thomas, Christopher M. Morris

The paper investigates dopaminergic and serotonergic changes in the subgenual cingulate cortex of dementia with Lewy bodies patients with and without depression, finding reduced dopaminergic innervation and markers in depressed cases.

Translational Psychiatry · Mar 20, 2025Peer-reviewedNeuroscience

Genetic modifiers of risk and age at onset in GBA associated Parkinson disease and Lewy body dementia

Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, Karl Heilbron, Sara Bandrés‐Ciga, Manuela M. X. Tan, Jesse Raphael Gibbs, Dena G. Hernandez, Ravindran Kumaran, Rebekah G. Langston, Luis Bonet‐Ponce, Roy N. Alcalay, Sharon Hassin‐Baer, Lior Greenbaum, Hirotaka Iwaki, , Andrew Singleton

The paper identifies genetic modifiers of risk and age at onset in GBA-associated Parkinson disease and Lewy body dementia using large case-control datasets and genome-wide association studies.

Brain · Oct 23, 2019Peer-reviewedGenetics

CXCR4 involvement in neurodegenerative diseases

Luke W. Bonham, Celeste M M. Karch, Chun Chieh Fan, Chin Hong Tan, Ethan G. Geier, Yunpeng Wang, Natalie Wen, Iris Broce, Yi Li, Matthew J. Barkovich, Raffaele Ferrari, John Hardy, Parastoo Momeni, Günter U. Höglinger, Ulrich Müller, , Murray Grossman

The paper identifies a genetic variant near CXCR4 associated with increased risk for PSP and PD, showing dysregulation of CXCR4 and microglia-related genes in neurodegenerative diseases.

Translational Psychiatry · Apr 11, 2018Peer-reviewedGenetics