Full list of publications can be found on Pubmed and Google Scholar.

Selected Publications:

1. ALS/Frontotemporal Dementia (FTD) and Stem Cell Models of Disease

C9ORF72 poly-PR disrupts expression of ALS/FTD-implicated STMN2 through SRSF7

Wang KW*, Smeyers J*, Eggan K, Budnik B, Mordes DA. ACTA Neuropathologica Com., 2025.

Pluripotent stem cell strategies for rebuilding the human brain

Limone F, Klim JR, Mordes DA. Frontiers in Aging Neuroscience, 2022.

Absence of Survival and Motor Deficits in 500 Repeat C9ORF72 BAC Mice

Mordes DA*, Morrison BM*, Ament XH, Cantrell C, Mok J, Eggan P, Xue C, Wang J, Eggan K, Rothstein JD. Neuron, 2020.

Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients

Mordes DA, Prudencio M, Goodman LD, Klim JR, Moccia R, Limone F, Pietilainen O, Chowdhary K, Dickson DW, Rademakers R, Bonini NM, Petrucelli L, Eggan K. ACTA Neuropathologica Comm., 2018.

Two familial ALS proteins function in prevention/repair of transcription-associated DNA damage

Hill, Mordes et al., PNAS.

2. Neuropathology of ALS and Neurodegenerative Diseases

Single-nucleus sequencing reveals enriched expression of genetic risk factors in extratelencephalic neurons sensitive to degeneration in ALS

Limone F*, Mordes DA*, Couto A, Joseph BJ, Mitchell JM, Therrien M, Ghosh SD, Meyer D, Zhang Y, Goldman M, Bortolin L, Cobos I, Stevens B, McCarroll SA, Kadiu I, Burberry A, Pietiläinen O, Eggan K. Nature Aging. 2024.

Phosphorylation of tau at a single residue inhibits binding to the E3 ubiquitin ligase, CHIP

Nadel CM, Pokhrel S, Wucherer K, Oehler A, Thwin AC, Basu K, Callahan MD, Southworth DR, Mordes DA, Craik CS, Gestwicki JE. Nature Communications. 2024.

3. Movement Disorders and Alpha-synuclein Pathology

Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism

Prusiner SB, Woerman AL, Mordes DA, Watts JC, Rampersaud R, Berry DB, Patel S, Oehler A, Lowe JK, Kravitz SN, Geschwind DH, Glidden DV, Halliday GM, Middleton LT, Gentleman SM, Grinberg LT, Giles K. PNAS, 2015.

Familial Parkinson's point mutation abolishes multiple system atrophy prion replication

Woerman AL, Kazmi SA, Patel S, Aoyagi A, Oehler A, Widjaja K, Mordes DA, Olson SH, Prusiner SB. PNAS, 2018.

Kinetics of α-synuclein prions preceding neuropathological inclusions in multiple system atrophy

Woerman AL, Patel S, Kazmi SA, Oehler A, Lee J, Mordes DA, Olson SH, Prusiner SB. PLoS Pathogens, 2020.