Jeff Iliff, PhD

Personal Statement

I focus on neurodegeneration and traumatic brain injury research at the VA Puget Sound and at the UW Alzheimer’s Disease Research Center.

My work has probed the ‘glymphatic’ system, a brain-wide network of perivascular spaces that facilitates the clearance of waste products, including amyloid beta and tau, from the brain interstitium during sleep. Previously at OHSU, my group demonstrated that the glymphatic system fails in the aging brain and in the young brain after traumatic brain injury. The studies suggest that impairment of glymphatic function may be one factor that renders the aging brain vulnerable to protein aggregation and neurodegeneration and may link brain trauma early in life with the development of dementia in the decades that follow. My ongoing work seeks to define the molecular and cellular underpinnings of impaired glymphatic function in the aging and post-traumatic brain, and to use novel MRI-based imaging approaches to extend these findings into clinical Alzheimer’s disease and post-traumatic populations.

As the leader of the ADRC’s new Research Education Component, I oversee the effort to train and develop a community of clinical, basic and translational Alzheimer’s disease researchers with the necessary clinical, scientific and technical competence to effectively collaborate to define the mechanistic and biological underpinnings of Alzheimer’s and related dementia, and to translate this understanding to improve the lives of those living with memory loss and dementia.

Department Affiliations

Recent Publications

Hormonal Modulation of Subjective Sleep Quality and Perivascular Space Volume Across the Menstrual Cycle: An Observational Dense-Sampling Study.
(2026 Sep 8)
bioRxiv
Apter D, Elberse JD, Stankeviciute L, Weis S, Elmenhorst D, Iliff J, Eickhoff SB, Heller C, Tahmasian M

When disease illuminates physiology: mapping hidden fluid pathways in the human brain.
(2026 Sep 24)
Brain
Ford JN, Bouffard MA, Buch KA, Iliff JJ

Aquaporin-4 mis-localization decreases glymphatic clearance of α-synuclein in an alpha-syntrophin knock out mouse model and promotes α-synuclein pathology and aggregate propagation.
(2026)
Brain Commun 8(5): fcag327
Braun M, Simon MJ, Jang J, Sanderson K, Swierz J, Sevao M, Pincus AB, Schaser AJ, Elliott JE, Lim MM, Unni VK, Schindler AG, Keene CD, Latimer CS, Iliff JJ

Aquaporin-4 mislocalization from astrocyte endfeet prolongs survival in a prion-cerebral amyloid angiopathy model.
(2026 Jul 17)
bioRxiv
Flores S, Wilpitz A, Ojeda-Juarez D, Wang J, Danque G, Sumowski P, Funk G, Malik A, Pizzo D, Richards E, Iliff JJ, Sigurdson CJ

Diurnal choroid plexus function in mice depends on sex, age, and amyloid-β status.
(2026 May 20)
Commun Biol 9(1):
Jansson D, O'Boyle R, Pedersen TJ, Gino E, Sevao M, Vered R, Suchland KL, Zhou B, Fame R, Keil SA, Braun M, Iliff J

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