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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 22, 2021
MarkVCID cerebral small vessel consortium: I. Enrollment, clinical, fluid protocolsDonna Wilcock, Gregory Jicha, Deborah Blacker, et al.Journal of Magnetic Resonance Imaging : JMRI|September 26, 2021
Deep Generative Medical Image Harmonization for Improving Cross-Site Generalization in Deep Learning PredictorsVishnu M Bashyam, Jimit Doshi, Guray Erus, et al.Proceedings of the National Academy of Sciences of the United States of America|June 5, 2021
Sequence of the supernumerary B chromosome of maize provides insight into its drive mechanism and evolutionNicolas Blavet, Hua Yang, Handong Su, et al.Nature Communications|March 20, 2025
Machine learning reveals distinct neuroanatomical signatures of cardiovascular and metabolic diseases in cognitively unimpaired individualsSindhuja Tirumalai Govindarajan, Elizabeth Mamourian, Guray Erus, et al.Brain : a Journal of Neurology|June 28, 2020
MRI signatures of brain age and disease over the lifespan based on a deep brain network and 14 468 individuals worldwideVishnu M Bashyam, Guray Erus, Jimit Doshi, et al.Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
Brain age identification from diffusion MRI synergistically predicts neurodegenerative diseaseChenyu Gao, Michael E Kim, Karthik Ramadass, et al.Nature Genetics|November 24, 2020
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traitsAvik Choudhuri, Eirini Trompouki, Brian J Abraham, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2015
GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's diseaseIgnacio F Mata, James B Leverenz, Daniel Weintraub, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 6, 2013
Assessment of cognition in early dementiaNina B Silverberg, Laurie M Ryan, Maria C Carrillo, et al.JAMA Neurology|August 30, 2016
Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson DiseaseMarie Y Davis, Catherine O Johnson, James B Leverenz, et al.Pageof 107