The Neuropsychology Core (NC) will provide objective, standardized, and quantitative neuropsychological evaluations of patients and normal volunteers who sere as subjects in MADRC studies. These evaluations will serve as a basis for diagnostic accuracy and the development of operationally defined study variables and, thus, further our understanding of the pathophysiology of neurodegenerative disorders and dementia more generally. The NC will document changes in patient behavior over time, and coordinate the collection of neuropsychological data in projects and at satellite diagnostic and treatment centers (SDTCs) of the MADRC. This core will be responsible for training personnel at SDTCs and in specific projects that will be engaged in psychometric and other psychological applications and that are approved by the MADRC Executive Committee. The NC will participate in the selection of personnel for these projects, assignment of these personnel to functional units of the MADRC, and oversight of their ongoing activities once they are assigned. The NC will collaborate with NIH sponsored multicenter projects such as CERAD and ADCSU. The NC will provide consultation to existing projects and cores and assist in the development of future projects and center modifications. It will assist, when appropriate, in the design of projects, in their implementation, analyses, and communication of results. The NC will also provide the MADRC with expertise in behavioral measurement and behavioral principles in general, including normal conditions as well as psychopathological states. This will serve as a basis for training and consultation to other components of the MADRC, including MADRC sponsored conferences and the Community Outreach Education Program (COEP). In these endeavors, the NC will work collaboratively with the Clinical and Education and Information Transfer Cores as well as other projects of the MADRC.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center (P50)
Project #
5P50AG008671-09
Application #
6234217
Study Section
Project Start
1997-07-01
Project End
1998-05-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
9
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Sims, Rebecca (see original citation for additional authors) (2017) Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nat Genet 49:1373-1384
Michaud, Tzeyu L; High, Robin; Charlton, Mary E et al. (2017) Dependence Stage and Pharmacoeconomic Outcomes in Patients With Alzheimer Disease. Alzheimer Dis Assoc Disord 31:209-217
Monin, Joan K; Poulin, Michael J; Brown, Stephanie L et al. (2017) Spouses' daily feelings of appreciation and self-reported well-being. Health Psychol 36:1135-1139
Jun, Gyungah R; Chung, Jaeyoon; Mez, Jesse et al. (2017) Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimers Dement 13:727-738
Cary, Brian P; Brooks, Allen F; Fawaz, Maria V et al. (2016) Synthesis and Evaluation of [(18)F]RAGER: A First Generation Small-Molecule PET Radioligand Targeting the Receptor for Advanced Glycation Endproducts. ACS Chem Neurosci 7:391-8
Karch, Celeste M; Ezerskiy, Lubov A; Bertelsen, Sarah et al. (2016) Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci. PLoS One 11:e0148717
Mez, Jesse; Mukherjee, Shubhabrata; Thornton, Timothy et al. (2016) The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable. Neurobiol Aging 41:115-121
Ridge, Perry G; Hoyt, Kaitlyn B; Boehme, Kevin et al. (2016) Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiol Aging 41:200.e13-200.e20
Hohman, Timothy J; Bush, William S; Jiang, Lan et al. (2016) Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiol Aging 38:141-150
Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M et al. (2016) A novel Alzheimer disease locus located near the gene encoding tau protein. Mol Psychiatry 21:108-17

Showing the most recent 10 out of 274 publications