We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the
NIH Research Portfolio Online Reporting Tools and the
NSF Award Database.
The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
You can help! If you notice any innacuracies, please
sign in and mark grants as correct or incorrect matches.
Sign in to see low-probability grants and correct any errors in linkage between grants and researchers.
High-probability grants
According to our matching algorithm, Anthony T. Yachnis is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
2015 — 2019 |
Yachnis, Anthony |
P50Activity Code Description: To support any part of the full range of research and development from very basic to clinical; may involve ancillary supportive activities such as protracted patient care necessary to the primary research or R&D effort. The spectrum of activities comprises a multidisciplinary attack on a specific disease entity or biomedical problem area. These grants differ from program project grants in that they are usually developed in response to an announcement of the programmatic needs of an Institute or Division and subsequently receive continuous attention from its staff. Centers may also serve as regional or national resources for special research purposes. |
Core D: Neuropathology Core
SUMMARY (Core D) In order to support the goals of the University of Florida-Mount Sinai Medical Center Alzheimer s Disease Research Center (UF-MSMC ADRC) the Neuropathology Core (Core D) will perform diagnostic evaluations and quantitative analyses of the brains collected from deceased individuals that participate in the clinical studies. These are critical functions of an ADRC as a definite diagnosis of AD still requires a thorough post- mortem evaluation. The Neuropathology Core will also collect and provide genetic information, brain tissue samples, biospecimens and DNA that will be integrated within or utilized by other components of the UF- MSMC ADRC. The specific aims of the Neuropathology Core are: Aim 1. Perform brain autopsies on participants of the UF-MSMC ADRC in a timely fashion and in accordance with the National Institute on Aging-Alzheimer s Association consensus guidelines. Aim 2. Provide neuropathologic data and genetic information to be included in the database to support clinical studies. Aim 3. Collect and bank fixed and frozen brain specimens, DNA and biospecimens (plasma, serum and cerebrospinal fluid) in accordance with the biospecimen best practice guidelines. A final diagnosis will be achieved by clinic-pathological consensus conferences to be held monthly with the Clinical Core (Core B). This will also serve as an important educational component that will integrate with the Outreach, Recruitment and Education Core (Core E). Brain tissue and other biological materials collected will be stored and provided to support research projects from approved investigators of the UF-MSMC ADRC and to qualified external investigators as well as a portion being sent to NCRAD. Genetic data will be provided to NIAGADS and the neuropathologic data will be provided to the National Alzheimer Coordinating Center (NACC) through the Data Management and Statistical Core (Core C).
|
0.915 |