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, Seth J. Gillihan is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
2005 — 2006 |
Gillihan, Seth J |
F31Activity Code Description: To provide predoctoral individuals with supervised research training in specified health and health-related areas leading toward the research degree (e.g., Ph.D.). |
Serotonin Transporter Genotype and Mood Regulation @ University of Pennsylvania
DESCRIPTION (provided by applicant): Given the enormous public health problem that depressive disorders represent there is significant benefit to be derived from the identification of depression vulnerability (DV) risk factors, including the development of preventive interventions. Recent research has found that allelic variation in the serotonin transporter gene-linked polymorphic region (5-HTTLPR) is related to depression outcomes under conditions of stress, with greater DV associated with the short (s) versus long (I) allele. For the current proposal a genetic high-risk design will be used: Individuals will be recruited who have the "high DV risk" (s/s) or "low DV risk" (I/I) genotype. The major aim of the proposal is to test the hypothesis that short-term mood-related behavioral outcomes vary as a function of an individual's 5-HTTLPR genotype, with poorer (i.e., DV) outcomes associated with the short (s) versus long (I) allele. These outcomes include, among others, greater reactivity to negative mood inducing events and poorer ability to recover from an acute negative mood. The identification of these hypothesized behavioral differences would represent significant progress toward developing interventions that reduce the risk of depression in those individuals identified as "at risk."
|
1 |