Abstract

The Human Translational Applications Core (P30-HTAC) supports the Consortium for Neuropsychiatric Phenomics (CNP) by providing services of three integrated units: (1) Human Recruitment and Phenotyping Unit;(2) Neuroimaging Unit;and (3) Statistics and Database Management Unit. The Human Recruitment and Phenotyping Unit serves the CNP by recruiting all human subjects and conducting all diagnostic, behavioral, personality, and cognitive data needed by Components 3 and 4. The human samples include a group of 2000 healthy people (referred to as the """"""""LA2K""""""""), and 100 individuals in each of three diagnostic groups (comprising people with the diagnoses of schizophrenia, bipolar disorder, and attention deficit/hyperactivity disorder), including people of both European and Hispanic/Latino ancestries. The Neuroimaging Unit will be responsible for sthe conduct of structural and functional neuroimaging aspects (including structural magnetic resonance imaging, functional magnetic resonance imaging, and diffusion tensor imaging) required for Components 3 and 4, acquiring all relevant data and providing analysis expertise to investigators within these components. The Statistics and Database Management Unit provides a range of statistical resource coordination, database management, and project management functions to all other CNP components. Each of the units within the P30-HTAC maintains standards to assure quality of CNP data. Collectively the three units of the P30-HTAC provide high quality services to the CNP with efficiency difficult for any individual project to achieve. The P30-HTAC further integrates delivery of these services to sustain the synergy and interactions across components within the CNP. The P30-HTAC also has scientific aims beyond its service roles: its units actively seeks to develop new methods in human behavioral and cognitive assessment, neuroimaging, and statistical methods for optimal phenotype definition and identification of relations between phenotypes and genotypes.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Linked Center Core Grant (PL1)
Project #
5PL1MH083271-05
Application #
8101070
Study Section
Special Emphasis Panel (ZRR1-SRC (99))
Program Officer
Rumsey, Judith M
Project Start
2007-09-29
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2013-06-30
Support Year
5
Fiscal Year
2011
Total Cost
$500,977
Indirect Cost

  Institution

Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095

  Publications

Orban, Pierre; Dansereau, Christian; Desbois, Laurence et al. (2018) Multisite generalizability of schizophrenia diagnosis classification based on functional brain connectivity. Schizophr Res 192:167-171
Ibrahim, Amira F A; Montojo, Caroline A; Haut, Kristen M et al. (2017) Spatial working memory in neurofibromatosis 1: Altered neural activity and functional connectivity. Neuroimage Clin 15:801-811
Trampush, J W; Yang, M L Z; Yu, J et al. (2017) GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Mol Psychiatry 22:336-345
Lam, Max; Trampush, Joey W; Yu, Jin et al. (2017) Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. Cell Rep 21:2597-2613
Anderson, Ariana E; Mansolf, Maxwell; Reise, Steven P et al. (2017) Measuring pathology using the PANSS across diagnoses: Inconsistency of the positive symptom domain across schizophrenia, schizoaffective, and bipolar disorder. Psychiatry Res 258:207-216
Poldrack, R A; Congdon, E; Triplett, W et al. (2016) A phenome-wide examination of neural and cognitive function. Sci Data 3:160110
Montojo, C A; Jalbrzikowski, M; Congdon, E et al. (2015) Neural substrates of inhibitory control deficits in 22q11.2 deletion syndrome. Cereb Cortex 25:1069-79
Robertson, Chelsea L; Ishibashi, Kenji; Mandelkern, Mark A et al. (2015) Striatal D1- and D2-type dopamine receptors are linked to motor response inhibition in human subjects. J Neurosci 35:5990-7
Montojo, C A; Congdon, E; Hwang, L et al. (2015) Neural mechanisms of response inhibition and impulsivity in 22q11.2 deletion carriers and idiopathic attention deficit hyperactivity disorder. Neuroimage Clin 9:310-21
Haut, Kristen M; Karlsgodt, Katherine H; Bilder, Robert M et al. (2015) Memory systems in schizophrenia: Modularity is preserved but deficits are generalized. Schizophr Res 168:223-30

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