The Core A (Administrative Core) is a large core that comprises sub-groups of administration, distinct resources of human materials, and data analyses/database construction. For efficient and central operation of the overall center, we have integrated these distinct components under the leadership of Core A PI, who also serves as the center director. This Core has three major aims: administrative leadership, organization of human bio-resources, and data organization/database maintenance.
In Aim 1, this Core will lead financial administration, organization of human and animal subject protocols, and coordination of research meetings and annual retreat inside this Center. This Core will provide scientific leadership to the entire Center by centrally organizing scientific issues towards uniform conclusions inside the Center, and coordinating collaborative research and material exchange with investigators outside the Center. This Core will maintain the web page of the P50 Conte center, organize education and outreach plans. Lastly, this Core will lead the Center in research rigor and integrity and make sure the members to observe data/resource sharing policies.
In Aim 2, this Core will organize and provide the center investigators with several types of established human resources, including three case-control sample sets for genetic study, the datasets of RNA-sequencing from human brains, blood from two prospective cohort samples, and human induced pluripotent stem cells.
In Aim 3, this Core will continue development of a database in which the multiple types of data obtained in Projects will be systematically stored to support investigators for data sharing, analysis, and preservation. This is also a basis of data and resource sharing within the scientific community as well as public outreach. In summary, believe that this Core will continuously play a key role by providing the central service in administrative coordination, organization of human bio-resources, and data management/database maintenance. This core will lead research rigor and integrity on behalf of the Center. We will emphasize educational and public outreach plans, according to the successful protocol that we have built in the current P50.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH094268-08
Application #
9544311
Study Section
Special Emphasis Panel (ZMH1)
Project Start
Project End
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
8
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Li, Ye; Viscidi, Raphael P; Kannan, Geetha et al. (2018) Chronic Toxoplasma gondii Infection Induces Anti-N-Methyl-d-Aspartate Receptor Autoantibodies and Associated Behavioral Changes and Neuropathology. Infect Immun 86:
Lindgren, Maija; Torniainen-Holm, Minna; Härkänen, Tommi et al. (2018) The association between toxoplasma and the psychosis continuum in a general population setting. Schizophr Res 193:329-335
Sedlak, Thomas W; Nucifora, Leslie G; Koga, Minori et al. (2018) Sulforaphane Augments Glutathione and Influences Brain Metabolites in Human Subjects: A Clinical Pilot Study. Mol Neuropsychiatry 3:214-222
McFarland, Ross; Wang, Zi Teng; Jouroukhin, Yan et al. (2018) AAH2 gene is not required for dopamine-dependent neurochemical and behavioral abnormalities produced by Toxoplasma infection in mouse. Behav Brain Res 347:193-200
Severance, Emily G; Yolken, Robert H (2018) Deciphering microbiome and neuroactive immune gene interactions in schizophrenia. Neurobiol Dis :
Sumitomo, Akiko; Yukitake, Hiroshi; Hirai, Kazuko et al. (2018) Ulk2 controls cortical excitatory-inhibitory balance via autophagic regulation of p62 and GABAA receptor trafficking in pyramidal neurons. Hum Mol Genet 27:3165-3176
Endo, Ryo; Takashima, Noriko; Nekooki-Machida, Yoko et al. (2018) TAR DNA-Binding Protein 43 and Disrupted in Schizophrenia 1 Coaggregation Disrupts Dendritic Local Translation and Mental Function in Frontotemporal Lobar Degeneration. Biol Psychiatry 84:509-521
Koh, Ming Teng; Ahrens, Paige S; Gallagher, Michela (2018) A greater tendency for representation mediated learning in a ketamine mouse model of schizophrenia. Behav Neurosci 132:106-113
Gusev, Alexander; Mancuso, Nicholas; Won, Hyejung et al. (2018) Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. Nat Genet 50:538-548
Koh, Ming Teng; Shao, Yi; Rosenzweig-Lipson, Sharon et al. (2018) Treatment with levetiracetam improves cognition in a ketamine rat model of schizophrenia. Schizophr Res 193:119-125

Showing the most recent 10 out of 190 publications