Administrative Core The Administrative Core is our overarching organizational unit and serves as the main communication arm of the Mount Sinai Lab Hub, working directly with the CHEAR Coordinating Center (CC) and NIH program staff. We will collaborate and communicate with the other Lab Hubs on QA/QC development. We will coordinate internally to maximize efficiency and will alter our priorities as directed by the CC (i.e. if areas of chemical analysis specialization develop or new biomarkers are needed). We will organize monthly Executive Steering Committee (ESC) meetings of the Resource/Core Leaders and other key personnel to coordinate intra-Hub work flow including planning receipt of sample shipments, re-labeling, tracking, and entry to our laboratory information management system (LIMS) system. ESC meetings will include CC staff to aid in communication of special programmatic needs to specific Hub components (e.g. a programmatic need to develop an assay for an emerging chemical of interest may arise as a directive to the Developmental Core and Targeted Resource). We will organize PI/Client consultation meetings in which we review the parent study for design, sample specimen availability, phenotypes, and requested types of exposures to be measured. We will then make recommendations to best fit the PI/Client's goals, while addressing any scientific or technical issues that may limit feasibility prior to conducting assay analysis. We will also track the progress of on-going jobs and generate regular reports to the Coordinating Center and to NIH program. We will coordinate data reporting with the CHEAR Data Center (DC), ensuring that our databases are properly formatted and contain the appropriate metadata. We will also collaborate with the DC and Client/PI in the interpretation of results (i.e. QA/QC issues) and the statistical analysis of exposure/phenotype relationships. We will organize and implement an annual Lab Hub workshop that will engage existing and potential clients in Exposure Biology assay methodologies and inform users on how to access our web based LIMS interface for tracking job progress through the Lab Hub system. In sum, we will 1) coordinate communication internally within the Lab Hub and externally with the Coordinating Center, Data Center, PI/Clients and NIH program; 2) develop the procedures, protocols and system checks to ensure samples flow to the correct Resource/Core and that QA/QC protocols are followed rigorously; 3) maintain a LIMS system that is user friendly, facilitates sample tracking, prevents mismatches between samples and results, and integrates with the needs of the Data Center; 4) provide scientific consultation services to PI/Clients that maximizes the information and quality of their study results; 5) ensure that feedback communication occurs between Clients and Resources/Cores and that this information is relayed transparently to the CC and NIH and 6) ensure transparent fiscal management of the Lab Hub program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Resource-Related Research Multi-Component Projects and Centers Cooperative Agreements (U2C)
Project #
1U2CES026561-01
Application #
9062193
Study Section
Special Emphasis Panel (ZES1-LWJ-J (UC))
Project Start
2015-09-30
Project End
2019-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
1
Fiscal Year
2015
Total Cost
$519,997
Indirect Cost
$213,213
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Wright, Robert O; Teitelbaum, Susan; Thompson, Claudia et al. (2018) The child health exposure analysis resource as a vehicle to measure environment in the environmental influences on child health outcomes program. Curr Opin Pediatr 30:285-291
Sanders, Alison P; Saland, Jeffrey M; Wright, Robert O et al. (2018) Perinatal and childhood exposure to environmental chemicals and blood pressure in children: a review of literature 2007-2017. Pediatr Res 84:165-180
Curtin, Paul; Austin, Christine; Curtin, Austen et al. (2018) Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder. Sci Adv 4:eaat1293
Smith, Tanya M; Austin, Christine; Hinde, Katie et al. (2017) Cyclical nursing patterns in wild orangutans. Sci Adv 3:e1601517
Wright, Robert O (2017) Environment, susceptibility windows, development, and child health. Curr Opin Pediatr 29:211-217
Andra, Syam S; Austin, Christine; Patel, Dhavalkumar et al. (2017) Trends in the application of high-resolution mass spectrometry for human biomonitoring: An analytical primer to studying the environmental chemical space of the human exposome. Environ Int 100:32-61
Wolff, Mary S; Buckley, Jessie P; Engel, Stephanie M et al. (2017) Emerging exposures of developmental toxicants. Curr Opin Pediatr 29:218-224
Evrard, Solene M; Lecce, Laura; Michelis, Katherine C et al. (2016) Endothelial to mesenchymal transition is common in atherosclerotic lesions and is associated with plaque instability. Nat Commun 7:11853
Kappil, Maya; Wright, Robert O; Sanders, Alison P (2016) Developmental Origins of Common Disease: Epigenetic Contributions to Obesity. Annu Rev Genomics Hum Genet 17:177-92
Andra, Syam S; Austin, Christine; Yang, Juan et al. (2016) Recent advances in simultaneous analysis of bisphenol A and its conjugates in human matrices: Exposure biomarker perspectives. Sci Total Environ 572:770-781

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