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Authors
Fang, Fang
Zhou, Linran
Perng, Wei
Marsit, Carmen J.
Knight, Anna K.
Cardenas, Andres
Aung, Max T.
Hivert, Marie-France
Aris, Izzuddin M.
Goodrich, Jaclyn M.
Smith, Alicia K.
Gaylord, Abigail
Fry, Rebecca C.
Oken, Emily
O’Connor, George
Ruden, Douglas M.
Trasande, Leonardo
Herbstman, Julie B.
Camargo, Carlos A. Jr.
Bush, Nicole R.
Dunlop, Anne L.
Dabelea, Dana M.
Karagas, Margaret R.
Breton, Carrie V.
Ober, Carole
Everson, Todd M.
Page, Grier P.
Ladd-Acosta, Christine
,
Smith, P. B.
Newby, L. K.
Jacobson, L. P.
Catellier, D. J.
Gershon, R.
Cella, D.
Laham, F. R.
Mansbach, J. M.
Wu, S.
Spergel, J. M.
Celedón, J. C.
Puls, H. T.
Teach, S. J.
Porter, S. C.
Waynik, I. Y.
Iyer, S. S.
Samuels-Kalow, M. E.
D.Thompson, A.
Stevenson, M. D.
Bauer, C. S.
Inhofe, N. R.
Boos, M.
Macias, C. G.
Gern, J.
Jackson, D.
Bacharier, L.
Kattan, M.
Wood, R.
Rivera-Spoljaric, K.
Bacharier, L.
Bastain, T.
Farzan, S.
Habre, R.
Karr, C.
Tylavsky, F.
Mason, A.
Zhao, Q.
Sathyanarayana, S.
Bush, N.
LeWinn, K. Z.
Lester, B.
Carter, B.
Pastyrnak, S.
Neal, C.
Smith, L.
Helderman, J.
McEvoy, C.
Tepper, R.
Lyall, K.
Volk, H.
Schmidt, R.
Croen, L.
O’Shea, M.
Vaidya, R.
Obeid, R.
Rollins, C.
Bear, K.
Pastyrnak, S.
Lenski, M.
Singh, R.
Msall, M.
Frazier, J.
Gogcu, S.
Montgomery, A.
Kuban, K.
Douglass, L.
Jara, H.
Joseph, R.
Kerver, J. M.
Perera, F.
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Funding
Funding for this research was provided by:
Center for Clinical and Translational Research (KL2-TR002534)
NIH Office of the Director (R01MD009064, UH3OD023286, UH3OD023305, UH3OD023290, UH3OD023253, R01MD009064, R01DK076648, UH3OD023275, UH3OD023287)
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Article History
Received: 8 June 2023
Accepted: 12 August 2023
First Online: 2 September 2023
Declarations
:
: The ECHO-wide Cohort Data Collection Protocol operates under a single Institutional Review Board (IRB) administered by the Western Institutional Review Board (WIRB) Copernicus Group IRB, which is registered with both the Office for Human Research Protections (OHRP) and the FDA as IRB00000533. Compliance with regulatory requirements for the ECHO-wide Cohort Data Collection Protocol at participating cohort sites is the responsibility of properly constituted Institutional Review Boards, which can either be the ECHO single IRB or the ECHO cohort's local IRB. These governing IRBs review ECHO protocols, as well as informed consent/assent forms, HIPAA authorization forms, recruitment materials, and other relevant information before any ECHO-wide Cohort Data Collection Protocol-related procedures or activities can begin. The ECHO Data Analysis Center's work is approved by the Institutional Review Board at the Johns Hopkins Bloomberg School of Public Health. ECHO Cohort Investigators, or their designated study personnel, obtained written informed consent from all participants in the current study for both ECHO-wide Cohort Data Collection Protocol participation and participation in their specific cohorts.
: Not applicable.
: The authors declare no competing interests.
