Sherris, Allison R.
Loftus, Christine T.
Szpiro, Adam A.
Dearborn, Logan C.
Hazlehurst, Marnie F.
Carroll, Kecia N.
Moore, Paul E.
Adgent, Margaret A.
Barrett, Emily S.
Bush, Nicole R.
Day, Drew B.
Kannan, Kurunthachalam
LeWinn, Kaja Z.
Nguyen, Ruby H. N.
Ni, Yu
Riederer, Anne M.
Robinson, Morgan
Sathyanarayana, Sheela
Zhao, Qi
Karr, Catherine J.
Funding for this research was provided by:
NIH (UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271, UG3/UH3OD023271)
National Institutes of Health,United States (R01ES25169, R01ES25169, R01ES25169)
National Institute of Environmental Health Sciences (T32ES015459)
National Institutes of Health (R01HL132338, R01HL132338, UG3/UH3OD023305, UG3/UH3OD023305, R01ES016863, R01HL132338)
National Institutes of Health, United States (P30ES005022, P30ES007033)
Article History
Received: 30 June 2023
Accepted: 23 February 2024
First Online: 8 March 2024
Declarations
:
: The CANDLE study was approved by the University of Tennessee Health Science Center Institutional Review Board (IRB), and TIDES study procedures were approved by IRBs at each study site as well as the TIDES coordinating center. Pregnant women provided informed consent at enrollment. The current analysis was conducted by the ECHO PATHWAYS Consortium and was approved by the University of Washington IRB.
: The authors declare no competing interests.