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Organophosphate Flame Retardants in Pregnant Women: Sources, Occurrence, and Potential Risks to Pregnancy Outcomes
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/em.22322openalex-snapshot
Tris(1,3‐dichloro‐2‐propyl) phosphate disturbs mouse embryonic development by inducing apoptosis and abnormal DNA methylation
inferredcites →https://doi.org/10.1002/jat.2550130408openalex-snapshot
Whole‐body autoradiographic disposition, elimination and placental transport of [14C]Tri‐o‐cresyl phosphate in mice
inferredcites →https://doi.org/10.1002/jat.3569openalex-snapshot
Early‐life exposure to Tris(1,3‐dichloroisopropyl) phosphate induces dose‐dependent suppression of sexual behavior in male rats
inferredcites →https://doi.org/10.1002/jbt.21439openalex-snapshot
Accumulation and Endocrine Disrupting Effects of the Flame Retardant Mixture Firemaster ® 550 in Rats: An Exploratory Assessment
inferredcites →https://doi.org/10.1002/jcp.28729openalex-snapshot
Acute exposure to triphenyl phosphate inhibits the proliferation and cardiac differentiation of mouse embryonic stem cells and zebrafish embryos
inferredcites →https://doi.org/10.1007/s00128-021-03454-7openalex-snapshot
Industrial Production of Organophosphate Flame Retardants (OPFRs): Big Knowledge Gaps Need to Be Filled?
inferredcites →https://doi.org/10.1007/s00204-018-2275-zopenalex-snapshot
Recent biomonitoring reports on phosphate ester flame retardants: a short review
inferredcites →https://doi.org/10.1007/s11356-012-1237-xopenalex-snapshot
Organophosphorus flame retardants in house dust from the Philippines: occurrence and assessment of human exposure
inferredcites →https://doi.org/10.1007/s11356-021-15861-8openalex-snapshot
A review of environmental occurrence, analysis, bioaccumulation, and toxicity of organophosphate esters
inferredcites →https://doi.org/10.1007/s11906-018-0888-5openalex-snapshot
Environmental Toxicant Exposure and Hypertensive Disorders of Pregnancy: Recent Findings
inferredcites →https://doi.org/10.1007/s40572-019-00258-0openalex-snapshot
Organophosphate Esters: Are These Flame Retardants and Plasticizers Affecting Children’s Health?
inferredcites →https://doi.org/10.1007/s40572-021-00317-5openalex-snapshot
Racial/Ethnic Disparities in Pregnancy and Prenatal Exposure to Endocrine-Disrupting Chemicals Commonly Used in Personal Care Products
inferredcites →https://doi.org/10.1016/0140-6736(90)92159-fopenalex-snapshot
Recurrent miscarriage I: definition and epidemiology
inferredcites →https://doi.org/10.1016/j.aogh.2016.01.004openalex-snapshot
Health Consequences of Environmental Exposures: Causal Thinking in Global Environmental Epidemiology
inferredcites →https://doi.org/10.1016/j.aquatox.2012.02.019openalex-snapshot
Endocrine disruption potentials of organophosphate flame retardants and related mechanisms in H295R and MVLN cell lines and in zebrafish
inferredcites →https://doi.org/10.1016/j.aquatox.2012.11.009openalex-snapshot
Exposure of zebrafish embryos/larvae to TDCPP alters concentrations of thyroid hormones and transcriptions of genes involved in the hypothalamic–pituitary–thyroid axis
inferredcites →https://doi.org/10.1016/j.aquatox.2012.12.010openalex-snapshot
Effects of tris(1,3-dichloro-2-propyl) phosphate and triphenyl phosphate on receptor-associated mRNA expression in zebrafish embryos/larvae
inferredcites →https://doi.org/10.1016/j.aquatox.2015.01.027openalex-snapshot
Aryl organophosphate flame retardants induced cardiotoxicity during zebrafish embryogenesis: By disturbing expression of the transcriptional regulators
inferredcites →https://doi.org/10.1016/j.aquatox.2017.07.015openalex-snapshot
Acute exposure to tris (2-butoxyethyl) phosphate (TBOEP) affects growth and development of embryo-larval zebrafish
inferredcites →https://doi.org/10.1016/j.aquatox.2017.09.003openalex-snapshot
Tris(1,3-dichloro-2-propyl) phosphate disrupts axonal growth, cholinergic system and motor behavior in early life zebrafish
inferredcites →https://doi.org/10.1016/j.aquatox.2018.05.010openalex-snapshot
Exposure to tris(1,3-dichloro-2-propyl) phosphate for Two generations decreases fecundity of zebrafish at environmentally relevant concentrations
inferredcites →https://doi.org/10.1016/j.aquatox.2018.08.001openalex-snapshot
Developmental neurotoxicity of triphenyl phosphate in zebrafish larvae
inferredcites →https://doi.org/10.1016/j.chemosphere.2010.09.013openalex-snapshot
Kinetic differences of legacy organochlorine pesticides and polychlorinated biphenyls in Vietnamese human breast milk
inferredcites →https://doi.org/10.1016/j.chemosphere.2014.02.033openalex-snapshot
Organophosphorus flame retardants (PFRs) in human breast milk from several Asian countries
inferredcites →https://doi.org/10.1016/j.chemosphere.2015.09.049openalex-snapshot
Kinetics of tris (1-chloro-2-propyl) phosphate (TCIPP) metabolism in human liver microsomes and serum
inferredcites →https://doi.org/10.1016/j.chemosphere.2015.11.084openalex-snapshot
Inhalation a significant exposure route for chlorinated organophosphate flame retardants
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.03.003openalex-snapshot
Review of OPFRs in animals and humans: Absorption, bioaccumulation, metabolism, and internal exposure research
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.04.016openalex-snapshot
Organophosphate esters in dust samples collected from Danish homes and daycare centers
inferredcites →https://doi.org/10.1016/j.chemosphere.2016.10.058openalex-snapshot
Novel method to determine the lipid content of breast milk
inferredcites →https://doi.org/10.1016/j.chemosphere.2017.09.037openalex-snapshot
Current-use flame retardants: Maternal exposure and neurodevelopment in children of the CHAMACOS cohort
inferredcites →https://doi.org/10.1016/j.chemosphere.2018.12.008openalex-snapshot
Differential exposure to organophosphate flame retardants in mother-child pairs
inferredcites →https://doi.org/10.1016/j.chemosphere.2018.12.198openalex-snapshot
The adverse effect of TCIPP and TCEP on neurodevelopment of zebrafish embryos/larvae
inferredcites →https://doi.org/10.1016/j.chemosphere.2019.04.085openalex-snapshot
Polyurethane heat preservation materials: The significant sources of organophosphorus flame retardants
inferredcites →https://doi.org/10.1016/j.chemosphere.2020.129375openalex-snapshot
Exposure to organophosphate flame esters during early pregnancy and risk of spontaneous abortion: A case-control study
inferredcites →https://doi.org/10.1016/j.ecoenv.2018.11.038openalex-snapshot
Presence and human exposure assessment of organophosphate flame retardants (OPEs) in indoor dust and air in Beijing, China
inferredcites →https://doi.org/10.1016/j.ecoenv.2018.11.058openalex-snapshot
Effects of tris(1,3-dichloro-2-propyl) phosphate (TDCPP) and triphenyl phosphate (TPP) on sex-dependent alterations of thyroid hormones in adult zebrafish
inferredcites →https://doi.org/10.1016/j.ecoenv.2019.04.056openalex-snapshot
Acute exposure to triphenyl phosphate (TPhP) disturbs ocular development and muscular organization in zebrafish larvae
inferredcites →https://doi.org/10.1016/j.ecoenv.2019.109449openalex-snapshot
Tris(1,3-dichloro-2-propyl)phosphate (TDCIPP) disrupts zebrafish tail fin development
inferredcites →https://doi.org/10.1016/j.ecoenv.2020.111263openalex-snapshot
Effects of tris(2-chloroethyl) phosphate exposure on chicken embryos in a shell-less incubation system
inferredcites →https://doi.org/10.1016/j.ecoenv.2021.112904openalex-snapshot
Graphene-triphenyl phosphate (TPP) co-exposure in the marine environment: Interference with metabolism and immune regulation in mussel Mytilus galloprovincialis
inferredcites →https://doi.org/10.1016/j.ecoenv.2022.113707openalex-snapshot
Occupational exposure to organophosphate esters in e-waste dismantling workers: Risk assessment and influencing factors screening
inferredcites →https://doi.org/10.1016/j.envint.2009.08.002openalex-snapshot
Concentrations and determinants of outdoor, indoor and personal nitrogen dioxide in pregnant women from two Spanish birth cohorts
inferredcites →https://doi.org/10.1016/j.envint.2013.11.013openalex-snapshot
Urinary metabolites of organophosphate flame retardants and their variability in pregnant women
inferredcites →https://doi.org/10.1016/j.envint.2015.07.021openalex-snapshot
Estimation of exposure to atmospheric pollutants during pregnancy integrating space–time activity and indoor air levels: Does it make a difference?
inferredcites →https://doi.org/10.1016/j.envint.2016.10.007openalex-snapshot
Predictors of urinary flame retardant concentration among pregnant women
inferredcites →https://doi.org/10.1016/j.envint.2017.01.020openalex-snapshot
Associations between urinary diphenyl phosphate and thyroid function
inferredcites →https://doi.org/10.1016/j.envint.2017.03.009openalex-snapshot
Assessment of dietary exposure to organohalogen contaminants, legacy and emerging flame retardants in a Norwegian cohort
inferredcites →https://doi.org/10.1016/j.envint.2017.11.019openalex-snapshot
Urinary metabolites of organophosphate esters: Concentrations and age trends in Australian children
inferredcites →https://doi.org/10.1016/j.envint.2017.12.005openalex-snapshot
Paternal urinary concentrations of organophosphate flame retardant metabolites, fertility measures, and pregnancy outcomes among couples undergoing in vitro fertilization
inferredcites →https://doi.org/10.1016/j.envint.2018.04.016openalex-snapshot
Prenatal exposure to organophosphates and associations with birthweight and gestational length
inferredcites →https://doi.org/10.1016/j.envint.2018.07.015openalex-snapshot
Identifying the PECO: A framework for formulating good questions to explore the association of environmental and other exposures with health outcomes
inferredcites →https://doi.org/10.1016/j.envint.2018.07.018openalex-snapshot
Associations between allergic symptoms and phosphate flame retardants in dust and their urinary metabolites among school children
inferredcites →https://doi.org/10.1016/j.envint.2018.10.021openalex-snapshot
Are cell phones an indicator of personal exposure to organophosphate flame retardants and plasticizers?
inferredcites →https://doi.org/10.1016/j.envint.2019.03.009openalex-snapshot
A review on organophosphate Ester (OPE) flame retardants and plasticizers in foodstuffs: Levels, distribution, human dietary exposure, and future directions
inferredcites →https://doi.org/10.1016/j.envint.2019.104914openalex-snapshot
Organophosphate flame retardants (OPFRs) induce genotoxicity in vivo: A survey on apoptosis, DNA methylation, DNA oxidative damage, liver metabolites, and transcriptomics
inferredcites →https://doi.org/10.1016/j.envint.2019.105178openalex-snapshot
Organophosphate esters in indoor dust from 12 countries: Concentrations, composition profiles, and human exposure
inferredcites →https://doi.org/10.1016/j.envint.2019.105293openalex-snapshot
Early-life exposure to the organophosphorus flame-retardant tris (1,3-dichloro-2-propyl) phosphate induces delayed neurotoxicity associated with DNA methylation in adult zebrafish
inferredcites →https://doi.org/10.1016/j.envint.2019.105321openalex-snapshot
Estimating renal and hepatic clearance rates of organophosphate esters in humans: Impacts of intrinsic metabolism and binding affinity with plasma proteins
inferredcites →https://doi.org/10.1016/j.envint.2020.105919openalex-snapshot
Bioaccumulation and trophic transfer of organophosphate esters in tropical marine food web, South China Sea
inferredcites →https://doi.org/10.1016/j.envint.2020.106215openalex-snapshot
Exposure to organophosphate ester flame retardants and plasticizers during pregnancy: Thyroid endocrine disruption and mediation role of oxidative stress
inferredcites →https://doi.org/10.1016/j.envint.2020.106224openalex-snapshot
A review of the transplacental transfer of persistent halogenated organic pollutants: Transfer characteristics, influential factors, and mechanisms
inferredcites →https://doi.org/10.1016/j.envint.2021.106640openalex-snapshot
Prenatal exposure to organophosphate esters and neonatal thyroid-stimulating hormone levels: A birth cohort study in Wuhan, China
inferredcites →https://doi.org/10.1016/j.envint.2021.106860openalex-snapshot
Occurrence of novel organophosphate esters derived from organophosphite antioxidants in an e-waste dismantling area: Associations between hand wipes and dust
inferredcites →https://doi.org/10.1016/j.envint.2022.107590openalex-snapshot
Accumulation of microplastics and Tcep pollutants in agricultural soil: Exploring the links between metabolites and gut microbiota in earthworm homeostasis
inferredcites →https://doi.org/10.1016/j.envpol.2013.07.030openalex-snapshot
Mercury concentrations in human placenta, umbilical cord, cord blood and amniotic fluid and their relations with body parameters of newborns
inferredcites →https://doi.org/10.1016/j.envpol.2015.11.051openalex-snapshot
Thyroid hormone-disrupting activity and ecological risk assessment of phosphorus-containing flame retardants by in vitro, in vivo and in silico approaches
inferredcites →https://doi.org/10.1016/j.envpol.2016.04.049openalex-snapshot
Effects of tris(2-butoxyethyl) phosphate exposure on endocrine systems and reproduction of zebrafish (Danio rerio)
inferredcites →https://doi.org/10.1016/j.envpol.2017.06.089openalex-snapshot
Occurrence and fate of organophosphate ester flame retardants and plasticizers in indoor air and dust of Nepal: Implication for human exposure
inferredcites →https://doi.org/10.1016/j.envpol.2017.07.002openalex-snapshot
Probing the relationship between external and internal human exposure of organophosphate flame retardants using pharmacokinetic modelling
inferredcites →https://doi.org/10.1016/j.envpol.2018.04.086openalex-snapshot
Concentrations and variability of organophosphate esters, halogenated flame retardants, and polybrominated diphenyl ethers in indoor and outdoor air in Stockholm, Sweden
inferredcites →https://doi.org/10.1016/j.envpol.2018.08.051openalex-snapshot
Urinary metabolites of organophosphate flame retardants in 0–5-year-old children: Potential exposure risk for inpatients and home-stay infants
inferredcites →https://doi.org/10.1016/j.envpol.2018.12.020openalex-snapshot
Organophosphate esters in the water, sediments, surface soils, and tree bark surrounding a manufacturing plant in north China
inferredcites →https://doi.org/10.1016/j.envpol.2018.12.053openalex-snapshot
Effects of triphenyl phosphate exposure during fetal development on obesity and metabolic dysfunctions in adult mice: Impaired lipid metabolism and intestinal dysbiosis
inferredcites →https://doi.org/10.1016/j.envpol.2018.12.066openalex-snapshot
Exposure to tris(1,3-dichloro-2-propyl) phosphate (TDCPP) induces vascular toxicity through Nrf2-VEGF pathway in zebrafish and human umbilical vein endothelial cells
inferredcites →https://doi.org/10.1016/j.envpol.2019.05.110openalex-snapshot
Early life exposure to triphenyl phosphate: Effects on thyroid function, growth, and resting metabolic rate of Japanese quail (Coturnix japonica) chicks
inferredcites →https://doi.org/10.1016/j.envpol.2019.113695openalex-snapshot
Assessment of the effects of early life exposure to triphenyl phosphate on fear, boldness, aggression, and activity in Japanese quail (Coturnix japonica) chicks
inferredcites →https://doi.org/10.1016/j.envpol.2021.117532openalex-snapshot
Characteristics and risk assessment of organophosphate esters and phthalates in soils and vegetation from Dalian, northeast China
inferredcites →https://doi.org/10.1016/j.envres.2009.03.008openalex-snapshot
Determinants of organochlorine levels detectable in the amniotic fluid of women from Tenerife Island (Canary Islands, Spain)
inferredcites →https://doi.org/10.1016/j.envres.2016.12.033openalex-snapshot
Birds and flame retardants: A review of the toxic effects on birds of historical and novel flame retardants
inferredcites →https://doi.org/10.1016/j.envres.2019.108756openalex-snapshot
The association of urinary organophosphate ester metabolites and self-reported personal care and household product use among pregnant women in Puerto Rico
inferredcites →https://doi.org/10.1016/j.envres.2020.109255openalex-snapshot
Organophosphate esters in a cohort of pregnant women: Variability and predictors of exposure
inferredcites →https://doi.org/10.1016/j.envres.2020.109874openalex-snapshot
Exposure to organophosphate esters, phthalates, and alternative plasticizers in association with uterine fibroids
inferredcites →https://doi.org/10.1016/j.envres.2021.112220openalex-snapshot
Maternal urinary OPE metabolite concentrations and blood pressure during pregnancy: The HOME study
inferredcites →https://doi.org/10.1016/j.etap.2015.06.021openalex-snapshot
Exposure of male mice to two kinds of organophosphate flame retardants (OPFRs) induced oxidative stress and endocrine disruption
inferredcites →https://doi.org/10.1016/j.etap.2021.103600openalex-snapshot
Effects of environmentally relevant concentrations of tris (2-chloroethyl) phosphate (TCEP) on early life stages of zebrafish (Danio rerio)
inferredcites →https://doi.org/10.1016/j.etap.2021.103699openalex-snapshot
Effects of tris (2-chloroethyl) phosphate (TCEP) on survival, growth, histological changes and gene expressions in juvenile yellow catfish Pelteobagrus fulvidraco
inferredcites →https://doi.org/10.1016/j.fertnstert.2018.06.045openalex-snapshot
Organophosphate flame-retardant metabolite concentrations and pregnancy loss among women conceiving with assisted reproductive technology
inferredcites →https://doi.org/10.1016/j.jhazmat.2020.124020openalex-snapshot
The risk and impact of organophosphate esters on the development of female-specific cancers: Comparative analysis of patients with benign and malignant tumors
inferredcites →https://doi.org/10.1016/j.jhazmat.2020.124754openalex-snapshot
Trimester-specific effects of maternal exposure to organophosphate flame retardants on offspring size at birth: A prospective cohort study in China
inferredcites →https://doi.org/10.1016/j.jhazmat.2020.124856openalex-snapshot
Prenatal exposure to halogenated, aryl, and alkyl organophosphate esters and child neurodevelopment at two years of age
inferredcites →https://doi.org/10.1016/j.jhazmat.2021.126279openalex-snapshot
Human internal exposure to organophosphate esters: A short review of urinary monitoring on the basis of biological metabolism research
inferredcites →https://doi.org/10.1016/j.jhazmat.2022.129728openalex-snapshot
Percutaneous absorption and exposure risk assessment of organophosphate esters in children’s toys
inferredcites →https://doi.org/10.1016/j.ntt.2015.08.004openalex-snapshot
Neurotoxicological and thyroid evaluations of rats developmentally exposed to tris(1,3-dichloro-2-propyl)phosphate (TDCIPP) and tris(2-chloro-2-ethyl)phosphate (TCEP)
inferredcites →https://doi.org/10.1016/j.ntt.2018.10.002openalex-snapshot
Toxicity profiling of flame retardants in zebrafish embryos using a battery of assays for developmental toxicity, neurotoxicity, cardiotoxicity and hepatotoxicity toward human relevance
inferredcites →https://doi.org/10.1016/j.placenta.2015.11.013openalex-snapshot
Effects of prenatal maternal stress on serotonin and fetal development
inferredcites →https://doi.org/10.1016/j.reprotox.2007.03.003openalex-snapshot
Concentrations of xenobiotic chemicals in the maternal-fetal unit
inferredcites →https://doi.org/10.1016/j.reprotox.2016.07.009openalex-snapshot
Perinatal triphenyl phosphate exposure accelerates type 2 diabetes onset and increases adipose accumulation in UCD-type 2 diabetes mellitus rats
inferredcites →https://doi.org/10.1016/j.scitotenv.2016.02.171openalex-snapshot
Organophosphate ester flame retardants and plasticizers in human placenta in Eastern China
inferredcites →https://doi.org/10.1016/j.scitotenv.2019.06.442openalex-snapshot
Polybrominated diphenyl ethers and novel brominated flame retardants in human milk from the general population in Beijing, China: Occurrence, temporal trends, nursing infants' exposure and risk assessment
inferredcites →https://doi.org/10.1016/j.scitotenv.2019.134798openalex-snapshot
An exploratory analysis of urinary organophosphate ester metabolites and oxidative stress among pregnant women in Puerto Rico
inferredcites →https://doi.org/10.1016/j.scitotenv.2019.135328openalex-snapshot
Occurrence and distribution of organophosphate esters in sediment from northern Chinese coastal waters
inferredcites →https://doi.org/10.1016/j.scitotenv.2020.139071openalex-snapshot
A review of organophosphate flame retardants and plasticizers in the environment: Analysis, occurrence and risk assessment
inferredcites →https://doi.org/10.1016/j.scitotenv.2021.145404openalex-snapshot
Organophosphorus flame retardants in breast milk from Beijing, China: Occurrence, nursing infant's exposure and risk assessment
inferredcites →https://doi.org/10.1016/j.scitotenv.2021.148837openalex-snapshot
A review on organophosphate flame retardants in the environment: Occurrence, accumulation, metabolism and toxicity
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.154271openalex-snapshot
Organophosphate esters in agro-foods: Occurrence, sources and emerging challenges
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.154272openalex-snapshot
Organophosphate esters and their diester metabolites in infant formulas and baby supplementary foods collected in Beijing, China: Occurrence and the implications for infant exposure
inferredcites →https://doi.org/10.1016/j.scitotenv.2022.160915openalex-snapshot
Organophosphate esters in Chinese rice: Occurrence, distribution, and human exposure risks
inferredcites →https://doi.org/10.1016/j.sste.2022.100502openalex-snapshot
Time-activity and daily mobility patterns during pregnancy and early postpartum – evidence from the MADRES cohort
inferredcites →https://doi.org/10.1016/j.taap.2014.06.024openalex-snapshot
Tris(2-butoxyethyl)phosphate and triethyl phosphate alter embryonic development, hepatic mRNA expression, thyroid hormone levels, and circulating bile acid concentrations in chicken embryos
inferredcites →https://doi.org/10.1016/j.toxlet.2013.08.012openalex-snapshot
First insights in the metabolism of phosphate flame retardants and plasticizers using human liver fractions
inferredcites →https://doi.org/10.1016/j.yhbeh.2020.104759openalex-snapshot
Maternal exposure to organophosphate flame retardants alters locomotor and anxiety-like behavior in male and female adult offspring
inferredcites →https://doi.org/10.1017/s0007114507764747openalex-snapshot
Dietary fat intakes for pregnant and lactating women
inferredcites →https://doi.org/10.1021/acs.est.0c06095openalex-snapshot
Transplacental Behaviors of Organophosphate Tri- and Diesters Based on Paired Human Maternal and Cord Whole Blood: Efficiencies and Impact Factors
inferredcites →https://doi.org/10.1021/acs.est.6b00365openalex-snapshot
Organophosphate Esters in Canadian Arctic Air: Occurrence, Levels and Trends
inferredcites →https://doi.org/10.1021/acs.est.7b00872openalex-snapshot
Activation of Peroxisome Proliferator-Activated Receptor Gamma and Disruption of Progesterone Synthesis of 2-Ethylhexyl Diphenyl Phosphate in Human Placental Choriocarcinoma Cells: Comparison with Triphenyl Phosphate
inferredcites →https://doi.org/10.1021/acs.est.7b01122openalex-snapshot
Organophosphorus Flame Retardants in Pregnant Women and Their Transfer to Chorionic Villi
inferredcites →https://doi.org/10.1021/acs.est.7b01289openalex-snapshot
Organophosphate Esters in Air, Snow, and Seawater in the North Atlantic and the Arctic
inferredcites →https://doi.org/10.1021/acs.est.7b06395openalex-snapshot
Occurrence of Organophosphorus Flame Retardants and Plasticizers (PFRs) in Belgian Foodstuffs and Estimation of the Dietary Exposure of the Adult Population
inferredcites →https://doi.org/10.1021/acs.est.8b00838openalex-snapshot
Distribution of Phthalate Metabolites between Paired Maternal–Fetal Samples
inferredcites →https://doi.org/10.1021/acs.est.8b03043openalex-snapshot
Concentrations of Organophosphate Esters and Their Specific Metabolites in Food in Southeast Queensland, Australia: Is Dietary Exposure an Important Pathway of Organophosphate Esters and Their Metabolites?
inferredcites →https://doi.org/10.1021/acs.est.8b07238openalex-snapshot
Diphenyl Phosphate-Induced Toxicity During Embryonic Development
inferredcites →https://doi.org/10.1021/acs.est.9b00715openalex-snapshot
Prenatal Exposure to Per- and Polyfluoroalkyl Substances (PFASs) and Association between the Placental Transfer Efficiencies and Dissociation Constant of Serum Proteins–PFAS Complexes
inferredcites →https://doi.org/10.1021/acs.est.9b05669openalex-snapshot
Triphenyl Phosphate at Environmental Levels Retarded Ovary Development and Reduced Egg Production in Japanese Medaka (Oryzias latipes)
inferredcites →https://doi.org/10.1021/acs.est.9b06026openalex-snapshot
Prenatal Exposure to Organophosphate Flame Retardants and the Risk of Low Birth Weight: A Nested Case-Control Study in China
inferredcites →https://doi.org/10.1021/acs.estlett.0c00916openalex-snapshot
Organophosphate Esters and Their Metabolites in Breast Milk from the United States: Breastfeeding Is an Important Exposure Pathway for Infants
inferredcites →https://doi.org/10.1021/acs.estlett.1c00210openalex-snapshot
Early Life Exposure to Tris(2-butoxyethyl) Phosphate (TBOEP) Is Related to the Development of Childhood Asthma
inferredcites →https://doi.org/10.1021/acs.estlett.9b00394openalex-snapshot
Organophosphorus Flame Retardants and Plasticizers in Breast Milk from the United States
inferredcites →https://doi.org/10.1021/acs.jafc.1c05697openalex-snapshot
Occurrence and Dietary Intake of Organophosphate Esters via Animal-Origin Food Consumption in China: Results of a Chinese Total Diet Study
inferredcites →https://doi.org/10.1021/acs.jafc.2c03603openalex-snapshot
Organophosphate Esters in Foodstuffs from Multiple Provinces in China: Possible Sources during Food Processing and Implications for Human Exposure
inferredcites →https://doi.org/10.1021/acs.jafc.8b06114openalex-snapshot
Concentrations and Dietary Exposure to Organophosphate Esters in Foodstuffs from Albany, New York, United States
inferredcites →https://doi.org/10.1021/es405337gopenalex-snapshot
Organophosphate Ester (OPE) Flame Retardants and Plasticizers in the Open Mediterranean and Black Seas Atmosphere
inferredcites →https://doi.org/10.1021/es801070popenalex-snapshot
Alternate and New Brominated Flame Retardants Detected in U.S. House Dust
inferredcites →https://doi.org/10.1038/jes.2008.24openalex-snapshot
Time–activity patterns of pregnant women and changes during the course of pregnancy
inferredcites →https://doi.org/10.1038/s41370-019-0122-9openalex-snapshot
The association of urinary phosphorous-containing flame retardant metabolites and self-reported personal care and household product use among couples seeking fertility treatment
inferredcites →https://doi.org/10.1038/s41370-021-00327-3openalex-snapshot
Personal care product use among diverse women in California: Taking Stock Study
inferredcites →https://doi.org/10.1038/s41598-017-07216-6openalex-snapshot
Sex Specific Placental Accumulation and Behavioral Effects of Developmental Firemaster 550 Exposure in Wistar Rats
inferredcites →https://doi.org/10.1039/b921910bopenalex-snapshot
Organophosphorus flame retardants and plasticizers in marine and fresh water biota and in human milk
inferredcites →https://doi.org/10.1039/c8em00389kopenalex-snapshot
A pilot study of metabolites of organophosphorus flame retardants in paired maternal urine and amniotic fluid samples: potential exposure risks of tributyl phosphate to pregnant women
inferredcites →https://doi.org/10.1056/nejm199908193410801openalex-snapshot
Maternal Thyroid Deficiency during Pregnancy and Subsequent Neuropsychological Development of the Child
inferredcites →https://doi.org/10.1080/10643389.2022.2050147openalex-snapshot
Endocrine disrupting toxicity of aryl organophosphate esters and mode of action
inferredcites →https://doi.org/10.1080/10643389.2022.2087428openalex-snapshot
Review on age-specific exposure to organophosphate esters: Multiple exposure pathways and microenvironments
inferredcites →https://doi.org/10.1080/10937404.2014.884956openalex-snapshot
Relationships of Chemical Concentrations in Maternal and Cord Blood: A Review of Available Data
inferredcites →https://doi.org/10.1093/aje/kwab086openalex-snapshot
Maternal Urinary Organophosphate Esters and Alterations in Maternal and Neonatal Thyroid Hormones
inferredcites →https://doi.org/10.1093/toxsci/kft020openalex-snapshot
Aryl Phosphate Esters Within a Major PentaBDE Replacement Product Induce Cardiotoxicity in Developing Zebrafish Embryos: Potential Role of the Aryl Hydrocarbon Receptor
inferredcites →https://doi.org/10.1093/toxsci/kft100openalex-snapshot
In Ovo Effects of Two Organophosphate Flame Retardants—TCPP and TDCPP—on Pipping Success, Development, mRNA Expression, and Thyroid Hormone Levels in Chicken Embryos
inferredcites →https://doi.org/10.1093/toxsci/kfw122openalex-snapshot
Editor’s Highlight: Transplacental and Lactational Transfer of Firemaster® 550 Components in Dosed Wistar Rats
inferredcites →https://doi.org/10.1093/toxsci/kfy037openalex-snapshot
Disruption of Nuclear Receptor Signaling Alters Triphenyl Phosphate-Induced Cardiotoxicity in Zebrafish Embryos
inferredcites →https://doi.org/10.1111/mcn.12916openalex-snapshot
Dietary guideline adherence during preconception and pregnancy: A systematic review
inferredcites →https://doi.org/10.1177/0734904107083553openalex-snapshot
The Potential for Volatile Phosphorus-containing Flame Retardants in Textile Back-coatings
inferredcites →https://doi.org/10.1186/s12884-014-0373-3openalex-snapshot
Reported dietary intake in early pregnant compared to non-pregnant women – a cross-sectional study
inferredcites →https://doi.org/10.1186/s12885-018-4553-9openalex-snapshot
A case-control study of exposure to organophosphate flame retardants and risk of thyroid cancer in women
inferredcites →https://doi.org/10.1186/s12940-017-0224-6openalex-snapshot
Cross-sectional study of social behaviors in preschool children and exposure to flame retardants
inferredcites →https://doi.org/10.1186/s12940-017-0247-zopenalex-snapshot
Variability and predictors of urinary concentrations of organophosphate flame retardant metabolites among pregnant women in Rhode Island
inferredcites →https://doi.org/10.1186/s12940-020-00610-0openalex-snapshot
Predictors and reproducibility of urinary organophosphate ester metabolite concentrations during pregnancy and associations with birth outcomes in an urban population
inferredcites →https://doi.org/10.1186/s12940-020-00648-0openalex-snapshot
Maternal urinary concentrations of organophosphate ester metabolites: associations with gestational weight gain, early life anthropometry, and infant eating behaviors among mothers-infant pairs in Rhode Island
inferredcites →https://doi.org/10.1186/s12940-021-00724-zopenalex-snapshot
Prenatal exposure to consumer product chemical mixtures and size for gestational age at delivery
inferredcites →https://doi.org/10.1210/en.2015-1350openalex-snapshot
Life-Long Implications of Developmental Exposure to Environmental Stressors: New Perspectives
inferredcites →https://doi.org/10.1210/er.2013-1122openalex-snapshot
Implications of Prenatal Steroid Perturbations for Neurodevelopment, Behavior, and Autism
inferredcites →https://doi.org/10.1289/ehp.00108s3511openalex-snapshot
Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models.
inferredcites →https://doi.org/10.1289/ehp.0901332openalex-snapshot
House Dust Concentrations of Organophosphate Flame Retardants in Relation to Hormone Levels and Semen Quality Parameters
inferredcites →https://doi.org/10.1289/ehp.10972openalex-snapshot
Estimating Individual-Level Exposure to Airborne Polycyclic Aromatic Hydrocarbons throughout the Gestational Period Based on Personal, Indoor, and Outdoor Monitoring
inferredcites →https://doi.org/10.1289/ehp.1205316openalex-snapshot
Early Zebrafish Embryogenesis Is Susceptible to Developmental TDCPP Exposure
inferredcites →https://doi.org/10.1289/ehp.1409288openalex-snapshot
Perfluorooctane Sulfonate Concentrations in Amniotic Fluid, Biomarkers of Fetal Leydig Cell Function, and Cryptorchidism and Hypospadias in Danish Boys (1980–1996)
inferredcites →https://doi.org/10.1289/ehp1021openalex-snapshot
Urinary Concentrations of Organophosphate Flame Retardant Metabolites and Pregnancy Outcomes among Women Undergoing in Vitro Fertilization
inferredcites →https://doi.org/10.1289/ehp1953openalex-snapshot
Environmental Chemicals in Breast Milk and Formula: Exposure and Risk Assessment Implications
inferredcites →https://doi.org/10.1289/ehp358openalex-snapshot
Project TENDR: Targeting Environmental Neuro-Developmental Risks The TENDR Consensus Statement
inferredcites →https://doi.org/10.1530/ec-17-0373openalex-snapshot
EDC IMPACT: Molecular effects of developmental FM 550 exposure in Wistar rat placenta and fetal forebrain
inferredcites →https://doi.org/10.20937/rica.2019.35.02.02openalex-snapshot
PERSISTENT ORGANIC POLLUTANTS IN SERUM AND BREAST MILK OF FERTILE-AGED WOMEN
inferredcites →https://doi.org/10.2165/00003088-200443080-00001openalex-snapshot
Drug Transfer and Metabolism by the Human Placenta
inferredcites →https://doi.org/10.2741/e279openalex-snapshot
Endocrine disruptors environmental oxygen epigenetics and pregnancy
inferredcites →https://doi.org/10.3389/fpubh.2020.547239openalex-snapshot
Assessment of Multipollutant Exposures During Pregnancy Using Silicone Wristbands
inferredcites →https://doi.org/10.3390/ijerph17186713openalex-snapshot
Organophosphorus Flame Retardants: A Global Review of Indoor Contamination and Human Exposure in Europe and Epidemiological Evidence
inferredcites →https://doi.org/10.5830/cvja-2016-021openalex-snapshot
Physiological changes in pregnancy
inferredcites →https://doi.org/10.7717/peerj.4156openalex-snapshot
Tris(1,3-dichloro-2-propyl) phosphate disrupts dorsoventral patterning in zebrafish embryos
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/smll.202401982openalex-snapshot
Partitioning of an Enzyme‐Polymer Surfactant Nanocomplex into Lipid‐Rich Cellular Compartments Drives In Situ Hydrolysis of Organophosphates
inferred← citeshttps://doi.org/10.1007/s00204-026-04445-5openalex-snapshot
Triphenyl phosphate promotes lipid accumulation in human mesenchymal stem cells through metabolic stress pathways
inferred← citeshttps://doi.org/10.1016/j.cej.2026.182922openalex-snapshot
Coupling ambient mechanical agitation with photocatalysis through defective TiO2 for organophosphate flame-retardants removal and phosphorus recovery
inferred← citeshttps://doi.org/10.1016/j.chroma.2026.467397openalex-snapshot
Advances in the biomonitoring of flame retardants in human matrices
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115685openalex-snapshot
Toxicity assessment of organophosphate flame retardant triphenyl phosphate (TPHP) on intestines in mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115815openalex-snapshot
Multigenerational effects and mutagenicity of three flame retardants on germ cells in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116524openalex-snapshot
Association of co-exposure to organophosphate esters and per- and polyfluoroalkyl substances and mixture with cardiovascular-kidney-liver-metabolic biomarkers among Chinese adults
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117618openalex-snapshot
Prenatal exposure to a mixture of organophosphate ester and organophosphorus pesticides in relation to child neurodevelopment in the Shanghai Birth Cohort
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.117877openalex-snapshot
New insights into the mechanism of triphenyl phosphate and its metabolite diphenyl phosphate in diabetic kidney disease
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118927openalex-snapshot
Prenatal exposure to organophosphorus flame retardants and birth outcomes: A cross-sectional study in an e-waste area in China
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119289openalex-snapshot
The associated long-term disturbance of diethyl phosphonate on the growth phenotype, gut microbiota and SCFAs of offspring rats
inferred← citeshttps://doi.org/10.1016/j.emcon.2025.100536openalex-snapshot
Elucidation of chemicals of emerging concern in placenta by non-targeted and suspect screening approaches
inferred← citeshttps://doi.org/10.1016/j.enceco.2025.12.017openalex-snapshot
The differential cardiotoxicity effects and molecular mechanisms induced by two emerging organophosphorus flame retardants (EHDPP and DPHP) with similar parent structures in zebrafish
inferred← citeshttps://doi.org/10.1016/j.envint.2024.109165openalex-snapshot
Occupational exposure to traditional and emerging organophosphate esters: A comparison of levels across different sources and blood distribution
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110172openalex-snapshot
Nontargeted screening identifies mixtures of environmental pollutants that are associated with perturbations to amino acid and fatty acid metabolic pathways during early pregnancy
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.125212openalex-snapshot
Identification and seasonal variation of PM2.5-bound organophosphate flame retardants from industrial parks and the associated human health risk
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.125633openalex-snapshot
Legacy and emerging organophosphate flame retardants (OPFRs) in water and sediment from the Pearl River Delta to the adjacent coastal waters of the South China Sea: Spatioseasonal variations, flux estimation and ecological risk
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.125858openalex-snapshot
PBScreen: A server for the high-throughput screening of placental barrier–permeable contaminants based on multifusion deep learning
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.126300openalex-snapshot
Association of organophosphate flame retardants exposure with liver function and the contrasting mediating roles of inflammatory and oxidative stress pathways
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.126873openalex-snapshot
Estimated exposure of flame-retardants in Spanish toddlers: a modelling approach
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128739openalex-snapshot
Pregnancy exposure to organophosphate flame retardants and alterations in maternal and newborn thyroid hormone levels
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128808openalex-snapshot
Prenatal parabens exposure and infantile Eczema: Mediation by IL-17A, effect modification by breastfeeding, and evidence from network toxicology
inferred← citeshttps://doi.org/10.1016/j.envpol.2026.128951openalex-snapshot
Probabilistic and sensitive dietary risk assessment of sixteen legacy and emerging organophosphorus flame retardants in the Taiwanese populations: A food market basket study
inferred← citeshttps://doi.org/10.1016/j.envres.2024.119159openalex-snapshot
Prenatal triphenyl phosphate exposure impairs placentation and induces preeclampsia-like symptoms in mice
inferred← citeshttps://doi.org/10.1016/j.envres.2024.120141openalex-snapshot
Gestational exposure to organophosphate esters and autism spectrum disorder and other non-typical development in a cohort with elevated familial likelihood
inferred← citeshttps://doi.org/10.1016/j.envres.2025.121646openalex-snapshot
Gestational exposures to mixtures of multiple chemical classes and autism spectrum disorder in the MARBLES study
inferred← citeshttps://doi.org/10.1016/j.envres.2026.124940openalex-snapshot
Prenatal exposure to organophosphate ester flame retardants and plasticizers and maternal immune responses in three ECHO cohorts
inferred← citeshttps://doi.org/10.1016/j.ijheh.2024.114336openalex-snapshot
Prenatal exposure to a mixture of organophosphate flame retardants and infant neurodevelopment: A prospective cohort study in Shandong, China
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134818openalex-snapshot
Emerging N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and 6PPD quinone in paired human plasma and urine from Tianjin, China: Preliminary assessment with demographic factors
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138633openalex-snapshot
Traditional and novel organophosphate esters in atmosphere of greenhouse covered with mulch films: Seasonal variations, partitioning and exposure risks
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138906openalex-snapshot
Quantitative identification and prioritization of combined effects of multiple endocrine disrupting compound exposure on oxidative stress
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.139496openalex-snapshot
Human exposure to organophosphate esters (OPEs): A meta-analytic review of levels and distribution
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141827openalex-snapshot
Trihexyl phosphate exposure disrupts mitophagy and activates mtDNA-cGAS-STING signaling to drive pyroptosis and steroidogenic impairment in Leydig cells
inferred← citeshttps://doi.org/10.1016/j.microc.2024.110074openalex-snapshot
Spindle barium chromate coupled with luminol chemiluminiscence for determining phosphorus and triphenyl phosphate
inferred← citeshttps://doi.org/10.1016/j.ntt.2026.107711openalex-snapshot
Neurobehavioral and metabolic consequences of embryonic triphenyl phosphate exposure across the lifespan in zebrafish
inferred← citeshttps://doi.org/10.1016/j.ocecoaman.2024.107262openalex-snapshot
Urban mangroves at risk: Understanding organophosphate flame retardant pollution at different urban function zones in shenzhen
inferred← citeshttps://doi.org/10.1016/j.pmatsci.2025.101529openalex-snapshot
Flame-retardant strategies for lignocellulose: recent progress and prospect
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170562openalex-snapshot
Effects of uptake pathways on the accumulation, translocation, and metabolism of OPEs in rice: An emphasis on foliar uptake
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.171044openalex-snapshot
Microplastics in maternal amniotic fluid and their associations with gestational age
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.180501openalex-snapshot
Associations between brominated and organophosphate flame retardant levels and inflammatory biomarkers in maternal blood, cord blood, and placental tissue at mid-gestation
inferred← citeshttps://doi.org/10.1016/j.steroids.2026.109851openalex-snapshot
Menopause-specific associations of organophosphate esters with sex hormones among US women
inferred← citeshttps://doi.org/10.1016/j.talanta.2025.128088openalex-snapshot
Simultaneous determination of multiple endocrine disrupting chemicals in human amniotic fluid samples by solid phase extraction coupled with liquid chromatography tandem mass spectrometry (LC-MS/MS)
inferred← citeshttps://doi.org/10.1016/j.tox.2024.154019openalex-snapshot
A review on sustainable management strategies for navigating the piling e-waste crisis and associated environmental threats
inferred← citeshttps://doi.org/10.1016/j.toxlet.2026.111895openalex-snapshot
A stimulating effect induced by Bisphenol A bis (diphenylphosphate) in HepG2 cells via vascular endothelial growth factor (VEGF)/VEGF receptor axis
inferred← citeshttps://doi.org/10.1021/acs.est.3c06487openalex-snapshot
Synthetic Antioxidants as Contaminants of Emerging Concern in Indoor Environments: Knowns and Unknowns
inferred← citeshttps://doi.org/10.1021/acs.est.3c11032openalex-snapshot
First Insight into Fetal Exposure to Legacy and Emerging Plasticizers Revealed by Infant Hair and Meconium: Occurrence, Biotransformation, and Accumulation
inferred← citeshttps://doi.org/10.1021/acs.est.4c01927openalex-snapshot
Embryonic Exposure to Organophosphate Flame Retardants (OPFRs) Differentially Induces Cardiotoxicity in Rare Minnow (Gobiocypris rarus)
inferred← citeshttps://doi.org/10.1021/acs.est.4c04180openalex-snapshot
Identification of Primary Organophosphate Esters Contributing to Enhanced Risk of Gestational Diabetes Mellitus Based on a Case-Control Study
inferred← citeshttps://doi.org/10.1021/acs.est.4c04782openalex-snapshot
Biotransformation, Bioaccumulation, and Bioelimination of Triphenyl Phosphate and Its Dominant Metabolite Diphenyl Phosphate In Vivo
inferred← citeshttps://doi.org/10.1021/acs.est.4c09436openalex-snapshot
Tris(2-chloroethyl) Phosphate Leads to Unbalanced Circulating Erythrocyte in Mice by Activating both Medullary and Extramedullary Erythropoiesis
inferred← citeshttps://doi.org/10.1021/acs.est.4c10800openalex-snapshot
Prenatal Triphenyl Phosphate Exposure and Hyperlipidemia in Offspring: Role of Trophoblast-Derived Extracellular Vesicle PPARγ
inferred← citeshttps://doi.org/10.1021/acs.est.4c14153openalex-snapshot
Analogue-Specific Transplacental Transfer of Organophosphate Flame Retardants in ICR Mouse Mediated by Active Transport
inferred← citeshttps://doi.org/10.1021/acs.est.4c14787openalex-snapshot
Artificial Intelligence for the Discovery of Safe and Effective Flame Retardants
inferred← citeshttps://doi.org/10.1021/acs.est.5c11158openalex-snapshot
Cardiovascular Health Risks of Organophosphate Flame Retardant Exposure: A Narrative Review of the Available Evidence
inferred← citeshttps://doi.org/10.1021/acs.est.5c14462openalex-snapshot
Gestational Exposure to Tri- n -butyl Phosphate Induces Maternal Insulin Resistance and Glucose Intolerance by Antagonizing Estrogen Receptor Alpha
inferred← citeshttps://doi.org/10.1021/envhealth.5c00018openalex-snapshot
Prenatal Persistent Exposure to Organophosphate Esters and Early Childhood Brain Development: A Longitudinal Analysis
inferred← citeshttps://doi.org/10.1080/15376516.2026.2634933openalex-snapshot
Integrating NHANES and network toxicology to assess the impact of organophosphate flame retardants on cardiovascular disease
inferred← citeshttps://doi.org/10.1210/endocr/bqag051openalex-snapshot
Perinatal organophosphate flame-retardant exposure alters adult stress axis and avoidance behavior in mice
inferred← citeshttps://doi.org/10.1289/ehp14634openalex-snapshot
Organophosphorus Flame Retardants and Metabolic Disruption: An in Silico , in Vitro , and in Vivo Study Focusing on Adiponectin Receptors
inferred← citeshttps://doi.org/10.3389/fmats.2025.1508000openalex-snapshot
The development and application of contemporary phosphorus flame retardants: a review
inferred← citeshttps://doi.org/10.3389/fphar.2024.1475244openalex-snapshot
Analysis of the evolution of placental oxidative stress research from a bibliometric perspective
inferred← citeshttps://doi.org/10.3390/ijms27198769openalex-snapshot
Construction of Adverse Outcome Pathway (AOP) for Triphenyl Phosphate (TPHP)–Induced Autism Spectrum Disorder (ASD) and Risk Identification of Neurodevelopmental Toxicity of Aryl Organophosphorus Flame Retardants (OPFRs) Based on Multidimensional Bioinformatic Data
inferred← citeshttps://doi.org/10.3390/molecules31071067openalex-snapshot
Health Risks of Organophosphate Flame Retardants (OPFRs) in Facial Cosmetic Sponges via Dermal Exposure
inferred← citeshttps://doi.org/10.46234/ccdcw2024.105openalex-snapshot
Potential Adverse Outcome Pathways of Chlorinated Organophosphate Flame Retardants
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