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1 r set of atmospheric inversions and biosphere models, which were adjusted for a consistent flux definition, showed a high
2                                                 Prevalences were adjusted for age and CD4 cell count.
3                                Common variants (MAF > 0.05) were adjusted for age at cancer diagnosis, CED, and top princ
4                                                     Our HRs were adjusted for age, baseline educational level, marital st
5                                                    Analyses were adjusted for age, gender, education and social class, an
6                                        Multivariable models were adjusted for age, gender, race, diagnosis, central corne
7                                                    Analyses were adjusted for age, race, breast density, baseline examina
8                                        Association analyses were adjusted for age, sex, and principal components in a lin
9                               Cox models for these outcomes were adjusted for age, sex, body mass index, hypertension, di
10                                          All risk estimates were adjusted for age, sex, comorbidity, type of antireflux s
11                                                Associations were adjusted for age, sex, education, diabetes status, and c
12                                                         HRs were adjusted for age, sex, educational level, marital status
13 g as a covariate, whereas in the pharmacogenomic study, HRs were adjusted for age, sex, history of myocardial infarction,
14                Seroprevalence 95% confidence intervals (CI) were adjusted for assay sensitivity and specificity.
15                                           Regression models were adjusted for baseline function and patient and tumor cha
16                                                      Models were adjusted for confounders, including other Healthy Eating
17                                                    Analyses were adjusted for confounding by time, cluster effects, and p
18                                                    Analyses were adjusted for confounding using inverse probability of tr
19                                                    Analyses were adjusted for covariates and multiple hypothesis testing.
20  relative risks (aRRs) and absolute risk differences (ARDs) were adjusted for demographic characteristics and comorbiditi
21                                                All analyses were adjusted for demographics and standard COPD risk factors
22                                  Logistic regression models were adjusted for education, other early life characteristics
23 tients with SZ were studied cross-sectionally, and analyses were adjusted for effects of confounding variables.
24                                                      Models were adjusted for estimated cell type proportions, age, sex,
25                                           Survival analyses were adjusted for guarantee-time bias controlling for known p
26                                                    Analyses were adjusted for income, parental education, maternal skin c
27                                           Regression models were adjusted for individual sociodemographic and clinical ch
28                                                  All models were adjusted for individual-level predictors including age,
29                                      All costs and benefits were adjusted for inflation to 2019 United States dollars and
30 on of the amyloid precursor protein after the latter values were adjusted for kinetic isotope effects.
31                    Associations between FeNO and HIV status were adjusted for known potential confounders.
32 acts, all associations became non-significant when analyses were adjusted for multiple comparisons.
33  disease category was analyzed separately, and the P values were adjusted for multiple comparisons.
34 cs were compared across tertiles; P values for significance were adjusted for multiple comparisons.
35                     Multivariable linear probability models were adjusted for patient and hospital characteristics.
36                                         Linear mixed models were adjusted for postpartum age and infant sex.
37                                                  All models were adjusted for potential confounders, including demographi
38                                                    Outcomes were adjusted for prognostic variables and analyzed using Cox
39                                                      Models were adjusted for sex, age, education, and income (total effe
40                                                      Models were adjusted for sex, age, education, baseline test score, B
41  Incidence rate ratios (IRRs) and absolute risk differences were adjusted for sex, age, smoking status, obesity, socioeco
42  cognitive scores between participants with and without HIV were adjusted for sex, education, age, country of birth, fath
43                                                      Models were adjusted for sociodemographics, cardiovascular disease r
44                                Logistic regression analyses were adjusted for surgical factors and patients' preoperative
45                                                     Results were adjusted for the effects of other common infections, ass
46 idual familial aggregation of breast and ovarian cancer and were adjusted for the family-specific ascertainment schemes.
47                                                      Models were adjusted for traditional risk factors, low-density lipop
48 s healthcare access and quality and diet, but these factors were adjusted for with use of county-specific random intercep
49 conomic status, gestational age, breast-feeding, and gender were adjusted for within each multi-variable model.
50                                                      Models were adjusted for within-ICU correlation, patient- and ICU-le