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The effect of gender was estimated in the full sample adjusting for sociodemographic factors and diagnostic distribution.
Multivariate analyses were conducted to estimate differences in EQ-5D scores across the sample adjusting for age, sex, and race.
Analyses were conducted in the pooled sample adjusting for self-reported ethnicity; sensitivity analyses were repeated in NHW only to rule out population stratification.
BAF and LRR thresholds are calculated both globally and locally for each sample, adjusting for quality-related variation between samples and chromosomes.
Positive values indicate an increase in methylation with GDM bChange in methylation associated with GDM across pyrosequenced loci modeled using linear mixed models with a random intercept for sample, adjusting for the same covariates.
Associations with GDM across pyrosequenced loci were modeled using linear mixed models with a random intercept for sample, adjusting for maternal age, pre-pregnancy BMI, infant sex, maternal smoking, and self-reported ethnicity.
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aMayo sample adjusted for age and region of residence (Minnesota, Iowa, Wisconsin, Illinois, North Dakota and South Dakota); SEARCH sample adjusted for age; pooled Mayo + SEARCH sample adjusted for age and study.
aMayo Clinic sample adjusted for age and region of residence (Minnesota, Iowa, Wisconsin, Illinois, North Dakota and South Dakota); SEARCH sample adjusted for age; pooled Mayo Clinic + SEARCH sample adjusted for age and study.
It may be interpreted directly as the proportion of discriminations made in the sample, adjusted for the length of the scale.
Table 2 presents an overview of the socioeconomic distribution of health care utilization in the sample, adjusted for age, gender, self-reported health and municipality size.
Table 2 gives HR with 95% CIs for all endpoints with aspirin treatment compared with no aspirin in the whole sample, adjusted for covariates as given in the table by stratification with a propensity score.
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