This thesis contributes to the research field of causal inference, where the effect of a treatment on an outcome is of interest is concerned. Many such effects cannot be estimated through randomised experiments. For example, the effect of higher education on future income needs to be estimated using observational data. In the estimation, assumptions are made to make individuals that get higher education comparable with those not getting higher education, to make the effect estimable. Another assumption often made in causal inference (both in randomised an nonrandomised studies) is that the treatment received by one individual has no effect on the outcome of others. If this assumption is not met, the meaning of the causal effect of the treatment may be unclear. In the first paper the effect of college choice on income is investigated using Swedish register data, by comparing graduates from old and new Swedish universities. A semiparametric method of estimation is used, thereby relaxing functional assumptions for the data. One assumption often made in causal inference in observational studies is that individuals in different treatment groups are comparable, given that a set of pretreatment variables have been adjusted for in the analysis. This so called unconfoundedness assumption is in principle not possible to test and, therefore, in the second paper we propose a Bayesian sensitivity analysis of the unconfoundedness assumption. This analysis is then performed on the results from the first paper. In the third paper of the thesis, we study profile likelihood as a tool for semiparametric estimation of a causal effect of a treatment. A semiparametric version of the Bayesian sensitivity analysis of the unconfoundedness assumption proposed in Paper II is also performed using profile likelihood. The last paper of the thesis is concerned with the estimation of direct and indirect causal effects of a treatment where interference between units is present, i.e., where the treatment of one individual affects the outcome of other individuals. We give unbiased estimators of these direct and indirect effects for situations where treatment probabilities vary between individuals. We also illustrate in a simulation study how direct and indirect causal effects can be estimated when treatment probabilities need to be estimated using background information on individuals.

<p>This thesis makes contributions to the statistical research field of causal inference in observational studies. The results obtained are directly applicable in many scientific fields where effects of treatments are investigated and yet controlled experiments are difficult or impossible to implement.</p><p>In the first paper we define a partially specified directed acyclic graph (DAG) describing the independence structure of the variables under study. Using the DAG we show that given that unconfoundedness holds we can use the observed data to select minimal sets of covariates to control for. General covariate selection algorithms are proposed to target the defined minimal subsets.</p><p>The results of the first paper are generalized in Paper II to include the presence of unobserved covariates. Morevoer, the identification assumptions from the first paper are relaxed.</p><p>To implement the covariate selection without parametric assumptions we propose in the third paper the use of a model-free variable selection method from the framework of sufficient dimension reduction. By simulation the performance of the proposed selection methods are investigated. Additionally, we study finite sample properties of treatment effect estimators based on the selected covariate sets.</p><p>In paper IV we investigate misspecifications of parametric models of a scalar summary of the covariates, the propensity score. Motivated by common model specification strategies we describe misspecifications of parametric models for which unbiased estimators of the treatment effect are available. Consequences of the misspecification for the efficiency of treatment effect estimators are also studied.</p>

This thesis makes contributions to the statistical research field of causal inference in observational studies. The results obtained are directly applicable in many scientific fields where effects of treatments are investigated and yet controlled experiments are difficult or impossible to implement. In the first paper we define a partially specified directed acyclic graph (DAG) describing the independence structure of the variables under study. Using the DAG we show that given that unconfoundedness holds we can use the observed data to select minimal sets of covariates to control for. General covariate selection algorithms are proposed to target the defined minimal subsets. The results of the first paper are generalized in Paper II to include the presence of unobserved covariates. Morevoer, the identification assumptions from the first paper are relaxed. To implement the covariate selection without parametric assumptions we propose in the third paper the use of a model-free variable selection method from the framework of sufficient dimension reduction. By simulation the performance of the proposed selection methods are investigated. Additionally, we study finite sample properties of treatment effect estimators based on the selected covariate sets. In paper IV we investigate misspecifications of parametric models of a scalar summary of the covariates, the propensity score. Motivated by common model specification strategies we describe misspecifications of parametric models for which unbiased estimators of the treatment effect are available. Consequences of the misspecification for the efficiency of treatment effect estimators are also studied.