Diagnosing diffuse liver disease first involves measurement of blood enzymes followed by biopsy. However, blood markers lack spatial and diagnostic specificity and biopsy is highly risky and variable. Although structural changes have been evaluated using diffusion weighted imaging (DWI), the technique is minimally quantitative. Quantitative MR diffusion approaches, such as intra-voxel incoherent motion (IVIM) and diffusion tensor imaging (DTI) have been proposed to better characterize diseased liver. However, the so called pseudo-hepatic artefact due to cardiac motion, drastically affects DWI results. The overall goals of this thesis were thus to evaluate the pseudo-hepatic anisotropy artefact on the quality of diffusion tensor (DT) and IVIM metrics, and to identify potential solutions. Intra- and intersession DTI repeatability was evaluated in healthy human livers when varying the number of diffusion encoding gradients (NGD) and number of signal averages (NSA). Although no further advantage was observed with increasing NGD beyond 6 directions, increased NSA improved intra- and inter-session repeatability. The pseudo-hepatic artefact resulted in increased fractional anisotropy (FA) and tensor eigenvalues (λ1, λ2, λ3), most prominent in the left liver lobe during systole of the cardiac cycle. Without taking advantage of tensor directional information, increasing the acquired NGD slightly improved IVIM fit quality thus helping to minimize the pseudo-hepatic artefact. Combining IVIM and DTI resulted in FA values closer to the hypothesized value of 0.0, which, based on liver microstructure is most logical. Although both IVIM-DTI and DTI-IVIM exhibited similar fit R2 values, the latter failed more often, especially near major blood vessels. Thus, IVIM-DTI was concluded to be more robust and thus the better approach. / Thesis / Doctor of Philosophy (PhD)