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5. Atypical Brain Aging and Its Association With Working Memory Performance in Major Depressive Disorder

7. Extracellular fluid viscosity enhances cell migration and cancer dissemination

8. Predicting intelligence based on cortical WM/GM contrast, cortical thickness and volumetry

9. Addition of MRI or DRE to clinical data and risk prediction for clinically significant prostate cancer.

11. Atypical brain aging and its association with working memory performance in major depressive disorder

13. Cohort profile: the TrueNTH Global Registry - an international registry to monitor and improve localised prostate cancer health outcomes.

17. The FinnBrain Multimodal Neonatal Template and Atlas Collection: T1, T2, and DTI brain templates, and accompanying cortical and subcortical atlases

24. Cellular heterogeneity profiling by hyaluronan probes reveals an invasive but slow-growing breast tumor subset

28. Cover Image

33. Infant Left Amygdala Volume Is Negatively Associated with Fecal Microbiota Diversity

34. Prenatal maternal depressive symptoms are associated with neonatal left amygdala microstructure in a sex‐dependent way

35. Association of cumulative prenatal adversity with infant subcortical structure volumes and child problem behavior and its moderation by a coexpression polygenic risk score of the serotonin system

41. Supplementary Movie 1 from Integrin-Free Tetraspanin CD151 Can Inhibit Tumor Cell Motility upon Clustering and Is a Clinical Indicator of Prostate Cancer Progression

42. Data from Integrin-Free Tetraspanin CD151 Can Inhibit Tumor Cell Motility upon Clustering and Is a Clinical Indicator of Prostate Cancer Progression

45. Supplementary Tables 1 through 3 from Integrin-Free Tetraspanin CD151 Can Inhibit Tumor Cell Motility upon Clustering and Is a Clinical Indicator of Prostate Cancer Progression

47. Supplementary Figure and Movie Legend from Integrin-Free Tetraspanin CD151 Can Inhibit Tumor Cell Motility upon Clustering and Is a Clinical Indicator of Prostate Cancer Progression

50. Sex differences, asymmetry, and age‐related white matter development in infants and 5‐year‐olds as assessed with tract‐based spatial statistics

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