Catherine Mankiw

TL;DR: This work uses a rare neuroimaging dataset to deconvolve the interwoven effects of sex, sex chromosome complement, and brain size on human cerebellar organization, and reveals topographically variegated scaling relationships between regional Cerebellar volume andbrain size in humans.

TL;DR: This work uses structural neuroimaging to measure a global sulcation index (SI), brain size‐independent sulcal lengthening in males versus females, and insensitivity of overall folding architecture to SCD, and provides a novel context for future studies of human cortical folding in health and disease.

TL;DR: T trajectories of volume and shape change for the amygdala and hippocampus are defined by applying a multi-atlas segmentation pipeline and semi-parametric mixed-effects spline modeling to 1,529 longitudinally-acquired structural MRI brain scans from a large, single-center cohort of youth.

TL;DR: By adding granularity to the understanding of neurodevelopmental difficulties in XYY, these findings assist targeted clinical assessment of newly identified cases, motivate greater provision of specialized multidisciplinary support, and inform future efforts to integrate behavioral phenotypes inXYY with neurobiology.

TL;DR: T trajectories of volume and shape change for the amygdala and hippocampus are defined by applying a multi-atlas segmentation pipeline (MAGeT-Brain) and semi-parametric mixed-effects spline modeling to 1,529 longitudinally-acquired structural MRI brain scans from a large, single-center cohort of 792 youth between the ages of 5 and 25 years old and provide a new framework for understanding amygdalo-hippocampal organization in human development.