Investigations on principles of brain organization in health and disease have gained significant traction over the last decade. One important approach to understanding principles of brain organization is through evaluating so-called gradients of brain organization, also called axes or dimensions [1]. Gradients describe modes of smooth variations of regional and inter-regional brain features (such as connectivity and covariance with other regions) across the cortical mantle, but can also be implemented in subcortical areas such as thalamus and striatum, and cerebellum [2, 3, 4]. So far, gradient-based approaches have gained key insights in associations between brain organization and genetic variation, histology, neurotransmitter receptors/transporter distributions, developmental change, aging, plasticity, and cognition [5, 6, 7,8, 9, 10, 11]. Moreover, the gradient framework can be applied in disorder, to understand how and which principles of brain organization are differing in a case-control setting, or explore how different disorders show shared co-alteration patterns [12, 13, 14,15]. However, important questions in this field on generalizability and heterogeneity of gradients across the lifespan and states, as well as clinical alterations, and system-level perspectives on symptoms and healthy brain function, cannot be fully addressed without scaling up of investigations to much larger and more diverse samples, which may be achieved by taking advantage of available data collected at multiple sites. The ENIGMA-Gradient working group aims to use the ENIGMA collaborative model to address questions related to associations between organizational axes in brain structure and function in healthy and clinical samples, beginning with a focus on normative and cross-disorder gradients. The aims of this group include:
Chairs: