Biophysical network models and the human connectome.

A core goal of human connectomics is to characterise the neural pathways that underlie brain function. This can be largely achieved noninvasively by inferring white matter connectivity using diffusion MRI data. However, there are challenges. First, diffusion tractography is blind to directed connect...

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Main Authors: Woolrich, M, Stephan, K
Format: Journal article
Language:English
Published: 2013
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author Woolrich, M
Stephan, K
author_facet Woolrich, M
Stephan, K
author_sort Woolrich, M
collection OXFORD
description A core goal of human connectomics is to characterise the neural pathways that underlie brain function. This can be largely achieved noninvasively by inferring white matter connectivity using diffusion MRI data. However, there are challenges. First, diffusion tractography is blind to directed connections, or whether a connection is expressed functionally. Second, we need to be able to go beyond the characterization of anatomical pathways, to understand distributed brain function that results from them. In particular, we need to characterise effective connectivity using functional imaging modalities, such as FMRI and M/EEG, to understand its context-sensitivity (e.g., modulation by task), and how it changes with synaptic plasticity. Here, we consider the critical role that biophysical network models have to play in meeting these challenges, by providing a principled way to conciliate information from anatomical and functional data. They also provide biophysically meaningful parameters, through which we can better understand brain function. In a translational setting, well-validated models may shed light on the mechanisms of individual disease processes.
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spelling oxford-uuid:673ffe8d-c752-4602-bc57-faa1823dfe302022-03-26T18:36:58ZBiophysical network models and the human connectome.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:673ffe8d-c752-4602-bc57-faa1823dfe30EnglishSymplectic Elements at Oxford2013Woolrich, MStephan, KA core goal of human connectomics is to characterise the neural pathways that underlie brain function. This can be largely achieved noninvasively by inferring white matter connectivity using diffusion MRI data. However, there are challenges. First, diffusion tractography is blind to directed connections, or whether a connection is expressed functionally. Second, we need to be able to go beyond the characterization of anatomical pathways, to understand distributed brain function that results from them. In particular, we need to characterise effective connectivity using functional imaging modalities, such as FMRI and M/EEG, to understand its context-sensitivity (e.g., modulation by task), and how it changes with synaptic plasticity. Here, we consider the critical role that biophysical network models have to play in meeting these challenges, by providing a principled way to conciliate information from anatomical and functional data. They also provide biophysically meaningful parameters, through which we can better understand brain function. In a translational setting, well-validated models may shed light on the mechanisms of individual disease processes.
spellingShingle Woolrich, M
Stephan, K
Biophysical network models and the human connectome.
title Biophysical network models and the human connectome.
title_full Biophysical network models and the human connectome.
title_fullStr Biophysical network models and the human connectome.
title_full_unstemmed Biophysical network models and the human connectome.
title_short Biophysical network models and the human connectome.
title_sort biophysical network models and the human connectome
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AT stephank biophysicalnetworkmodelsandthehumanconnectome