| Literature DB >> 24262376 |
Benoit Da Mota1, Virgile Fritsch2, Gaël Varoquaux2, Tobias Banaschewski3, Gareth J Barker4, Arun L W Bokde5, Uli Bromberg6, Patricia Conrod7, Jürgen Gallinat8, Hugh Garavan9, Jean-Luc Martinot10, Frauke Nees3, Tomas Paus11, Zdenka Pausova12, Marcella Rietschel3, Michael N Smolka13, Andreas Ströhle8, Vincent Frouin14, Jean-Baptiste Poline15, Bertrand Thirion16.
Abstract
Neuroimaging group analyses are used to relate inter-subject signal differences observed in brain imaging with behavioral or genetic variables and to assess risks factors of brain diseases. The lack of stability and of sensitivity of current voxel-based analysis schemes may however lead to non-reproducible results. We introduce a new approach to overcome the limitations of standard methods, in which active voxels are detected according to a consensus on several random parcellations of the brain images, while a permutation test controls the false positive risk. Both on synthetic and real data, this approach shows higher sensitivity, better accuracy and higher reproducibility than state-of-the-art methods. In a neuroimaging-genetic application, we find that it succeeds in detecting a significant association between a genetic variant next to the COMT gene and the BOLD signal in the left thalamus for a functional Magnetic Resonance Imaging contrast associated with incorrect responses of the subjects from a Stop Signal Task protocol.Entities:
Keywords: Group analysis; Multiple comparisons; Parcellation; Permutations; Reproducibility
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Year: 2013 PMID: 24262376 DOI: 10.1016/j.neuroimage.2013.11.012
Source DB: PubMed Journal: Neuroimage ISSN: 1053-8119 Impact factor: 6.556