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Matthew Allin

Researcher at King's College London

Publications -  71
Citations -  4640

Matthew Allin is an academic researcher from King's College London. The author has contributed to research in topics: Psychosis & White matter. The author has an hindex of 36, co-authored 71 publications receiving 4273 citations. Previous affiliations of Matthew Allin include Centre for Mental Health & Camden and Islington NHS Foundation Trust.

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Atlasing location, asymmetry and inter-subject variability of white matter tracts in the human brain with MR diffusion tractography.

TL;DR: It is suggested that DTI-derived maps can be used together with a previous histological atlas to establish the relationship of focal lesions with nearby tracts and improve clinico-anatomical correlation.
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Symmetries in human brain language pathways correlate with verbal recall

TL;DR: It is suggested that the degree of lateralization of perisylvian pathways is heterogeneous in the normal population and, paradoxically, bilateral representation, not extreme lateralization, might ultimately be advantageous for specific cognitive functions.
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Cognitive and motor function and the size of the cerebellum in adolescents born very pre-term.

TL;DR: There were significant associations between cerebellar volume and several cognitive test scores, in particular the Wechsler Intelligence Scale for Children-Revised, the Kaufman Assessment Battery for Children and the Schonnel reading age, which provides further evidence implicating the cerebellum in cognition.
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Preterm birth and structural brain alterations in early adulthood

TL;DR: The results reveal that VPT birth continues to be associated with altered structural brain anatomy in early adult life, although it remains to be ascertained whether these changes reflect neurodevelopmental delays or long lasting structural alterations due to prematurity.
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Gender Differences in White Matter Microstructure

TL;DR: The size of the differences was substantial, suggesting gender may be a potentially significant confound in unbalanced clinical studies and the higher FA in women may reflect greater efficiency of a smaller corpus callosum.