Author

Jacqueline Smith

Cardiff UniversityORCID 0000-0002-2191-5571Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:imaging· 2 Approach:statistical model· 2 Research Focus:differential expression· 1

Frequent Co-Authors

David E.J. LindeniD· 2 shared Jérémy HalliD· 2 shared Marianne B. M. van den BreeiD· 2 shared Mark DrakesmithiD· 2 shared Michael John OweniD· 2 shared Nigel M. WilliamsiD· 2 shared Stefanie Caroline LindeniD· 2 shared Alister BairdiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersNeuroscience

David E.J. LindenORCID

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2 papers

Recent·Most cited

Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk

Diana C. Dima, Rachael Adams, Stefanie Caroline Linden, Alister Baird, Jacqueline Smith, Sonya F. Foley, Gavin Perry, Bethany C. Routley, Lorenzo Magazzini, Mark Drakesmith, Nigel M. Williams, Joanne L. Doherty, Marianne B. M. van den Bree, Michael John Owen, Jérémy Hall, , Krish D. Singh

This study investigates electrophysiological network changes in adults with neurodevelopmental risk copy number variants using MEG, finding decreased connectivity and network segregation differences.

Translational Psychiatry · Sep 21, 2020Peer-reviewedNeuroscience

Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white matter structures

Mark Drakesmith, Greg D. Parker, Jacqueline Smith, Stefanie Caroline Linden, Elliott Rees, Nigel M. Williams, Michael John Owen, Marianne B. M. van den Bree, Jérémy Hall, Derek Kenton Jones, David E.J. Linden

The paper investigates how genetic risk for schizophrenia and developmental delay relates to structural brain abnormalities in midline white matter.

Translational Psychiatry · Feb 25, 2019Peer-reviewedNeuroscience