J. Doherty

发表

Celso, Naomi J. Goodrich-Hunsaker, Arango, 2019 .

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

Paul M. Thompson, Christopher R. K. Ching, Neda Jahanshad, 2019, Molecular Psychiatry.

Genomic and Imaging Biomarkers in Schizophrenia.

D. Linden, J. Hall, J. Walters, 2018, Current topics in behavioral neurosciences.

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.

Dmitry Isaev, Kosha Ruparel, Eileen Daly, 2020, The American journal of psychiatry.

In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome

Derek K. Jones, Erika P. Raven, R. Kievit, 2020, Molecular psychiatry.

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

Paul M. Thompson, Jessica A. Turner, Christopher R. K. Ching, 2018, Molecular Psychiatry.

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

Dan J Stein, Lachlan T. Strike, Thomas W. Mühleisen, 2020, JAMA psychiatry.

Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics

Courtney A. Durdle, E. Zackai, M. Owen, 2021, Cerebral cortex.

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice

M. Owen, J. Doherty, 2014, Genome Medicine.

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs

Courtney A. Durdle, Dan J Stein, Thomas W. Mühleisen, 2021, Human brain mapping.

Psychiatric disorders in children with 16p11.2 deletion and duplication

W. Chung, D. Skuse, M. Owen, 2019, Translational Psychiatry.

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

Lachlan T. Strike, Thomas W. Mühleisen, A. McRae, 2021, Translational Psychiatry.

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.

W. Chung, L. Gallagher, M. Owen, 2020, The American journal of psychiatry.

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

David E. J. Linden, Mark Drakesmith, Joanne Doherty, 2019, bioRxiv.

Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome

Paul M. Thompson, Christopher R. K. Ching, Julio E. Villalon-Reina, 2018, Symposium on Medical Information Processing and Analysis.

Altered White Matter Microstructure in 22q11.2 Deletion Syndrome: A Multi-Site Diffusion Tensor Imaging Study Running Title: DTI in 22q11.2 Deletion Syndrome

Celso, Courtney A. Durdle, Arango, 2019 .

The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome

M. Owen, M. Niarchou, S. Chawner, 2019, Journal of psychiatric research.

What can we learn from the high rates of schizophrenia in people with 22q11.2 deletion syndrome?

M. Owen, J. Doherty, 2016, World psychiatry : official journal of the World Psychiatric Association.

7 A GENETIC FIRST APPROACH TO DISSECTING THE HETEROGENEITY OF AUTISM: PHENOTYPIC COMPARISON OF AUTISM RISK COPY NUMBER VARIANTS

W. Chung, C. Bearden, W. Kates, 2019, European Neuropsychopharmacology.

Advances in our understanding of the genetics of childhood neurodevelopmental disorders

A. Thapar, M. Cooper, J. Doherty, 2018, Evidence-Based Mental Health.

Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndrome

D. Linden, S. Chawner, M. V. D. van den Bree, 2021, medRxiv.

Changes in Gray Matter Volume and White Matter Microstructure in Adolescents with Obsessive-Compulsive Disorder

Paul M. Matthews, Mojtaba Zarei, Isobel Heyman, 2011, Biological Psychiatry.

Childhood cognitive development in 22q11.2 deletion syndrome: case–control study

M. Owen, J. Walters, M. Niarchou, 2017, British Journal of Psychiatry.

Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication

W. Chung, D. Skuse, M. Owen, 2019, Translational Psychiatry.

The Research Domain Criteria: moving the goalposts to change the game

M. Owen, J. Doherty, 2014, British Journal of Psychiatry.

Reduced Subjective Response to Acute Ethanol Administration Among Young Men with a Broad Bipolar Phenotype

R. Rogers, G. Goodwin, C. Tzagarakis, 2012, Neuropsychopharmacology.

Tractometry-based Anomaly Detection for Single-subject White Matter Analysis pdf

Derek K. Jones, Maxime Chamberland, Sila Genc, 2020, ArXiv.

Detecting microstructural deviations in individuals with deep diffusion MRI tractometry

Erika P. Raven, K. Hamandi, C. Tax, 2021, Nature Computational Science.

Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders

M. Owen, D. Linden, K. Singh, 2023, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology.

Beyond the Global Brain Differences: Intra-individual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers

Dan J Stein, Lachlan T. Strike, Vince D. Calhoun, 2023, Biological Psychiatry.