Doherty, Joanne L.

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

Doherty, J. L., & Owen, M. J. (2014) · Genome Medicine

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 228

Changes in gray matter volume and white matter microstructure in adolescents with obsessive-compulsive disorder

Zarei, M., Mataix-Cols, D., Heyman, I., Hough, M., Doherty, J., Burge, L., Winmill, L., Nijhawan, S., Matthews, P. M., & James, A. (2011) · Biological Psychiatry

Obsessive-Compulsive Spectrum DisordersNeural and Behavioral Psychology Studies

Cited by 160

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

Niarchou, M., Chawner, S. J. R. A., Doherty, J. L., Maillard, A. M., Jacquemont, S., Chung, W. K., Green-Snyder, L., Bernier, R. A., Goin-Kochel, R. P., Hanson, E., et al. (2019) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 156

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

Chawner, S. J. R. A., Doherty, J. L., Anney, R. J. L., Antshel, K. M., Bearden, C. E., Bernier, R., Chung, W. K., Clements, C. C., Curran, S. R., Cuturilo, G., et al. (2021) · American Journal of Psychiatry

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities

Cited by 95

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

Writing Committee for the ENIGMA-CNV Working Group, van der Meer, D., Sønderby, I. E., Kaufmann, T., Walters, G. B., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., et al. (2020) · JAMA Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 87

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

Sønderby, I. E., Ching, C. R. K., Thomopoulos, S. I., van der Meer, D., Sun, D., Villalon‐Reina, J. E., Agartz, I., Amunts, K., Arango, C., Armstrong, N. J., et al. (2022) · Human Brain Mapping

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 67

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

Raven, E. P., Veraart, J., Kievit, R. A., Genc, S., Ward, I. L., Hall, J., Cunningham, A., Doherty, J., van den Bree, M. B. M., & Jones, D. K. (2023) · Molecular Psychiatry

Advanced Neuroimaging Techniques and ApplicationsGenomic variations and chromosomal abnormalities

Cited by 21

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

Dima, D. C., Adams, R., Linden, S. C., Baird, A., Smith, J., Foley, S., Perry, G., Routley, B. C., Magazzini, L., Drakesmith, M., et al. (2020) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesFunctional Brain Connectivity Studies

Cited by 14