Gallagher, Louise
Centre for Addiction and Mental Health · University of Toronto · Trinity College Dublin · Hospital for Sick Children
24 papers on CoChatORCID 0000-0001-9462-2836
Most cited papers
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The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism
Di Martino, A., Yan, C.-G., Li, Q., Denio, E., Castellanos, F. X., Alaerts, K., Anderson, J. S., Assaf, M., Bookheimer, S. Y., Dapretto, M., et al. (2014) · Molecular Psychiatry
Functional Brain Connectivity StudiesAutism Spectrum Disorder Research
Cited by 2,780
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Synaptic, transcriptional and chromatin genes disrupted in autism
Study, T. D., De Rubeis, S., Autism, H. M. C. F., UK10K Consortium, The Autism Sequencing Consortium, He, X., Goldberg, A. P., Poultney, C. S., Samocha, K., Ercument Cicek, A., et al. (2014) · Nature
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,746
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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2018) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,323
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2020) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,321
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Functional impact of global rare copy number variation in autism spectrum disorders
Pinto, D., Pagnamenta, A. T., Klei, L., Anney, R., Merico, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., et al. (2010) · Nature
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 2,013
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The UK10K project identifies rare variants in health and disease
The UK10K Consortium, Writing group, Walter, K., Min, J. L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J. R. B., Xu, C., et al. (2015) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 1,040
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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Pinto, D., Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., Thiruvahindrapuram, B., Xu, X., Ziman, R., Wang, Z., et al. (2014) · The American Journal of Human Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 969
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
C Yuen, R. K., Merico, D., Bookman, M., L Howe, J., Thiruvahindrapuram, B., Patel, R. V., Whitney, J., Deflaux, N., Bingham, J., Wang, Z., et al. (2017) · Nature Neuroscience
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 844
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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Mefford, H. C., Sharp, A. J., Baker, C., Itsara, A., Jiang, Z., Buysse, K., Huang, S., Maloney, V. K., Crolla, J. A., Baralle, D., et al. (2008) · New England Journal of Medicine
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 804
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Microduplications of 16p11.2 are associated with schizophrenia
Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 711
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A genome-wide scan for common alleles affecting risk for autism
Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., Sykes, N., Pagnamenta, A. T., et al. (2010) · Human Molecular Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 593
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Individual common variants exert weak effects on the risk for autism spectrum disorders
Anney, R., Klei, L., Pinto, D., Almeida, J., Bacchelli, E., Baird, G., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., et al. (2012) · Human Molecular Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 375
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Dopaminergic-neuropeptide interactions in the social brain
Skuse, D. H., & Gallagher, L. (2009) · Trends in Cognitive Sciences
Neuroendocrine regulation and behaviorNeurotransmitter Receptor Influence on Behavior
Cited by 340
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Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention
Johnson, K. A., Robertson, I. H., Kelly, S. P., Silk, T. J., Barry, E., Dáibhis, A., Watchorn, A., Keavey, M., Fitzgerald, M., Gallagher, L., et al. (2007) · Neuropsychologia
Attention Deficit Hyperactivity DisorderNeural and Behavioral Psychology Studies
Cited by 259
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Sex and gender in neurodevelopmental conditions
Bölte, S., Neufeld, J., Marschik, P. B., Williams, Z. J., Gallagher, L., & Lai, M.-C. (2023) · Nature Reviews Neurology
Sex and Gender in HealthcareSexual Differentiation and Disorders
Cited by 249
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Subcortical brain volume, regional cortical thickness, and cortical surface area across disorders: findings from the ENIGMA ADHD, ASD, and OCD working groups
Boedhoe, P. S. W., van Rooij, D., Hoogman, M., Twisk, J. W. R., Schmaal, L., Abe, Y., Alonso, P., Ameis, S. H., Anikin, A., Anticevic, A., et al. (2020) · American Journal of Psychiatry
Attention Deficit Hyperactivity DisorderAutism Spectrum Disorder Research
Cited by 201
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Casey, J. P., Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., et al. (2012) · Human Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 200
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Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
Noor, A., Whibley, A., Marshall, C. R., Gianakopoulos, P. J., Piton, A., Carson, A. R., Orlic-Milacic, M., Lionel, A. C., Sato, D., Pinto, D., et al. (2010) · Science Translational Medicine
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 193
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Social and monetary reward processing in autism spectrum disorders
Delmonte, S., Balsters, J. H., McGrath, J., Fitzgerald, J., Brennan, S., Fagan, A. J., & Gallagher, L. (2012) · Molecular Autism
Autism Spectrum Disorder ResearchNeural and Behavioral Psychology Studies
Cited by 180
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Gait Deviations in Children with Autism Spectrum Disorders: A Review
Kindregan, D., Gallagher, L., & Gormley, J. (2015) · Autism Research and Treatment
Autism Spectrum Disorder ResearchChildren's Physical and Motor Development
Cited by 146
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Whole-genome sequence-based analysis of thyroid function
Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., et al. (2015) · Nature Communications
Genetic Associations and EpidemiologyThyroid Disorders and Treatments
Cited by 104
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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
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Disrupted prediction errors index social deficits in autism spectrum disorder
Balsters, J. H., Apps, M. A. J., Bolis, D., Lehner, R., Gallagher, L., & Wenderoth, N. (2017) · Brain
Autism Spectrum Disorder ResearchAction Observation and Synchronization
Cited by 85
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Mental health aspects of autistic spectrum disorders in children
Skokauskas, N., & Gallagher, L. (2012) · Journal of Intellectual Disability Research
Autism Spectrum Disorder ResearchFamily and Disability Support Research
Cited by 75
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