Medicina Legal, Psiquiatría y Patología
Departamento
Hospital for Sick Children
Toronto, CanadáPublicaciones en colaboración con investigadores/as de Hospital for Sick Children (23)
2022
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A clinically compatible drug-screening platform based on organotypic cultures identifies vulnerabilities to prevent and treat brain metastasis
EMBO molecular medicine, Vol. 14, Núm. 3, pp. e14552
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A normative chart for cognitive development in a genetically selected population
Neuropsychopharmacology, Vol. 47, Núm. 7, pp. 1379-1386
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Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure
Human Brain Mapping, Vol. 43, Núm. 1, pp. 37-55
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Effect of disease related biases on the subjective assessment of social functioning in Alzheimer's disease and schizophrenia patients
Journal of Psychiatric Research, Vol. 145, pp. 302-308
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Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Human Brain Mapping, Vol. 43, Núm. 1, pp. 300-328
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FXR1 -related congenital myopathy: expansion of the clinical and genetic spectrum
Journal of Medical Genetics, Vol. 59, Núm. 11, pp. 1069-1074
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Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium
Molecular Psychiatry, Vol. 27, Núm. 4, pp. 2114-2125
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Virtual Ontogeny of Cortical Growth Preceding Mental Illness
Biological Psychiatry, Vol. 92, Núm. 4, pp. 299-313
2021
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Author Correction: Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets (Nature Communications, (2019), 10, 1, (4958), 10.1038/s41467-019-13005-8)
Nature Communications
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Molecular Psychiatry, Vol. 26, Núm. 8, pp. 4496-4510
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Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders
JAMA Psychiatry, Vol. 78, Núm. 1, pp. 47-63
2020
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A framework for assessing neuropsychiatric phenotypes by using smartphone-based location data
Translational Psychiatry, Vol. 10, Núm. 1
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Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study
Molecular Psychiatry, Vol. 25, Núm. 11, pp. 2818-2831
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Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder (Nature Neuroscience, (2017), 20, 9, (1217-1224), 10.1038/nn.4598)
Nature Neuroscience
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
Nature Medicine, Vol. 26, Núm. 12, pp. 1912-1918
2019
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Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets
Nature Communications, Vol. 10, Núm. 1
2018
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Cortical and subcortical brain morphometry differences between patients with autism spectrum disorder and healthy individuals across the lifespan: Results from the ENIGMA ASD working group
American Journal of Psychiatry, Vol. 175, Núm. 4, pp. 359-369
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Preventive strategies for mental health
The Lancet Psychiatry, Vol. 5, Núm. 7, pp. 591-604
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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome
American Journal of Medical Genetics, Part A, Vol. 176, Núm. 10, pp. 2182-2191