Publicaciones en colaboración con investigadores/as de Hospital for Sick Children (20)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. A normative chart for cognitive development in a genetically selected population

    Neuropsychopharmacology, Vol. 47, Núm. 7, pp. 1379-1386

  2. Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

    Human Brain Mapping, Vol. 43, Núm. 1, pp. 37-55

  3. 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

  4. 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

  5. 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

  6. Virtual Ontogeny of Cortical Growth Preceding Mental Illness

    Biological Psychiatry, Vol. 92, Núm. 4, pp. 299-313

2021

  1. 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

  2. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    Molecular Psychiatry, Vol. 26, Núm. 8, pp. 4496-4510

  3. Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders

    JAMA Psychiatry, Vol. 78, Núm. 1, pp. 47-63

2020

  1. A framework for assessing neuropsychiatric phenotypes by using smartphone-based location data

    Translational Psychiatry, Vol. 10, Núm. 1

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

    Molecular Psychiatry, Vol. 25, Núm. 11, pp. 2818-2831

  3. 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

  4. 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

  1. Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets

    Nature Communications, Vol. 10, Núm. 1

2018

  1. 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

  2. Preventive strategies for mental health

    The Lancet Psychiatry, Vol. 5, Núm. 7, pp. 591-604

  3. Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome

    American Journal of Medical Genetics, Part A, Vol. 176, Núm. 10, pp. 2182-2191

  4. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

    American Journal of Medical Genetics, Part A, Vol. 176, Núm. 10, pp. 2172-2181

2017

  1. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

    Nature Neuroscience, Vol. 20, Núm. 9, pp. 1217-1224