Medicina
Facultad
Toronto General Hospital
Toronto, CanadáPublicaciones en colaboración con investigadores/as de Toronto General Hospital (36)
2022
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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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Early short course of neuromuscular blocking agents in patients with COVID-19 ARDS: a propensity score analysis
Critical Care, Vol. 26, Núm. 1
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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
2021
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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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Myocardial T1 and T2 Mapping by Magnetic Resonance in Patients With Immune Checkpoint Inhibitor–Associated Myocarditis
Journal of the American College of Cardiology, Vol. 77, Núm. 12, pp. 1503-1516
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Natural influenza infection produces a greater diversity of humoral responses than vaccination in immunosuppressed transplant recipients
American Journal of Transplantation, Vol. 21, Núm. 8, pp. 2709-2718
2020
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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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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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Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)
Nature Communications
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Shared heritability and functional enrichment across six solid cancers
Nature Communications, Vol. 10, Núm. 1
2018
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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
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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
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Erratum to: Risk factors for progression in children and young adults with IgA nephropathy: an analysis of 261 cases from the VALIGA European cohort (Pediatr Nephrol, 10.1007/s00467-016-3469-3)
Pediatric Nephrology
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Improved survival among ICU-hospitalized patients with community-acquired pneumonia by unidentified organisms: a multicenter case–control study
European Journal of Clinical Microbiology and Infectious Diseases, Vol. 36, Núm. 1, pp. 123-130
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Risk factors for progression in children and young adults with IgA nephropathy: an analysis of 261 cases from the VALIGA European cohort
Pediatric Nephrology, Vol. 32, Núm. 1, pp. 139-150
2016
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Long-Term Outcome of Patients with Chronic Thromboembolic Pulmonary Hypertension : Results from an International Prospective Registry
Circulation, Vol. 133, Núm. 9, pp. 859-871
2015
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Consistency of benefit from an early invasive strategy after fibrinolysis: A patient-level meta-analysis
Heart, Vol. 101, Núm. 19, pp. 1554-1561
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Role of atrial tissue remodeling on rotor dynamics: An in vitro study
American Journal of Physiology - Heart and Circulatory Physiology, Vol. 309, Núm. 11, pp. H1964-H1973
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Utility of a monitoring strategy for human herpesviruses 6 and 7 viremia after liver transplantation: A randomized clinical trial
Transplantation, Vol. 99, Núm. 1, pp. 106-113