Publications

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2019
Fontes K, Rohlicek CV, Saint-Martin C, Gilbert G, Easson K, Majnemer A, Marelli A, M Chakravarty M, Brossard-Racine M.  2019.  Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease.. Hum Brain Mapp. 40(12):3548-3560.
M Y Chau C, Ranger M, Bichin M, Park MTae M, Amaral RSC, Chakravarty M, Poskitt K, Synnes AR, Miller SP, Grunau RE.  2019.  Hippocampus, Amygdala, and Thalamus Volumes in Very Preterm Children at 8 Years: Neonatal Pain and Genetic Variation.. Front Behav Neurosci. 13:51.
Leclair MC, Deveaux F, Roy L, Goulet M-H, Latimer E, Crocker AG.  2019.  The Impact of Housing First on Criminal Justice Outcomes among Homeless People with Mental Illness: A Systematic Review.. Can J Psychiatry. :706743718815902.
Etter M, Goose A, Nossal M, Chishom-Nelson J, Heck C, Joober R, Boksa P, Lal S, Shah JL, Andersson N et al..  2019.  Improving youth mental wellness services in an Indigenous context in Ulukhaktok, Northwest Territories: ACCESS Open Minds Project.. Early Interv Psychiatry. 13 Suppl 1:35-41.
Kervezee L, Cermakian N, Boivin DB.  2019.  Individual metabolomic signatures of circadian misalignment during simulated night shifts in humans.. PLoS Biol. 17(6):e3000303.
Czamara D, Eraslan G, Page CM, Lahti J, Lahti-Pulkkinen M, Hämäläinen E, Kajantie E, Laivuori H, Villa PM, Reynolds RM et al..  2019.  Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns.. Nat Commun. 10(1):2548.
Jones SLee, Dufoix R, Laplante DP, Elgbeili G, Patel R, M Chakravarty M, King S, Pruessner JC.  2019.  Larger Amygdala Volume Mediates the Association Between Prenatal Maternal Stress and Higher Levels of Externalizing Behaviors: Sex Specific Effects in Project Ice Storm.. Front Hum Neurosci. 13:144.
Bedford SA, Park MTae M, Devenyi GA, Tullo S, Germann J, Patel R, Anagnostou E, Baron-Cohen S, Bullmore ET, Chura LR et al..  2019.  Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.. Mol Psychiatry.
Bedford SA, Park MTae M, Devenyi GA, Tullo S, Germann J, Patel R, Anagnostou E, Baron-Cohen S, Bullmore ET, Chura LR et al..  2019.  Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.. Mol Psychiatry.
Bedford SA, Park MTae M, Devenyi GA, Tullo S, Germann J, Patel R, Anagnostou E, Baron-Cohen S, Bullmore ET, Chura LR et al..  2019.  Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.. Mol Psychiatry.
Gallino D, Devenyi GA, Germann J, Guma E, Anastassiadis C, M Chakravarty M.  2019.  Longitudinal assessment of the neuroanatomical consequences of deep brain stimulation: Application of fornical DBS in an Alzheimer's mouse model.. Brain Res. 1715:213-223.
Lleó A, Alcolea D, Martínez-Lage P, Scheltens P, Parnetti L, Poirier J, Simonsen AH, Verbeek MM, Rosa-Neto P, Slot RER et al..  2019.  Longitudinal cerebrospinal fluid biomarker trajectories along the Alzheimer's disease continuum in the BIOMARKAPD study.. Alzheimers Dement. 15(6):742-753.
Hirsiger S, Hänggi J, Germann J, Vonmoos M, Preller KH, Engeli EJE, Kirschner M, Reinhard C, Hulka LM, Baumgartner MR et al..  2019.  Longitudinal changes in cocaine intake and cognition are linked to cortical thickness adaptations in cocaine users.. Neuroimage Clin. :101652.
Carmichael V, Adamson G, Sitter KC, Whitley R.  2019.  Media coverage of mental illness: a comparison of citizen journalism vs. professional journalism portrayals.. J Ment Health. :1-7.
Carmichael V, Whitley R.  2019.  Media coverage of Robin Williams' suicide in the United States: A contributor to contagion? PLoS One. 14(5):e0216543.
Bordeleau M, Carrier M, Luheshi GN, Tremblay M-È.  2019.  Microglia along sex lines: From brain colonization, maturation and function, to implication in neurodevelopmental disorders.. Semin Cell Dev Biol.
Torres-Berrío A, Nouel D, Cuesta S, Parise EM, Restrepo-Lozano JMaria, Larochelle P, Nestler EJ, Flores C.  2019.  MiR-218: a molecular switch and potential biomarker of susceptibility to stress.. Mol Psychiatry.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.. Am J Hum Genet. 104(5):815-834.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.. Am J Hum Genet. 104(5):815-834.
Bell S, Rousseau J, Peng H, Aouabed Z, Priam P, Théroux J-F, Jefri M, Tanti A, Wu H, Kolobova I et al..  2019.  Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons.. Am J Hum Genet. 104(5):815-834.

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