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2019
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Oliveira RDe Barros, Turecki G, Dion PA et al..  2019.  Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.. PLoS One. 14(11):e0225186.
Iyer SN, Shah JL, Boksa P, Lal S, Joober R, Andersson N, Fuhrer R, Abdel-Baki A, Beaton AM, Reaume-Zimmer P et al..  2019.  A minimum evaluation protocol and stepped-wedge cluster randomized trial of ACCESS Open Minds, a large Canadian youth mental health services transformation project. BMC psychiatry. 19(1):273-273.
Iyer SN, Shah JL, Boksa P, Lal S, Joober R, Andersson N, Fuhrer R, Abdel-Baki A, Beaton AM, Reaume-Zimmer P et al..  2019.  A minimum evaluation protocol and stepped-wedge cluster randomized trial of ACCESS Open Minds, a large Canadian youth mental health services transformation project.. BMC Psychiatry. 19(1):273.
MJ Fleury, Sabetti J, Bamvita JM, Grenier G.  2019.  Modeling variables associated with personal recovery among service users with mental disorders using community-based services.. Int J Soc Psychiatry. 65(2):123-135.
Tullo S, Patel R, Devenyi GA, Salaciak A, Bedford SA, Farzin S, Wlodarski N, Tardif CL, Breitner JCS, M Chakravarty M.  2019.  MR-based age-related effects on the striatum, globus pallidus, and thalamus in healthy individuals across the adult lifespan.. Hum Brain Mapp.
Accogli A, Yang R, Blain-Juste M-E, Braverman N, Shah JL, Trakadis Y.  2019.   Mutation and Mosaic Turner Syndrome in a Female Patient With Intellectual Disability and Psychiatric Features.. J Neuropsychiatry Clin Neurosci. 31(3):272-275.
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.
Hodge CPaquin, Gauvin L, St-Hilaire A, Israel M, Azzi M, Kahan E, Thaler L, Dansereau E, Steiger H.  2019.  A naturalistic comparison of two inpatient treatment protocols for adults with anorexia nervosa: Does reducing duration of treatment and external controls compromise outcome? Int J Eat Disord. 52(9):1015-1023.
Hodge CPaquin, Gauvin L, St-Hilaire A, Israel M, Azzi M, Kahan E, Thaler L, Dansereau E, Steiger H.  2019.  A naturalistic comparison of two inpatient treatment protocols for adults with anorexia nervosa: Does reducing duration of treatment and external controls compromise outcome? Int J Eat Disord. 52(9):1015-1023.
Ong M-L, Tuan TA, Poh J, Teh AL, Chen L, Pan H, MacIsaac JL, Kobor MS, Chong YS, Kwek K et al..  2019.  Neonatal amygdalae and hippocampi are influenced by genotype and prenatal environment, and reflected in the neonatal DNA methylome.. Genes Brain Behav. :e12576.
Vosberg DE, Beaulé V, Torres-Berrío A, Cooke D, Chalupa A, Jaworska N, Cox SML, Larcher K, Zhang Y, Allard D et al..  2019.  Neural function in DCC mutation carriers with and without mirror movements.. Ann Neurol. 85(3):433-442.
Bimpisidis Z, König N, Stagkourakis S, Zell V, Vlcek B, Dumas S, Giros B, Broberger C, Hnasko TS, Wallén-Mackenzie Å.  2019.  The NeuroD6 Subtype of VTA Neurons Contributes to Psychostimulant Sensitization and Behavioral Reinforcement.. eNeuro. 6(3)
W Y Tam E, Chau V, Lavoie R, M Chakravarty M, Guo T, Synnes A, Zwicker J, Grunau R, Miller SP.  2019.  Neurologic Examination Findings Associated With Small Cerebellar Volumes After Prematurity.. J Child Neurol. :883073819847925.
Hadoux X, Hui F, Lim JKH, Masters CL, Pébay A, Chevalier S, Ha J, Loi S, Fowler CJ, Rowe C et al..  2019.  Non-invasive in vivo hyperspectral imaging of the retina for potential biomarker use in Alzheimer's disease.. Nat Commun. 10(1):4227.
Hadoux X, Hui F, Lim JKH, Masters CL, Pébay A, Chevalier S, Ha J, Loi S, Fowler CJ, Rowe C et al..  2019.  Non-invasive in vivo hyperspectral imaging of the retina for potential biomarker use in Alzheimer's disease.. Nat Commun. 10(1):4227.
Unternaehrer E, Cost KTombeau, Jonas W, Dhir SK, Bouvette-Turcot A-A, Gaudreau H, Dass SHari, Lydon JE, Steiner M, Szatmari P et al..  2019.  Once and Again : History of Rearing Experiences and Psychosocial Parenting Resources at Six Months in Primiparous Mothers.. Hum Nat. 30(4):448-476.
Unternaehrer E, Cost KTombeau, Jonas W, Dhir SK, Bouvette-Turcot A-A, Gaudreau H, Dass SHari, Lydon JE, Steiner M, Szatmari P et al..  2019.  Once and Again : History of Rearing Experiences and Psychosocial Parenting Resources at Six Months in Primiparous Mothers.. Hum Nat. 30(4):448-476.
Lévesque M, Chen L-Y, Etter G, Shiri Z, Wang S, Williams S, Avoli M.  2019.  Paradoxical effects of optogenetic stimulation in mesial temporal lobe epilepsy.. Ann Neurol. 86(5):714-728.
Majnemer A, Rohlicek C, Dahan-Oliel N, Sahakian S, Mazer B, Maltais DB, Schmitz N.  2019.  Participation in leisure activities in adolescents with congenital heart defects. Developmental Medicine & Child NeurologyDevelopmental Medicine & Child NeurologyDev Med Child Neurol. n/a(n/a)
Majnemer A, Rohlicek C, Dahan-Oliel N, Sahakian S, Mazer B, Maltais DB, Schmitz N.  2019.  Participation in leisure activities in adolescents with congenital heart defects. Developmental Medicine & Child NeurologyDevelopmental Medicine & Child NeurologyDev Med Child Neurol. n/a(n/a)

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