Publications

Export 14 results:
Auteur Title Type [ Année(Asc)]
Filtres: Mot-clé is Phenotype  [Enlever les filtres]
2020
Uechi L, Jalali M, Wilbur JD, French JL, Jumbe NL, Meaney MJ, Gluckman PD, Karnani N, Sakhanenko NA, Galas DJ.  2020.  Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards deciphering developmental mechanisms.. PLoS One. 15(12):e0242684.
2016
Bisht K, Sharma KP, Lecours C, Sánchez MGabriela, Hajj HEl, Milior G, Olmos-Alonso A, Gómez-Nicola D, Luheshi G, Vallières L et al..  2016.  Dark microglia: A new phenotype predominantly associated with pathological states.. Glia. 64(5):826-39.
Hou L, Heilbronner U, Degenhardt F, Adli M, Akiyama K, Akula N, Ardau R, Arias B, Backlund L, Banzato CEM et al..  2016.  Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.. Lancet. 387(10023):1085-93.
2015
Gammer I, Bedford R, Elsabbagh M, Garwood H, Pasco G, Tucker L, Volein A, Johnson MH, Charman T.  2015.  Behavioural markers for autism in infancy: scores on the Autism Observational Scale for Infants in a prospective study of at-risk siblings.. Infant Behav Dev. 38:107-15.
Romdhani H, Hwang H, Paradis G, Roy-Gagnon M-H, Labbe A.  2015.  Pathway-based association study of multiple candidate genes and multiple traits using structural equation models.. Genet Epidemiol. 39(2):101-13.
2014
Yetnikoff L, Pokinko M, Arvanitogiannis A, Flores C.  2014.  Adolescence: a time of transition for the phenotype of dcc heterozygous mice.. Psychopharmacology (Berl). 231(8):1705-14.
Dubois B, Feldman HH, Jacova C, Hampel H, Molinuevo JLuis, Blennow K, DeKosky ST, Gauthier S, Selkoe D, Bateman R et al..  2014.  Advancing research diagnostic criteria for Alzheimer's disease: the IWG-2 criteria.. Lancet Neurol. 13(6):614-29.
Pedneault M, Labbe A, Roy-Gagnon M-H, Low NC, Dugas E, Engert JC, O'Loughlin J.  2014.  The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke.. Addict Behav. 39(1):316-20.
Zarchi O, Diamond A, Weinberger R, Abbott D, Carmel M, Frisch A, Michaelovsky E, Gruber R, Green T, Weizman A et al..  2014.  A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.. Eur Psychiatry. 29(4):203-10.
Cassoff J, Bhatti JA, Gruber R.  2014.  The effect of sleep restriction on neurobehavioural functioning in normally developing children and adolescents: insights from the Attention, Behaviour and Sleep Laboratory.. Pathol Biol (Paris). 62(5):319-31.
O'Loughlin J, Sylvestre M-P, Labbe A, Low NC, Roy-Gagnon M-H, Dugas EN, Karp I, Engert JC.  2014.  Genetic variants and early cigarette smoking and nicotine dependence phenotypes in adolescents.. PLoS One. 9(12):e115716.
Georgiades S, Boyle M, Szatmari P, Hanna S, Duku E, Zwaigenbaum L, Bryson S, Fombonne E, Volden J, Mirenda P et al..  2014.  Modeling the phenotypic architecture of autism symptoms from time of diagnosis to age 6.. J Autism Dev Disord. 44(12):3045-55.
Walder DJ, Laplante DP, Sousa-Pires A, Veru F, Brunet A, King S.  2014.  Prenatal maternal stress predicts autism traits in 6½ year-old children: Project Ice Storm.. Psychiatry Res. 219(2):353-60.
Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ et al..  2014.  Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.. Am J Hum Genet. 94(6):870-83.