Publications

Export 19 results:
Auteur Title [ Type(Desc)] Année
Filtres: Mot-clé is Genotype  [Enlever les filtres]
Journal Article
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.
Grant A, Fathalli F, Rouleau G, Joober R, Flores C.  2012.  Association between schizophrenia and genetic variation in DCC: a case-control study.. Schizophr Res. 137(1-3):26-31.
Silveira PPelufo, Portella AKrumel, Kennedy JL, Gaudreau H, Davis C, Steiner M, Soares CN, Matthews SG, Sokolowski MB, Dubé L et al..  2014.  Association between the seven-repeat allele of the dopamine-4 receptor gene (DRD4) and spontaneous food intake in pre-school children.. Appetite. 73:15-22.
Choudhry Z, Sengupta S, Thakur G, Page V, Schmitz N, Grizenko N, Joober R.  2014.  Catechol-o-methyltransferase gene and executive function in children with ADHD.. J Atten Disord. 18(3):202-11.
Lin X, Teh ALing, Chen L, Lim IYubin, Tan PFang, MacIsaac JL, Morin AM, Yap F, Tan KHian, Saw SMei et al..  2017.  Choice of surrogate tissue influences neonatal EWAS findings.. BMC Med. 15(1):211.
Merner N, d'Arc BForgeot, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF, Michaud JL, Mottron L et al..  2016.  A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.. Am J Med Genet A. 170A(5):1225-35.
Teh ALing, Pan H, Chen L, Ong M-L, Dogra S, Wong J, MacIsaac JL, Mah SM, McEwen LM, Saw S-M et al..  2014.  The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.. Genome Res. 24(7):1064-74.
Bouvette-Turcot A-A, Pluess M, Bernier A, Pennestri M-H, Levitan R, Sokolowski MB, Kennedy JL, Minde K, Steiner M, Pokhvisneva I et al..  2015.  Effects of Genotype and Sleep on Temperament.. Pediatrics. 136(4):e914-21.
Silveira PP, Gaudreau H, Atkinson L, Fleming AS, Sokolowski MB, Steiner M, Kennedy JL, Meaney MJ, Levitan RD, Dubé L.  2016.  Genetic Differential Susceptibility to Socioeconomic Status and Childhood Obesogenic Behavior: Why Targeted Prevention May Be the Best Societal Investment.. JAMA Pediatr. 170(4):359-64.
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.
Pan H, Lin X, Wu Y, Chen L, Teh ALing, Soh SE, Lee YSeng, Tint MThway, MacIsaac JL, Morin AM et al..  2015.  HIF3A association with adiposity: the story begins before birth.. Epigenomics. 7(6):937-50.
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.
Wazana A, Moss E, Jolicoeur-Martineau A, Graffi J, Tsabari G, Lecompte V, Pascuzzo K, Babineau V, Gordon-Green C, Mileva V et al..  2015.  The interplay of birth weight, dopamine receptor D4 gene (DRD4), and early maternal care in the prediction of disorganized attachment at 36 months of age.. Dev Psychopathol. 27(4 Pt 1):1145-61.
O'Donnell K, Glover V, Holbrook JD, O'Connor TG.  2014.  Maternal prenatal anxiety and child brain-derived neurotrophic factor (BDNF) genotype: effects on internalizing symptoms from 4 to 15 years of age.. Dev Psychopathol. 26(4 Pt 2):1255-66.
Checknita D, Maussion G, Labonté B, Comai S, Tremblay RE, Vitaro F, Turecki N, Bertazzo A, Gobbi G, Côté G et al..  2015.  Monoamine oxidase A gene promoter methylation and transcriptional downregulation in an offender population with antisocial personality disorder.. Br J Psychiatry. 206(3):216-22.
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.
Manitt C, Labelle-Dumais C, Eng C, Grant A, Mimee A, Stroh T, Flores C.  2010.  Peri-pubertal emergence of UNC-5 homologue expression by dopamine neurons in rodents.. PLoS One. 5(7):e11463.
Zhang R, Li X, Ramaswami G, Smith KS, Turecki G, Montgomery SB, Li JBilly.  2014.  Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.. Nat Methods. 11(1):51-4.
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.