Publications

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[ Author(Desc)] Title Type Year
Filters: Keyword is Polymorphism, Single Nucleotide  [Clear All Filters]
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A
Albanna A, Choudhry Z, Harvey P-O, Fathalli F, Cassidy C, Sengupta SM, Iyer SN, Rho A, Lepage M, Malla A et al..  2014.  TCF4 gene polymorphism and cognitive performance in patients with first episode psychosis.. Schizophr Res. 152(1):124-9.
B
Bombardier A, Beauchemin M, Gosselin N, Poirier J, De Beaumont L.  2016.  Altered Episodic Memory in Introverted Young Adults Carrying the BDNFMet Allele.. Int J Mol Sci. 17(11)
Bouvette-Turcot A-A, Fleming AS, Wazana A, Sokolowski MB, Gaudreau H, Gonzalez A, Deslauriers J, Kennedy JL, Steiner M, Meaney MJ.  2015.  Maternal childhood adversity and child temperament: an association moderated by child 5-HTTLPR genotype.. Genes Brain Behav. 14(3):229-37.
C
Cassidy C, Buchy L, Bodnar M, Dell'elce J, Choudhry Z, Fathalli F, Sengupta S, Fox R, Malla A, Lepage M et al..  2014.  Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis.. J Psychiatry Neurosci. 39(1):31-9.
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.
D
De Schutter JW, Park J, Leung CYuen, Gormley P, Lin Y-S, Hu Z, Berghuis AM, Poirier J, Tsantrizos YS.  2014.  Multistage screening reveals chameleon ligands of the human farnesyl pyrophosphate synthase: implications to drug discovery for neurodegenerative diseases.. J Med Chem. 57(13):5764-76.
F
Felsky D, Szeszko P, Yu L, Honer WG, De Jager PL, Schneider JA, Malhotra AK, Lencz T, Ikuta T, Pipitone J et al..  2014.  The SORL1 gene and convergent neural risk for Alzheimer's disease across the human lifespan.. Mol Psychiatry. 19(10):1125-32.
G
Galfalvy H, Haghighi F, Hodgkinson C, Goldman D, Oquendo MA, Burke A, Huang Y-Y, Giegling I, Rujescu D, Bureau A et al..  2015.  A genome-wide association study of suicidal behavior.. Am J Med Genet B Neuropsychiatr Genet. 168(7):557-63.
Girard SL, Dion PA, Bourassa CV, Geoffroy S, Lachance-Touchette P, Barhdadi A, Langlois M, Joober R, Krebs M-O, Dubé M-P et al..  2015.  Mutation burden of rare variants in schizophrenia candidate genes.. PLoS One. 10(6):e0128988.
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.
Gross JA, Bureau A, Croteau J, Galfalvy H, Oquendo MA, Haghighi F, Mérette C, Giegling I, Hodgkinson C, Goldman D et al..  2015.  A genome-wide copy number variant study of suicidal behavior.. PLoS One. 10(5):e0128369.
H
Hannon E, Spiers H, Viana J, Pidsley R, Burrage J, Murphy TM, Troakes C, Turecki G, O'Donovan MC, Schalkwyk LC et al..  2016.  Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci.. Nat Neurosci. 19(1):48-54.
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.
L
Leduc V, Théroux L, Dea D, Dufour R, Poirier J.  2016.  Effects of rs3846662 Variants on HMGCR mRNA and Protein Levels and on Markers of Alzheimer's Disease Pathology.. J Mol Neurosci. 58(1):109-19.
M
Mühleisen TW, Leber M, Schulze TG, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Forstner AJ, Schumacher J, Breuer R et al..  2014.  Genome-wide association study reveals two new risk loci for bipolar disorder.. Nat Commun. 5:3339.
N
Niola P, Gross JA, Lopez JPablo, Chillotti C, Deiana V, Manchia M, Georgitsi M, Patrinos GP, Alda M, Turecki G et al..  2014.  Lithium-induced differential expression of SAT1 in suicide completers and controls is not correlated with polymorphisms in the promoter region of the gene.. Psychiatry Res. 220(3):1167-8.
O
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.
P
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.
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.
Peterson D, Munger C, Crowley J, Corcoran C, Cruchaga C, Goate AM, Norton MC, Green RC, Munger RG, Breitner JCS et al..  2014.  Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study.. Alzheimers Dement. 10(3):366-71.
Q
Qiu A, Tuan TAnh, Ong MLyn, Li Y, Chen H, Rifkin-Graboi A, Broekman BFP, Kwek K, Saw S-M, Chong Y-S et al..  2015.  COMT haplotypes modulate associations of antenatal maternal anxiety and neonatal cortical morphology.. Am J Psychiatry. 172(2):163-72.
R
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.
T
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.