Publications

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Auteur Title [ Type(Desc)] Année
Filtres: Auteur is MacIsaac, Julia L  [Enlever les filtres]
Journal Article
Forest M, O'Donnell K, Voisin G, Gaudreau H, MacIsaac JL, McEwen LM, Silveira PPelufo, Steiner M, Kobor MS, Meaney MJ et al..  2018.  Agreement in DNA methylation levels from the Illumina 450K array across batches, tissues, and time.. Epigenetics. 13(1):19-32.
Chen L, Pan H, Tuan TAnh, Teh ALing, MacIsaac JL, Mah SM, McEwen LM, Li Y, Chen H, Broekman BFP et al..  2015.  Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes.. Dev Psychopathol. 27(1):137-50.
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.
Teh ALing, Pan H, Lin X, Lim YIves, Patro CPawan Kuma, Cheong CYujing, Gong M, MacIsaac JL, Kwoh C-K, Meaney MJ et al..  2016.  Comparison of Methyl-capture Sequencing vs. Infinium 450K methylation array for methylome analysis in clinical samples.. Epigenetics. 11(1):36-48.
Lin X, Lim IYubin, Wu Y, Teh ALing, Chen L, Aris IM, Soh SE, Tint MThway, MacIsaac JL, Morin AM et al..  2017.  Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome.. BMC Med. 15(1):50.
Lim IYubin, Lin X, Teh ALing, Wu Y, Chen L, He M, Chan S-Y, MacIsaac JL, K Y Chan J, Tan KHian et al..  2021.  Dichotomy in the Impact of Elevated Maternal Glucose Levels on Neonatal Epigenome.. J Clin Endocrinol Metab.
O'Donnell K, Chen L, MacIsaac JL, McEwen LM, Nguyen T, Beckmann K, Zhu Y, Chen LMing, Brooks-Gunn J, Goldman D et al..  2018.  DNA methylome variation in a perinatal nurse-visitation program that reduces child maltreatment: a 27-year follow-up.. Transl Psychiatry. 8(1):15.
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.
Klein KOros, Grinek S, Bernatsky S, Bouchard L, Ciampi A, Colmegna I, Fortin J-P, Gao L, Hivert M-F, Hudson M et al..  2016.  funtooNorm: an R package for normalization of DNA methylation data when there are multiple cell or tissue types.. Bioinformatics. 32(4):593-5.
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.
Ong M-L, Tan PYean, MacIsaac JL, Mah SM, Buschdorf JPaul, Cheong CY, Stünkel W, Chan L, Gluckman PD, Chng K et al..  2014.  Infinium monkeys: Infinium 450K array for the Cynomolgus macaque (Macaca fascicularis).. G3 (Bethesda). 4(7):1227-34.
Tollenaar MS, Beijers R, Garg E, Nguyen TTThao, Lin DTS, MacIsaac JL, Shalev I, Kobor MS, Meaney MJ, O'Donnell K et al..  2021.  Internalizing symptoms associate with the pace of epigenetic aging in childhood.. Biol Psychol. 159:108021.
Chen LM, Tollenaar MS, Dass SAHari, Bouvette-Turcot A-A, Pokhvisneva I, Gaudreau H, Parent C, Diorio J, McEwen LM, MacIsaac JL et al..  2020.  Maternal antenatal depression and child mental health: Moderation by genomic risk for attention-deficit/hyperactivity disorder.. Dev Psychopathol. 32(5):1810-1821.
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.
McEwen LM, O'Donnell K, McGill MG, Edgar RD, Jones MJ, MacIsaac JL, Lin DTse Shen, Ramadori K, Morin A, Gladish N et al..  2019.  The PedBE clock accurately estimates DNA methylation age in pediatric buccal cells.. Proc Natl Acad Sci U S A.
Chen LM, Yao N, Garg E, Zhu Y, Nguyen TTT, Pokhvisneva I, Dass SAHari, Unternaehrer E, Gaudreau H, Forest M et al..  2018.  PRS-on-Spark (PRSoS): a novel, efficient and flexible approach for generating polygenic risk scores.. BMC Bioinformatics. 19(1):295.