Julia Pinsonneault - Publications


25 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Mascarenhas R, Pietrzak M, Smith RM, Webb A, Wang D, Papp AC, Pinsonneault JK, Seweryn M, Rempala G, Sadee W. Allele-Selective Transcriptome Recruitment to Polysomes Primed for Translation: Protein-Coding and Noncoding RNAs, and RNA Isoforms. Plos One. 10: e0136798. PMID 26331722 DOI: 10.1371/Journal.Pone.0136798  0.64
2015 Hampson E, Phillips SD, Duff-Canning SJ, Evans KL, Merrill M, Pinsonneault JK, Sadée W, Soares CN, Steiner M. Working memory in pregnant women: Relation to estrogen and antepartum depression. Hormones and Behavior. PMID 26187710 DOI: 10.1016/J.Yhbeh.2015.07.006  0.64
2014 Barrie ES, Weinshenker D, Verma A, Pendergrass SA, Lange LA, Ritchie MD, Wilson JG, Kuivaniemi H, Tromp G, Carey DJ, Gerhard GS, Brilliant MH, Hebbring SJ, Cubells JF, Pinsonneault JK, et al. Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity. Circulation Research. 115: 1017-25. PMID 25326128 DOI: 10.1161/Circresaha.116.304398  0.64
2014 Gadow KD, Smith RM, Pinsonneault JK. Serotonin 2A receptor gene (HTR2A) regulatory variants: possible association with severity of depression symptoms in children with autism spectrum disorder. Cognitive and Behavioral Neurology : Official Journal of the Society For Behavioral and Cognitive Neurology. 27: 107-16. PMID 24968012 DOI: 10.1097/Wnn.0000000000000028  0.64
2014 Gadow KD, Pinsonneault JK, Perlman G, Sadee W. Association of dopamine gene variants, emotion dysregulation and ADHD in autism spectrum disorder. Research in Developmental Disabilities. 35: 1658-65. PMID 24780147 DOI: 10.1016/J.Ridd.2014.04.007  0.64
2013 Pinsonneault JK, Sullivan D, Sadee W, Soares CN, Hampson E, Steiner M. Association study of the estrogen receptor gene ESR1 with postpartum depression--a pilot study. Archives of Women's Mental Health. 16: 499-509. PMID 23917948 DOI: 10.1007/S00737-013-0373-8  0.64
2013 Sullivan D, Pinsonneault JK, Papp AC, Zhu H, Lemeshow S, Mash DC, Sadee W. Dopamine transporter DAT and receptor DRD2 variants affect risk of lethal cocaine abuse: a gene-gene-environment interaction. Translational Psychiatry. 3: e222. PMID 23340505 DOI: 10.1038/Tp.2012.146  0.64
2012 Papp AC, Pinsonneault JK, Wang D, Newman LC, Gong Y, Johnson JA, Pepine CJ, Kumari M, Hingorani AD, Talmud PJ, Shah S, Humphries SE, Sadee W. Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. Plos One. 7: e31930. PMID 22403620 DOI: 10.1371/journal.pone.0031930  0.64
2011 Pinsonneault JK, Han DD, Burdick KE, Kataki M, Bertolino A, Malhotra AK, Gu HH, Sadee W. Dopamine transporter gene variant affecting expression in human brain is associated with bipolar disorder. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 36: 1644-55. PMID 21525861 DOI: 10.1038/Npp.2011.45  0.64
2011 Sadee W, Wang D, Papp AC, Pinsonneault JK, Smith RM, Moyer RA, Johnson AD. Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapy. Clinical Pharmacology and Therapeutics. 89: 355-65. PMID 21289622 DOI: 10.1038/Clpt.2010.314  0.64
2009 Bertolino A, Fazio L, Caforio G, Blasi G, Rampino A, Romano R, Di Giorgio A, Taurisano P, Papp A, Pinsonneault J, Wang D, Nardini M, Popolizio T, Sadee W. Functional variants of the dopamine receptor D2 gene modulate prefronto-striatal phenotypes in schizophrenia. Brain : a Journal of Neurology. 132: 417-25. PMID 18829695 DOI: 10.1093/brain/awn248  0.64
2008 Johnson AD, Zhang Y, Papp AC, Pinsonneault JK, Lim JE, Saffen D, Dai Z, Wang D, Sadée W. Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues. Pharmacogenetics and Genomics. 18: 781-91. PMID 18698231 DOI: 10.1097/Fpc.0B013E3283050107  0.64
2007 Lim JE, Pinsonneault J, Sadee W, Saffen D. Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons. Molecular Psychiatry. 12: 491-501. PMID 17453063 DOI: 10.1038/sj.mp.4001923  0.64
2007 Pinsonneault J, Sadée W. Sex Differences in Pharmacogenomics as a Tool to Study CNS Disorders Sex Differences in the Brain: From Genes to Behavior. DOI: 10.1093/acprof:oso/9780195311587.003.0005  0.64
2006 Pinsonneault JK, Papp AC, Sadée W. Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors. Human Molecular Genetics. 15: 2636-49. PMID 16893905 DOI: 10.1093/hmg/ddl192  0.64
2006 Lim JE, Papp A, Pinsonneault J, Sadée W, Saffen D. Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR. Molecular Psychiatry. 11: 649-62. PMID 16432527 DOI: 10.1038/sj.mp.4001797  0.64
2006 Anderle P, Nielsen CU, Pinsonneault J, Krog PL, Brodin B, Sadée W. Genetic variants of the human dipeptide transporter PEPT1. The Journal of Pharmacology and Experimental Therapeutics. 316: 636-46. PMID 16258023 DOI: 10.1124/jpet.105.094615  0.64
2005 Bahadduri PM, D'Souza VM, Pinsonneault JK, Sadée W, Bao S, Knoell DL, Swaan PW. Functional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epithelium. American Journal of Respiratory Cell and Molecular Biology. 32: 319-25. PMID 15626774 DOI: 10.1165/Rcmb.2004-0322Oc  0.64
2004 Pinsonneault J, Nielsen CU, Sadée W. Genetic variants of the human H+/dipeptide transporter PEPT2: analysis of haplotype functions. The Journal of Pharmacology and Experimental Therapeutics. 311: 1088-96. PMID 15282265 DOI: 10.1124/jpet.104.073098  0.64
2003 Pinsonneault J, Sadée W. Pharmacogenomics of multigenic diseases: sex-specific differences in disease and treatment outcome. Aaps Pharmsci. 5: E29. PMID 15198517 DOI: 10.1208/ps050429  0.64
2003 Papp AC, Pinsonneault JK, Cooke G, Sadée W. Single nucleotide polymorphism genotyping using allele-specific PCR and fluorescence melting curves. Biotechniques. 34: 1068-72. PMID 12765033  0.64
1997 Hassan B, Li L, Bremer KA, Chang W, Pinsonneault J, Vaessin H. Prospero is a panneural transcription factor that modulates homeodomain protein activity. Proceedings of the National Academy of Sciences of the United States of America. 94: 10991-6. PMID 9380747 DOI: 10.1073/pnas.94.20.10991  0.64
1997 Pinsonneault J, Florence B, Vaessin H, McGinnis W. A model for extradenticle function as a switch that changes HOX proteins from repressors to activators. The Embo Journal. 16: 2032-42. PMID 9155029 DOI: 10.1093/emboj/16.8.2032  0.64
1995 Derbyshire V, Pinsonneault JK, Joyce CM. Structure-function analysis of 3'-->5'-exonuclease of DNA polymerases. Methods in Enzymology. 262: 363-85. PMID 8594362 DOI: 10.1016/0076-6879(95)62030-3  0.64
1994 Zeng C, Pinsonneault J, Gellon G, McGinnis N, McGinnis W. Deformed protein binding sites and cofactor binding sites are required for the function of a small segment-specific regulatory element in Drosophila embryos. The Embo Journal. 13: 2362-77. PMID 7910795 DOI: 10.1002/J.1460-2075.1994.Tb06520.X  0.64
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