Paul Valdmanis

Publications

• Expression determinants of mammalian argonaute proteins in mediating gene silencing. Valdmanis PN, Gu S, Schüermann N, Sethupathy P, Grimm D, Kay MA. Nucleic Acids Res. 2012; 40 (8): 3704-13
• The loop position of shRNAs and pre-miRNAs is critical for the accuracy of dicer processing in vivo. Gu S, Jin L, Zhang Y, Huang Y, Zhang F, Valdmanis PN, Kay MA. Cell. 2012; 151 (4): 900-11
• rAAV-mediated tumorigenesis: still unresolved after an AAV assault. Valdmanis PN, Lisowski L, Kay MA. Mol Ther. 2012; 20 (11): 2014-7
• A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. Valdmanis PN, Dupré N, Lachance M, Stochmanski SJ, Belzil VV, Dion PA, Thiffault I, Brais B, Weston L, Saint-Amant L, Samuels ME, Rouleau GA. Brain. 2011; 134 (Pt 2): 602-7
• Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis. Daoud H, Valdmanis PN, Gros-Louis F, Belzil V, Spiegelman D, Henrion E, Diallo O, Desjarlais A, Gauthier J, Camu W, Dion PA, Rouleau GA. Arch Neurol. 2011; 68 (5): 587-93
• Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis. Daoud H, Valdmanis PN, Dion PA, Rouleau GA. Amyotroph Lateral Scler. 2010; 11 (4): 389-91