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Human Gene Therapy|January 12, 2017
Future of rAAV Gene Therapy: Platform for RNAi, Gene Editing, and BeyondPaul N Valdmanis, Mark A KayNeurology|January 9, 2008
Genetics of familial amyotrophic lateral sclerosisPaul N Valdmanis, Guy A RouleauJournal of Visualized Experiments : Jove|September 10, 2019
A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source ToolsMeredith M Course, Kathryn Gudsnuk, Paul N ValdmanisArchives of Neurology|March 12, 2008
A locus for primary lateral sclerosis on chromosome 4ptel-4p16.1Paul N Valdmanis, Nicolas Dupré, Guy A RouleauBioinformatics Advances|May 11, 2023
TRviz: a Python library for decomposing and visualizing tandem repeat sequencesJonghun Park, Eli Kaufman, Paul N Valdmanis, et al.Human Mutation|December 24, 2008
The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative diseasePaul N Valdmanis, Dominique J Verlaan, Guy A RouleauExperimental & Molecular Medicine|July 10, 2023
Emerging roles of tRNA-derived small RNAs in cancer biologySaebyeol Lee, Jungeun Kim, Paul N Valdmanis, et al.Annals of Neurology|December 13, 2007
Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?Edor Kabashi, Paul N Valdmanis, Patrick Dion, et al.Current Neurology and Neuroscience Reports|April 8, 2009
Recent advances in the genetics of amyotrophic lateral sclerosisPaul N Valdmanis, Hussein Daoud, Patrick A Dion, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|December 17, 2009
Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosisHussein Daoud, Paul N Valdmanis, Patrick A Dion, et al.Pageof 6