About

Name

Francois Bolduc

University

University of Alberta

Email

[email protected]

Roles and Connections

Primary Role

Faculty

Most Cited Publications

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B, "Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia." American journal of human genetics 98,5 (2016 May 5): 1038-1046
Jacob FD, Ramaswamy V, Andersen J, Bolduc FV, "Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature." European journal of human genetics : EJHG 17,12 (2009 Dec): 1577-81
Choi CH, Schoenfeld BP, Weisz ED, Bell AJ, Chambers DB, Hinchey J, Choi RJ, Hinchey P, Kollaros M, Gertner MJ, Ferrick NJ, Terlizzi AM, Yohn N, Koenigsberg E, Liebelt DA, Zukin RS, Woo NH, Tranfaglia MR, Louneva N, Arnold SE, Siegel SJ, Bolduc FV, McDonald TV, Jongens TA, McBride SM, "PDE-4 inhibition rescues aberrant synaptic plasticity in Drosophila and mouse models of fragile X syndrome." The Journal of neuroscience : the official journal of the Society for Neuroscience 35,1 (2015 Jan 7): 396-408