François V. Bolduc - Concepedia

Author

François V. Bolduc

Also Known As

, Bolduc, Francois, F Bolduc, F V Bolduc, F. Bolduc, F. V. Bolduc, Francois Bolduc, Francois V Bolduc, Francois V. Bolduc, Francois V. Bolduc

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

University of Alberta Women and Children’s Health Research Institute McGill University University of Pennsylvania Cold Spring Harbor Laboratory

About

François V. Bolduc is an author at University of Alberta specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	15	1.1K
2	Engineering	4	4	254
3	Social Sciences	2	2	98
4	Health Sciences	1	1	38
5	Public Health	1	1	33

François V. Bolduc

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory François V. Bolduc, Kimberly Bell, Hilary Cox, Nature Neuroscience Genome InstabilityDevelopmental BiologyGeneticsFragile X SpectrumGenomic Mechanism	2008	208
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsMolecular Genetics	2016	113
Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders Surya T. Madabattula, Joel C. Strautman, Andrew Bysice, Journal of Visualized Experiments EngineeringGeneticsMolecular BiologyDisease Gene IdentificationLocomotive Defects	2015	110
A <i>Drosophila</i> model for Angelman syndrome Yaning Wu, François V. Bolduc, Kimberly Bell, Proceedings of the National Academy of Sciences Developmental BiologyDevelopmental GeneticsGeneticsAngelman SyndromeMedicine	2008	100
Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model Rachel E. Monyak, Dow Emerson, Brian P. Schoenfeld, Molecular Psychiatry GeneticsHomeostatic MechanismInsulin SignalingCircadian RhythmNeurogenetics	2016	94
Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype Nuria C. Bramswig, Oana Caluseriu, H.‐J. Lüdecke, Human Genetics Genetic DisorderMedicineGeneticsEvolutionary BiologyCoffin–siris Syndrome-like Phenotype	2017	74
Relationships Between Wintering Waterbirds and Invertebrates, Sediments and Hydrology of Coastal Marsh Ponds François V. Bolduc, Alan D. Afton Waterbirds Coastal ManagementWetland EcologyEngineeringWater DepthFreshwater Ecosystem	2004	66
Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders Surya T. Madabattula, Joel C. Strautman, Andrew Bysice, Journal of Visualized Experiments EngineeringGeneticsMolecular BiologyDisease Gene IdentificationLocomotive Defects	2015	58
PDE-4 Inhibition Rescues Aberrant Synaptic Plasticity in<i>Drosophila</i>and Mouse Models of Fragile X Syndrome Catherine H. Choi, Brian P. Schoenfeld, Eliana D Weisz, Journal of Neuroscience GeneticsSynaptic TransmissionStructural PlasticitySynaptic SignalingSocial Sciences	2015	55
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability Benjamin Cogné, Sophie Ehresmann, Éliane Beauregard‐Lacroix, The American Journal of Human Genetics Neurodevelopmental DisordersChromatinSyndromic AutismGenetic DisorderGenetics	2019	51

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