| Year |
Citation |
Score |
| 2023 |
Bui TA, Rosenfelt CS, Whitlock KH, Leclercq M, Weber S, Droit A, Wiebe SA, Pei J, Bolduc FV. Long-term Memory Testing in Children With Typical Development and Neurodevelopmental Disorders: Remote Web-based Image Task Feasibility Study. Jmir Pediatrics and Parenting. 6: e39720. PMID 37155237 DOI: 10.2196/39720 |
0.316 |
|
| 2021 |
Bui TA, Shatto J, Cuppens T, Droit A, Bolduc FV. Phenotypic Trade-Offs: Deciphering the Impact of Neurodiversity on Drug Development in Fragile X Syndrome. Frontiers in Psychiatry. 12: 730987. PMID 34733188 DOI: 10.3389/fpsyt.2021.730987 |
0.311 |
|
| 2020 |
Husain RA, Grimmel M, Wagner M, Hennings JC, Marx C, Feichtinger RG, Saadi A, Rostásy K, Radelfahr F, Bevot A, Döbler-Neumann M, Hartmann H, Colleaux L, Cordts I, Kobeleva X, ... ... Bolduc F, et al. Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia. American Journal of Human Genetics. PMID 32707086 DOI: 10.1016/J.Ajhg.2020.06.015 |
0.342 |
|
| 2019 |
Cogné B, Ehresmann S, Beauregard-Lacroix E, Rousseau J, Besnard T, Garcia T, Petrovski S, Avni S, McWalter K, Blackburn PR, Sanders SJ, Uguen K, Harris J, Cohen JS, Blyth M, ... ... Bolduc F, et al. Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability. American Journal of Human Genetics. PMID 30827496 DOI: 10.1016/J.Ajhg.2019.01.010 |
0.389 |
|
| 2018 |
Androschuk A, He RX, Weber S, Rosenfelt C, Bolduc FV. Stress Odorant Sensory Response Dysfunction in Fragile X Syndrome Mutants. Frontiers in Molecular Neuroscience. 11: 242. PMID 30135642 DOI: 10.3389/fnmol.2018.00242 |
0.399 |
|
| 2017 |
Bramswig NC, Caluseriu O, Lüdecke HJ, Bolduc FV, Noel NC, Wieland T, Surowy HM, Christen HJ, Engels H, Strom TM, Wieczorek D. Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype. Human Genetics. 136: 297-305. PMID 28124119 DOI: 10.1007/s00439-017-1757-z |
0.32 |
|
| 2016 |
Choi CH, Schoenfeld BP, Bell AJ, Hinchey J, Rosenfelt C, Gertner MJ, Campbell SR, Emerson D, Hinchey P, Kollaros M, Ferrick NJ, Chambers DB, Langer S, Sust S, Malik A, ... ... Bolduc FV, et al. Multiple Drug Treatments That Increase cAMP Signaling Restore Long-Term Memory and Aberrant Signaling in Fragile X Syndrome Models. Frontiers in Behavioral Neuroscience. 10: 136. PMID 27445731 DOI: 10.3389/Fnbeh.2016.00136 |
0.373 |
|
| 2016 |
Monyak RE, Emerson D, Schoenfeld BP, Zheng X, Chambers DB, Rosenfelt C, Langer S, Hinchey P, Choi CH, McDonald TV, Bolduc FV, Sehgal A, McBride SM, Jongens TA. Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model. Molecular Psychiatry. PMID 27090306 DOI: 10.1038/Mp.2016.51 |
0.349 |
|
| 2015 |
Madabattula ST, Strautman JC, Bysice AM, O'Sullivan JA, Androschuk A, Rosenfelt C, Doucet K, Rouleau G, Bolduc F. Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders. Journal of Visualized Experiments : Jove. e52741. PMID 26132637 DOI: 10.3791/52741 |
0.405 |
|
| 2015 |
Androschuk A, Al-Jabri B, Bolduc FV. From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment. Frontiers in Psychiatry. 6: 85. PMID 26089803 DOI: 10.3389/fpsyt.2015.00085 |
0.4 |
|
| 2015 |
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, ... ... Bolduc FV, et al. 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: 396-408. PMID 25568131 DOI: 10.1523/Jneurosci.1356-12.2015 |
0.343 |
|
| 2010 |
Bolduc FV, Valente D, Nguyen AT, Mitra PP, Tully T. An assay for social interaction in Drosophila fragile X mutants. Fly. 4: 216-25. PMID 20519966 DOI: 10.4161/fly.4.3.12280 |
0.493 |
|
| 2010 |
Bolduc FV, Bell K, Rosenfelt C, Cox H, Tully T. Fragile x mental retardation 1 and filamin a interact genetically in Drosophila long-term memory. Frontiers in Neural Circuits. 3: 22. PMID 20190856 DOI: 10.3389/neuro.04.022.2009 |
0.574 |
|
| 2009 |
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: 1577-81. PMID 19623215 DOI: 10.1038/ejhg.2009.95 |
0.356 |
|
| 2009 |
Bolduc FV, Tully T. Fruit flies and intellectual disability. Fly. 3: 91-104. PMID 19182539 DOI: 10.4161/fly.3.1.7812 |
0.513 |
|
| 2008 |
Bolduc FV, Bell K, Cox H, Broadie KS, Tully T. Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory. Nature Neuroscience. 11: 1143-5. PMID 18776892 DOI: 10.1038/nn.2175 |
0.482 |
|
| 2008 |
Wu Y, Bolduc FV, Bell K, Tully T, Fang Y, Sehgal A, Fischer JA. A Drosophila model for Angelman syndrome. Proceedings of the National Academy of Sciences of the United States of America. 105: 12399-404. PMID 18701717 DOI: 10.1073/Pnas.0805291105 |
0.519 |
|
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