Publications

Ward-Flanagan, R; Scavuzzo, C; Mandhane, PJ; Bolduc, FV; Dickson, CT. (2020). Prenatal fruit juice exposure enhances memory consolidation in male post-weanling Sprague-Dawley rats. PLoS One. Jan 15(1): 1-18.
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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, Lehman A, Berg J, Li MH, Kini U, Joss S, von der Lippe C, Gordon CT, Humberson JB, Robak L, Scott DA, Sutton VR, Skraban CM, Johnston JJ, Poduri A, Nordenskjöld M, Shashi V, Gerkes EH, Bongers EMHF, Gilissen C, Zarate YA, Kvarnung M, Lally KP, Kulch PA, Daniels B, Hernandez-Garcia A, Stong N, McGaughran J, Retterer K, Tveten K, Sullivan J, Geisheker MR, Stray-Pedersen A, Tarpinian JM, Klee EW, Sapp JC, Zyskind J, Holla ØL, Bedoukian E, Filippini F, Guimier A, Picard A, Busk ØL, Punetha J, Pfundt R, Lindstrand A, Nordgren A, Kalb F, Desai M, Ebanks AH, Jhangiani SN, Dewan T, Coban Akdemir ZH, Telegrafi A, Zackai EH, Begtrup A, Song X, Toutain A, Wentzensen IM, Odent S, Bonneau D, Latypova X, Deb W; CAUSES Study, Redon S, Bilan F, Legendre M, Troyer C, Whitlock K, Caluseriu O, Murphree MI, Pichurin PN, Agre K, Gavrilova R, Rinne T, Park M, Shain C, Heinzen EL, Xiao R, Amiel J, Lyonnet S, Isidor B, Biesecker LG, Lowenstein D, Posey JE, Denommé-Pichon AS; Deciphering Developmental Disorders study, Férec C, Yang XJ, Rosenfeld JA, Gilbert-Dussardier B, Audebert-Bellanger S, Redon R, Stessman HAF, Nellaker C, Yang Y, Lupski JR, Goldstein DB, Eichler EE, Bolduc F, Bézieau S, Küry S, Campeau PM. Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability. Am J Hum Genet. 2019 Mar 7;104(3):530-541. doi: 10.1016/j.ajhg.2019.01.010. Epub 2019 Feb 28. PMID: 30827496; PMCID: PMC6407527.
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Androschuk A, He RX, Weber S, Rosenfelt C, Bolduc FV (2018). Stress Odorant Sensory Response Dysfunction in Drosophila Fragile X Syndrome Mutants. Front Mol Neurosci. 2018 Aug 8;11:242
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Monyak RE, Emerson D, Schoenfeld BO, Zheng X, Chambers DB, Rosenfelt C, Langer S, Hinchey P, Choi CH, McDonald TV, Bolduc FV, Seghal A, McBride SMJ, Jongens RA (2017). Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile x model. Molecular Psychiatry. 2017 Aug;22:1140-8.
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Raun M, Mailo J, Spinelli E, He X, McAvena S, Brand L, O'Sullivan J, Andersen J, Richer L, Tang-Wai R, Bolduc FV (2017). Quantitative phenotypic and network analysis of 1q44 microdeletion for microcephaly. Am J Med Genet A. 2017 Apr;173(4):972-7.
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Choi CH, Schoenfeld BP, Bell AJ, Hinchey K, Rosenfelt C, Gertner MJ, Campbell SR, Emerson D, Hinchey P, Kollaros M, Ferrick NJ, Chambers DB, Langer S, Sust S, Malik A, Terlizzi AM, Liebelt DA, Ferreiro D, Sharma A, Koenigsberg E, Choi RJ, Louneva N, Arnold SE, Featherstone RE, Siegel SJ, Zukin RS, McDonald TV, Bolduc FV, Jongens TA, McBride SM (2016). Multiple Drug Treatments That Increase cAMP Signaling Restore Long-Term Memory and Aberrant Signaling in Fragile X Syndrome Models. Front Behav Neurosi. 2016 Jun 30;10:136.
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Julien C, Lissouba A, Madabattula S, Fardghassemi Y, Rosenfelt C, Androschuk A, Strautman J, Wong C, Bysine A, O'Sullivan J, Rouleau GA, Drapeau P, Parker JA, Bodluc FV (2016). Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms. Hum Mol Genet. 2016 Mar 15;25(6):1088-99.
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Bolduc FV, Lau A, Rosenfelt C, Langer S, Wang N, Smithson L, Lefebvre D, Alexander RT, Dickson CT, Li L, Becker AB, Subbarao P, Turvey SE, Pei J, Sears MR, Mandhane PJ, CHILD Study Investigators (2016). Cognitive Enhancement in Infants Associated with Increased Maternal Fruit Intake During Pregnancy: Results from a Birth Cohort Study with Validation in an Animal Model. FBioMedicine. 2016 Jun;6:221-40.
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Gan-Or Z, Bouslam N, Birouk M, 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 FA, Ouled Amar Bencheikh B (2016).Mutations in CAPN1 Cause Autosomnal-Recessive Hereditary Spastic Paraplegia. Am J Hum Genet. 2016 Jun 2;98(6):1271.
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McLeod SA, Wee W, Jacob FD, Chapados I, Bolduc FV (2016). Recurrent Diplopia in a Pediatric Patient with Bickerstaff Brainstem Encephalitis. Case Rep Neurol Med. 2016 May;2016:5240274.
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He X, Caluseriu O, Srivastava R, Denny AM, Bolduc FV (2015). Reversible white matter lesions associated with mutant EHMT1 and Kleefstra syndrome. Neurol Genet. 2016 April;2(2):e58.
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Vander Pluym JH, O'Sullivan J, Andrew G, Bolduc FV (2015). Genomic characterization of chromosome 8 & pericentric trisomy. Clin Cae Rep. 2015 Jul;3(7):570-7.
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Madabattula ST, Strautman JC, Bysice AM, O'Sullivan JA, Androschuk A, Rosenfelt C, Doucet K, Rouleau G, Bolduc FV, (2015). Quantitative Analysis of Climbing Defects in Drosophila Model of Neurodegenerative Disorders. J Vis Exp. 2015 Jun 13;(100):e52741.
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Androschuk A, Al-Jabri B, Bolduc FV (2015). From Learning to Memory: What Flies Can Tell Us About Intellectual Disability Treatment. Front Psychiatry. 2015 Jun 3;6:85.
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Chambers DB, Androschuk A, Rosenfelt C, Langer S, Harding M, Bolduc FV (2015). Insulin signaling is acutely required for long-term memory in Drosophila. Front Neurol Circuits. 2015;9:8.
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Choi CH, Schoenfeld NP, Weisz ED, Bell AJ, Chambers DB, Hinchey J, Choi RJ, Hinchey P, Kollaros M, Gertner MJ, Ferrick NJ, Terlizzi AM, Koenigsberg E, Liebelt DA, Zukin RS, Woo NH, Tranfaglia MR, Louneva N, Arnold SE, Siegel SJ, Bolduc FV McDonald TV, Jongens TA, McBride SM (2015). PDE-4 inhibition rescues aberrant synaptic plasticity in Drosophila and mouse models of fragile X syndrome. J Neurosci. 2015 Jan 7;35(1):396-408.
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Ramaswamy V, Jacob FD, Bolduc FV (2011). Rearrangement of chromosome 14q with associated white matter disease. Pediatr Neurol. 2011 Aug;45(2):117-20.
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Ramaswamy V, Castillo M, Bolduc FV (2010). Developmental disability: duplication of zinc finger transcription factors 673 and 674. Pediatr Neurol. 2010 Sep;43(3):209-12.
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Bolduc FV, Valente D, Nguyen AT, Mitra PP, Tully T (2010). An assay for social interaction in Drosophila fragile X mutants. Fly(Austin). 2010-Jul-Sep;4(3):216-25.
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Bolduc FV, Bell K, Rosenfelt C, Cox H, Tully T (2010). Fragile X mental retardation 1 and filamin A interact genetically in Drosophila long-term memory. Front Neural Circuits. 2010 Jan 8;3:22.
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Jacob FD, Ramaswamy V, Andersen J, Bolduc FV (2009). Atypical Rett syndrome with selective FIXG1 deletion detected by comparative genomic hybridization: case report and review and literature. Eur J Hum Genet. 2009 Dec;17(12):1577-81.
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Bolduc FV, Tully T (2009). Fruit flies and intellectual disability. Fly(Austin). 2009 Jan-Mar;3(1):91-104.
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Bolduc FV, Bell K, Cox H, Broadie KS, Tully T (2008). Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory. Nat Neurosci. 2008 Oct;11(10):1143-5.
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Wu Y, Bolduc FV, Bell K, Tully T, Fang Y, Sehgal A, Fischer JA (2008). A Drosophila model for Angelman syndrome. Proc Natl Acad Sci U S A. 2008 Aug 26;105(34):12399-404.
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Bolduc FV, Shevell MI (2005). Corrected head circumference centiles as a possible predictor of developmental performance in high-risk neonatal intensive care unit survivors. Dev Med Child Neurol. 2005 Nov;46(11):766-70.
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