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- Publications -
(ASD-CARC Researchers, ASPIRE Training Program Trainees, Other Trainees)
2010
Cohen IL, Rovito Gomez T, Gonzalez MG, Lennon EM, Karmel BZ & Gardner JM (2010) Parent PDD Behavior Inventory Profiles of Young Children Classified According to Autism Diagnostic Observation Schedule-Generic and Autism Diagnostic Interview-Revised Criteria. Journal of Autism and Developmental Disorders, 40(2). 246-254.
Cohen IL, Tsiouris JA, Flory MJ, Kim SY, Freedland R, Heaney G, Pettinger J, & Brown TW. (2010) A large scale study of the psychometric characteristics of the IBR Modified Overt Aggression Scale: Findings and evidence for increased self-destructive behaviors in adult females with autism spectrum disorder. .Journal of Autism and Developmental Disorders. 40(5). 599-609.
Malisza KL, Clancy C, Shiloff D, Foreman D, Holden J, Jones C, Paulson K, Summers R, Yu CT, Chudley AE. (2010). Functional Evaluation of Hidden Figures Object Analysis in Children with Autistic Disorder. Journal of Autism and Developmental Disorders. Epub ahead of print.
McGuinness TM, Lewis S. (in press) Update on Autism and Vaccines. J Psychosoc Nurs Ment Health Serv. 2010 May 26:1-4.
Regehr K, & Feldman MA (in press). Parent-selected interventions for infants at-risk for autism spectrum disorder and their affected siblings. Behavioral Interventions.
Ward-King J, Cohen IL, Penning H, Holden JJ. (2010). Brief Report: Telephone Administration of the Autism Diagnostic Interview-Revised: Reliability and Suitability for Use in Research. Journal of Autism and Developmental Disorders. Epub ahead of print.
Wegiel J, Kuchna I, Nowicki K, Imaki H, Wegiel J, Marchi E, Ma SY, Chauhan A, Chauhan V, Bobrowicz TW, de Leon M, Louis LA, Cohen IL, London E, Brown WT, & Wisniewski T. (2010). The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. Acta Neuropathol. 119(6). 755-750.
2009
Hiebert R, Martin GL, Yu CT, Thorsteinsson JR, Martin TL. (2009) Predicting compliance of children with and without developmental delay. Canadian Journal of Behavioural Science/Revue canadienne des sciences du comportement. 41(1), 31-36.
Mazur-Kolecka B, Cohen IL, Jenkins EC, Flory M, Merz G, Brown WT, &
Frackowiak J. (2009). Sera from children with Autism alter proliferation of human neuronal progenitor cells exposed to oxidation. Neurotoxicity Research, 16(1). 87-95.
Qiao Y, Riendeau N, Koochek M, Liu X, Harvard C, Hildebrand MJ, Holden JJ, Lewis ME, Rajcan-Separovic E. (2009) Phenomic determinants of genomic variation in autism spectrum disorders. J Med Genet. 2009 Oct;46(10):680-8. Epub 2009 Jul 21.
Ouellette-Kuntz HM, Coo H, Lam M, Yu CT, Breitenbach MM, Hennessey PE, Holden JJ, Brown HK, Noonan AL, Gauthier RB, Crews LR. (2009) Age at diagnosis of autism spectrum disorders in four regions of Canada. Can J Public Health. 2009 Jul-Aug;100(4):268-73.
Thiessen C, Fazzio D, Arnal L, Martin GL, Yu CT, Keilback L. (2009) Evaluation of a self-instructional manual for conducting discrete-trials teaching with children with autism. Behavior Modification. Vol 33(3), May 2009, pp. 360-373
Thomson K, Martin GL, Arnal L, Fazzio D, Yu CT. (2009) Instructing individuals to deliver discrete-trials teaching to children with autism spectrum disorders: A review. Research in Autism Spectrum Disorders. Vol 3(3), Jul-Sep 2009, pp. 590-606
2008
Anisman H, Merali Z, Stead JD. Experiential and genetic contributions to depressive- and anxiety-like disorders: clinical and experimental studies. Neurosci Biobehav Rev. 2008 Aug;32(6):1185-206.
Boycott KM, Parboosingh JS, Chodirker BN, Lowry RB, McLeod DR, Morris J, Greenberg CR, Chudley AE, Bernier FP, Midgley J, Møller LB, Innes AM. Clinical genetics and the Hutterite population: a review of Mendelian disorders. Am J Med Genet A. 2008 Apr 15;146A(8):1088-98. Review.
Chodirker BN, Chudley AE. Routine genetic testing for Asperger syndrome. Genet Med. 2008 Nov;10(11):843-5; author reply 845.
Coo H, Ouellette-Kuntz H, Lloyd JE, Kasmara L, Holden JJ, Lewis ME. Trends in autism prevalence: diagnostic substitution revisited. J Autism Dev Disord. 2008 Jul;38(6):1036-46. (PMID: 17975721)
D'Souza CA, Chopra V, Varhol R, Xie YY, Bohacec S, Zhao Y, Lee LL, Bilenky M, Portales-Casamar E, He A, Wasserman WW, Goldowitz D, Marra MA, Holt RA, Simpson EM, Jones SJ. Identification of a set of genes showing regionally enriched expression in the mouse brain. BMC Neurosci. 2008 Jul 14;9:66.
Gibson WT, Harvard C, Qiao Y, Somerville MJ, Lewis ME, Rajcan-Separovic E. Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3. Am J Med Genet A. 2008 Jan 15;146A(2):225-32. Can J Clin Pharmacol. 2008 Summer;15(2):e344-66.
Goh YI, Chudley AE, Clarren SK, Koren G, Orrbine E, Rosales T, Rosenbaum C. Development of Canadian screening tools for fetal alcohol spectrum disorder. Taskforce for Development of FASD Screening Tools. Can J Clin Pharmacol. 2008 Summer;15(2):e344-66.
Hammond P, Forster-Gibson C, Chudley AE, Allanson JE, Hutton TJ, Farrell SA, McKenzie J, Holden JJ, Lewis ME. Face-brain asymmetry in autism spectrum disorders. Mol Psychiatry. 2008 Jun;13(6):614-23. (PMID: 18317467)
Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ. A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. (PMID: 18205172)
Hettinger JA, Liu X, Holden JJ.The G22A polymorphism of the ADA gene and susceptibility to autism spectrum disorders. J Autism Dev Disord. 2008 Jan;38(1):14-9. (PMID: 17340203)
Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ. The DLX1and DLX2 genes and susceptibility to autism spectrum disorders. Eur J Hum Genet. 2008 Aug 27. (PMID: 18728693)
Martin GL, Thorsteinsson JR, Yu CT, Martin TL, Vause T. The assessment of basic learning abilities test for predicting learning of persons with intellectual disabilities: a review. Behav Modif. 2008 Mar;32(2):228-47. Review.
Merali Z, Anisman H, James JS, Kent P, Schulkin J. Effects of corticosterone on corticotrophin-releasing hormone and gastrin-releasing peptide release in response to an aversive stimulus in two regions of the forebrain (central nucleus of the amygdala and prefrontal cortex). Eur J Neurosci. 2008 Jul;28(1):165-72.
Merali Z, Cayer C, Kent P, Anisman H. Nesfatin-1 increases anxiety- and fear-related behaviors in the rat. Psychopharmacology (Berl). 2008 Nov;201(1):115-23.
Mistry M, Pavlidis P. Gene Ontology term overlap as a measure of gene functional similarity. BMC Bioinformatics. 2008 Aug 4;9:327.
Mittleman G, Goldowitz D, Heck DH, Blaha CD. Cerebellar modulation of frontal cortex dopamine efflux in mice: relevance to autism and schizophrenia. Synapse. 2008 Jul;62(7):544-50.
Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, Lewis ME. Autism-associated familial microdeletion of Xp11.22. Clin Genet. 2008 Aug;74(2):134-44. (PMID: 18498374)
Rusnak AJ, Hadfield MI, Chudley AE, Marles SL, Reid GJ, Chodirker BN. Increased Nuchal Translucency Thickness: A Potential Indicator for Ritscher-Schinzel Syndrome. Fetal Diagn Ther. 2008 Oct 28;24(4):395-399.
Stark KL, Xu B, Bagchi A, Lai WS, Liu H, Hsu R, Wan X, Pavlidis P, Mills AA, Karayiorgou M, Gogos JA. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat Genet. 2008 Jun;40(6):751-60.
Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E. Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH. Mol Cytogenet. 2008 Nov 11;1(1):23. (PMID: 19000322)
2007
Bao L, Peirce JL, Zhou M, Li H, Goldowitz D, Williams RW, Lu L, Cui Y. An integrative genomics strategy for systematic characterization of genetic loci modulating phenotypes. Hum Mol Genet. 2007 Jun 1;16(11):1381-90.
Feldman M, McDonald L, Serbin L, Stack D, Secco ML, Yu CT. Predictors of depressive symptoms in primary caregivers of young children with or at risk for developmental delay. J Intellect Disabil Res. 2007 Aug;51(Pt 8):606-19.
Fisch GS, Carpenter N, Howard-Peebles PN, Holden JJ, Tarleton J, Simensen R, Nance W. Studies of age-correlated features of cognitive-behavioral development in children and adolescents with genetic disorders. Am J Med Genet A. 2007 Oct 15;143A(20):2478-89. (PMID: 17853466)
Ouellette-Kuntz H, Coo H, Lloyd JE, Kasmara L, Holden JJ, Lewis ME. Trends in special education code assignment for autism: implications for prevalence estimates. J Autism Dev Disord. 2007 Nov;37(10):1941-8. (PMID: 17216561)
Qiao Y, Liu X, Harvard C, Nolin SL, Brown WT, Koochek M, Holden JJ, Lewis ME, Rajcan-Separovic E. Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis. BMC Genomics. 2007 Jun 12;8:167. (PMID: 17565693)
Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1. J Med Genet. 2007 Apr;44(4):269-76. (PMID: 16963482)
Shen JJ, Lee PH, Holden JJ, Shatkay H. Using cluster ensemble and validation to identify subtypes of pervasive developmental disorders. AMIA Annu Symp Proc. 2007 Oct 11:666-70. (PMID: 18693920)
Thorsteinsson JR, Martin GL, Yu CT, Spevack S, Martin TL, Lee MS.Predicting learning ability of people with intellectual disabilities: assessment of basic learning abilities test versus caregivers' predictions. Am J Ment Retard. 2007 Mar;112(2):130-9.
2006
Bebko JM, Weiss JA, Demark JL, Gomez P. Discrimination of temporal synchrony in intermodal events by children with autism and children with developmental disabilities without autism. J Child Psychol Psychiatry. 2006 Jan;47(1):88-98.
Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH. Clin Genet. 2006 Feb;69(2):124-34. (PMID: 16433693)
Lopez-Rangel E, Lewis ME. Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders. Clin Genet. 2006 Jan;69(1):21-2.
Loretta Secco M, Askin D, Yu CT, Garinger J, Mulaire-Cloutier C, Scharf L, Schwartzman L, Konyk D, Feldman MA. Factors affecting parenting stress among biologically vulnerable toddlers. Issues Compr Pediatr Nurs. 2006 Jul-Sep;29(3):131-56.
Mercer L, Creighton S, Holden JJ, Lewis ME. Parental perspectives on the causes of an autism spectrum disorder in their children. J Genet Couns. 2006 Feb;15(1):41-50. (PMID: 16547798)
2005
Bebko JM, Demark JL, Im-Bolter N, MacKewn A. Transfer, control, and automatic processing in a complex motor task: an examination of bounce juggling. J Mot Behav. 2005 Nov;37(6):465-74.
Curlis Y, Zhang C, Holden JJ, Loesch PK, Mitchell RJ. Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size FMR1 alleles. Hum Biol. 2005 Feb;77(1):137-51. (PMID: 16114822)
de Vries C, Yu CT, Sakko G, Wirth KM, Walters KL, Marion C, Martin GL. Predicting the relative efficacy of verbal, pictorial, and tangible stimuli for assessing preferences of leisure activities. Am J Ment Retard. 2005 Mar;110(2):145-54.
D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM. Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions. Mol Psychiatry. 2005 Nov;10(11):1006-16. (PMID: 16027737)
Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E.A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH. Clin Genet. 2005 Apr;67(4):341-51. (PMID: 15733271)
Lopez-Rangel E
