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Publications by ASD-CARC Researchers and Trainees
(ASD-CARC Researchers, ASPIRE Training Program Trainees, Other Trainees)
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, 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)
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 and Lewis MES. Noonan syndrome and autoimmune disorders. Am. J. Med. Genet. 2005 139A:239-242.
Mitchell RJ, Holden JJ, Zhang C, Curlis Y, Slater HR, Burgess T, Kirkby KC, Carmichael A, Heading KD, Loesch DZ. FMR1 alleles in Tasmania: a screening study of the special educational needs population. Clin Genet. 2005 Jan;67(1):38-46. (PMID: 15617547)
Ouellette-Kuntz H, Garcin N, Lewis ME, Minnes P, Martin C, Holden JJ. Addressing health disparities through promoting equity for individuals with intellectual disability. Can J Public Health. 2005 Mar-Apr;96 Suppl 2:S8-22. Review. (PMID: 16078552)
Perry A, Condillac RA, Freeman NL, Dunn-Geier J, Belair J. Multi-site study of the Childhood Autism
Rating Scale (CARS) in five clinical groups of young children. J Autism Dev Disord. 2005 Oct;35(5):625-34.
Stepp ML, Cason AL, Finnis M, Mangelsdorf M, Holinski-Feder E, Macgregor D, MacMillan A, Holden JJ, Gecz J, Stevenson RE, Schwartz CE. XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene. BMC Med Genet. 2005 Apr 25;6:16. (PMID: 15850492)
Tyson C, Harvard C, Locker R, Friedman JM, Langlois S, Lewis ME, Van Allen M, Somerville M, Arbour L, Clarke L, McGilivray B, Yong SL, Siegel-Bartel J, Rajcan-Separovic E. Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH. Am J Med Genet A. 2005 Dec 15;139(3):173-85.
2004:
Feldman MA, Atkinson L, Foti-Gervais L, Condillac R. Formal versus informal interventions for challenging behaviour in persons with intellectual disabilities. J Intellect Disabil Res. 2004 Jan;48(1):60-8.
Kogan CS, Boutet I, Cornish K, Zangenehpour S, Mullen KT, Holden JJ, Der Kaloustian VM, Andermann E, Chaudhuri A. . Differential impact of the FMR1 gene on visual processing in fragile X syndrome. Brain. 2004 Mar;127(Pt 3):591-601. (PMID: 14736752)
Lewis MES. Putting mind over matter: Rethinking current strategies for unmasking the genetics of mental illness. Clin. Genet. 2004: 66:177-182.
Lewis MES. Genes, screens and improved means for the diagnosis and anticipatory care of individuals with congenital intellectual disability (ID). Clin.Genet 2004 65:1-6.
Sakko G, Martin TL, Vause T, Martin GL, Yu CT. Visual-visual nonidentity matching assessment: a worthwhile addition to the assessment of basic learning abilities test. Am J Ment Retard. 2004 Jan;109(1):44-52.
Tyson C, McGillivray B, Chijiwa C, Rajcan-Separovic E. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH. Am J Med Genet A. 2004 Sep 1;129A(3):254-60.
2003:
Bebko JM, Calderon R, Treder R. The Language Proficiency Profile-2: Assessment of the Global Communication Skills of Deaf Children Across Languages and Modalities of Expression. J Deaf Stud Deaf Educ. 2003 Autumn;8(4):438-451.
Bebko JM, Demark JL, Osborne PA, Majumder S, Ricciuti CJ, Rhee T. Acquisition and automatization of a complex task: an examination of three-ball cascade juggling. J Mot Behav. 2003 Jun;35(2):109-18. Erratum in: J Mot Behav. 2003 Sep;35(3):245.
Cohen IL, Liu X, Schutz C, White BN, Jenkins EC, Brown WT, Holden JJ. Association of autism severity with a monoamine oxidase A functional polymorphism. Clin Genet. 2003 Sep;64(3):190-7. (PMID: 12919132)
Goldstein G, Bebko JM. The Profile of Multiple Language Proficiencies: A Measure for Evaluating Language Samples of Deaf Children. J Deaf Stud Deaf Educ. 2003 Autumn;8(4):452-463.
Lewis MES. The complicity of segmental duplicity in human genetic disease. Clin.Genet. (2003).(63): 262-267.
Li J, Jiang T, Bejjani B, Rajcan-Separovic E, Cai WW. High-resolution human genome scanning using whole-genome BAC arrays. Cold Spring Harb Symp Quant Biol. 2003;68:323-9.
2002:
Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ. Reelin gene alleles and susceptibility to autism spectrum disorders. Mol Psychiatry. 2002;7(9):1012-7.(PMID: 12399956)
Schutz CK, Polley D, Robinson PD, Chalifoux M, Macciardi F, White BN, Holden JJ. Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method. Am J Med Genet. 2002 Apr 15;109(1):36-41. (PMID: 11932990)
2001:
Faradz SM, Leggo J, Murray A, Lam-Po-Tang PR, Buckley MF, Holden JJ. Distribution of FMR1 and FMR2 alleles in Japanese individuals with developmental disability and confirmation of a specific AGG-interruption pattern in Asian populations. Ann Hum Genet. 2001 Mar;65(Pt 2):127-35. (PMID: 11427173)
© 2005, 2006, 2007 ASD-CARC - GRIDS Ltd. All rights reserved.
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