Skip to main content Accessibility help
×
Home
  • Print publication year: 2016
  • Online publication date: March 2016

Chapter 18 - Behavioral phenotypes/genetic syndromes

from Section 4 - Special topics
Abbeduto, L., Warren, S.F., Conners, F.A. (2007). Language development in Down syndrome: from the prelinguistic period to the acquisition of literacy. Mental Retardation and Developmental Disabilities Research Reviews, 13, 247261.
Baumgardner, T.L., Reiss, A.L., Freund, L.S., Abrams, M.T. (1995). Specification of the neurobehavioral phenotype in males with Fragile X syndrome. Pediatrics, 95, 744752.
Boer, H., Holland, A., Whittington, J., et al. (2002). Psychotic illness in people with PWS due to chromosome 15 maternal uniparental disomy. Lancet, 359, 135.
Bunton, K. and Leddy, M. (2011). An evaluation of articulatory working space area in vowel production of adults with Down syndrome. Clinical Linguistics and Phonetics, 25, 321334.
Cherniske, E.M. Carpenter, T.O., Klaiman, C., et al. (2004). Multisystem study of 20 older adults with Williams syndrome. American Journal of Medical Genetics Part A, 131, 255264.
Clarke, D.J., Boer, H., Whittington, J., et al. (2002). Prader–Willi syndrome, compulsive and ritualistic behaviors: the first population-based study. British Journal of Psychiatry, 180, 358362.
Cordeiro, L., Ballinger, E., Hagerman, R., Hessl, D. (2011). Clinical assessment of DSM-IV anxiety disorders in Fragile X syndrome: prevalence and characterization. Journal of Neurodevelopmental Disorders, 3(1), 5767.
Dankner, N. and Dykens, E.M. (2012). Anxiety in intellectual disabilities: challenges and next steps. International Review of Research in Developmental Disabilities, 42, 5784.
Descheemaeker, M.J., Vogels, A, Govers, V., et al. (2002). Prader–Willi syndrome: new insights in the behavioural and psychiatric spectrum. Journal of Intellectual Disability Research, 46, 4150.
Descheemaeker, M.J., Govers, V., Vermeulen, P., Fryns, J.-P. (2006). Pervasive developmental disorders in Prader–Willi syndrome: the Leuven experience in 59 subjects and controls. American Journal of Medical Genetics Part A, 140, 11361142.
Devenny, D. and Matthews, A. (2011). Regression: atypical loss of attained functioning in children and adolescents with Down syndrome. International Review of Research in Developmental Disabilities, 41, 233264.
Dimitropoulos, A., Feurer, I.D., Butler, M.G., Thompson, T. (2001). Emergence of compulsive behavior and tantrums in children with Prader–Willi syndrome. American Journal on Mental Retardation, 106, 3951.
Dykens, E.M. (1995). Measuring behavioral phenotypes: provocations from the “new genetics.” American Journal on Mental Retardation, 99, 522532.
Dykens, E.M. (2003). Anxiety, fears, and phobias in persons with Williams syndrome. Developmental Neuropsychology, 23, 291316.
Dykens, E.M. (2004). Maladaptive and compulsive behavior in Prader–Willi syndrome: new insights from older adults. American Journal on Mental Retardation, 109, 142153.
Dykens, E.M. (2007). Psychiatric and behavioral disorders in persons with Down syndrome. Mental Retardation and Developmental Disabilities Research Reviews, 13, 272278.
Dykens, E.M. and Clarke, D.J. (1997). Correlates of maladaptive behavior in individuals with 5p-(cri-du-chat) syndrome. Developmental Medicine and Child Neurology, 39, 752756.
Dykens, E.M. and Kasari, C. (1997). Maladaptive behavior in children with Prader–Willi syndrome, Down syndrome, and non-specific mental retardation. American Journal on Mental Retardation, 102, 228237.
Dykens, E.M. and Roof, E. (2008). Behavior in Prader–Willi syndrome: relationship to genetic subtypes and age. Journal of Child Psychology and Psychiatry, 49, 10011008.
Dykens, E.M. and Shah, B. (2003). Psychiatric disorders in Prader–Willi syndrome: epidemiology and treatment. CNS Drugs, 17, 167178.
Dykens, E.M., Hodapp, R.M., Leckman, J.F. (1987). Strengths and weaknesses in intellectual functioning of males with Fragile X syndrome. American Journal of Mental Deficiency, 92, 234236.
Dykens, E.M., Hodapp, R.M., Walsh, K.K., Nash, L. (1992). Adaptive and maladaptive behavior in Prader–Willi syndrome. Journal of the American Academy of Child and Adolescent Psychiatry, 31, 11311136.
Dykens, E.M., Leckman, J.F., Cassidy, S.B. (1996). Obsessions and compulsions in Prader–Willi syndrome. Journal of Child Psychology and Psychiatry, 37, 9951002.
Dykens, E.M., Hodapp, R.M., Finucane, B. (2000). Genetics and Mental Retardation Syndromes: A New Look at Behavior and Treatments. Baltimore, MD: Paul H. Brookes Publishing Company.
Dykens, E.M., Maxwell, M.A., Pantino, E., Kossler, R., Roof, E. (2007). Assessment of hyperphagia in Prader–Willi syndrome. Obesity, 15, 18161826.
Dykens, E.M., Lee, E., Roof, E. (2011). Prader–Willi syndrome and autism spectrum disorders: an evolving story. Journal of Neurodevelopmental Disorders, 3, 225237.
Dykens, E.M., Shah, B., Davis, B., Baker, C., Fife, T., Fitzpatrick, J. (2015). Psychiatric disorders in adolescents and young adults with Down syndrome and other intellectual disabilities. Journal of Neurodevelopmental Disorders, 7, 9.
Einfeld, S.L., Tonge, B.J., Rees, V.W. (2001). Longitudinal course of behavioral and emotional problems in Williams syndrome. American Journal on Mental Retardation, 106(1), 7381.
Fidler, D.J. (ed.) (2011). Early development in neurogenetic disorders. International Review of Research in Developmental Disorders, 40, 1318.
Finucane, B.R. and Haas-Givler, B. (2009). Smith–Magenis syndrome: genetic basis and clinical implications. Journal of Mental Health Research in Intellectual Disabilities, 2, 134148.
Fletcher, R., Loschen, E., Stavrakaki, C. (eds.) (2007). Diagnostic Manual – Intellectual Disability (DM-ID): A Textbook of Diagnosis of Mental Disorders in Persons with Intellectual Disability. Kingston, NY: NADD Press.
Grosse, S.D. (2010). Sociodemographic characteristics of families of children with Down syndrome and the economic impacts of child disability on families. International Review of Research on Mental Retardation, 39, 257294.
Hodapp, R.M. (1997). Direct and indirect behavioral effects of different genetic disorders of mental retardation. American Journal on Mental Retardation, 102, 6779.
Hodapp, R.M. and Dykens, E.M. (1994). Mental retardation’s two cultures of behavioral research. American Journal on Mental Retardation, 98, 675687.
Hodapp, R.M. and Dykens, E.M. (2012). Genetic disorders of intellectual disability: expanding our concepts of phenotypes and of family outcomes. Journal of Genetic Counseling, 21, 761769.
Hodapp, R.M. and Urbano, R.C. (2008). Demographics of African-American and European-American mothers of newborns with Down syndrome. Journal of Policy and Practice in Intellectual Disabilities, 5, 187193.
Hodapp, R.M., Burke, M.M., Urbano, R.C. (2012). What’s age got to do with it? Implications of maternal age on families of offspring with Down syndrome. International Review of Research in Developmental Disabilities, 42, 109145.
Hogart, A., Wu, D., LaSalle, J.M., Schanen, C. (2010). The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease, 38, 181191.
Holland, A, Whittington, J, Hitton, E, (2003). The paradox of Prader–Willi syndrome: a genetic model of starvation. Lancet, 362, 989991.
Kemper, M.B., Hagerman, R.J., Altshul-Stark, D. (1988). Cognitive profiles of boys with Fragile X syndrome. American Journal of Medical Genetics, 30, 191200.
Leyfer, O.T., Woodruff-Borden, J., Klein-Tasman, B.P., Fricke, J.S., Mervis, C.B. (2006). Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141, 615622.
Moskowitz, L.J., Mulder, E., Walsh, C.E., et al. (2013). A multimethod assessment of anxiety and problem behavior in children with autism spectrum disorders and intellectual disability. American Journal on Intellectual and Developmental Disabilities, 116, 419434.
Myers, B.A. and Pueschel, S.M. (1991). Psychiatric disorders in persons with Down syndrome. Journal of Nervous and Mental Disease, 179(10), 609613.
Opitz, J.M. (1985). The developmental field concept. American Journal of Medical Genetics, 21(1), 1.
Patterson, D. (2009). Molecular genetic analysis of Down syndrome. Human Genetics, 126, 195214.
Porter, H. and Tharpe, A.M. (2010). Hearing loss among persons with Down syndrome. International Review of Research in Mental Retardation, 39, 195220.
Prasher, V.P. (2002). Disintegrative syndrome in young adults. Irish Journal of Psychological Medicine, 19(3), 101.
Schanen, N.C. (2006). Epigenetics of autism spectrum disorder. Human Molecular Genetics, 15, R138R150.
Sharp, A.J., Migliavacca, E., Dupre, Y., et al. (2010). Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15. Genome Research, 20, 12711278.
Schretlen, D.J., Ward, J., Yun, J., et al. (2005). Behavioral aspects of Lesch–Nyhan disease and its variants. Developmental Medicine and Child Neurology, 47, 673677.
Sigafoos, J., O’Reilly, M.F., Lancioni, G.E. (2009). Editorial: cri-du-chat. Developmental Neurorehabilitation, 12, 119121.
Soni, S., Whittington, J., Holland, A.J., et al. (2007). The course and outcome of psychiatric illness in people with Prader–Willi syndrome: implications for management and treatment. Journal of Intellectual Disability Research, 51, 3242.
Stein, D.S., Munir, K.M., Karweck, A.J., Davidson, E.J., Stein, M.T. (2013). Developmental regression, depression, and psychosocial stress in an adolescent with Down syndrome. Journal of Developmental and Behavioral Pediatrics, 34, 216218.
Van Acker, R. (1991). Rett syndrome: a review of current knowledge. Journal of Autism and Developmental Disorders, 21, 381406.
Veltman, M.W., Craig, E.E., Bolton, P.F. (2005). Autism spectrum disorders in Prader–Willi and Angelman syndromes: a systematic review. Psychiatric Genetics, 15, 243254.
Webb, T., Maina, E.N., Soni, S., et al. (2008). In search of the psychosis gene in people with Prader–Willi syndrome. American Journal of Medical Genetics Part A, 146, 843853.
Woodruff-Borden, J., Kistler, D.J., Henderson, D.R., Crawford, N.A., Mervis, C.B. (2010). Longitudinal course of anxiety in children and adolescents with Williams syndrome. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 154, 277290.
Worley, G., Crissman, B., Cardogan, E., Kishnani, P. (2013). New onset autistic regression, cognitive decline and insomnia in older children and adolescents with Down syndrome. Presentation to the Down Syndrome Medical Interest Group–USA, Denver, CO.