Aging & Developmental Disabilities Publications
Journal Articles
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Esbensen, A., Seltzer, M.M., & Krauss, M.W. (2008). Stability and change in health, functional abilities and behavior problems among adults with and without Down syndrome. American Journal on Mental Retardation, 113, 263-277.
Esbensen, A.J., Seltzer, M.M., & Greenberg, J.S. (2007). Factors predicting mortality in midlife adults with and without Down syndrome living with family. Journal of Intellectual Disability Research, 51, 1039-1050.
Orsmond, G.I. & Seltzer, M.M. (2007). Siblings of individuals with autism or Down syndrome: Effects on adult lives. Journal of Intellectual Disability Research. 51, 682-696.
Esbensen, A. J., Seltzer, M. M., & Greenberg, J. S. (2006). Depressive symptoms of adults with mild to moderate intellectual disability and its relation to maternal well-being. Journal of Policy and Practice in Intellectual Disabilities 3, 229-237.
Esbensen, A.J., Seltzer, M.M., Greenberg, J.S., & Benson, B.A. (2005). Psychometric evaluation of a self-report measure of depression for individuals with mental retardation. American Journal of Mental Retardation, 110, 469-481.
Seltzer, M.M. & Krauss, M.W. (2001). Quality of life of adults with mental retardation/developmental disabilities who live with family. Mental Retardation and Developmental Disabilities Research Reviews, 7, 105-114.
Seltzer, M.M., Krauss, M.W., Hong, J., & Orsmond, G.I. (2001). Continuity or discontinuity of family involvement following residential transitions of adults with mental retardation. Mental Retardation, 39, 181-194.
Orsmond, G.I., & Seltzer, M.M. (2000). Brothers and sisters of adults with mental retardation: The gendered nature of the sibling relationship. American Journal on Mental Retardation, 105, 486-508.
Essex, E.L., Seltzer, M.M., & Krauss, M.W. (1999). Differences in coping effectiveness and well-being among aging mothers and fathers of adults with mental retardation. American Journal on Mental Retardation, 104, 545-563.
Freedman, R. I., Griffiths, D., Krauss, M. W., & Seltzer, M. M. (1999). Patterns of respite use by aging parents of adults with mental retardation. Mental Retardation, 37,93-103.
Seltzer, M. M. & Heller, T. (1997). Families and caregiving across the life course: Research advances on the influence of context. Family Relations, 46, 321-323.
Seltzer, M. M., Greenberg, J. S., Krauss, M. W., Gordon, R. M., & Judge, K. (1997). Siblings of adults with mental retardation or mental illness: Effects on lifestyle and psychological well-being. Family Relations, 46, 395-405.
Essex, E. L., Seltzer, M. M., & Krauss, M. W. (1997). Residential transitions of adults with mental retardation: Predictors of waiting list use and placement. American Journal on Mental Retardation, 101, 613-629.
Freedman, R. I., Krauss, M. W., & Seltzer, M. M. (1997). Aging parents residential plans for adult children with mental retardation. Mental Retardation, 35, 114-123.
Seltzer, M. M., Greenberg, J. S., Krauss, M. W., & Hong, J. (1997). Predictors and outcomes of the end of co-resident caregiving in aging families of adults with mental retardation or mental illness. Family Relations, 46, 13-22
reprinted in A. J. Walker, M. Manoogian-O Dell, L. McGraw, & D. White (Eds.) (2001). Families in later life: Connections and transitions (pp. 212-217). Thousand Oaks, CA, Pine Forge Press.
Krauss, M. W., Seltzer, M. M., Gordon, R., & Friedman, D.H. (1996). Binding ties: The roles of adult siblings of persons with mental retardation. Mental Retardation, 34, 83-93.
Seltzer, M. M., Krauss, MW., Walsh, P., Conliffe, C., Larson, B., Birkbeck, G., Hong, J., & Choi, S. C. (1995). Cross-national comparisons of aging mothers of adults with intellectual disabilities. Journal of Intellectual Disability Research, 39, 408-418.
Seltzer, M. M., Greenberg, J. S., & Krauss, M. W. (1995). A comparison of coping strategies of aging mothers of adults with mental illness or mental retardation. Psychology and Aging, 10, 64-75.
Greenberg, J. S., Seltzer, M. M., & Greenley, J. R. (1993). Aging parents of adults with disabilities: The gratifications and frustrations of later life caregiving. The Gerontologist, 33, 542-550.
Krauss, M. W., & Seltzer, M. M. (1993). Current well-being and future plans of older caregiving mothers. Irish Journal of Psychology, 14, 47-64.
Seltzer, M. M., Krauss, M. W., & Tsunematsu, N. (1993). Adults with Down syndrome and their aging mothers: Diagnostic group differences. American Journal on Mental Retardation, 97, 464-508.
Krauss, M. W., Seltzer, M. M., & Goodman, S. J. (1992). Social support networks of adults with retardation who live at home. American Journal on Mental Retardation, 96, 432-441.
Seltzer, G. B., Begun, A., Seltzer, M. M., & Krauss, M. W. (1991). The impacts of siblings on adults with mental retardation and their aging mothers. Family Relations, 40, 310-317.
Erickson, M., Krauss, M. W., & Seltzer, M. M. (1989). Perceptions of old age among a sample of aging mentally retarded persons. Journal of Applied Gerontology, 8, 251-260.
Book Chapters
| Esbensen, A.J., Seltzer, M.M., & Abbeduto, L. (2007). Family well-being in Down syndrome and fragile X syndrome. In J. E. Roberts, R. Chapman, & S. Warren (Eds.), Speech and language development and intervention in Down syndrome and fragile X syndrome (pp. 275-295). Baltimore, MD: Brookes. | ![]() |
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| Robison, D., Krauss, M.W., & Seltzer, M.M. (2001). Does parenting ever end? Experiences of parents of adults with Down syndrome. In S. Pueschel (Ed.), A parent's guide to Down syndrome: Toward a brighter future. Baltimore, MD Paul H. Brookes. | ![]() |
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| Essex, E.L., Seltzer, M.M., & Krauss, M.W. (2001). Fathers as caregivers for adult children with mental retardation. In B.J. Kramer & E.H. Thompson (Eds.), Men as caregivers: Theory, research, and service implications. New York: Springer. | ![]() |
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| Seltzer, M. M., & Greenberg, J. S. (1999). The caregiving context: The intersection of social and individual influences in the experience of family caregiving. In C. D. Ryff & J. Marshall (Eds.), The self and society in aging process. New York: Springer. | ![]() |
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Krauss, M. W., Greenberg, J. S., & Seltzer, M. M. (1999). Aging in adults with developmental disabilities and severe and persistent mental illness. In J. J. Gallo, & J. Busby-Whitehead, P. V. Rabins, R. A. Silliman, & J. B. Murphy, (Eds.), Reichel's care of the elderly: Clinical aspects of aging (fifth edition). Baltimore: Williams & Wilkins.
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| Krauss, M. W., & Seltzer, M. M. (1999). An unanticipated life: The impact of lifelong caregiving. In H. Bersani (Ed.), Responding to the challenge: International trends and current issues in developmental disabilities. Brookline, MA: Brookline Books. | ![]() |
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Seltzer, M. M., & Krauss, M. W. (1998). Families of adults with Down syndrome. In J. F. Miller, L. A. Leavitt, & M. Leddy (Eds.), Communication development in young children with Down syndrome. Baltimore: Paul H. Brookes.
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Seltzer, M. M. (1998). Service utilization patterns and organization of the service delivery system for persons with mental retardation and other developmental disabilities. In S. Allen & V. Mor (Eds.), Living in the community with disability: A cross-group perspective. New York: Springer.
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| Seltzer, M. M., (1997). Later life parenting by older mothers of adults with disabilities. In E. Bleckman (Ed.), Behavioral Medicine for women: A comprehensive handbook. NY: Guildford Publications. | ![]() |
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| Krauss, M. W., & Seltzer, M. M. (1997). Life course perspectives on mental retardation research: The case of family caregiving. In J. A. Burack, R. M. Hodapp, & E. Zigler (Eds.), Handbook on mental retardation and development. NY: Cambridge University Press. | ![]() |
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Gordon, R. M., Seltzer, M. M., & Krauss, M. W. (1997). The aftermath of parental death: Changes in the context and quality of life. In R. L. Schalock (Ed.), Quality of life: Its application to persons with disabilities. Washington, DC: American Association on Mental Retardation.
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| Seltzer, M. M., Krauss, M. W., Choi, S. C., Hong, J. (1996). Midlife and later life parenting of adult children with mental retardation. In C. D. Ryff & M. M. Seltzer (Eds.), The parental experience at midlife. Chicago: University of Chicago Press. | ![]() |
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Krauss, M. W., & Seltzer, M. M. (1995). Long-term caring: Family experience over the life course. In D. Rosenthal & L. Nadel (Eds.), Down syndrome: Living and learning in the community. New York: John Wiley.
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Krauss, M. W., & Seltzer, M. M. (1994). Taking stock: Expected gains from a lifespan perspective on mental retardation. In M. M. Seltzer, M. W. Krauss, & M. P. Janicki (Eds). Life course perspectives on adulthood and aging. Washington, DC: American Association on Mental Retardation.
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Seltzer, M. M., & Krauss, M. W. (1994). Aging parents with co-resident adult children: The impact of lifelong caregiving. In M. M. Seltzer, M. W. Krauss, & M. P. Janicki (Eds.), Life course perspectives on adulthood and old age. Washington, DC: American Association on Mental Retardation.
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| Seltzer, M. M., & Ryff, C. D. (1994). Parenting across the lifespan: The normative and nonnormative cases. In D. L. Featherman, R. Lerner, & M. Perlmutter (Eds.), Life-span development and behavior (Vol. 12). Hillsdale, NJ: Lawrence Erlbaum. | ||
| Krauss, M. W., & Seltzer, M. M. (1993). Coping strategies among older mothers of adults with retardation: A life span developmental perspective. In A. P. Turnbull, J. M. Patterson, S. K. Behr, D. L. Murphy, J. G. Marquis, & M. J. Blue-Banning (Eds.), Cognitive coping, families, and disability: Participatory research in action. Baltimore: Paul H. Brookes. | ![]() |
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Seltzer, M. M., & Krauss, M. W. (1993). Adult sibling relationships of persons with mental retardation. In Z. Stoneman & P. Berman (Eds.), Siblings of individuals with mental retardation, physical disabilities, and chronic illness. Baltimore: Paul H. Brookes. |
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| Seltzer, M. M., and Seltzer, G. B. (1992). Aging in persons with developmental disabilities. In F. J. Turner (Ed.), Mental health and the elderly. NY: The Free Press. | ![]() |
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Seltzer, M. M (1992). Family caregiving across the full life span. In L. Rowitz (Ed.), Mental retardation in the year 2000. New York: Springer-Verlag.
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| Seltzer, M. M. (1992). Aging in persons with developmental disabilities. In J. E. Birren, R. B. Sloane, & G. D. Cohen (Eds.), Handbook of mental health and aging. New York: Academic Press. | ||
| Seltzer, M. M., Krauss, M. W., & Heller, T. (1991). Family caregiving over the life course. In M.P. Janicki, & M. M. Seltzer (Eds.), Aging and developmental disabilities: Challenges for the 1990s. Washington, DC: Special Interest Group on Aging, AAMR. | ||
| Janicki, M. P., Krauss, M. W. & Seltzer, M. M. (1988). Context, models, and issues for community residences. In M. P. Janicki, M. W. Krauss, & M. M. Seltzer (Eds.), Community residences for persons with developmental disabilities: Here to stay. Baltimore: Paul H. Brookes. | ||
| Janicki, M. P., Krauss, M. W. & Seltzer, M. M. (1988). Agenda for service policy, and research. In M.P. Janicki, M. W. Krauss, & M. M. Seltzer (Eds.), Community residences for persons with developmental disabilities: Here to stay. Baltimore: Paul H. Brookes. | ||















