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Noelker, L. S., Castora-Binkley, M., Rose, M. S., Browdie, R., & Ejaz, F. K. (2010). Strengthening the direct care workforce: Preliminary recommendations from a national panel of experts in long-term care. Public Policy & Aging Report, 20(1), 22-26. doi:10.1093/ppar/20.1.22
Piiparinen, R., & Whitlatch, C. J. (2011). Existential loss as a determinant to well-being in the dementia caregiving dyad: A conceptual model. Dementia, 10(2), 185-201.
Sebern, M. D., Sulemanjee, N., Sebern, M. J., Garnier-Villarreal, M., & Whitlatch, C. J. (2017). Does an intervention designed to improve self-management, social support and awareness of palliative-care address needs of persons with heart failure, family caregivers and clinicians? Journal of Clinical Nursing, 27(3-4), e643-e657. doi:10.1111/jocn.14115.
Looman, W. J., Noelker, L. S., Schur, D., Whitlatch, C. J. & Ejaz, F. K. (2002). Impact of family members on nurse assistants: What helps, what hurts. American Journal of Alzheimer's Disease and Other Dementias, 17(6), 350-356. doi:10.1177/153331750201700606
Whitlatch, C. J. (1998). Distress and burden for family caregivers. In A. Wimo, B. Jonsson, G. Karlsson, & B. Winblad (Eds.), Health Economics of Dementia (pp. 123-137). London: John Wiley & Sons, Ltd.