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Cited by

• 1994Instruments measuring family or caregiver burden in severe mental illness202 cited
• 2000Caregiving in schizophrenia: development, internal consistency and reliability of the Involvement Evaluation Questionnaire – European Version198 cited
• 1997Positive and negative symptom behaviors and caregiver burden in the relatives of persons with schizophrenia184 cited
• 2003Family caregiving in depression: impact on caregivers' daily life, distress, and help seeking179 cited
• 1994Attributions, expressed emotion, and patient relapse: An attributional model of relatives' response to schizophrenic illness170 cited
• 2008Primary caregivers of schizophrenia outpatients: Burden and predictor variables162 cited
• 1996Ethnicity, social status, and families' experiences of caring for a mentally ill family member162 cited
• 2004Asking, Witnessing, Interpreting, Knowing: Conducting Qualitative Research in Community Psychology137 cited
• 2006The impact of caregivers’ characteristics, patients’ conditions and regional differences on family burden in schizophrenia: a longitudinal analysis125 cited
• 2014The Recovery Framework as a Way of Understanding Families' Responses to Mental Illness: Balancing Different Needs and Recovery Journeys115 cited
• 1990Community care of the seriously mentally ill: Continuing problems and current issues115 cited
• 2002Navigating the Storm of Mental Illness: Phases in the Family’s Journey111 cited