Quality of Life Research

Papers
(The H4-Index of Quality of Life Research is 23. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-10-01 to 2025-10-01.)
ArticleCitations
Trajectories of dyadic quality of life in young to middle-aged stroke couples: a longitudinal study73
Functional and psychosocial impact of COVID-19 pandemic on rheumatic patients’ quality of life in Saudi Arabia70
A patient first perspective of sleep disturbance across therapeutic areas: a systematic literature review of qualitative studies49
Quality of life among people living with mental illness and predictors in Africa: a systematic review and meta-analysis47
Effect of caregiver burden on the quality of life of informal caregivers of people with cystic fibrosis in the United Kingdom: a cross-sectional study46
Measurement invariance of physical, mental, and social health PROMIS measures across individuals with spinal cord injury and traumatic brain injury44
Psychometric properties of patient-reported outcome measures assessing recovery from hand fractures: a systematic review41
Applicability of the PRISMA-COSMIN guidelines for systematic reviews of outcome measurement instruments to ISOQOL’s special interest group for clinical practice38
Development of algorithms for estimating the Child Health Utility 9D from Caregiver Priorities and Child Health Index of Life with Disabilities36
Mediational roles of stress-coping factors in the relationship between patient-perceived communication quality and physical functioning: racial difference between Chinese and Non-Hispanic White Americ35
Psychometric properties of kidney disease quality of life-36 (KDQOL-36) in dialysis patients in Indonesia35
Quality of mobility measures among individuals with acquired brain injury: an umbrella review35
Understanding the unique patient—causal singularism and patient reported outcomes34
Comparative analysis of pediatric anxiety measures in clinical sample: evaluation of the PROMIS pediatric anxiety short forms32
Use of a generic Paediatric Patient Reported Outcome Measure (P-PROM) in Routine hospital Outpatient Care for Kids (ROCK): A qualitative exploration of adolescent, caregiver and service provider persp32
What does better look like in individuals with severe neurodevelopmental impairments? A qualitative descriptive study on SCN2A-related developmental and epileptic encephalopathy32
Dynamics and determinants of long-term quality of life in children and adolescents with type 1 diabetes: real-world evidence from China30
Self-reported quality of recovery after radical prostatectomy—a prospective cohort study28
Valuing health‐related quality of life: an EQ‐5D‐5L value set for Morocco27
Can patient-reported data improve predictions about who will be a high-need, high-cost patient in British Columbia?24
Patient-reported mental health and well-being trajectories in oncology patients during radiation therapy: an exploratory retrospective cohort analysis using the Ontario Cancer Registry24
Commentary on “Predictors of survival among head and neck cancer patients after radiotherapy based on health-related quality of life indices and symptoms-specific outcomes: a systematic review”24
Unsupervised item response theory models for assessing sample heterogeneity in patient-reported outcomes measures24
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