Journal of Policy and Practice in Intellectual Disabilities

Papers
(The median citation count of Journal of Policy and Practice in Intellectual Disabilities is 1. 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 2020-11-01 to 2024-11-01.)
ArticleCitations
Digital inclusion and participation of people with intellectual disabilities during COVID‐19: A rapid review and international bricolage74
Same Progress for All? Inclusive Education, the United Nations Convention on the Rights of Persons With Disabilities and Students With Intellectual Disability in European Countries47
The mental health and well‐being of adults with intellectual disability during theCOVID‐19 pandemic: A narrative review39
The Experiences of Carers of Adults With Intellectual Disabilities During the First COVID‐19 Lockdown Period25
Preventing, mitigating, and managing future pandemics for people with an intellectual and developmental disability ‐ Learnings from COVID‐19: A scoping review23
Remote Support for Adults with Intellectual Disability During COVID‐19: From a Caregiver's Perspective21
State of the Field: The Need for Self‐Report Measures of Health and Quality of Life for People With Intellectual and Developmental Disabilities17
The Divide Between Inclusive Education Policy and Practice in Australia and the Way Forward17
Preliminary Findings From a Nationwide, Multicenter Mental Health Service for Adults and Older Adolescents With Autism Spectrum Disorder and ID16
Supporting the needs of people with intellectual and developmental disabilities 1 year into the COVID‐19 pandemic: An international, mixed methods study of nurses' perspectives13
Needs of Direct Support Professionals to Support People With Intellectual Disabilities in Leading a Healthy Lifestyle12
Applying the CRPD to People With Intellectual and Developmental Disability With Behaviors of Concern During COVID‐1912
Implications of COVID‐19 Regulations for People With Visual and Intellectual Disabilities: Lessons to Learn From Visiting Restrictions11
Culturally adapting a parent psychoeducational intervention for Chinese immigrant families of young children with autism spectrum disorder11
Inclusive Education in Asia: Insights From Some Country Case Studies11
Parents taking action adapted to parents of Black autistic children: Pilot results10
Key learnings from COVID‐19 to sustain quality of life for families of individuals with IDD10
Housing Design and Modifications for Individuals With Intellectual and Developmental Disabilities and Complex Behavioral Needs: Scoping Review10
What Constitutes Good Quality End‐of‐Life Care? Perspectives of People With Intellectual Disabilities and Their Families10
Using the quality of life framework to operationalize and assess the CRPD articles and the Sustainable Development Goals9
Online training for parents of children with developmental disabilities in a low‐resource community: A pilot feasibility study8
COVID‐19: Evolving challenges and opportunities for residential and vocational intellectual disability service providers8
Emerging from the shadows: Digital stories of self‐advocates with intellectual disabilities7
Determining Frailty in People With Intellectual Disabilities in the COVID‐19 Pandemic7
Predictors of the Attitudes of Preservice Teachers Toward Teaching Students With Down Syndrome in Regular Schools in Ghana7
Using a self‐guided app to provide communication strategies for caregivers of young children with developmental disorders: A pilot investigation6
A study of caregiver support services: Perspectives of family caregivers of persons with intellectual disabilities in Singapore6
‘In the beginning it was difficult but things got easier’: Service use experiences of family members of people with disability from Iraqi and Syrian refugee backgrounds6
Cultural and Linguistic Diversity Among Children and Families Referred for Diagnostic Evaluation of Developmental Delay and Disability: Implications for Service Delivery6
The Elusive Inclusive University: What Does This Look Like for Students With Intellectual Disability? An Irish Perspective6
Examining the Effectiveness of a Legislative Advocacy Program for Parents of Individuals With Intellectual and Developmental Disabilities6
Some observations on remote delivery of eye‐movement desensitisation and reprocessing to people with intellectual disabilities6
Recruitment and work arrangements for employees with intellectual disability in competitive employment5
Geographical Networks in the Divergence of Australian Positive Behavior Support Policy5
From Plot Twists, Progress, and the Persistence of Segregated Education: The Continuing Struggle for Inclusive Education in Relation to Students With Intellectual Disabilities5
The Use of Restrictive Measures in Community Services for People With Intellectual Disabilities in Sweden5
Right to Information for People with Intellectual Disability in Australian Mental Health Policy4
Healthcare of Persons With Complex Developmental Disabilities From Three European Experiences: France, Italy, and Norway4
Documenting the advocacy experiences among eight Latina mothers of children with intellectual and developmental disabilities4
The Quality of Life Supports Model as a major component in applying the quality of life paradigm4
Implementation of remote support services: Pre‐COVID‐193
What are the priorities for health data for adults with intellectual and developmental disabilities? It varies by whom you ask3
Perceived stress moderates the relationship between family support and family quality of life among parents of children living with intellectual and developmental disabilities3
Best practices in evaluating work integration social enterprises for persons with intellectual disabilities: A scoping review3
Connecting locally: An examination of the role of service providers in supporting the social inclusion of adults with intellectual disabilities in their neighbourhoods3
Adapting parent‐focused interventions for diverse caregivers of children with intellectual and developmental disabilities: Lessons learned during global crises3
What Are the Experiences of People with Neurodevelopmental Disorders Receiving Outpatient Mental Health Services in Singapore?3
A Survey of Befriending Services for People With Intellectual Disabilities in the United Kingdom3
Siblings of children with intellectual and developmental disabilities: Quality of life perceptions from Catalonia3
Speech and language therapy services for people with Down syndrome: The disparity between research and practice3
Experiences of Reciprocal Caring Among Adults With an Intellectual Disability Caring for an Older Family Member3
Ethics framework and recommendations to support capabilities of people with intellectual and developmental disabilities during pandemics3
Personal emergency response systems and people with intellectual and developmental disabilities in the United States2
Integrated Emotion‐Oriented Care for Older People With ID: Defining and Understanding Intervention Components of a Person‐Centered Approach2
Spirituality, disability, and quality of life2
Mexican–American caregivers' perceptions of a culturally adapted transition planning program for youth with autism2
Remote monitoring support services for people with intellectual and developmental disabilities2
Research and training priorities of staff supporting individuals with intellectual disabilities with or without autism2
Self‐determination and quality of life of people with intellectual and developmental disabilities: Past, present, and future of close research paths2
What Promotes Transfer of Staff Training Related to Challenging Behavior Displayed by Adults With Intellectual Disabilities?2
Reasons for collaborating in inclusive research projects: The perspectives of researchers with experiential knowledge, academic researchers and principal investigators2
Augmentative and alternative communication continuing education programs for multidisciplinary teams—Does it make a difference?2
‘Say hi to the lady on the television’: A review of clinic presentations and comparison of telepsychiatry and in‐person mental health assessments for people with intellectual disability in rural New S2
Does family quality of life get better as the years go by? A comparative mixed‐methods study between early years and school‐aged children with disability in Australia2
The content validity of the Behavioural Appraisal Scales in people with profound intellectual and multiple disabilities: A Delphi study2
Chronicity of Challenging Behaviors in Persons with Severe/Profound Intellectual Disabilities Who Received Active Treatment During a 20‐Year Period2
Expressions of a humanistic orientation among service providers supporting adults with intellectual and developmental disabilities2
Health care for people with intellectual disability in Spain2
Using the consensus group method to select the best screening tools for autism and intellectual disability for use with Nigerian adolescents1
How Mothers of Adults With Profound Intellectual Disabilities Experience Their Everyday Life? A Qualitative Retrospective Study From Poland1
Neighbourhood deprivation and access to early intervention and support for families of children with intellectual and developmental disabilities1
The development of a trauma informed care framework for residential services for adults with an intellectual disability: Implications for policy and practice1
Understanding quality of life of persons with profound intellectual and multiple disabilities1
Healthcare for people with intellectual disabilities in the Netherlands1
The humanistic perspective as “a lighthouse” for the perception of QOL/FQOL and its application1
Ten‐year impact of a Down syndrome pediatric clinic1
Issue Information1
Intellectual disability healthcare in Australia: Progress, challenges, and future directions1
Parents helping a child with disability learn at home during COVID‐19: Experiences from Slovenia and Canada1
What teachers know about teaching reading to students with developmental disabilities: A survey of special educators1
The influence of context on the conceptualization, measurement, and application of the concept of quality of life1
Physical activity and physical and mental health in middle‐aged adults with Down syndrome1
How do Fathers With ID Experience Their Children Being Removed from Their Care Through the English Court System?1
Pain and distress in people with severe or profound ID in Victoria, Australia: Utility of behavioural assessment tools1
Norwegian perspectives on health care for people with intellectual and developmental disabilities1
Designing genetic studies for people with intellectual disabilities: Practical lessons from a pilot study1
Nursing staff and nursing managers' experiences of using the interRAI ID instrument in assessing the service needs of persons with intellectual disabilities in housing services1
Healthcare provision for Swedish persons with intellectual and developmental disabilities1
The role of microboards in enhancing quality of life for children with intellectual disability and their families1
Policy on sexual abuse: A survey study amongst managers of care facilities for individuals with intellectual disability in the Netherlands1
Mental age and intellectual disability: Psychologists' perspectives on the use of the term ‘mental age’ as it relates to adults with an intellectual disability1
COVID‐19 pandemic experiences of group home residents with intellectual disabilities: Findings from inclusive, qualitative interviews with self‐advocates in Massachusetts1
A national census of forensic in‐patients with intellectual disability and five‐year follow‐up1
Multilevel Governance and the Implementation of Inclusion Policy for Older Adults With Intellectual and Developmental Disabilities in Canada1
As far as possible: The relationship between public awareness, social distance, and stigma towards people with intellectual disability1
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