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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Caregiver burden and family functioning in different neurological diseases
Francesco Tramonti, Luca Bonfiglio, Paolo Bongioanni, et al.
Psychology Health & Medicine (2018) Vol. 24, Iss. 1, pp. 27-34
Closed Access | Times Cited: 94

Showing 1-25 of 94 citing articles:

Informal Caregiver Burnout? Development of a Theoretical Framework to Understand the Impact of Caregiving
Pierre Gérain, Emmanuelle Zech
Frontiers in Psychology (2019) Vol. 10
Open Access | Times Cited: 243
Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions
Rebecca Maguire, Phil Maguire
Current Neurology and Neuroscience Reports (2020) Vol. 20, Iss. 7
Open Access | Times Cited: 79
A roadmap toward promoting and improving brain health in Europe and closing the awareness and funding gap
Paul Boon, Thomas Berger, Matilde Leonardi, et al.
European Journal of Neurology (2025) Vol. 32, Iss. 1
Open Access | Times Cited: 1
Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives
Pavel Schischlevskij, Isabell Cordts, René Günther, et al.
Brain Sciences (2021) Vol. 11, Iss. 6, pp. 748-748
Open Access | Times Cited: 42
Associação da espiritualidade, qualidade de vida e depressão em familiares de idosos com demências
Luana Vitro Barreto, Maria Goreti da Silva Cruz, Meiry Fernanda Pinto Okuno, et al.
Acta Paulista de Enfermagem (2023) Vol. 36
Open Access | Times Cited: 21
Family caregiver experiences and needs across health conditions, relationships, and the lifespan: a Qualitative analysis
Sarah Neller, Megan Hebdon, Emily Wickens, et al.
International Journal of Qualitative Studies on Health and Well-Being (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 6
Long-term effect of apomorphine infusion in advanced Parkinson’s disease: a real-life study
Bruna Meira, Bertrand Degos, Elise Corsetti, et al.
npj Parkinson s Disease (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 39
Caregiver Burden and Quality of Life in Late Stage Parkinson’s Disease
Kristina Rosqvist, Anette Schrag, Per Odin
Brain Sciences (2022) Vol. 12, Iss. 1, pp. 111-111
Open Access | Times Cited: 27
Listening to Caregivers’ Voices: The Informal Family Caregiver Burden of Caring for Chronically Ill Bedridden Elderly Patients
Jinpitcha Mamom, Hanvedes Daovisan
International Journal of Environmental Research and Public Health (2022) Vol. 19, Iss. 1, pp. 567-567
Open Access | Times Cited: 25
Conducting Polymer-Hydrogel Interpenetrating Networks for Improving the Electrode–Neural Interface
Mengying Yan, Lulu Wang, Yiyong Wu, et al.
ACS Applied Materials & Interfaces (2023) Vol. 15, Iss. 35, pp. 41310-41323
Closed Access | Times Cited: 14
Analyzing the Cohesion and Adaptability of Families of Children with Intellectual Disability Using the FACES-20Esp Scale
Esther Vela Llauradó, Laura Serrano Fernández, Laura Martín Martínez
SAGE Open (2025) Vol. 15, Iss. 1
Open Access
Non-motor Symptoms and Treatments in Parkinson’s Disease
Jennifer G. Goldman
Neurologic Clinics (2025) Vol. 43, Iss. 2, pp. 291-317
Closed Access
Comprehensive assessment of caregiver burden and strain in early-stage Parkinson’s disease: An exploratory study
Maria Grazia Maggio, Laura Culicetto, Lilla Bonanno, et al.
Journal of Health Psychology (2025)
Closed Access
Association between chronic illnesses in older adults and caregiver burden: a cross sectional study in the United States
Yeajin Ham, Yeonju Jin, Ickpyo Hong, et al.
Aging & Mental Health (2025), pp. 1-7
Closed Access
The caregiver burden of idiopathic inflammatory myopathies
Parker Brady, R. Hernandez, Amber Salter, et al.
Quality of Life Research (2025)
Closed Access
Treatment of Nonmotor Symptoms Associated with Parkinson Disease
Jennifer G. Goldman, Carlos M. González Guerra
Neurologic Clinics (2020) Vol. 38, Iss. 2, pp. 269-292
Closed Access | Times Cited: 34
A review on neuropharmacological role of erucic acid: an omega-9 fatty acid from edible oils
J. B. Senthil Kumar, Bhawna Sharma
Nutritional Neuroscience (2020) Vol. 25, Iss. 5, pp. 1041-1055
Closed Access | Times Cited: 32
Multiple sclerosis caregiving: A systematic scoping review to map current state of knowledge
Roshanth Rajachandrakumar, Marcia Finlayson
Health & Social Care in the Community (2021) Vol. 30, Iss. 4
Open Access | Times Cited: 28
The effect of a students led caregiving support program on depression, sleep quality and quality of life of the caregivers and patients with stroke
Esra Doğru Hüzmeli, Murat Güntel, Hatice Tambağ, et al.
Disability and Rehabilitation (2025), pp. 1-11
Closed Access
Potential neurological manifestations of COVID-19: a narrative review
Joseph V. Pergolizzi, Robert B. Raffa, Giustino Varrassi, et al.
Postgraduate Medicine (2020) Vol. 134, Iss. 4, pp. 395-405
Open Access | Times Cited: 30
Systems thinking and the biopsychosocial approach: A multilevel framework for patient‐centred care
Francesco Tramonti, Franco Giorgi, Annibale Fanali
Systems Research and Behavioral Science (2020) Vol. 38, Iss. 2, pp. 215-230
Closed Access | Times Cited: 28
Responsibilization and value conflicts in healthcare co-creation: a public service logic perspective
Jim Broch Skarli
Public Management Review (2021) Vol. 25, Iss. 7, pp. 1238-1259
Closed Access | Times Cited: 24
A Comprehensive Literature Search of Digital Health Technology Use in Neurological Conditions: Review of Digital Tools to Promote Self-management and Support
John H. Spreadbury, Alexandra Young, Christopher Kipps
Journal of Medical Internet Research (2022) Vol. 24, Iss. 7, pp. e31929-e31929
Open Access | Times Cited: 16
Perceived benefits from peer‐support among family caregivers of people with amyotrophic lateral sclerosis and cognitive impairments in a palliative rehabilitation blended online learning programme
Lene Klem Olesen, Karen la Cour, Sally Thorne, et al.
Journal of Evaluation in Clinical Practice (2023) Vol. 29, Iss. 4, pp. 602-613
Open Access | Times Cited: 9
Association between apathy and caregiver burden in patients with amyotrophic lateral sclerosis: a cross-sectional study
Zhenxiang Gong, Wenhua Deng, Zehui Li, et al.
BMJ Open (2024) Vol. 14, Iss. 9, pp. e080803-e080803
Open Access | Times Cited: 3
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