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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:

Silent voices: Family caregivers' narratives of involvement in palliative care
Anett Skorpen Tarberg, Marit Kvangarsnes, Torstein Hole, et al.
Nursing Open (2019) Vol. 6, Iss. 4, pp. 1446-1454
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

Compassion in healthcare: an updated scoping review of the literature
Sydney Malenfant, Priya Jaggi, Alix Hayden, et al.
BMC Palliative Care (2022) Vol. 21, Iss. 1
Open Access | Times Cited: 93
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: 24
What are family caregivers’ experiences of coordinating end-of-life care at home? A narrative review
Harriet Nicholls, Matthew C. Carey, Kevin Hambridge
Palliative & Supportive Care (2025) Vol. 23
Closed Access
A care ethical perspective on family caregiver burden and support
Maaike M. Haan, Jelle van Gurp, Marianne Boenink, et al.
Nursing Ethics (2025)
Closed Access
Nurse assistants’ perception of caring for older persons who are dying in their own home
Magdalena Annersten Gershater, Josefin Brenner, Malin Nordberg, et al.
BMC Palliative Care (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 3
Nurses’ experiences of compassionate care in the palliative pathway
Anett Skorpen Tarberg, Bodil J. Landstad, Torstein Hole, et al.
Journal of Clinical Nursing (2020) Vol. 29, Iss. 23-24, pp. 4818-4826
Open Access | Times Cited: 27
Experiences of bereaved family caregivers with shared decision making in palliative cancer treatment: a qualitative interview study
Sanne P. C. van Oosterhout, Daisy J. M. Ermers, Floor K. Ploos van Amstel, et al.
BMC Palliative Care (2021) Vol. 20, Iss. 1
Open Access | Times Cited: 25
Higher levels of unmet support needs in spouses are associated with poorer quality of life – a descriptive cross-sectional study in the context of palliative home care
Maria Norinder, Kristofer Årestedt, Susanne Lind, et al.
BMC Palliative Care (2021) Vol. 20, Iss. 1
Open Access | Times Cited: 24
Family and health-care professionals managing medicines for patients with serious and terminal illness at home: a qualitative study
Kristian Pollock, Eleanor Wilson, Glenys Caswell, et al.
Health Services and Delivery Research (2021) Vol. 9, Iss. 14, pp. 1-162
Open Access | Times Cited: 21
Support received by family members before, at and after an ill person’s death
Anna O’Sullivan, Anette Alvariza, Joakim Öhlén, et al.
BMC Palliative Care (2021) Vol. 20, Iss. 1
Open Access | Times Cited: 20
Italian nursing students' attitudes towards care of the dying patient: A multi-center descriptive study
Chiara Mastroianni, Anna Marchetti, Daniela D’Angelo, et al.
Nurse Education Today (2021) Vol. 104, pp. 104991-104991
Closed Access | Times Cited: 20
Physicians' perceptions of patient participation and the involvement of family caregivers in the palliative care pathway
Anett Skorpen Tarberg, Morten Thronæs, Bodil J. Landstad, et al.
Health Expectations (2022) Vol. 25, Iss. 4, pp. 1945-1953
Open Access | Times Cited: 12
Spiritual Distress, Hopelessness, and Depression in Palliative Care: Simultaneous Concept Analysis
Helga Martins, Rita Santos Silva, Joana Bragança, et al.
Healthcare (2024) Vol. 12, Iss. 10, pp. 960-960
Open Access | Times Cited: 2
Mediating role of self‐efficacy between unmet needs and quality of life in palliative cancer caregivers
Huilin Cheng, Doris Y. P. Leung, Po Shan Ko, et al.
Psycho-Oncology (2023) Vol. 32, Iss. 3, pp. 457-464
Closed Access | Times Cited: 6
Who cares for the carers? carerhelp: development and evaluation of an online resource to support the wellbeing of those caring for family members at the end of their life
Jennifer Tieman, Peter Hudson, Kristina Thomas, et al.
BMC Palliative Care (2023) Vol. 22, Iss. 1
Open Access | Times Cited: 6
Perspectives in preparedness of family caregivers of patients with cancer providing end-of-life care in the home: A narrative review of qualitative studies
Emily Ongko, Jennifer Philip, Nienke Zomerdijk
Palliative & Supportive Care (2023), pp. 1-11
Open Access | Times Cited: 6
‘It’s not just about me’: a qualitative study of couples’ narratives about home death when one of the partners is dying of cancer
Margareta Aurén-Møkleby, Lisbeth Thoresen, Anne Marit Mengshoel, et al.
Palliative Care and Social Practice (2023) Vol. 17
Open Access | Times Cited: 6
The Life Experiences Among Primary Family Caregivers of Home-Based Palliative Care
Meng‐Ping Wu, Sheng‐Jean Huang, Lee‐Ing Tsao
American Journal of Hospice and Palliative Medicine® (2020) Vol. 37, Iss. 10, pp. 816-822
Closed Access | Times Cited: 17
EXPERIENCE OF FAMILIES FACING CANCER IN PALLIATIVE CARE
Cínthia Cristina Oliveski, Nara Marilene Oliveira Girardon-Perlini, Silvana Bastos Cogo, et al.
Texto & Contexto - Enfermagem (2021) Vol. 30
Open Access | Times Cited: 14
Smiles behind the masks: A systematic review and narrative synthesis exploring how family members of seriously ill or dying patients are supported during infectious disease outbreaks
Melissa J. Bloomer, Catherine Walshe
Palliative Medicine (2021) Vol. 35, Iss. 8, pp. 1452-1467
Open Access | Times Cited: 13
Feeling called to care: a qualitative interview study on normativity in family caregivers’ experiences in Dutch home settings in a palliative care context
Maaike M. Haan, Gert Olthuis, Jelle van Gurp
BMC Palliative Care (2021) Vol. 20, Iss. 1
Open Access | Times Cited: 13
An emotional roller coaster - family members’ experiences of being a caregiver throughout a cancer trajectory
Monica Solberg, Geir Vegard Berg, Hege Andreassen
International Journal of Qualitative Studies on Health and Well-Being (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 9
Family members’ participation in palliative inpatient care: An integrative review
J. Saarinen, Kaisa Mishina, Anu Soikkeli‐Jalonen, et al.
Scandinavian Journal of Caring Sciences (2021) Vol. 37, Iss. 4, pp. 897-908
Closed Access | Times Cited: 12
Bridging comic art and research: lessons from an interdisciplinary collaboration project in a palliative care context
Maaike M. Haan, Gert Olthuis, Marianne Boenink, et al.
Medical Humanities (2024) Vol. 50, Iss. 3, pp. 475-485
Closed Access | Times Cited: 1
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