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Journal of Palliative Care & Medicine received 2035 citations as per Google Scholar report
Articles published in Journal of Palliative Care & Medicine have been cited by esteemed scholars and scientists all around the world. Journal of Palliative Care & Medicine has got h-index 20, which means every article in Journal of Palliative Care & Medicine has got 20 average citations.
Following are the list of articles that have cited the articles published in Journal of Palliative Care & Medicine.
2024 | 2023 | 2022 | 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | |
---|---|---|---|---|---|---|---|---|---|
Total published articles |
110 | 95 | 58 | 60 | 25 | 25 | 24 | 32 | 56 |
Research, Review articles and Editorials |
30 | 70 | 34 | 14 | 12 | 14 | 0 | 0 | 0 |
Research communications, Review communications, Editorial communications, Case reports and Commentary |
18 | 10 | 7 | 15 | 5 | 0 | 0 | 0 | 0 |
Conference proceedings |
0 | 6 | 6 | 0 | 0 | 0 | 106 | 80 | 39 |
Citations received as per Google Scholar, other indexing platforms and portals |
85 | 143 | 186 | 192 | 212 | 117 | 205 | 182 | 166 |
Journal total citations count | 2035 |
Journal impact factor | 4.51 |
Journal 5 years impact factor | 6.49 |
Journal cite score | 6.19 |
Journal h-index | 20 |
Journal h-index since 2019 | 46 |
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Shanmugasundaram S. Unmet needs of the Indian family members of terminally ill patients receiving palliative care services. Journal of Hospice & Palliative Nursing. 2015 Dec 1;17(6):536-43. |
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Rasouli-Ghahfarkhi SM, Molahosseini S. Stress and its related factors in families of patients with cancer. Chronic Diseases Journal. 2015 May 21;3(2):45-54. |
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Y?ld?z E, Dedeli O, Pakyuz SC. Evaluation of care burden and quality of life among family caregivers of patients with cancer/An examination of the care burden and quality of life of family members who care for cancer patients. Journal of Education and Research in Nursing. 2016 Sep 1;13(3):216-26. |
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?tef?nu? AM, Vintil? M, Sârbescu P. Perception of disease, dyadic coping and the quality of life of oncology patients in the active treatment phase and their life partners: Study protocol of an approach based on the actorâpartner interdependence model. European Journal of Cancer Care. 2021 Nov;30(6):e13374. |
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Galvis-López CR, Aponte-Garzón LH, Pinzón-Rocha ML. Perception of the quality of life of caregivers of patients attending a program for the chronically, Villavicencio, Colombia. Aquichan. 2016 Jan;16(1):104-15. |
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Rao SR, Gupta M, Salins N. The Concept of Respite in Palliative Care: Definitions and Discussions. Current Oncology Reports. 2021 Feb;23(2):1-6. |
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Dhiliwal SR, Ghoshal A, Dighe MP, Damani A, Deodhar J, Chandorkar S, Muckaden MA. Development of a model of Home-based Cancer Palliative Care Services in Mumbai-Analysis of Real-world Research Data over 5 Years. Indian Journal of Palliative Care.:1-31. |
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Patel A, Bhatnagar S, Ratre B. Patient centric integrative supportive care model at a tertiary cancer care center of India. Indian Journal of Medical Sciences. 2021 May 1;73(2). |
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Ofosu-Poku R, Owusu-Ansah M, Antwi J. Referral of patients with nonmalignant chronic diseases to specialist palliative care: a study in a teaching Hospital in Ghana. International journal of chronic diseases. 2020 Mar 15;2020. |
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Hawkins-Taylor C, Mollman S, Walstrom B, Kerkvliet J, Minton M, Anderson D, Berke C. Perceptions of palliative care: voices from rural South Dakota. American Journal of Hospice and Palliative Medicine®. 2021 Jun;38(6):557-65. |
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Zeeshan M, Shaikh S, Ahmer Z. How frequent is burnout among informal caregivers of disabled children? Findings from a cross?sectional study in Karachi, Pakistan. Child: Care, Health and Development. 2021 Dec 3. |
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Zeeshan M, Shaikh S, Ahmer Z. How frequent is burnout among informal caregivers of disabled children? Findings from a cross?sectional study in Karachi, Pakistan. Child: Care, Health and Development. 2021 Dec 3. |
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Dambi JM. Evaluation of the mental health profile of caregivers of children with cerebral palsy in a low-resourced setting: development, translation and validation of patient-reported outcome measures. |
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Nyback MH. Generic and professional caring in a Chinese setting: an ethnopraphic study. |
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Masoudifar Z, Mojen LK, Rassouli M, Nasiri M, Patterson P, Mc Donald F, Eshghi P. Psychometric properties of the Persian version of the Sibling Cancer Needs Instrument (SCNI). Asian Pacific journal of cancer prevention: APJCP. 2018;19(12):3457. |
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Maddocks S, Moodley K, Hanass-Hancock J, Cobbing S, Chetty V. Children living with HIV-related disabilities in a resource-poor community in South Africa: Caregiver perceptions of caring and rehabilitation. AIDS care. 2020 Apr 2;32(4):471-9. |
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Kilic ST, Oz F. Family caregiversâ involvement in caring with cancer and their quality of life. Asian Pacific journal of cancer prevention: APJCP. 2019;20(6):1735. |
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Shoghi M, Shahbazi B, Seyedfatemi N. The effect of the family-centered empowerment model (FCEM) on the care burden of the parents of children diagnosed with cancer. Asian Pacific journal of cancer prevention: APJCP. 2019;20(6):1757. |
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Mori A, Goren A, Gilloteau I, DiBonaventura MD. Quantifying the burden of caregiving for patients with cancer in Europe. Annals of Oncology. 2012 Sep 1;23:ixe25-6. |
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Dambi JM, Mandizvidza C, Chiwaridzo M, Nhunzvi C, Tadyanemhandu C. Does an educational workshop have an impact on caregiversâ levels of knowledge about cerebral palsy? A comparative, descriptive cross-sectional survey of Zimbabwean caregivers. Malawi medical journal. 2016;28(4):167-73. |
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