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Deepa Bhat

Biographic Data

ID197988
NAMEDeepa Bhat
GIVEN NAMESDeepa
FAMILY NAMEBhat
SIGNATUREBHAT D
AFFILIATIONSJSS Academy of Higher Education and Research
ORCID0000-0002-4928-1718
VERIFIEDYes
TOTAL WORKS6
TOTAL CITATIONS0
AUTHOR COUNT6
EDITOR COUNT0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Beyond the Diagnosis

    Open Access•V Swathi, Pooja Aggarwal et al.•ARTICLE•Journal of Racial and Ethnic…•2026

    BACKGROUND: Sickle cell disease (SCD) is an inherited blood disorder characterized by the presence of sickle-shaped erythrocytes, leading to haemolytic anemia, vaso-occlusive crises, and multi-organ complications. In this study, we describe the lived experiences of persons with SCD (PwSCD) and their caregivers within their social and cultural contexts, aiming to uncover the factors that limit effective healthcare for tribal communities in India. …

  • Socioeconomic health and impact of sickle cell disease and vaso-occlusive crises in India

    Open Access•Dipty Jain, Tulika Seth et al.•ARTICLE•BMJ Global Health•2025

    BACKGROUND: Sickle cell disease (SCD) with vaso-occlusive pain crisis (VOC) has a major impact on healthcare resource utilisation and poses a significant financial burden for the patients. This study examines the economic implications of managing VOC in individuals with SCD in India, from the perspectives of patients, healthcare system and society. METHODS: This cross-sectional, observational study included 1000 patients with SCD across 14 centre…

  • Health System-Led Multimodal and Multilevel Interventions to Reduce Sickle Cell Disease-Related Stigma Among Tribal Populations in India

    Open Access•Shaily B Surti, Y Sharma et al.•ARTICLE•Journal of Racial and Ethnic…•2025•References: 33

  • Indian Council of Medical Research (ICMR)-Sickle Cell Disease (SCD) Stigma Scale for India (ISSSI)

    Open Access•Deepa Bhat, Y Sharma et al.•ARTICLE•Journal of Racial and Ethnic…•2024•References: 43

  • Peripheral health workers’ knowledge and experience related to sickle cell disease

    Open Access•Bontha Veerraju Babu, Parikipandla Sridevi et al.•ARTICLE•Journal of Community Genetics•2022

  • Sickle cell disease-related knowledge and perceptions of traditional healers in tribal communities in India

    Open Access•Bontha Veerraju Babu, Parikipandla Sridevi et al.•ARTICLE•Journal of Community Genetics•2022

No prominent works on this page.

  • Peripheral health workers’ knowledge and experience related to sickle cell disease

    Open Access•Bontha Veerraju Babu, Parikipandla Sridevi et al.•ARTICLE•Journal of Community Genetics•2022

  • Sickle cell disease-related knowledge and perceptions of traditional healers in tribal communities in India

    Open Access•Bontha Veerraju Babu, Parikipandla Sridevi et al.•ARTICLE•Journal of Community Genetics•2022

  • Indian Council of Medical Research (ICMR)-Sickle Cell Disease (SCD) Stigma Scale for India (ISSSI)

    Open Access•Deepa Bhat, Y Sharma et al.•ARTICLE•Journal of Racial and Ethnic…•2024•References: 43

  • Socioeconomic health and impact of sickle cell disease and vaso-occlusive crises in India

    Open Access•Dipty Jain, Tulika Seth et al.•ARTICLE•BMJ Global Health•2025

    BACKGROUND: Sickle cell disease (SCD) with vaso-occlusive pain crisis (VOC) has a major impact on healthcare resource utilisation and poses a significant financial burden for the patients. This study examines the economic implications of managing VOC in individuals with SCD in India, from the perspectives of patients, healthcare system and society. METHODS: This cross-sectional, observational study included 1000 patients with SCD across 14 centre…

  • Health System-Led Multimodal and Multilevel Interventions to Reduce Sickle Cell Disease-Related Stigma Among Tribal Populations in India

    Open Access•Shaily B Surti, Y Sharma et al.•ARTICLE•Journal of Racial and Ethnic…•2025•References: 33

  • Beyond the Diagnosis

    Open Access•V Swathi, Pooja Aggarwal et al.•ARTICLE•Journal of Racial and Ethnic…•2026

    BACKGROUND: Sickle cell disease (SCD) is an inherited blood disorder characterized by the presence of sickle-shaped erythrocytes, leading to haemolytic anemia, vaso-occlusive crises, and multi-organ complications. In this study, we describe the lived experiences of persons with SCD (PwSCD) and their caregivers within their social and cultural contexts, aiming to uncover the factors that limit effective healthcare for tribal communities in India. …

Hemoglobinopathies and Related Disorders (6 works) · Disease (5 works) · Iron Metabolism and Disorders (5 works) · Medicine (4 works) · Public health (4 works) · Family medicine (3 works) · Health care (3 works) · Pathology (3 works) · Qualitative research (3 works) · Alternative medicine (2 works)

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