“Registries are not only a tool for data collection, they are for action”: Cancer registration and gaps in data for health equity in six population‐based registries in India-Reference-Cited by-同舟云学术

“Registries are not only a tool for data collection, they are for action”: Cancer registration and gaps in data for health equity in six population‐based registries in India

Published:2020-12-29 Issue:9 Volume:148 Page:2171-2183
ISSN:0020-7136
Container-title:International Journal of Cancer
language:en
Short-container-title:Intl Journal of Cancer

Author:

Bhatia Amiya¹²^ORCID,Victora Cesar Gomes³^ORCID,Beckfield Jason⁴^ORCID,Budukh Atul⁵^ORCID,Krieger Nancy¹^ORCID

Affiliation:

1. Department of Social and Behavioral Sciences Harvard T. H. Chan School of Public Health Boston Massachusetts USA

2. Department of Global Health and Development London School of Hygiene and Tropical Medicine London UK

3. International Center for Equity in Health Federal University of Pelotas Pelotas (RS) Brazil

4. Department of Sociology Harvard University Cambridge Massachusetts USA

5. Centre for Cancer Epidemiology Tata Memorial Center, Homi Bhabha National Institute Mumbai Maharashtra India

Publisher

Wiley

Subject

Cancer Research,Oncology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ijc.33391

Reference50 articles.

1. International Agency for Research on Cancer.Global Initiative for Cancer Registry Development (GICR) vol. 2018: International Agency for Research on Cancer (IARC)http://gicr.iarc.fr/en/2018.

2. Global cancer transitions according to the Human Development Index (2008–2030): a population-based study

3. Three countries—half of the global cancer burden

4. Cancer registration in developing countries: luxury or necessity?

5. Planning and developing population‐based cancer registration in low‐ and middle‐income settings International Agency for Research on;Bray F;Cancer,2015

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