Publications

Publication Type
Our Work
Authors
Date Range
Journal Article
This study reviewed AANHPI disaggregated data collection methods in large, U.S. population-based surveys, summarized disaggregated data reporting practices in the peer-reviewed literature, and conducted key informant interviews with 23 members of the National Network of Health Surveys who lead state/local and national surveys to identify challenges to data collection.
Journal Article
This study reviewed AANHPI disaggregated data collection methods in large, U.S. population-based surveys, summarized disaggregated data reporting practices in the peer-reviewed literature, and conducted key informant interviews with 23 members of the National Network of Health Surveys who lead state/local and national surveys to identify challenges to data collection.
Journal Article
Population-level health outcomes and measures of well-being are often described relative to broad racial/ethnic categories such as white or Caucasian; Black or African American; Latino or Hispanic; Asian American; Native Hawaiian and Pacific Islander; or American Indian and Alaska Native.
Journal Article
Population-level health outcomes and measures of well-being are often described relative to broad racial/ethnic categories such as white or Caucasian; Black or African American; Latino or Hispanic; Asian American; Native Hawaiian and Pacific Islander; or American Indian and Alaska Native.
Policy Brief
American Indian and Alaska Native (AIAN) people are underrepresented and often invisible in public health data and research. AIAN health data capacity is impeded by the quality of information collected, released, and reported on AIANs in population-based surveys. AIANs are either put in a residual “other” category or, typically, depicted as single-race non-Latinx AIANs.
Policy Brief
American Indian and Alaska Native (AIAN) people are underrepresented and often invisible in public health data and research. AIAN health data capacity is impeded by the quality of information collected, released, and reported on AIANs in population-based surveys. AIANs are either put in a residual “other” category or, typically, depicted as single-race non-Latinx AIANs.
Policy Research Report
The purpose of the current study was to identify barriers faced by women whose cancer has metastasized, and to propose possible solutions for system or policy changes that can improve care for metastatic breast cancer patients.
Policy Research Report
The purpose of the current study was to identify barriers faced by women whose cancer has metastasized, and to propose possible solutions for system or policy changes that can improve care for metastatic breast cancer patients.
Research Report
National health surveillance instruments are intended to monitor important health issues and health status of all populations in the United States. Several population subgroups have disparities in health conditions and health care. To effectively create programs and policies to address these issues requires accurate identification of key population subgroups.
Research Report
National health surveillance instruments are intended to monitor important health issues and health status of all populations in the United States. Several population subgroups have disparities in health conditions and health care. To effectively create programs and policies to address these issues requires accurate identification of key population subgroups.
Policy Brief
This policy brief examines the association of school discipline practices with feelings of school connectedness and civic engagement.
Policy Brief
This policy brief examines the association of school discipline practices with feelings of school connectedness and civic engagement.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports on barriers created when health coverage plans change resulting in loss of providers, specific benefits and more.   Read the related report, Addressing Barriers to Breast Cancer Care in California: Levers for Policy Change.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports on barriers created when health coverage plans change resulting in loss of providers, specific benefits and more.   Read the related report, Addressing Barriers to Breast Cancer Care in California: Levers for Policy Change.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports the specific barriers faced by low-income women, including provider shortages and time limits on public program treatment.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports the specific barriers faced by low-income women, including provider shortages and time limits on public program treatment.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports the on the need for patient navigators for breast cancer survivors both during and after treatment. Read the related report, Addressing Barriers to Breast Cancer Care in California: Levers for Policy Change.
Fact Sheet
This fact sheet summarizes one of three key findings from a study of barriers to breast cancer care in California. Specifically, it reports the on the need for patient navigators for breast cancer survivors both during and after treatment. Read the related report, Addressing Barriers to Breast Cancer Care in California: Levers for Policy Change.
Policy Research Report
[UPDATED REPORT as of MARCH 2018] In 2018, over 29,000 women will be diagnosed with breast cancer in California and an estimated 4,500 will die of the disease. While the Affordable Care Act (ACA) has successfully expanded access to health insurance and breast cancer care, numerous population subgroups remain uninsured, and many others may lack adequate coverage for treatment and management of their breast cancer.
Policy Research Report
[UPDATED REPORT as of MARCH 2018] In 2018, over 29,000 women will be diagnosed with breast cancer in California and an estimated 4,500 will die of the disease. While the Affordable Care Act (ACA) has successfully expanded access to health insurance and breast cancer care, numerous population subgroups remain uninsured, and many others may lack adequate coverage for treatment and management of their breast cancer.