American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2002 (ICPSR 3893)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2003 (ICPSR 4117)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2004 (ICPSR 4370)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2005 (ICPSR 4587)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2006 (ICPSR 22101)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2007 (ICPSR 24503)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2008 (ICPSR 29263)
American Community Survey (ACS): Public Use Microdata Sample (PUMS), 2009 (ICPSR 33802)
American Community Survey (ACS): Three-Year Public Use Microdata Sample (PUMS), 2005-2007 (ICPSR 25042)
Annual Housing Survey, 1975 [United States]: Travel-to-Work [SMSAs] (ICPSR 7849)
Annual Housing Survey, 1976 [United States]: Travel-to-Work [SMSAs] (ICPSR 8136)
Annual Housing Survey, 1977 [United States]: Travel-to-Work [SMSAs] (ICPSR 8322)
Annual Housing Survey, 1978 [United States]: SMSA File (ICPSR 9017)
Annual Housing Survey, 1980 [United States]: SMSA Files (ICPSR 8257)
Annual Housing Survey, 1982 [United States]: SMSA Files (ICPSR 8310)
Behavioral Risk Factor Surveillance System (BRFSS), 2003 (ICPSR 34085)
Behavioral Risk Factor Surveillance System (BRFSS) Asthma Call-Back Survey, 2009 (ICPSR 34300)
Asthma is one of the nation's most common and costly chronic conditions, affecting over 38 million Americans at some time in their lives. Managing asthma requires a long term, multifaceted approach, including patient education, behavior changes, asthma trigger avoidance, pharmacological therapy, and frequent medical follow-up. This study provides asthma data available at the state and local level to direct and evaluate interventions undertaken by asthma control programs located in the state health departments. Improved tracking for asthma is critical for planning and evaluating efforts to reduce the health burden from the disease.
The Behavioral Risk Factor Surveillance System (BRFSS) is a state-based system of health surveys that collects information on health risk behaviors, preventive health practices, and health care access primarily related to chronic disease and injury. For many states, the BRFSS is the only available source of timely, accurate data on health-related behaviors. BRFSS was established in 1984 by the Centers for Disease Control and Prevention (CDC); currently data are collected monthly in all 50 states, the District of Columbia, Puerto Rico, the United States Virgin Islands, and Guam. More than 350,000 adults are interviewed each year, making the BRFSS the largest telephone health survey in the world. States use BRFSS data to identify emerging health problems, establish and track health objectives, and develop and evaluate public health policies and programs. The BRFSS is a cross-sectional telephone survey conducted by state health departments with technical and methodological assistance provided by CDC. States conduct monthly telephone surveillance using a standardized questionnaire to determine the distribution of risk behaviors and health practices among adults. Responses are forwarded to CDC, where the monthly data are aggregated for each state, returned with standard tabulations, and published at the year's end by each state. The BRFSS questionnaire was developed jointly by CDC's Behavioral Surveillance Branch (BSB) and the states. Data derived from the questionnaire provide health departments, public health officials, and policymakers with necessary behavioral information. When combined with mortality and morbidity statistics, these data enable public health officials to establish policies and priorities and to initiate and assess health promotion strategies. Demographic variables include race, age, sex, education level, marital status, employment status, and income level.
Census of Population and Housing, 1980 [United States]: P.L. 94-171 Population Counts (ICPSR 7854)
Census of Population and Housing, 1990 [United States]: Summary Tape File 420, Place of Work 20 Destinations File (ICPSR 6212)
Census of Population and Housing, 2000 [United States]: Summary File 1, States (ICPSR 3194)
Census of Population and Housing, 2000 [United States]: Summary File 2, Advance National (ICPSR 13288)
Census of Population and Housing, 2000 [United States]: Summary File 2, Final National (ICPSR 13403)
Census of Population and Housing, 2000 [United States]: Summary File 2, New Jersey (ICPSR 13263)
Census of Population and Housing, 2000 [United States]: Summary File 4, New Jersey (ICPSR 13542)
Census of Population and Housing: Summary Tape File 4A, United States, 1980 (ICPSR 8282)
Collaborative Multi-racial Post-election Survey (CMPS), 2008 (ICPSR 35163)
Comparative Study of Community Decision-Making (ICPSR 25)
County-Level Estimates of the Population Aged Sixty Years and Over by Age, Sex, and Race, 1977-1980 (ICPSR 7955)
Firearms, Violence, and Youth in California, Illinois, Louisiana, and New Jersey, 1991 (ICPSR 6484)
Latino National Survey (LNS), 2006 (ICPSR 20862)
Latino National Survey (LNS) Focus Group Data, 2006 (ICPSR 29601)
Mortality Detail and Multiple Cause of Death, 1981 (ICPSR 3874)
Multiple Cause of Death, 1968-1973 (ICPSR 3905)
Multiple Cause of Death, 1974-1978 (ICPSR 3906)
Multiple Cause of Death, 1979 (ICPSR 3895)
Multiple Cause of Death, 1980 (ICPSR 3897)
Multiple Cause of Death, 1982 (ICPSR 9880)
Natality Detail File, 2003 [United States] (ICPSR 4706)
Natality Detail File, 2004 [United States] (ICPSR 4707)
Natality Detail File, 2005 [United States] (ICPSR 22960)
Natality Detail File, 2006 [United States] (ICPSR 24941)
National Crime Surveys: Cities, 1972-1975 (ICPSR 7658)
Office of Revenue Sharing: Fifth Count File, 1970 (ICPSR 77)
Racial Attitudes in Fifteen American Cities, 1968 (ICPSR 3500)
Simulated Totals for Hispanic National Origin Groups [in Census 2000] by State, Place, County, and Census Tract: [United States] (ICPSR 3907)
Study of Women's Health Across the Nation (SWAN), 1998-2001: Family Medical History From Visits 02, 03, and 04 (ICPSR 30181)
Study of Women's Health Across the Nation (SWAN), 2001-2003: Visit 05 Dataset (ICPSR 30501)
Study of Women's Health Across the Nation (SWAN), 2002-2004: Visit 06 Dataset (ICPSR 31181)
Study of Women's Health Across the Nation (SWAN), 2006-2008: Visit 10 Dataset (ICPSR 32961)
Study of Women's Health Across the Nation (SWAN): Baseline Dataset, [United States], 1996-1997 (ICPSR 28762)
The Study of Women's Health Across the Nation (SWAN), is a multi-site longitudinal, epidemiologic study designed to examine the health of women during their middle years. The study examines the physical, biological, psychological, and social changes during this transitional period. The goal of SWAN's research is to help scientists, health care providers, and women learn how mid-life experiences affect health and quality of life during aging. The data include questions about doctor visits, medical conditions, medications, treatments, medical procedures, relationships, smoking, and menopause related information such as age at pre-, peri- and post-menopause, self-attitudes, feelings, and common physical problems associated with menopause.
The study is co-sponsored by the National Institute on Aging (NIA), the National Institute of Nursing Research (NINR), the National Institutes of Health (NIH), and the NIH Office of Research on Women's Health. The study began in 1994. Between 1996 and 1997, 3,302 participants joined SWAN through 7 designated research centers. The research centers are located in the following communities: Detroit, MI; Boston, MA; Chicago, IL; Oakland and Los Angeles, CA; Newark, NJ; and Pittsburgh, PA. SWAN participants represent five racial/ethnic groups and a variety of backgrounds and cultures. This is the next phase of data collection after the original collection of the screening data (ICPSR 4368).