Biblio

Found 7 results
Filters: Keyword is Data Collection  [Clear All Filters]
2024
Husson O, Janssen SHM, Reeve BB, Sodergren SC, Cheung CK, McCabe MG, Salsman JM, van der Graaf WTA, Darlington A-S. Protocol for the development of a Core Outcome Set (COS) for Adolescents and Young Adults (AYAs) with cancer. BMC Cancer. 2024 ;24(1):126.
2023
Ackley SF, Zimmerman SC, Flatt JD, Riley AR, Sevelius J, Duchowny KA. Discordance in chromosomal and self-reported sex in the UK Biobank: Implications for transgender- and intersex-inclusive data collection. Proc Natl Acad Sci U S A. 2023 ;120(18):e2218700120.
Chen L, Young M-EDe Trinida, Rodriguez MA, Kietzman K. Immigrants' Enforcement Experiences and Concern about Accessing Public Benefits or Services. J Immigr Minor Health. 2023 ;25(5):1077-1084.
2021
Cruz TM, Paine EAllen. Capturing patients, missing inequities: Data standardization on sexual orientation and gender identity across unequal clinical contexts. Soc Sci Med. 2021 ;285:114295.
Cruz TM, Smith SA. Health Equity Beyond Data: Health Care Worker Perceptions of Race, Ethnicity, and Language Data Collection in Electronic Health Records. Med Care. 2021 ;59(5):379-385.
2020
Popejoy AB, Crooks KR, Fullerton SM, Hindorff LA, Hooker GW, Koenig BA, Pino N, Ramos EM, Ritter DI, Wand H, et al. Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures. Am J Hum Genet. 2020 ;107(1):72-82.
2019
Canham SL, Fang MLan, Battersby L, Wada M. Understanding the functionality of housing-related support services through mapping methods and dialogue. Eval Program Plann. 2019 ;72:33-39.