| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1086039995 |
| P356 | DOI | 10.1007/S12687-017-0308-6 |
| P8608 | Fatcat ID | release_nl67c4imevcvfnv3tc3t3doayy |
| P932 | PMC publication ID | 5496846 |
| P698 | PubMed publication ID | 28623623 |
| P50 | author | Janet K. Williams | Q42583035 |
| P2093 | author name string | Elaine L Larson | |
| Elizabeth Gross Cohn | |||
| Nalo Hamilton | |||
| P2860 | cites work | Personalized medicine and human genetic diversity | Q26824838 |
| Towards a more representative morphology: clinical and ethical considerations for including diverse populations in diagnostic genetic atlases | Q28066788 | ||
| The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies | Q28742793 | ||
| Community-based dialogue: engaging communities of color in the United states' genetics policy conversation | Q33567698 | ||
| eMERGEing progress in genomics-the first seven years | Q33764758 | ||
| Biobanks in the United States: how to identify an undefined and rapidly evolving population | Q33828227 | ||
| Inclusion of racial and ethnic minorities in genetic research: advance the spirit by changing the rules? | Q33850128 | ||
| What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report | Q33970852 | ||
| Communicating genetic and genomic information: health literacy and numeracy considerations | Q34017520 | ||
| Underutilization of specimens in biobanks: an ethical as well as a practical concern? | Q34307647 | ||
| Informational content, literacy demands, and usability of websites offering health-related genetic tests directly to consumers | Q34379754 | ||
| Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records | Q34452478 | ||
| "Which box should I check?": examining standard check box approaches to measuring race and ethnicity | Q34509222 | ||
| Genome-wide association studies in diverse populations | Q34817128 | ||
| Age Differences in Genetic Knowledge, Health Literacy and Causal Beliefs for Health Conditions | Q35105527 | ||
| Recruitment of African American and white postmenopausal women into clinical trials: the beneficial effects of soy trial experience | Q35113878 | ||
| Long-term outcomes from a multiple-risk-factor diabetes trial for Latinas: ¡Viva Bien! | Q35384823 | ||
| Ethics and neuropsychiatric genetics: a review of major issues | Q35985180 | ||
| Disparities among Asians and native Hawaiians and Pacific Islanders with ischemic stroke | Q36687171 | ||
| Increasing participation in genomic research and biobanking through community-based capacity building | Q36751013 | ||
| Multi-ethnic minority nurses' knowledge and practice of genetics and genomics. | Q36942520 | ||
| Characterizing biobank organizations in the U.S.: results from a national survey | Q36997918 | ||
| Genomics for the world | Q37003231 | ||
| Research priorities in geriatric palliative care: multimorbidity | Q37029121 | ||
| Connecting communities to health research: development of the Project CONNECT minority research registry | Q37191664 | ||
| Intentions to donate to a biobank in a national sample of African Americans. | Q37248237 | ||
| Preexposure Prophylaxis for HIV Infection Integrated With Municipal- and Community-Based Sexual Health Services | Q37296618 | ||
| Biobanks containing clinical specimens: defining characteristics, policies, and practices | Q37647064 | ||
| Using health literacy guidelines to improve discharge education and the post-hospital transition: a quality improvement project | Q37702355 | ||
| After inclusion, information and inference: reporting on clinical trials results after 15 years of monitoring inclusion of women | Q37889293 | ||
| Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician | Q38133941 | ||
| The role of religious values in decisions about genetics and the public's health | Q38186586 | ||
| Genetics, biomarkers, hereditary cancer syndrome diagnosis, heterogeneity and treatment: a review | Q38211737 | ||
| Under-representation of minority ethnic groups in cardiovascular research: a semi-structured interview study | Q39551189 | ||
| Combining Community-Based Participatory Research (CBPR) with a Random-Sample Survey to Assess Smoking Prevalence in an Under-Served Community | Q39705091 | ||
| Family and cultural influences on cervical cancer screening among immigrant Latinas in Miami-Dade County, USA. | Q40208761 | ||
| Will Precision Medicine Move Us beyond Race? | Q41666847 | ||
| Expert and Advocacy Group Consensus Findings on the Horizon of Public Health Genetic Testing | Q42430542 | ||
| Evaluating the brief health literacy screen | Q42745132 | ||
| Enrollment of racial/ethnic minorities and women with HIV in clinical research studies of HIV medicines. | Q43904517 | ||
| Recruitment of black and Latina women to a randomized controlled trial | Q45419687 | ||
| Barriers to the use of genetic testing: a study of racial and ethnic disparities | Q46193893 | ||
| The continuing legacy of the Tuskegee Syphilis Study: considerations for clinical investigation | Q46384511 | ||
| Recruitment and retention strategies of African American and Latina American breast cancer survivors in a longitudinal psycho-oncology study | Q46574469 | ||
| Healthcare's minority report. Sullivan Commission, IOM try to make patient, hospital staff makeup more reflective of the nation's ever-changing population. | Q47312109 | ||
| Latina recruitment for cancer prevention education via Community Based Participatory Research strategies | Q47658366 | ||
| Can Research on the Genetics of Intelligence Be "Socially Neutral"? | Q47954129 | ||
| Costs associated with multimorbidity among VA patients | Q48347017 | ||
| Culturally sensitive approaches to recruitment and retention of Hispanics in the national lung screening trial. | Q50802156 | ||
| P433 | issue | 3 | |
| P921 | main subject | biobank | Q864217 |
| P304 | page(s) | 229-238 | |
| P577 | publication date | 2017-06-16 | |
| P1433 | published in | Journal of Community Genetics | Q15816656 |
| P1476 | title | Self-reported race and ethnicity of US biobank participants compared to the US Census | |
| P478 | volume | 8 |
| Q92468938 | Big Data in Context: Addressing the Twin Perils of Data Absenteeism and Chauvinism in the Context of Health Disparities Research |
| Q90092023 | Big data in digital healthcare: lessons learnt and recommendations for general practice |
| Q92518598 | Human Biospecimens Come from People |
| Q92473693 | Inclusion of Indigenous Australians in biobanks: a step to reducing inequity in health care |
| Q89429851 | Linking Education to Action: A Program to Increase Research Participation Among African American Women |
Search more.