scholarly article | Q13442814 |
P50 | author | John S. Luque | Q51153627 |
Gwendolyn P Quinn | Q57056453 | ||
Mariana Arevalo | Q58638754 | ||
Francisco A Montel-Ishino | Q84959491 | ||
P2093 | author name string | Shalanda A Bynum | |
Cathy D Meade | |||
Clement K Gwede | |||
Kristen J Wells | |||
Shalewa Noel-Thomas | |||
Tampa Bay Community Cancer Network Partners | |||
P2860 | cites work | Biobanks: Importance, Implications and Opportunities for Genetic Counselors | Q27010377 |
Screening for breast cancer: U.S. Preventive Services Task Force recommendation statement | Q28265041 | ||
On the eve of personalized medicine in oncology | Q28755254 | ||
Structuring public engagement for effective input in policy development on human tissue biobanking | Q33869885 | ||
Biobanking: the foundation of personalized medicine | Q34149758 | ||
False hopes and best data: consent to research and the therapeutic misconception | Q34172812 | ||
Legal and ethical consequences of international biobanking from a national perspective: the German BMB-EUCoop project | Q34329028 | ||
Shared decision making: developing the OPTION scale for measuring patient involvement | Q35101207 | ||
More than Tuskegee: Understanding Mistrust about Research Participation | Q35162760 | ||
Why surgical patients do not donate tissue for commercial research: review of records | Q35190929 | ||
A study of public opinion on the use of tissue samples from living subjects for clinical research | Q35587363 | ||
The emergence of epidemiology in the genomics age. | Q35866648 | ||
Ethical issues in tissue banking for research: a brief review of existing organizational policies | Q35888041 | ||
Accountability in population biobanking: comparative approaches | Q36150055 | ||
One-time general consent for research on biological samples | Q36412166 | ||
Impacting health disparities through community outreach: utilizing the CLEAN look (culture, literacy, education, assessment, and networking). | Q36715274 | ||
Patients' refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study | Q37131436 | ||
Biobanking: old activity or young discipline? | Q37327371 | ||
Informed consent in biobank research: a deliberative approach to the debate | Q37354492 | ||
Why might people donate tissue for cancer research? Insights from organ/tissue/blood donation and clinical research. | Q37354774 | ||
The debate over research on stored biological samples: what do sources think? | Q38433724 | ||
Informed consent for biorepositories: assessing prospective participants' understanding and opinions | Q40080444 | ||
New biorepository guidelines raise concerns. | Q43337241 | ||
The ethics of research using biobanks: reason to question the importance attributed to informed consent | Q44539720 | ||
Evaluation of educational materials from a social marketing campaign to promote folic acid use among Hispanic women: insight from Cuban and Puerto Rican ethnic subgroups | Q46534425 | ||
Cancer Care for Diverse Populations: Relevant Communications and Research | Q47372109 | ||
Cancer as rubbish: donation of tumor tissue for research | Q48201465 | ||
‘I'm not Really Read up on Genetics’: Biobanks and the Social Context of Informed Consent | Q56769695 | ||
For what am I participating? The need for communication after receiving consent from biobanking project participants: experience in Japan | Q56777267 | ||
Changing defaults in biobank research could save lives too | Q56780457 | ||
Public perspectives on informed consent for biobanking | Q56780965 | ||
Rhode Islanders’ attitudes towards the development of a statewide genetic biobank | Q60144202 | ||
Therapeutic misconception and the appreciation of risks in clinical trials | Q76388608 | ||
President Obama apologises to Guatemala over 1940s syphilis study | Q85156087 | ||
Genetic research and biobanks | Q85200325 | ||
Constructing Grounded Theory: A practical guide through qualitative analysis | Q88480597 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | biobank | Q864217 |
P304 | page(s) | 91-99 | |
P577 | publication date | 2012-03-01 | |
P1433 | published in | Journal of Cancer Education | Q15763651 |
P1476 | title | Formative research on perceptions of biobanking: what community members think | |
P478 | volume | 27 |
Q28384057 | "I did it for us and I would do it again": perspectives of rural latinos on providing biospecimens for research |
Q30820477 | "It's all about trust": reflections of researchers on the complexity and controversy surrounding biobanking in South Africa |
Q37126406 | 'Born in Michigan? You're in the biobank': engaging population biobank participants through Facebook advertisements |
Q53662245 | A Community-Driven Intervention for Improving Biospecimen Donation in African American Communities. |
Q93147560 | A Review of African Americans' Beliefs and Attitudes About Genomic Studies: Opportunities for Message Design |
Q36070168 | A Web-Based Platform for Educating Researchers About Bioethics and Biobanking |
Q31026335 | A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States. |
Q36332057 | A trade secret model for genomic biobanking |
Q27341847 | African Americans' and Hispanics' information needs about cancer care. |
Q64122007 | An Integrative Review of the Barriers to Indigenous Peoples Participation in Biobanking and Genomic Research |
Q92469443 | An invitation for optimal inclusivity: Investing in communities to advance equity in biomedical research and cancer care |
Q37171555 | Awareness and interest in biospecimen donation for cancer research: views from gatekeepers and prospective participants in the Latino community |
Q30592366 | Biobanking for research in surgery: are surgeons in charge for advancing translational research or mere assistants in biomaterial and data preservation? |
Q47111633 | Biobanking in Israel 2016-17; expressed perceptions versus real life enrollment |
Q37716299 | Cancer patient perceptions about biobanking and preferred timing of consent |
Q50319699 | Community Perceptions of Biobanking Participation: A Qualitative Study among Mexican-Americans in Three Texas Cities |
Q36556970 | Community-based partnership to identify keys to biospecimen research participation |
Q38734868 | Comparison of Health Communication Channels for Reaching Hispanics About Biobanking: a Pilot Trial |
Q33888377 | Contrasting the ethical perspectives of biospecimen research among individuals with familial risk for hereditary cancer and biomedical researchers: implications for researcher training. |
Q37638662 | Culturally appropriate education intervention on biospecimen research participation among Chinese Americans. |
Q41647555 | Development and Validation of the Biomedical Research Trust Scale (BRTS) in English and Spanish |
Q30574075 | Development and validation of the biobanking attitudes and knowledge survey (BANKS) |
Q37474861 | Development and validation of the biobanking attitudes and knowledge survey-Spanish (BANKS-SP). |
Q38887000 | Development of Plain Language Supplemental Materials for the Biobank Informed Consent Process |
Q36470922 | Differences in preferences for models of consent for biobanks between Black and White women. |
Q34156887 | Disparities in knowledge and willingness to donate research biospecimens: a mixed-methods study in an underserved urban community |
Q34156873 | Engaging diverse populations about biospecimen donation for cancer research |
Q37474840 | Engaging diverse populations in biospecimen donation: results from the Hoy y Mañana study |
Q89304744 | Enhancing Biospecimen Knowledge Among Health Care Providers and Representatives From Community Organizations |
Q38386387 | Establishing an Iso-Compliant Modern Cancer-Biobank in a Developing Country: A Model for International Cooperation. |
Q37075332 | Ethics of clear health communication: applying the CLEAN Look approach to communicate biobanking information for cancer research |
Q38663970 | Factors associated with participation by African Americans in a study of the genetics of glaucoma |
Q92404897 | Factors associated with willingness to provide biospecimens for genetics research among African American cancer survivors |
Q35894681 | Factors that affect willingness to donate blood for the purpose of biospecimen research in the Korean American community |
Q37058541 | Health professionals' opinions on supporting a cancer biobank: identification of barriers to combat biobanking pitfalls. |
Q36929336 | How to build an integrated biobank: the Washington University Translational Cardiovascular Biobank & Repository experience |
Q33727054 | Impact of a biospecimen collection seminar on willingness to donate biospecimens among Chinese Americans: results from a randomized, controlled community-based trial |
Q34145618 | Increasing Asian American participation in clinical trials by addressing community concerns. |
Q36751013 | Increasing participation in genomic research and biobanking through community-based capacity building |
Q36806938 | Introducing Biospecimen Science to Communities: Tools from Two Cities |
Q33654072 | Involving disparate populations in clinical trials and biobanking protocols: experiences from the community network program centers |
Q36997127 | Knowledge and willingness to provide research biospecimens among foreign-born Latinos using safety-net clinics |
Q35626670 | Oncology patients overwhelmingly support tissue banking |
Q37063857 | Personalized Medicine in the U.S. and Germany: Awareness, Acceptance, Use and Preconditions for the Wide Implementation into the Medical Standard. |
Q37385034 | Predictors of biospecimen donation in the Black Women's Health Study. |
Q28384441 | Secondary consent to biospecimen use in a prostate cancer biorepository |
Q90641951 | Sistas Taking a Stand for Breast Cancer Research (STAR) Study: A Community-Based Participatory Genetic Research Study to Enhance Participation and Breast Cancer Equity among African American Women in Memphis, TN |
Q30380219 | Sustainability in a Hospital-Based Biobank and University-Based DNA Biorepository: Strategic Roadmaps |
Q48187480 | The 22Rv1 prostate cancer cell line carries mixed genetic ancestry: Implications for prostate cancer health disparities research using pre-clinical models. |
Q36422729 | The National Cancer Institute's Community Networks Program Initiative to Reduce Cancer Health Disparities: Outcomes and Lessons Learned |
Q28607490 | To Share or Not to Share? A Survey of Biomedical Researchers in the U.S. Southwest, an Ethnically Diverse Region |
Q33632534 | Unexpected findings in the exploration of African American underrepresentation in biospecimen collection and biobanks |
Q92628335 | Using Mixed Methods to Examine Perceptions and Willingness to Participate in Bio-specimen Banking in Diverse Asian Americans |
Q64900308 | [Behavioral Medicine, Health Psychology and Psycho-oncology Puerto Rican Graduated Students Research Training Needs]. |