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Stakeholder engagement: a key component of integrating genomic information into electronic health recordsPharmacogenomics in diverse practice settings: implementation beyond major metropolitan areasInformed Consent in Genome-Scale Research: What Do Prospective Participants Think?Genomic research and wide data sharing: views of prospective participantsAttitudes toward genetic research review: results from a survey of human genetics researchersAttitudes toward genetic research review: results from a national survey of professionals involved in human subjects protectionReturn of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).Glad you asked: participants' opinions of re-consent for dbGap data submissionBroad data sharing in genetic research: views of institutional review board professionals.Reframing the goals of care conversation: "we're in a different place".Factors that influence mammography use among older American Indian and Alaska Native women.Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromesSilent loss and the clinical encounter: Parents' and physicians' experiences of stillbirth-a qualitative analysis.Research ethics. Research practice and participant preferences: the growing gulf.Patient-centered discussions about prostate cancer screening: a real-world approach.What patients value when oncologists give news of cancer recurrence: commentary on specific moments in audio-recorded conversations"Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic TestingLooking for Trouble and Finding It.Views on electronic cigarette use in tobacco screening and cessation in an Alaska Native healthcare settingPatients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their DeathCommunity engagement in biobanking: Experiences from the eMERGE Network.Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.Beneficence, clinical urgency, and the return of individual research results to relativesBuilding partnerships in community-based participatory research: budgetary and other cost considerations.Partnership with the Confederated Salish and Kootenai Tribes: Establishing an Advisory Committee for Pharmacogenetic Research.Essential elements of personalized medicine.Seeking Genomic Knowledge: The Case for Clinical Restraint."I did not want to give birth to a child who has HIV": Experiences using PrEP during pregnancy among HIV-uninfected Kenyan women in HIV-serodiscordant couples.Systems medicine and the public's health.Educational needs in genetic medicine: primary care perspectives.Perceptions of pharmacogenetic research to guide tobacco cessation by patients, providers and leaders in a tribal healthcare setting.Choose your method: a comparison of phenomenology, discourse analysis, and grounded theory.Community dissemination and genetic research: moving beyond results reporting.
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P50
description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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type
label
Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan Brown Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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Susan B. Trinidad
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P1153
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0000-0002-5956-6557