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5711 - 5720 of 7239 Topics
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Publication
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment
J Genet CounsClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG007292, U24HG007307 -
Publication
Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq(®) cohort
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): HG200359 09 -
Publication
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG007292, U24HG007307 -
Publication
The potential price and access implications of the cost-utility and budget impact methodologies applied by NICE in England and ICER in the US for a novel gene therapy in Parkinson's disease
Journal of market access & health policy -
Publication
Contending with real and perceived intrusiveness in digital phenotyping research
American Journal of Bioethics -
Publication
Qualitative study of system-level factors related to genomic implementation
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01-HG007266, U01-HG007269, U01-HG007253, U01-HG007762, U01-HG007282, U01-HG007775, U01-HG007278 -
Publication
Challenges in the use of direct-to-consumer personal genome testing in children
Am J Bioeth -
Publication
Stakeholder engagement: A key component of integrating genomic information into electronic health records
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG006382, U01HG006375, UO1HG006389-01, U01HG04599, U01HG006379, U01HG006380, UL1RR029887, U01HG006388, U01… -
Publication
Patient understanding of pharmacogenomic test results in clinical care
Patient Education and Counseling -
Publication
Development and evaluation of a novel educational program for providers on the use of polygenic risk scores
Genetics in Medicine