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Publication
Stakeholder perspectives on implementing a universal Lynch syndrome screening program: A qualitative study of early barriers and facilitators
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): 5R01CA140377 -
Publication
Participant use and communication of findings from exome sequencing: A mixed-methods study
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. -
Publication
Returning pharmacogenetic secondary findings from genome sequencing: Let's not put the cart before the horse
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. -
Publication
Oncologists' and cancer patients' views on whole-exome sequencing and incidental findings: Results from the CanSeq study
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01HG006492, U01 HG007303, 120529-MRSG-11-006-01-CPPB -
Publication
Adopting genetics: Motivations and outcomes of personal genomic testing in adult adoptees
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): R01-HG005092, U01-HG006500, U19-HD077671, R01-HG002213 -
Publication
Family health history reporting is sensitive to small changes in wording
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): HG006615, HG006500, HD077671, HG006993 -
Publication
Overcalling secondary findings
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. -
Publication
Is "incidental finding" the best term?: A study of patients' preferences
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): U01 HG006507, U01 H007307, UO1 HG006487, U01 H007307 -
Publication
What are people willing to pay for whole-genome sequencing information, and who decides what they receive?
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): R01HG007063, 5P30CA082013-15, U01-HG006500 -
Publication
Eliciting preferences on secondary findings: The Preferences Instrument for Genomic Secondary Results
Genet MedClinical Sequencing Evidence-Generating Research (CSER) Consortium. Grant number(s): UM1 HG007301, R21 HG006612, UL1 TR000445