Search Results - "Miller, Ilana M"
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Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial
Published in American journal of human genetics (05-04-2018)“…In-person education and counseling for all people receiving genetic results is the predominant model of disclosure but is challenged by the growing volume of…”
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The PrU: Development and validation of a measure to assess personal utility of genomic results
Published in Genetics in medicine (01-03-2023)“…People report experiencing value from learning genomic results even in the absence of clinically actionable information. Such personal utility has emerged as a…”
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Knowledge, motivations, expectations, and traits of an African, African-American, and Afro-Caribbean sequencing cohort and comparisons to the original ClinSeq® cohort
Published in Genetics in medicine (01-06-2019)“…Purpose Racial minority populations are underrepresented in genomics research. This study enrolled African-descended individuals in a sequencing study and…”
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Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes
Published in Genetics in medicine (01-03-2019)“…Purpose Studies on returning variants of uncertain significance (VUS) results have predominantly included patients with a personal or family history of cancer…”
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Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore
Published in American journal of medical genetics. Part A (01-05-2019)“…This study explored patients' experiences and perceptions of living with thalassemia (an inherited hematologic disorder), perceptions of social stigma, and…”
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Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial
Published in Translational behavioral medicine (01-04-2020)“…Abstract How individuals perceive uncertainties in sequencing results may affect their clinical utility. The purpose of this study was to explore perceptions…”
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Health Behaviors Amongst Unaffected Participants Following Receipt of Variants of Uncertain Significance in Cardiomyopathy-Associated Genes
Published in Genetics in medicine (12-07-2018)Get full text
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