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| 33876469 | Preferences for and acceptability of receiving pharmacogenomic results by mail: A focus group study with a primarily African-American cohort. | J Genet Couns | 2021 |
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| 29971366 | Web-Based Platform vs Genetic Counselors in Educating Patients About Carrier Results From Exome Sequencing-Reply. | JAMA Intern Med | 2018 |
| 29848613 | Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications. | Circ Genom Precis Med | 2018 |
| 29476166 | Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes. | Eur J Hum Genet | 2018 |
| 29526281 | Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial. | Am J Hum Genet | 2018 |
| 29497922 | Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium. | J Genet Couns | 2018 |
| 29383714 | Disclosure of cardiac variants of uncertain significance results in an exome cohort. | Clin Genet | 2018 |
| 29356820 | Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial. | JAMA Intern Med | 2018 |
| 29745680 | Associations of perceived norms with intentions to learn genomic sequencing results: Roles for attitudes and ambivalence. | Health Psychol | 2018 |
| 29739461 | Clinical providers' experiences with returning results from genomic sequencing: an interview study. | BMC Med Genomics | 2018 |
| 29655271 | Correction to: PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing. | Clin Genet | 2018 |
| 28933792 | A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number. | Genet Med | 2018 |
| 28879629 | Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention. | J Genet Couns | 2018 |
| 27925165 | PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing. | Clin Genet | 2017 |
| 28218387 | Defining personal utility in genomics: A Delphi study. | Clin Genet | 2017 |
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| 26540156 | Participant use and communication of findings from exome sequencing: a mixed-methods study. | Genet Med | 2016 |
| 25313897 | Dispositional optimism and perceived risk interact to predict intentions to learn genome sequencing results. | Health Psychol | 2015 |
| 26186621 | Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology. | PLoS One | 2015 |
| 26046366 | Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations. | Am J Hum Genet | 2015 |
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| 25582989 | Information Avoidance Tendencies, Threat Management Resources, and Interest in Genetic Sequencing Feedback. | Ann Behav Med | 2015 |
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