| 32349224 | Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network. | J Pers Med | 2020 |
| 32413979 | Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network. | J Pers Med | 2020 |
| 30592300 | A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>. | Transfusion | 2019 |
| 30287922 | Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. | Genet Med | 2019 |
| 30670880 | Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. | Genet Med | 2019 |
| 29565423 | Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial. | Genet Med | 2018 |
| 29497922 | Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium. | J Genet Couns | 2018 |
| 28654958 | The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial. | Ann Intern Med | 2017 |
| 29030401 | A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients. | Circ Cardiovasc Genet | 2017 |
| 27181682 | Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. | Am J Hum Genet | 2016 |
| 27392080 | Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. | Am J Hum Genet | 2016 |
| 23881473 | Newborn screening: education, consent, and the residual blood spot. The position of the national society of genetic counselors. | J Genet Couns | 2014 |
| 24387990 | Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy. | Am J Hum Genet | 2014 |
| 25251809 | Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings. | Am J Med Genet A | 2014 |