|
| 37429778 | Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for Declining. | Clin Ther | 2023 |
| 36973832 | A systematic review of dissemination and implementation science capacity building programs around the globe. | Implement Sci Commun | 2023 |
| 36153628 | A citation analysis and scoping systematic review of the operationalization of the Practical, Robust Implementation and Sustainability Model (PRISM). | Implement Sci | 2022 |
| 34039980 | Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. | NPJ Genom Med | 2021 |
| 33888711 | Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. | NPJ Genom Med | 2021 |
| 34039997 | Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. | NPJ Genom Med | 2021 |
| 33063114 | A systematic literature review of Native American and Pacific Islanders' perspectives on health data privacy in the United States. | J Am Med Inform Assoc | 2020 |
| 33157008 | A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants. | Am J Hum Genet | 2020 |
| 31019026 | Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation. | Sci Transl Med | 2019 |
| 31564432 | A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants. | Am J Hum Genet | 2019 |
| 29644095 | Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization. | NPJ Genom Med | 2018 |
| 29449963 | The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants. | NPJ Genom Med | 2018 |
| 29266105 | Erratum: Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, <i>CYP2D6</i>, from whole-genome sequences. | NPJ Genom Med | 2017 |
| 28096516 | Newborn Sequencing in Genomic Medicine and Public Health. | Pediatrics | 2017 |
| 29263805 | Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, <i>CYP2D6</i>, from whole-genome sequences. | NPJ Genom Med | 2016 |
| 29263817 | Clinical detection of deletion structural variants in whole-genome sequences. | NPJ Genom Med | 2016 |
| 25937001 | Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings. | Lancet Respir Med | 2015 |
| 26419432 | A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases. | Genome Med | 2015 |