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| 36416152 | Development of Competency-based Online Genomic Medicine Training (COGENT). | Per Med | 2023 |
| 37655513 | Survey of the training needs of genetic assistants supports the creation of genetic assistant training programs. | J Genet Couns | 2023 |
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| 37267899 | eXclusionarY: 10 years later, where are the sex chromosomes in GWASs? | Am J Hum Genet | 2023 |
| 37071725 | Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. | Circ Genom Precis Med | 2023 |
| 36621880 | Returning integrated genomic risk and clinical recommendations: The eMERGE study. | Genet Med | 2023 |
| 38065071 | Genomic medicine year in review: 2023. | Am J Hum Genet | 2023 |
| 37655513 | Survey of the training needs of genetic assistants supports the creation of genetic assistant training programs. | J Genet Couns | 2023 |
| 37883979 | Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing. | Am J Hum Genet | 2023 |
| 37071725 | Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. | Circ Genom Precis Med | 2023 |
| 37267899 | eXclusionarY: 10 years later, where are the sex chromosomes in GWASs? | Am J Hum Genet | 2023 |
| 36621880 | Returning integrated genomic risk and clinical recommendations: The eMERGE study. | Genet Med | 2023 |
| 34930020 | Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. | Circulation | 2022 |
| 35943490 | Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results. | Genet Med | 2022 |
| 35485600 | A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources. | J Am Med Inform Assoc | 2022 |
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| 34906458 | The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort. | Genet Med | 2022 |
| 34930020 | Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. | Circulation | 2022 |
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| 34906458 | The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort. | Genet Med | 2022 |
| 34282949 | Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry. | Circ Genom Precis Med | 2021 |
| 36082306 | Workshop proceedings: GWAS summary statistics standards and sharing. | Cell Genom | 2021 |
| 34282949 | Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry. | Circ Genom Precis Med | 2021 |
| 33951936 | Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network. | Circ Heart Fail | 2021 |
| 34347061 | Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. | JAMA Netw Open | 2021 |
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| 34789511 | Should all babies have their genome sequenced at birth? | BMJ | 2021 |
| 36082306 | Workshop proceedings: GWAS summary statistics standards and sharing. | Cell Genom | 2021 |
| 34861172 | Genomic medicine year in review: 2021. | Am J Hum Genet | 2021 |
| 34789511 | Should all babies have their genome sequenced at birth? | BMJ | 2021 |
| 34347061 | Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. | JAMA Netw Open | 2021 |
| 33951936 | Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network. | Circ Heart Fail | 2021 |
| 32386537 | Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups. | Am J Hum Genet | 2020 |
| 32386537 | Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups. | Am J Hum Genet | 2020 |
| 33103095 | The International Hundred Thousand Plus Cohort Consortium: integrating large-scale cohorts to address global scientific challenges. | Lancet Digit Health | 2020 |
| 33275910 | Genomic Medicine Year in Review: 2020. | Am J Hum Genet | 2020 |
| 33116284 | Strategic vision for improving human health at The Forefront of Genomics. | Nature | 2020 |
| 33116284 | Strategic vision for improving human health at The Forefront of Genomics. | Nature | 2020 |
| 33275910 | Genomic Medicine Year in Review: 2020. | Am J Hum Genet | 2020 |
| 33103095 | The International Hundred Thousand Plus Cohort Consortium: integrating large-scale cohorts to address global scientific challenges. | Lancet Digit Health | 2020 |
| 30609404 | Integrating Genomics into Healthcare: A Global Responsibility. | Am J Hum Genet | 2019 |
| 32027834 | Genomic Medicine Year in Review: 2019. | Am J Hum Genet | 2019 |
| 30415494 | Return of secondary findings in genomic sequencing: Military implications. | Mol Genet Genomic Med | 2019 |
| 30609404 | Integrating Genomics into Healthcare: A Global Responsibility. | Am J Hum Genet | 2019 |
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