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| 38064200 | The motivation and process for developing a consortium-wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care. | Clin Transl Sci | 2024 |
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| 36350656 | The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource. | Nucleic Acids Res | 2023 |
| 36341765 | Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience. | Am J Med Genet A | 2023 |
| 37470118 | Parent-Reported Clinical Utility of Pediatric Genomic Sequencing. | Pediatrics | 2023 |
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| 37470118 | Parent-Reported Clinical Utility of Pediatric Genomic Sequencing. | Pediatrics | 2023 |
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| 35697829 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. | Commun Biol | 2022 |
| 34107879 | Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. | BMC Genomics | 2021 |
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| 34107879 | Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. | BMC Genomics | 2021 |
| 34870259 | Sequencing-based genome-wide association studies reporting standards. | Cell Genom | 2021 |
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| 32226016 | Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. | PLoS Genet | 2020 |
| 32439900 | Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. | Nat Commun | 2020 |
| 33948230 | Lessons learned about harmonizing survey measures for the CSER consortium. | J Clin Transl Sci | 2020 |
| 33230300 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2020 |
| 33108757 | Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies. | Am J Hum Genet | 2020 |
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| 33108757 | Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies. | Am J Hum Genet | 2020 |
| 33230300 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2020 |
| 32602732 | Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. | Circ Genom Precis Med | 2020 |
| 32439900 | Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. | Nat Commun | 2020 |
| 32171239 | Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. | BMC Genomics | 2020 |
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| 31891604 | A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans. | PLoS One | 2019 |
| 31719535 | Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. | Nat Commun | 2019 |
| 30445434 | The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019. | Nucleic Acids Res | 2019 |
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| 31217584 | Genetic analyses of diverse populations improves discovery for complex traits. | Nature | 2019 |
| 30906166 | Defining and Achieving Health Equity in Genomic Medicine. | Ethn Dis | 2019 |
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