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Population-Scale Discovery of Genetic Risk Factors
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Presidential Symposium & Address, ASHG 2022 Session Available On-Demand
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Presidential Symposium: Perspectives on diversity, race, inclusion and equity
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Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations
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Recurring Donation
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Regulatory features aid interpretation of 3’UTR variants
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Stability of Polygenic Scores Across Discovery GWAS
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Stakeholders’ Views on Returning Polygenic Risk Scores
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Successes in Community Engaged Research: Implementation of Recommendations in ASHG’s Guidance, Addressing Underrepresentation in Genomics Research through Community Engagement
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Taking the Next Step in Your Career with ASHG-NHGRI Fellowships
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Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding
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The impact of clinical genome sequencing in a global population with suspected rare genetic disease
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