Showing 1–12 of 33 results
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Cancer predisposition variants in All of Us
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Low-cost generation of clinical-grade, layperson-friendly pharmacogenetic passports
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Influence of rare variants on autism prevalence
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A Transchromosomic Rat Model of Down Syndrome
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Canonical splice site variants: more than meets the eye
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Common variant in Greenlanders impacts heart health
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CRISPR activation to study splice-altering variants
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Developing Polygenic Scores for Multi-Ancestry Populations
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Developmental Genomics of Congenital Limb Malformations
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Enhanced genetic diagnosis through RNA-seq analysis of transdifferentiated cells
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Evaluating and improving health equity and fairness of polygenic scores
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Exome CNV detection and classification in rare diseases
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