Search Results (10)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Expediting rare disease diagnosis: a call to bridge the gap between clinical and functional genomics. | Academic Article |
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| Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlation. | Academic Article |
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| Proteasome beta subunit pharmacogenomics: gene resequencing and functional genomics. | Academic Article |
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| Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterization. | Academic Article |
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| Identification of functional regulatory elements in the human genome using pooled CRISPR screens. | Academic Article |
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| Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells. | Academic Article |
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| Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants. | Academic Article |
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| Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients. | Academic Article |
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| Less Lumping, Smarter Splitting: Genomics and Metabolomics of Systemic Steroid Response in Bronchopulmonary Dysplasia | Grant |
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| Functional characterization of liver enhancers that regulate drug-associated transporters. | Academic Article |
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