Search Results (68)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| Pastinen, Tomi | Person |
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| Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. | Academic Article |
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| Developing a community-led rare disease ELSI research agenda. | Academic Article |
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| Downstream Exclusion in Rural Rare Disease Precision Medicine Research. | Academic Article |
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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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| Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts. | 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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| Sources of Unease About the Use of Genome Sequencing for Diagnosing Rare Diseases in Children. | Academic Article |
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| Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes. | Academic Article |
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| Cohen, Ana | Person |
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| Pyoderma Gangrenosum: A Rare Disease With Dire Consequences in Facial Aesthetic Surgery Patients. | Academic Article |
Why?
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| Congenital H-type tracheoesophageal fistula: A multicenter review of outcomes in a rare disease. | Academic Article |
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| Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. | Academic Article |
Why?
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| Psychosocial Considerations for the Child with Rare Disease: A Review with Recommendations and Calls to Action. | Academic Article |
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| Smail, Craig | Person |
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