Co-Authors
This is a "connection" page, showing publications co-authored by JENNIFER POSEY and SEBASTIAN OCHOA GONZALEZ.
Connection Strength
0.176
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An integrated platform for concurrent structural and single-nucleotide variants improves copy-number detection and reveals pathogenic alleles in undiagnosed Mendelian families. Genome Med. 2025 12 31; 18(1):16.
Score: 0.059
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GREGoR: accelerating genomics for rare diseases. Nature. 2025 11; 647(8089):331-342.
Score: 0.059
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Community-Driven Copy Number Variant Discovery at Scale: Results from a Rare Disease Genomics Hackathon. medRxiv. 2025 Aug 12.
Score: 0.058