Co-Authors
This is a "connection" page, showing publications co-authored by KIM WORLEY and LINDSAY BURRAGE.
Connection Strength
0.466
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The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. Am J Hum Genet. 2025 Nov 06; 112(11):2578-2590.
Score: 0.060
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Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. Elife. 2025 Aug 27; 13.
Score: 0.060
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Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders. EMBO Mol Med. 2025 Oct; 17(10):2562-2585.
Score: 0.060
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Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders. medRxiv. 2025 Jul 08.
Score: 0.059
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Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. medRxiv. 2025 May 29.
Score: 0.059
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The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics. medRxiv. 2025 Jan 29.
Score: 0.058
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Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 09 19; 33(19):1643-1647.
Score: 0.056
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The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing. Am J Hum Genet. 2024 05 02; 111(5):841-862.
Score: 0.054