Co-Authors
This is a "connection" page, showing publications co-authored by WILLIAM CRAIGEN and PENGFEI LIU.
Connection Strength
0.544
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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: 0.242
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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: 0.218
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Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. JAMA Pediatr. 2017 12 04; 171(12):e173438.
Score: 0.035
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Molecular findings among patients referred for clinical whole-exome sequencing. JAMA. 2014 Nov 12; 312(18):1870-9.
Score: 0.028
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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. J Med Genet. 2010 May; 47(5):332-41.
Score: 0.020