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Publications by David Yao
A Multiplexed Assay for Exon Recognition Reveals That an Unappreciated Fraction of Rare Genetic Variants Cause Large-Effect Splicing Disruptions
Molecular Cell
Cell Biology
Molecular Biology
Related publications
Exon Recognition in Vertebrate Splicing
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
S-Cap Extends Pathogenicity Prediction to Genetic Variants That Affect RNA Splicing
Nature Genetics
Genetics
Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies
Annals of Neurology
Neurology
Improved Detection of Rare Genetic Variants for Diseases
PLoS ONE
Multidisciplinary
406 an in Vitro Splicing Assay Reveals the Pathogenicity of Intronic Variants in ABCC6, the Gene at Fault in Pseudoxanthoma Elasticum
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
The Quest for Rare Variants: Pooled Multiplexed Next Generation Sequencing in Plants
Frontiers in Plant Science
Plant Science
The Exon a (C77G) Mutation Is a Common Cause of Abnormal CD45 Splicing in Humans
Journal of Immunology
Allergy
Immunology
Multiple Splicing Defects in an Intronic False Exon
Molecular and Cellular Biology
Cell Biology
Molecular Biology