Author

Christina P. Burghard

University of California, Los Angeles

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Research Focus:variant effect prediction· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Boon Xin Tan· 1 shared Daniel Bryan GoodmaniD· 1 shared David YaoiD· 1 shared Ei-Wen YangiD· 1 shared Eric M. JonesiD· 1 shared Jae Hoon BahniD· 1 shared Kimberly D. Insigne· 1 shared Kofi AmoahiD· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Boon Xin Tan

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GenomicsGenome ResearchPeer-reviewedMar 1, 2021

Allele-specific alternative splicing in human tissues

Kofi Amoah, Yun-Hua Esther Hsiao, Jae Hoon Bahn…·Xinshu Grace Xiao

The paper identifies allele-specific alternative splicing events across human tissues and develops a method to predict functional splicing-altering variants, finding many are linked to GWAS SNPs.

31 citations

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsbioRxivPreprintMar 10, 2018

Many rare genetic variants have unrecognized large-effect disruptions to exon recognition

Rocky Cheung, Kimberly D. Insigne, David Yao…·Sriram Kosuri

The paper identifies rare genetic variants that cause large disruptions to exon recognition, using a new assay called MFASS, and finds most of these variants are not in canonical splice sites.

5 citations

humanDNA methylation

𝕏 PostBluesky