Author

Jingyan Wu

Stanford Medicine

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· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Chenchen ZhuiD· 2 shared Han SuniD· 2 shared Lars Michael SteinmetziD· 2 shared Benjamin MederiD· 1 shared Francesca BrigantiiD· 1 shared Hong ZengiD· 1 shared Kevin R. RoyiD· 1 shared Michelle NguyeniD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 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

2 shared papersGenetics

Chenchen ZhuORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Single-molecule, full-length transcript isoform sequencing reveals disease mutation-associated RNA isoforms in cardiomyocytes

Chenchen Zhu, Jingyan Wu, Han Sun, Francesca Briganti, Benjamin Meder, Wei Wu, Lars Michael Steinmetz

The paper develops a pipeline to identify and quantify full-length RNA isoforms, revealing disease-associated isoforms in cardiomyocytes with RBM20 mutations.

Nature Communications · Jul 9, 2021Peer-reviewedGenetics

Transcript fusion between CDKN1A and RAB44 caused by exon skipping like mechanism due to disruption of a splice site

Han Sun, Michelle Nguyen, William F. Mueller, Zhuanfen Cheng, Hong Zeng, Chenchen Zhu, Jingyan Wu, Kevin R. Roy, Petra Jakob, Raeka S. Aiyar, Wu Wei, Lars Michael Steinmetz

The paper identifies a recurrent tumor-specific transcript fusion between CDKN1A and RAB44 caused by splice-site mutations and shows its correlation with TP53 inactivation and CDK activation.

bioRxiv · Feb 22, 2019 · PreprintGenetics