Author

Vivian Q. Xia

San Francisco General HospitalORCID 0000-0002-6540-3738Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Organism:mouse· 1 Organism:yeast· 1 Organism:zebrafish· 1

Frequent Co-Authors

Akhil PampanaiD· 1 shared Ambro van HoofiD· 1 shared Angelo PeloneroiD· 1 shared Anita H. CorbettiD· 1 shared Anne Michele SlavotinekiD· 1 shared Arun PadmanabhaniD· 1 shared Brian L. BlackiD· 1 shared Bryan Hill-Fung LauiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenomics

Akhil PampanaORCID

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2 papers

Recent·Most cited

CSDE1 is a Post-Transcriptional Regulator of the LDL Receptor

Geoffrey A. Smith, Arun Padmanabhan, Bryan Hill-Fung Lau, Akhil Pampana, Li Li, Clara Youngna Lee, Angelo Pelonero, Tomohiro Nishino, Nandhini Sadagopan, Vivian Q. Xia, Rajan Jain, Pradeep Natarajan, Roland S. Wu, Brian L. Black, Deepak Srivastava, , John S. Chorba

A genome-wide CRISPR screen identifies CSDE1 as a key regulator of hepatic LDLR mRNA decay in vivo, making it a promising target for heart disease.

Science Translational Medicine · Sep 14, 2022Peer-reviewedGenomics

Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness

Anne Michele Slavotinek, Doriana Misceo, Stephanie Htun, Linda Mathisen, Eirik Frengen, Michelle Foreman, Jennifer E. Hurtig, Liz Enyenihi, Maria C. Sterrett, Sara W. Leung, Dina Schneidman‐Duhovny, Juvianee I. Estrada‐Veras, Jacque L. Duncan, Charlotte A. Haaxma, Erik‐Jan Kamsteeg, , Anita H. Corbett

The paper reports three patients with biallelic EXOSC5 variants causing developmental delays, short stature, and cerebellar hypoplasia, and shows functional defects in RNA exosome activity.

Human Molecular Genetics · Jun 1, 2020Peer-reviewedGenetics