Author

Chongzhi Zang

Primary ORCID profile (0000-0003-4812-3627 · 31 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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

Same name, identified by ORCID

Chongzhi ZangiD31 papers · University of Virginia

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:fine-mapping· 1 Research Focus:polygenic risk· 1

Frequent Co-Authors

Alexander GuseviD· 2 shared Eli StahliD· 2 shared Gosia TrynkaiD· 2 shared Han Xu· 2 shared Mark Daly· 2 shared Soumya RaychaudhuriiD· 2 shared Stephan RipkeiD· 2 shared Alkes L Price· 1 shared

Activity by Year

2014-2015 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 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

Alexander GusevORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Partitioning heritability by functional category using GWAS summary statistics

Hilary Kiyo Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttilla, Han Xu, Chongzhi Zang, Kyle Farh, Stephan Ripke, Felix Day, ReproGen Consortium, Schizophrenia Working Group of the Psychiatric Genetics Consortium, RACI Consortium, , Alkes L. Price

This paper partitions heritability across functional genomic elements using GWAS summary statistics to identify trait-specific enrichments.

bioRxiv · Jan 23, 2015Genetics

Regulatory variants explain much more heritability than coding variants across 11 common diseases

Alexander Gusev, S Hong Lee, Benjamin M Neale, Gosia Trynka, Bjarni J Vilhjalmsson, Hilary Finucane, Han Xu, Chongzhi Zang, Stephan Ripke, Eli Stahl, n/a Schizophrenia Working Group of the PGC, n/a SWE-SCZ Consortium, Anna K Kahler, Christina M Hultman, Shaun M Purcell, , Alkes L Price

The paper shows regulatory variants explain significantly more heritability than coding variants for 11 diseases, using imputed data across 218 cell types.

bioRxiv · Apr 21, 2014 · PreprintGenetics