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Connecting genetic risk to disease endpoints through the human blood plasma proteome

Connecting genetic risk to disease endpoints through the human blood plasma proteome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_biorxiv_primary_086793

Connecting genetic risk to disease endpoints through the human blood plasma proteome

About this item

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

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Scope and Contents

Contents

Genome-wide association studies (GWAS) with intermediate phenotypes, like changes in metabolite and protein levels, provide functional evidence for mapping disease associations and translating them into clinical applications. However, although hundreds of genetic risk variants have been associated with complex disorders, the underlying molecular pa...

Alternative Titles

Full title

Connecting genetic risk to disease endpoints through the human blood plasma proteome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_biorxiv_primary_086793

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_biorxiv_primary_086793

Other Identifiers

ISSN

2692-8205

E-ISSN

2692-8205

DOI

10.1101/086793

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