Identification of PCSK9-like human gene knockouts using metabolomics, proteomics, and whole-genome sequencing in a consanguineous population.

consanguineous population drug target validation, drug target identification human gene knockouts metabolomics proteomics whole-genome sequencing

Journal

Cell genomics
ISSN: 2666-979X
Titre abrégé: Cell Genom
Pays: United States
ID NLM: 9918284260106676

Informations de publication

Date de publication:
11 Jan 2023
Historique:
received: 10 02 2022
revised: 16 07 2022
accepted: 25 10 2022
entrez: 13 2 2023
pubmed: 14 2 2023
medline: 14 2 2023
Statut: epublish

Résumé

Natural human knockouts of genes associated with desirable outcomes, such as

Identifiants

pubmed: 36777185
doi: 10.1016/j.xgen.2022.100218
pii: S2666-979X(22)00171-9
pmc: PMC9903797
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100218

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

E.B.F. is an employee of Pfizer.

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Auteurs

Aziz Belkadi (A)

Bioinformatics Core, Weill Cornell Medicine-Qatar, Education City, Doha 24144, Qatar.
Department of Biophysics and Physiology, Weill Cornell Medicine, New York, NY, USA.

Gaurav Thareja (G)

Bioinformatics Core, Weill Cornell Medicine-Qatar, Education City, Doha 24144, Qatar.
Department of Biophysics and Physiology, Weill Cornell Medicine, New York, NY, USA.

Fatemeh Abbaszadeh (F)

Hamada Medical Corporation, Doha, Qatar.

Ramin Badii (R)

Hamada Medical Corporation, Doha, Qatar.

Eric Fauman (E)

Pfizer, Boston, MA, USA.

Omar M E Albagha (OME)

College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.
Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Karsten Suhre (K)

Bioinformatics Core, Weill Cornell Medicine-Qatar, Education City, Doha 24144, Qatar.
Department of Biophysics and Physiology, Weill Cornell Medicine, New York, NY, USA.

Classifications MeSH