Keren J. Carss

BioPharmaceuticals R&D, AstraZeneca
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 64 publications

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Journal: Nature

Published: March 31, 2026

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Journal: Nature

Published: March 21, 2025

Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Journal: medRxiv : the preprint server for health sciences

Published: May 20, 2024

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Journal: Nature communications

Published: May 10, 2024

Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis.

Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis.

Journal: Nature genetics

Published: February 07, 2024

Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences.

Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences.

Journal: Nature genetics

Published: September 10, 2023

Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.

Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.

Journal: American journal of human genetics

Published: March 13, 2023

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.

Journal: Blood

Published: March 01, 2023

Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank.

Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank.

Journal: American journal of human genetics

Published: November 21, 2022

Rare variant associations with plasma protein levels in the UK Biobank.

Rare variant associations with plasma protein levels in the UK Biobank.

Journal: Nature

Published: October 05, 2022

Using human genetics to improve safety assessment of therapeutics.

Using human genetics to improve safety assessment of therapeutics.

Journal: Nature reviews. Drug discovery

Published: September 02, 2022

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.

Journal: Circulation. Genomic and precision medicine

Published: May 18, 2022

Showing 1-12 of 64

Last Updated: 09/26/2026