Loukas Moutsianas

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 36 publications

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026

Equity in genome sequencing for rare disease diagnosis: a cross-sectional analysis of data from the UK 100,000 Genomes Project.

Equity in genome sequencing for rare disease diagnosis: a cross-sectional analysis of data from the UK 100,000 Genomes Project.

Journal: EBioMedicine
Published: September 29, 2025

Equity in cancer genomics in the UK: a cross-sectional analysis of a national cancer cohort.

Equity in cancer genomics in the UK: a cross-sectional analysis of a national cancer cohort.

Journal: The Lancet. Oncology
Published: January 21, 2025

Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice.

Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: October 31, 2024

Common and rare variant analyses reveal genetic factors underlying idiopathic pulmonary fibrosis and its shared aetiology with severe COVID-19.

Common and rare variant analyses reveal genetic factors underlying idiopathic pulmonary fibrosis and its shared aetiology with severe COVID-19.

Journal: EBioMedicine
Published: August 22, 2024

Artificial intelligence for modelling infectious disease epidemics.

Artificial intelligence for modelling infectious disease epidemics.

Journal: Nature
Published: July 08, 2024

A Genomics England haplotype reference panel and imputation of UK Biobank.

A Genomics England haplotype reference panel and imputation of UK Biobank.

Journal: Nature genetics
Published: November 21, 2023

Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci.

Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci.

Journal: Nature communications
Published: August 22, 2023

Increased frequency of repeat expansion mutations across different populations.

Increased frequency of repeat expansion mutations across different populations.

Journal: medRxiv : the preprint server for health sciences
Published: July 18, 2023

Increased frequency of repeat expansion mutations across different populations.

Increased frequency of repeat expansion mutations across different populations.

Journal: Nature medicine
Published: June 22, 2023

The genomic landscape of familial glioma.

The genomic landscape of familial glioma.

Journal: Science advances
Published: April 28, 2023

Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.

Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.

Journal: Nature communications
Published: June 22, 2022
Showing 1-12 of 36

Last Updated: 09/26/2026