Katherine A. Fawcett
Leicester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 36 publications
Genome-wide association study of asthma with high treatment burden and/or worse outcomes defined using electronic healthcare data in UK Biobank.
Journal: ERJ open research
Published: February 27, 2026
The role of the ADRB2 Thr164Ile variant in lung function determination, plasma proteome variability and other phenotypes in UK Biobank.
Journal: ERJ open research
Published: March 11, 2025
Genome-wide association testing beyond SNPs.
Journal: Nature reviews. Genetics
Published: September 03, 2024
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Journal: Nature genetics
Published: April 19, 2024
Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Journal: Nature genetics
Published: September 25, 2023
Asthma exacerbations and eosinophilia in the UK Biobank: a genome-wide association study.
Journal: ERJ open research
Published: August 04, 2023
Seeing the trees for the wood: reducing heterogeneity in genomic studies of asthma.
Journal: The European respiratory journal
Published: October 04, 2022
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.
Journal: Nature communications
Published: September 20, 2022
DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies.
Journal: Bioinformatics (Oxford, England)
Published: August 30, 2022
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Journal: Nature genetics
Published: May 12, 2022
Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank.
Journal: BMC medical genomics
Published: February 27, 2022
Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5.
Journal: Frontiers in cell and developmental biology
Published: October 20, 2021
Last Updated: 09/26/2026