Christopher A. Odhams
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 11 publications
Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.
Journal: medRxiv : the preprint server for health sciences
Published: April 03, 2026
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.
Journal: EBioMedicine
Published: August 22, 2024
Whole-genome sequencing reveals host factors underlying critical COVID-19.
Journal: Nature
Published: September 02, 2021
Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severity.
Journal: Human molecular genetics
Published: December 13, 2019
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.
Journal: Nature communications
Published: July 10, 2019
De novo mutations implicate novel genes in systemic lupus erythematosus.
Journal: Human molecular genetics
Published: September 12, 2017
Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus.
Journal: Human molecular genetics
Published: August 05, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026