Mr Allan Motyer
Honorary (Fellow)
Department of Medical Biology (WEHI)
28 Scholarly works
3 Projects
HIGHLIGHTS
2025
Journal article
Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
DOI: 10.1186/s13073-025-01582-x2025
Journal article
Non-apoptotic caspase-8 is critical for orchestrating exaggerated inflammation during severe SARS-CoV-2 infection
DOI: 10.1038/s41467-025-65098-z2025
Journal article
Blood-Based T-Cell Diagnosis of Celiac Disease
DOI: 10.1053/j.gastro.2025.05.0222025
Journal article
Profiling the spatial architecture of multiple myeloma in human bone marrow trephine biopsy specimens with spatial transcriptomics
DOI: 10.1182/blood.20250288962025
Journal article
Purified oat protein can trigger acute symptoms linked to immune activation in coeliac disease patients but not histological deterioration
DOI: 10.1136/gutjnl-2024-3335892023
Research Grant
Characterising the Mutagenic Effects of Neuroinflammation in Primary Progressive MS
2020
Research Grant
Single Oligodendrocyte Genome Sequencing to Determine the Dynamics of Myelin Repair in Multiple Sclerosis
RECENT SCHOLARLY WORKS
2025
Journal article
Neuronal somatic mutations are increased in multiple sclerosis lesions
DOI: 10.1038/s41593-025-01895-52025
Journal article
Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals (Nature, (2024), 631, 8021, (583-592), 10.1038/s41586-024-07556-0)
DOI: 10.1038/s41586-024-08571-x2024
Journal article
A deep catalogue of protein-coding variation in 983,578 individuals
DOI: 10.1038/s41586-024-07556-02024
Journal article
Multiple Sclerosis Polygenic Risk Is Not Enriched in Three Multicase Families in Comparison to Population-Based Cases
DOI: 10.1155/2024/92689112021
Journal article
Large-Scale Imputation of KIR Copy Number and HLA Alleles in North American and European Psoriasis Case-Control Cohorts Reveals Association of Inhibitory KIR2DL2 With Psoriasis
DOI: 10.3389/fimmu.2021.684326
RECENT PROJECTS
2020
Research Grant
Single Oligodendrocyte Genome Sequencing to Determine the Dynamics of Myelin Repair in Multiple Sclerosis