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44 Publications listed
The alternative androgen receptor isoform A mitigates toxicity of polyglutamine-elongated mutant androgen receptor in spinal and bulbar muscular atrophy
Published 2026
Brain
Università degli Studi di Milano,
University of Padova,
Institute of Developmental and Regenerative Medicine, Department of Paediatrics, University of Oxford,
University of Pittsburgh Medical Center
10.1016/j.jare.2026.01.051
Chierichetti M, Andreotti R, Tedesco B, Ferrari V, Corna, et al,J Adv Res. 2026 Oct;88:959-976. doi: 10.1016/j.jare.2026.01.051. Epub 2026 Jan 19. PMID: 41564929.
Reference genomes and fossils revise bat family phylogeny and biogeography
Published 2026
Genomics
Senckenberg-Leibniz Institution for Biodiversity and Earth System Research,
University of Montpellier-CNRS-IRD,
The City College of New York
10.1038/s41586-026-11007-3
Morales AE, Liang Y, Thomas WR, Leushkin EV, et al. Nature. 2026 Oct;658(8134):141-152. doi: 10.1038/s41586-026-11007-3. Epub 2026 Sep 23. PMID: 42778608; PMCID: PMC13626947.
Functional analysis of TTN uORFs reveals context-dependent translational regulation
Published 2026
Genomics
Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford,
Oxford Organoid Hub, Sherrington Building, University of Oxford,
Institute of Developmental and Regenerative Medicine, Department of Paediatrics, University of Oxford,
Department of Paediatrics, MDUK Oxford Neuromuscular Centre & NIHR Oxford Biomedical Research Centre, University of Oxford
10.1016/j.omtn.2026.103077
Kirk RB, Sparrow AJ, Moya-Jódar M, Roberts TC, Toepfer CN, Watkins H., Mol Ther Nucleic Acids. 2026 Aug 28;37(4):103077. doi: 10.1016/j.omtn.2026.103077. PMID: 42761362; P
Perivascular Astrocytic Gliosis Induced by Retinal Gene Therapy
Published 2026
Eye
AAV2-CAG-REP1,
EGFR/STAT3,
FOXO3
Oxford Eye Hospital,
Nuffield Department of Clinical Neuroscience, University of Oxford,
University of Tübingen
10.1177/10430342261469741
Abdalla Elsayed MEA, Seitz IP, Fischer MD, MacLaren RE, Hum Gene Ther. 2026 Nov;37(21-22):1019-1026. doi: 10.1177/10430342261469741. Epub 2026 Aug 18. PMID: 42610332.
Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project
Published 2026
Genomics
AUTS2,
DLX5/6,
FN1
University of Edinburgh,
Centre for Human Genetics, University of Oxford,
Royal Devon University Healthcare NHS Foundation Trust,
North of Scotland Medical Genetic Service, NHS Grampian,
Queen Elizabeth University Hospital
10.1038/s41431-026-02210-x
Prasun Dutta, Alistair T. Pagnamenta, Christelle Robert et al, Eur J Hum Genet. 2026 Oct;34(10):1513-1523. doi: 10.1038/s41431-026-02210-x. Epub 2026 Aug 5. PMID: 42557338; PMCID: PMC13634035.