Author

Helen C. Baxter

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Daphne Lamirel· 2 shared A. R. Malinowski· 1 shared Alice Margaret TurneriD· 1 shared Andrew D. BretherickiD· 1 shared Andy Devereux-Cooke· 1 shared Anna Redshaw· 1 shared Anne Connolly· 1 shared Anniina M. TerviiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Daphne Lamirel

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Author profile →

2 papers

Recent·Most cited

Identification of Novel Reproducible Combinatorial Genetic Risk Factors for Myalgic Encephalomyelitis in the DecodeME Patient Cohort and Commonalities with Long COVID

Jason M. Sardell, Sayoni Das, Matthew W Pearson, Dmitry S. Kolobkov, A. R. Malinowski, LM Fullwood, Marianna Sanna, Helen C. Baxter, Kirsty E. McLellan, Michael Natt, Daphne Lamirel, S. Chowdhury, MA Strivens, Steve Gardner

This paper identifies 22,411 reproducible genetic signatures associated with ME in DecodeME cohorts and finds significant overlap with long COVID genes, suggesting shared mechanisms but distinct diseases.

Journal of Translational Medicine · Apr 21, 2026Peer-reviewedGenetic & Genomic Medicine

Initial findings from the DecodeME genome-wide association study of myalgic encephalomyelitis/chronic fatigue syndrome

Genetics Delivery Team, Thibaud Boutin, Andrew D. Bretherick, Joshua J Dibble, Esther Oluwada Ewaoluwagbemiga, Emma Northwood, Gemma L. Samms, Véronique Vitart, Project and Cohort Delivery Team, Øyvind Almelid, Tom Baker, Malgorzata Clyde, Anne Connolly, Diana Garcia, Shona M. Kerr, , Chris Paul Ponting

This study conducts a genome-wide association study (GWAS) of ME/CFS, identifying eight genetic loci associated with the disease, suggesting involvement of immune and neurological processes.

medRxiv · Aug 6, 2025 · PreprintGenetic & Genomic Medicine