Author

Parvinder K. Aley

University of OxfordORCID 0000-0002-0749-8329Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Adolfo García‐SastreiD· 1 shared Adriana TomićiD· 1 shared Alba EscaleraiD· 1 shared Andrew John PollardiD· 1 shared Anette‐Gabriele ZiegleriD· 1 shared Arancha de la Horra· 1 shared CHIM Study Group· 1 shared Christiane WinkleriD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperImmunology

Adolfo García‐SastreORCID

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2 papers

Recent·Most cited

Innate antiviral readiness drives the expansion of protective T stem cell memory against influenza

Ivan Tomic, David Ahern, Jeffrey Alan Tomalka, Alba Escalera, Teresa Aydillo, Matthew D. Pauly, Nadine Rouphael, Seema S. Lakdawala, Naseem Sadek, Elizabeth Clutterbuck, Nisha Singh, Parvinder K. Aley, Hannah Robinson, Spyridoula Marinou, Stephanie P. Hao, , Adriana Tomić

This study identifies innate antiviral readiness as a key driver of TSCM cell expansion, showing its predictive value for viral clearance and vaccine design.

bioRxiv · Dec 10, 2025 · PreprintImmunology

Successful incorporation of a genetic risk prediction research platform into routine newborn screening

Owen Bendor-Samuel, Tabitha Wishlade, Louise Willis, Parvinder K. Aley, Edward Choi, Rachel Craik, Yama Farooq Mujadidi, Ginny Mounce, Fenella Roseman, Arancha de la Horra, James Bland, Nazia Taj, Ian Smith, Anette‐Gabriele Ziegler, Ezio E. Bonifacio, , the GPPAD Study Group

The paper describes the integration of a genetic risk prediction platform into the NHS newborn screening program for Type 1 Diabetes, demonstrating a model for population-based genetic research.

Archives of Disease in Childhood · Sep 28, 2022Peer-reviewedGenetic & Genomic Medicine