Author

Graeme W. T. Newton

University of BristolORCID 0000-0003-4924-0112Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Achim KlessiD· 1 shared Aidan P. NickersoniD· 1 shared Anthony Edward PickeringiD· 1 shared Corin Charman· 1 shared James DunhamiD· 1 shared Keith Geoffrey PhillipsiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Achim KlessORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 12, 2025

Carriers of SCN9A variants linked to inherited and acquired pain syndromes show no alteration in the prevalence of pain or analgesic usage in the UK Biobank cohort

Graeme W. T. Newton, Corin Charman, Aidan P. Nickerson…·Anthony Edward Pickering

2 citations

humanwhole-exome sequencing

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