Author

Ian Smith

University of OxfordORCID 0000-0002-0511-9305Unclaimed ORCID profile · follow to get notified of new preprints

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Ian Smith1 paper

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Genetic & Genomic Medicine· 1

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Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:genome assembly· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

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Anette‐Gabriele ZiegleriD· 1 shared Arancha de la Horra· 1 shared Christiane WinkleriD· 1 shared Edward Choi· 1 shared Ezio E. BonifacioiD· 1 shared Fenella Roseman· 1 shared Florian HauptiD· 1 shared Ginny MounceiD· 1 shared

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2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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Anette‐Gabriele ZieglerORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineArchives of Disease in ChildhoodPeer-reviewedSep 28, 2022

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

Owen Bendor-Samuel, Tabitha Wishlade, Louise Willis…·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.

4 citations

humanDNA methylation

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