Author

Edward Choi

University of Oxford

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· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:genome assembly· 1 Organism:human· 1 Assay:protein structure· 1

Frequent Co-Authors

Aida Calderón‐RiveraiD· 1 shared Anette‐Gabriele ZiegleriD· 1 shared Arancha de la Horra· 1 shared Aubin MoutaliD· 1 shared Bryan D. MckiveriD· 1 shared Cheng Wu TangiD· 1 shared Christiane WinkleriD· 1 shared Cynthia L. MaduraiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Aida Calderón‐RiveraORCID

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Author profile →

2 papers

Recent·Most cited

Identification and targeting of a unique NaV1.7 domain driving chronic pain

Kimberly Gómez, Harrison J. Stratton, Paz Duran, Santiago Loya‐López, Cheng Wu Tang, Aida Calderón‐Rivera, Liberty François‐Moutal, May Khanna, Cynthia L. Madura, Shizhen Luo, Bryan D. Mckiver, Edward Choi, Dongzhi Ran, Lisa Boinon, Samantha Perez‐Miller, , Rajesh Khanna

The paper identifies a unique NaV1.7 domain that can be targeted to produce analgesia by disrupting its interaction with CRMP2.

Proceedings of the National Academy of Sciences · Jul 27, 2023Peer-reviewedNeuroscience

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