Author

Emily Wong

Human Longevity (United States)Primary ORCID profile (0009-0001-9695-9907 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Emily WongiD1 paper · The University of Western Australia

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Katrina LoomisiD· 1 shared Adam J. Mansfield· 1 shared Adam PlattiD· 1 shared Aimée M. DeatoniD· 1 shared Alan R. ShuldineriD· 1 shared Alex E. Lopez· 1 shared Alexander O. Flynn-Carroll· 1 shared Alicia C. Hawes· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Katrina LoomisORCID

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2 papers

Recent·Most cited

Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

Joseph D. Szustakowski, Suganthi Balasubramanian, Erika M. Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, , Adam Platt

The paper describes exome sequencing of 200,643 UK Biobank participants, providing a rich resource of coding variants for genetic and drug discovery research.

Nature Genetics · Jun 28, 2021Peer-reviewedGenetic & Genomic Medicine

The human functional genome defined by genetic diversity

Julia di Iulio, István Bartha, Emily Wong, Hung‐Chun Yu, Victor P. Lavrenko, Dongchan Yang, Inkyung Jung, Michael A. Hicks, Naisha Shah, Ewen F. Kirkness, Martin M. Fabani, William Biggs, Bing Ren, J. Craig Venter, Amalio Telenti

The paper analyzes genetic diversity across 11,257 human genomes to identify context-dependent conserved regions and their association with disease variants.

Nature Genetics · Feb 23, 2018Peer-reviewedGenomics