Author

Jessica Chong

University of Washington

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 2

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Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Amy Ginsburg· 1 shared Andrea J. CoheniD· 1 shared Anita Rauch· 1 shared Ashima Gulati· 1 shared Ben HeavneriD· 1 shared Benjamin Blankenmeister· 1 shared Brandon Garcia· 1 shared Casey A. GiffordiD· 1 shared

Activity by Year

2015-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Amy Ginsburg

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2 papers

Recent·Most cited

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Jessica X. Chong, Seth Berger, Samantha M. Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame, Megan H. Hawley, E. Andres Rivera-Munoz, Stephanie P. DiTroia, Siwaar Abouhala, Jessica Albert, Miguel Almalvez, Raquel Alvarez, Mutaz Amin, Peter Anderson, , Tanner D. Jensen

The paper develops criteria for identifying, sharing, and reporting novel candidate genes in clinical genomic testing to improve diagnostic yield for Mendelian conditions.

Genetics in Medicine · Jun 26, 2024Peer-reviewedGenetics

Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features

Jessica Chong, Joon-Ho Yu, Peter Lorentzen, Karen Park, Seema M Jamal, Holly K Tabor, Anita Rauch, Margarita Sifuentes Saenz, Eugen Boltshauser, Karynne E Patterson, Deborah A Nickerson, University of Washington Center for Mendelian Geno, Michael J Bamshad

This paper identifies de novo variants in KDM1A causing a new syndrome with developmental delay and distinctive facial features by leveraging social networking among families and researchers.

bioRxiv · Oct 3, 2015Genetics