Author

Xiaowei Sylvia Chen

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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Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Clyde FrancksiD· 2 shared Dianne F Newbury· 2 shared Simon E Fisher· 2 shared Alessandro GialluisiiD· 1 shared Alexander Hoischen· 1 shared Dario Gajewski· 1 shared Joris A Veltman· 1 shared Joses Ho· 1 shared

Activity by Year

2016-2017 · peak 1/yr

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10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Clyde FrancksORCID

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2 papers

Recent·Most cited

Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment

Xiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, Joris A Veltman, Nuala H Simpson, SLI Consortium, Clyde Francks, Dianne F Newbury, Simon E Fisher

The paper uses whole exome sequencing to identify novel gene variants and pathways associated with specific language impairment.

Scientific Reports · Apr 25, 2017Peer-reviewedGenetics

Finding functional disease-associated non-coding variation using next-generation sequencing

Paolo Devanna, Xiaowei Sylvia Chen, Joses Ho, Dario Gajewski, Alessandro Gialluisi, Clyde Francks, Simon E Fisher, Dianne F Newbury, Sonja C Vernes

The paper identifies a non-coding variant in a microRNA binding site associated with language impairment using whole exome sequencing data from a cohort of children.

bioRxiv · Jun 22, 2016Genetics