Author

Sonja C Vernes

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Genetics· 1

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

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Alessandro GialluisiiD· 1 shared Clyde FrancksiD· 1 shared Dario Gajewski· 1 shared Dianne F Newbury· 1 shared Joses Ho· 1 shared Paolo Devanna· 1 shared Simon E Fisher· 1 shared Xiaowei Sylvia Chen· 1 shared

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2016-2016 · peak 1/yr

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1 shared paperGenetics

Alessandro GialluisiORCID

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1 paper

Recent·Most cited

GeneticsbioRxivJun 22, 2016

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

Paolo Devanna, Xiaowei Sylvia Chen, Joses Ho…·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.

DOI 10.1038/mp.2017.30

humanwhole-exome sequencing

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