Author

Simon E Fisher

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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Genetics· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:imaging· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Clyde FrancksiD· 3 shared Dianne F Newbury· 2 shared Xiaowei Sylvia Chen· 2 shared Alessandro GialluisiiD· 1 shared Alexander Hoischen· 1 shared Barbara FrankeiD· 1 shared Daniel Brandeis· 1 shared Dario Gajewski· 1 shared

Activity by Year

2016-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersGenetics

Clyde FrancksORCID

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Author profile →

3 papers

Recent·Most cited

Mapping Cortical Brain Asymmetry in 17,141 Healthy Individuals Worldwide via the ENIGMA Consortium

Xiangzhen Kong, Samuel R. Mathias, Tulio M. Guadalupe, ENIGMA Laterality Working Group, David C. Glahn, Barbara Franke, Fabrice Crivello, Nathalie Tzourio‐Mazoyer, Simon E Fisher, Paul M. Thompson, Clyde Francks, et al, Daniel Brandeis, Silvia Brem, Susanne Walitza

The paper analyzes cerebral cortical asymmetry in 17,141 healthy individuals, finding widespread hemispheric and regional asymmetries, associations with sex, age, brain size, and heritability.

Proceedings of the National Academy of Sciences · May 29, 2018Peer-reviewedNeuroscience

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