Author

Gholson Lyon

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 Biochemistry· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Han FangiD· 2 shared Yiyang Wu· 2 shared Alan Rope· 1 shared David Mittelman· 1 shared Edward Yang· 1 shared Gareth Highnam· 1 shared Ivan Iossifov· 1 shared Jason A O'Rawe· 1 shared

Activity by Year

2015-2015 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Han FangORCID

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3 papers

Recent·Most cited

A variant in TAF1 is associated with a new syndrome with severe intellectual disability and characteristic dysmorphic features

Jason O'Rawe, Yiyang Wu, Alan Rope, Laura T. Jimenez Barrón, Jeffrey Swensen, Han Fang, David Mittelman, Gareth Highnam, Reid Robison, Edward Yang, Kai Wang, Gholson Lyon

The paper identifies a maternally inherited TAF1 variant in two brothers with severe intellectual disability and distinctive facial features, linking it to a new syndrome.

The American Journal of Human Genetics · Dec 1, 2015Peer-reviewedGenetics

The biological functions of Naa10—from amino-terminal acetylation to human disease

Max Doerfel, Gholson Lyon

This paper reviews the biological functions of Naa10, including its role in N-terminal acetylation, disease associations, and recent inhibitor developments.

Gene · Aug 1, 2015Peer-reviewedBiochemistry

Genome Wide Variant Analysis of Simplex Autism Families with an Integrative Clinical-Bioinformatics Pipeline

Laura T Jiménez-Barrón, Jason A O'Rawe, Yiyang Wu, Margaret Yoon, Han Fang, Ivan Iossifov, Gholson Lyon

This study uses an integrative clinical-bioinformatics pipeline to analyze genome-wide variants in simplex autism families, identifying candidate variants associated with ASD.

bioRxiv · May 11, 2015Genetics