Author

X.F. Colin C. Wong

Agency for Science, Technology and Research

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

Biology Disciplines

Click to filter author papers

Genetics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Organism:human· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:mouse· 1

Frequent Co-Authors

John CommoniD· 2 shared Simon L. I. J. DeniliD· 2 shared A. Quiggle· 1 shared Aileen SandilandsiD· 1 shared Alina D. SchmidtiD· 1 shared Angeline Su Ling Tay· 1 shared Avner ShemeriD· 1 shared Cristina de Guzman StrongiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

John CommonORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GeneticsbioRxivPreprintNov 5, 2019

An enhancer:involucrin regulatory module impacts human skin barrier adaptation out-of-Africa and modifies atopic dermatitis risk

Mary Elizabeth Mathyer, Erin A. Brettmann, Alina D. Schmidt…·Cristina de Guzman Strong

The paper identifies an enhancer-IVL regulatory module that evolved in humans and is associated with skin barrier adaptation and atopic dermatitis risk.

1 citation

humanmouse

𝕏 PostBluesky

GeneticsJournal of Allergy and Clinical ImmunologyPeer-reviewedOct 19, 2017

Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

X.F. Colin C. Wong, Simon L. I. J. Denil, Jia Nee Foo…·John Common

This paper develops a cost-effective and efficient sequencing protocol for the filaggrin gene to detect disease-associated variants across diverse populations.

49 citationstop 3%

humanwhole-exome sequencing

𝕏 PostBluesky