Author

Swetha Mohan

Primary ORCID profile (0000-0001-8463-1579 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Swetha MohaniD1 paper · National Centre for Biological Sciences

Biology Disciplines

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Organism:C. elegans· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Donald G Moerman· 1 shared Erica Li-LegeriD· 1 shared Federico Rosell· 1 shared Gert JanseniD· 1 shared Jerry Cai· 1 shared Mark Edgley· 1 shared Michel R Leroux· 1 shared Quintin Muncaster· 1 shared

Activity by Year

2016-2016 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Donald G Moerman

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1 paper

Recent·Most cited

Accelerating gene discovery by phenotyping whole-genome sequenced multi- mutation strains and using the sequence kernel association test (SKAT)

Tiffany A Timbers, Stephanie J Garland, Swetha Mohan, Stephane Flibotte, Mark Edgley, Quintin Muncaster, Vinci Au, Erica Li-Leger, Federico Rosell, Jerry Cai, Suzanne Rademakers, Gert Jansen, Donald G Moerman, Michel R Leroux

The paper uses a whole-genome sequenced multi-mutation C. elegans library with SKAT to identify genes associated with ciliated sensory neuron defects, uncovering novel genes like BGNT-1.1 linked to human ciliopathies.

PLOS Genetics · Aug 10, 2016Peer-reviewedGenomics