Author

Mathew Larson

Massachusetts General Hospital

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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Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Benjamin CurralliD· 1 shared Björn MenteniD· 1 shared Chelsea LowtheriD· 1 shared Claire E. Redin· 1 shared Dadi GaoiD· 1 shared Derek J.C. TaiiD· 1 shared Diane E. LucenteiD· 1 shared Erez Lieberman AideniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Benjamin CurrallORCID

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1 paper

Recent·Most cited

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models

Kiana Mohajeri, Rachita Yadav, Eva D’haene, Philip M. Boone, Serkan Erdin, Dadi Gao, Mariana Moysés‐Oliveira, Riya Bhavsar, Benjamin Currall, Kathryn O’Keefe, Nicholas D. Burt, Chelsea Lowther, Diane E. Lucente, Monica Salani, Mathew Larson, , Michael E. Talkowski

The paper investigates the effects of MEF2C mutations and chromatin structural variants on transcriptional and functional outcomes in neuronal models, revealing differential impacts based on mutation type and chromatin topology.

The American Journal of Human Genetics · Oct 24, 2022Peer-reviewedGenomics