Author

Benjamin R. Leadem

National Institutes of Health

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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Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:long-read sequencing· 1 Organism:mouse· 1

Frequent Co-Authors

Alexandre ReymondiD· 1 shared Alfredo BruscoiD· 1 shared Amanda G. NoyesiD· 1 shared Andrea BartuliiD· 1 shared Angela E. ScheuerleiD· 1 shared Anita M. RauchiD· 1 shared Ann DeaniD· 1 shared Anna HurstiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandre ReymondORCID

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2 papers

Recent·Most cited

Cell BiologyCell ReportsPeer-reviewedJun 17, 2024

An enhancer RNA recruits MLL1 to regulate transcription of Myb

Juhyun Kim, Luis Francisco Diaz, Matthew J. Miller…·Ann Dean

The paper identifies Myrlin, an enhancer RNA that recruits MLL1 to regulate Myb transcription during erythroid differentiation.

16 citations

mouselong-read sequencing

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Genetic & Genomic MedicinemedRxivPreprintSep 29, 2022

Deleterious, protein-altering variants in the X-linked transcriptional coregulator ZMYM3 in 22 individuals with a neurodevelopmental delay phenotype

Susan M. Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano…·Gregory M. Cooper

The paper identifies ZMYM3 variants in 22 individuals with neurodevelopmental delay, showing recurrent mutations, phenotypic overlap, and functional effects, supporting ZMYM3 as a novel NDD gene.

DOI 10.1101/2022.09.29.22279724

humanstatistical model

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