Author

Peng Huang

Children's Hospital of PhiladelphiaORCID 0000-0003-3008-851XUnclaimed ORCID profile · follow to get notified of new preprints

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Peng Huang2 papers · Sidney Kimmel Comprehensive Cancer Center

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Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Alessandra ChesiiD· 1 shared Alice S. Chen‐PlotkiniD· 1 shared Analise L. Gruenewald· 1 shared Andrew D. WellsiD· 1 shared Christopher D. BrowniD· 1 shared Elisabetta ManduchiiD· 1 shared Gerd A. BlobeliD· 1 shared Marijan PosaviiD· 1 shared

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2017-2017 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Alessandra ChesiORCID

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1 paper

Recent·Most cited

GeneticsThe American Journal of Human GeneticsPeer-reviewedOct 19, 2017

A dementia-associated risk variant near TMEM106B alters chromatin architecture and gene expression

Michael D. Gallagher, Marijan Posavi, Peng Huang…·Alice S. Chen‐Plotkin

The paper identifies a causal variant near TMEM106B that alters chromatin architecture and gene expression, linking it to frontotemporal lobar degeneration and neurodegenerative disease risk.

109 citationstop 3%

humanDNA methylation

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