Author

Bradley P. Coe

University of WashingtonORCID 0000-0001-8471-4016Unclaimed ORCID profile · follow to get notified of new preprints

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Bradley P. Coe1 paper

Biology Disciplines

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Genetics· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Evan E. EichleriD· 3 shared Arvis SulovariiD· 2 shared Amy B. WilfertiD· 1 shared Anand Srivastava· 1 shared Brian T. DoiD· 1 shared Cheen Euong AngiD· 1 shared Fereydoun HormozdiariiD· 1 shared Holly A.F. StessmaniD· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersGenetics

Evan E. EichlerORCID

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3 papers

Recent·Most cited

GeneticsbioRxivPreprintFeb 10, 2020

Recent ultra-rare inherited mutations identify novel autism candidate risk genes

Amy B. Wilfert, Tychele N. Turner, Shwetha Canchi Murali…·Evan E. Eichler

The paper identifies ultra-rare inherited mutations that are younger and preferentially transmitted to autism probands, revealing novel candidate genes and functional networks.

14 citations

humanwhole-genome sequencing

𝕏 PostBluesky

NeuroscienceeLifePeer-reviewedJan 10, 2019

The novel lncRNA lnc-NR2F1 is pro-neurogenic and mutated in human neurodevelopmental disorders

Cheen Euong Ang, Qing Ma, Orly L. Wapinski…·Howard Y. Chang

The paper identifies lnc-NR2F1 as a pro-neurogenic lncRNA mutated in neurodevelopmental disorders through genetic and functional studies.

75 citationstop 5%

humanstatistical model

𝕏 PostBluesky

GeneticsbioRxivPreprintOct 28, 2017

Neurodevelopmental disease genes implicated by de novo mutation and CNV morbidity

Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari…·Evan E. Eichler

The paper identifies 301 neurodevelopmental disease genes using de novo mutations and CNV data, finding overlaps with genomic disorder regions and highlighting new functional networks.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky