Author

Madeleine R. Geisheker

University of WashingtonORCID 0000-0002-4166-3236Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Approach:matrix factorization· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Evan E. EichleriD· 2 shared Ahmad S. Chatha· 1 shared Akhila BalasubramanianiD· 1 shared Alexander HsiehiD· 1 shared Alexies Camba· 1 shared Ali S. FatemiiD· 1 shared Alpha Amatya· 1 shared Amanda C. GulsrudiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Evan E. EichlerORCID

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2 papers

Recent·Most cited

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Pamela Feliciano, Xueya Zhou, Irina Astrovskaya, Tychele N. Turner, Tianyun Wang, Leo Brueggeman, Rebecca Barnard, Alexander Hsieh, LeeAnne Green Snyder, Donna Marie Muzny, Aniko Sabo, Richard A. Gibbs, Evan E. Eichler, Brian J. O’Roak, Jacob J. Michaelson, , Brenda Hauf

The paper reports exome sequencing of 457 ASD families, identifying 10.4% with known ASD genes and 3.4% with possibly associated variants, and provides statistical support for 34 ASD risk genes using the TADA framework.

npj Genomic Medicine · Aug 23, 2019Peer-reviewedGenetics

Neurodevelopmental disease genes implicated by de novo mutation and CNV morbidity

Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, Madeleine R. Geisheker, Fereydoun Hormozdiari, 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.

bioRxiv · Oct 28, 2017 · PreprintGenetics