Author

Jacob L. Taylor

Broad InstituteORCID 0009-0009-4660-6925Unclaimed 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:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Daniel J. WeineriD· 2 shared Elise RobinsoniD· 2 shared Emilie M. WigdoriD· 2 shared Jack A. KosmickiiD· 2 shared Mark J. DalyiD· 2 shared Preben Bo MortenseniD· 2 shared Alex Bloemendal· 1 shared Anders Dupont BørglumiD· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetics

Daniel J. WeinerORCID

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2 papers

Recent·Most cited

GeneticsNature CommunicationsPeer-reviewedJul 10, 2019

Paternal-age-related de novo mutations and risk for five disorders

Jacob L. Taylor, Jean-Christophe Debost, Sarah U. Morton…·Elise Robinson

The paper estimates the risk of five disorders from paternal-age-related de novo mutations using whole-exome-sequencing data and Danish registry data.

91 citationstop 2%

humanwhole-exome sequencing

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GeneticsNature GeneticsPeer-reviewedMay 15, 2017

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

iPSYCH-Broad Autism Group, Daniel J. Weiner, Emilie M. Wigdor…·Elise Robinson

The paper uses polygenic transmission disequilibrium to show common and rare variants act additively in autism risk, with polygenic risk over-transmitted to ASD cases but not unaffected siblings.

516 citationstop 1%

humanstatistical model

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