Author

Yaohua Xue

Weill Cornell MedicineORCID 0000-0002-7334-2541Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adrian Y. TaniD· 1 shared Alessandro RomaneliD· 1 shared Andrea SboneriD· 1 shared Colin C. PritchardiD· 1 shared Francesca DemichelisiD· 1 shared Hanna RennertiD· 1 shared Himisha BeltraniD· 1 shared Ivan H. IossifoviD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Adrian Y. TanORCID

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1 paper

Recent·Most cited

Discovery and reporting of clinically-relevant germline variants in advanced cancer patients assessed using whole-exome sequencing

Tuo Zhang, Alessandro Romanel, Kenneth Eng, Hanna Rennert, Adrian Y. Tan, Yaohua Xue, Joanna Cyrta, Juan Miguel Mosquera, Andrea Sboner, Ivan H. Iossifov, Steven M. Lipkin, Jenny Xiang, Xiaojun Feng, Peter S. Nelson, Himisha Beltran, , Olivier Elemento

This study reports that 17% of advanced cancer patients have clinically relevant germline variants, with higher rates of cancer-associated variants compared to control cohorts.

bioRxiv · Mar 1, 2017 · PreprintGenomics