Author

Zhongshan Li

Wenzhou Medical UniversityORCID 0000-0001-9645-7360Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Jinchen LiiD· 2 shared Xin HeiD· 2 shared Zhong Sheng SuniD· 2 shared A. Ercüment ÇiçekiD· 1 shared Evan T. GelleriD· 1 shared Fengbiao MaoiD· 1 shared Huajing TengiD· 1 shared Iuliana Ionita‐LazaiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenomics

Jinchen LiORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintNov 26, 2019

De novo mutations involved in post-transcriptional dysregulation contribute to four neuropsychiatric disorders

Fengbiao Mao, Lu Wang, Xiaolu Zhao…·Zhong Sheng Sun

The paper identifies de novo mutations affecting post-transcriptional regulation that contribute to four neuropsychiatric disorders.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsThe American Journal of Human GeneticsPeer-reviewedMay 10, 2018

A statistical framework for mapping risk genes from de novo mutations in whole-genome sequencing studies

Yuwen Liu, Yanyu Liang, A. Ercüment Çiçek…·Xin He

This paper introduces a statistical framework to identify risk genes from de novo mutations in whole-genome sequencing studies, finding new autism risk genes.

32 citations

humanwhole-genome sequencing

𝕏 PostBluesky