Author

Jincheng Wang

Center for Excellence in Brain Science and Intelligence TechnologyORCID 0009-0007-2826-6555Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Jincheng Wang1 paper · Chinese Academy of Sciences

Biology Disciplines

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Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:CRISPR screen· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Baolei YuaniD· 1 shared Chongwei BiiD· 1 shared Fei LiiD· 1 shared Fernanda Vargas Romero· 1 shared Gang YiiD· 1 shared Jinyu WuiD· 1 shared Juan Carlos Izpisúa BelmonteiD· 1 shared Juehua YuiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperMolecular Biology

Baolei YuanORCID

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2 papers

Recent·Most cited

Molecular BiologyBMC BiologyPeer-reviewedApr 29, 2024

Modulation of the microhomology-mediated end joining pathway suppresses large deletions and enhances homology-directed repair following CRISPR-Cas9-induced DNA breaks

Baolei Yuan, Chongwei Bi, Yeteng Tian…·Mo Li

This study shows that modulating the MMEJ pathway components RPA and POLQ can reduce large deletions and enhance HDR after CRISPR-Cas9 editing.

21 citations

humanCRISPR screen

𝕏 PostBluesky

NeurosciencebioRxivPreprintSep 30, 2021

De novo variants in Chinese ASD trios reveal genetic basis underlying autism without developmental delay and intellectual disabilities

Jincheng Wang, Juehua Yu, Mengdi Wang…·Zilong Qiu

This study identifies de novo variants in Chinese ASD trios, finding that ASD without DD/ID has fewer disruptive variants and novel risk genes not in existing databases.

1 citation

humanwhole-exome sequencing

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