Author

Jianqiang Bao

University of Science and Technology of ChinaORCID 0000-0003-1248-2687Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:gene regulatory network inference· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Asim AliiD· 1 shared Bingyan LiiD· 1 shared Bo XuiD· 1 shared Caoling XuiD· 1 shared Daren ZhaoiD· 1 shared Fengsong WangiD· 1 shared Furhan IqbaliD· 1 shared Han ZhaoiD· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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1 shared paperGenetics

Asim AliORCID

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3 papers

Recent·Most cited

Developmental BiologyeLifePeer-reviewedJun 19, 2023

Biallelic Variants in MAD2L1BP (p31comet) Cause Female Infertility Characterized by Oocyte Maturation Arrest

Lingli Huang, Wenqing Li, Xing‐Xing Dai…·Jianqiang Bao

This study identifies biallelic MAD2L1BP variants causing oocyte maturation arrest in female infertility and shows functional rescue with full-length cRNAs.

14 citations

humanwhole-exome sequencing

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Systems BiologyJournal of genetics and genomics/Journal of Genetics and GenomicsPeer-reviewedJan 21, 2023

Decoding transcriptional regulation via a human gene expression predictor

Yuzhou Wang, Yu Zhang, Yu Ning…·Shisong Ma

The paper develops a human gene expression predictor to decode transcriptional regulation by modeling TF-target gene relationships across tissues and conditions.

3 citations

humanbulk RNA-seq

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GeneticsbioRxivPreprintAug 5, 2020

FertilityOnline, a straight pipeline for functional gene annotation and disease mutation discovery, identifies novel infertility causative mutations in SYCE1 and STAG3

Jianing Gao, Huan Zhang, Xiaohua Jiang…·Yuanwei Zhang

FertilityOnline identifies novel infertility-causing mutations in SYCE1 and STAG3 by integrating functional gene annotations and enabling variant analysis for male infertility research.

DOI 10.1101/2020.08.05.238162

humanbulk RNA-seq

𝕏 PostBluesky