Author

Chen Ding

China Medical UniversityORCID 0000-0002-9195-2255Unclaimed ORCID profile · follow to get notified of new preprints

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Chen Ding2 papers

Biology Disciplines

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Genetics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:fungi (other)· 1 Organism:human· 1 Assay:metabolomics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bing ZhaiiD· 1 shared Bintao Qiu· 1 shared Chao Li· 1 shared Chun Feng· 1 shared Claudia M.B. CarvalhoiD· 1 shared Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study· 1 shared Gang LiuiD· 1 shared Guixing QiuiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperSystems Biology

Bing ZhaiORCID

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2 papers

Recent·Most cited

iCNG99: a validated genome-scale metabolic model of Cryptococcus neoformans strain H99

Chun Feng, Pengjie Hu, Yin Zhu, Weixin Ke, Xindi Gao, Chen Ding, Bing Zhai, Linqi Wang, Ziwei Dai

The paper develops and validates a genome-scale metabolic model for Cryptococcus neoformans strain H99, showing high precision in essential gene prediction and capturing metabolic adaptations relevant to drug tolerance and host survival.

bioRxiv · Apr 15, 2026 · PreprintSystems Biology

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

Mao Lin, Zhenlei Liu, Gang Liu, Sen Zhao, Chao Li, Wei‐Sheng Chen, Zeynep Coban‐Akdemir, Jiachen Lin, Xiaofei Song, Shengru Wang, Qiming Xu, Yanxue Zhao, Lianlei Wang, Yuanqiang Zhang, Zihui Yan, , Nan Wu

The paper investigates how different FBN1 truncating mutations cause distinct clinical phenotypes in Marfan syndrome and Marfanoid-progeroid-lipodystrophy syndrome through molecular and genetic analysis.

Molecular Genetics & Genomic Medicine · Nov 27, 2019Peer-reviewedGenetics