Author

Qiming Xu

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bintao Qiu· 1 shared Chao Li· 1 shared Chen DingiD· 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 James R. LupskiiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Bintao Qiu

Mutual co-authors in cluster

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1 paper

Recent·Most cited

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