Author

Yuzhi Zuo

Chinese Academy of Medical Sciences & Peking Union Medical CollegeORCID 0000-0003-2611-3575Unclaimed ORCID profile · follow to get notified of new preprints

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

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1 paper

Recent·Most cited

GeneticsMolecular Genetics & Genomic MedicinePeer-reviewedNov 27, 2019

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

Mao Lin, Zhenlei Liu, Gang Liu…·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.

28 citations

humanwhole-exome sequencing

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